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manufacturing quality technician iii
CMM Technician/Metrologist Level I, II or III
WAGSTAFF INC Spokane Valley, Washington
Wagstaff Description: Wagstaff manufactures equipment for aluminum producers, who process formed aluminum into parts and products you use every day. Pay: $26-$35 per hour, depending on experience As an employee of Wagstaff, you'll enjoy: Paid non-working holidays Monthly, site-wide BBQs Up to 8% retirement contribution Annual bonus program 1200 Sqft onsite gym, accessible 24/hrs a day Family friendly, company-wide events To review our full benefits summary, please visit Want to learn more about Wagstaff? Join us for a virtual tour! Job Summary Assists with the development, implementation and consistent application of Wagstaff's metrology program in collaboration with other departments throughout the production stream from design through manufacturing and inspection. Administers the consistent application of metrological concepts as defined in the ASME Y14.5 Dimension and Tolerancing standard. Work as a member of the Manufacturing Engineering team and in collaboration with Quality Assurance to develop design, manufacturing, inspection & calibration standards and methods associated with geometric form specifications (GD&T). Primary Job Responsibilities Assists with the development and maintenance of Wagstaff's metrology program Administers the implementation of the metrology program through the entire production stream including design, manufacturing, and inspection. Identifies sources of error contributing to uncertainty of results to determine reliability of measurement processes in quantitative terms. Redesigns or adjusts measurement processes as needed to minimize errors. Specifies measurement instrumentation needed to ensure effective inspections. Assists with developing calibration methods and techniques based on principles of measurement science, technical analysis of measurement problems, and accuracy and precision requirements. Mentors and trains other employees to enhance CMM skills Communicates with engineering, manufacturing, quality assurance, and laboratory personnel in design, implementation, evaluation, and revision of geometric dimensions and tolerances. Advises others on methods of resolving measurement problems Responsible for writing, maintaining, and updating calibration documentation and inspection records. Abide by company policies In order to achieve business objectives, work weeks in excess of 40 hours may be required Assist in developing and providing training for Quality Assurance programs and processes Assist in statistical studies and analysis Other duties as assigned Requirements: Associate's Degree in Quality, Engineering, Mathematics, or equivalent experience Minimum of 4 years of experience in using CMM or PCMM equipment Preferred experience with Laser Tracker or Laser Scanning equipment Thorough understanding of Dimension and Tolerancing standard ASME Y14.5 Experience with PolyWorks inspection software Formal training, or equivalent knowledge and skills, in gauging and inspection methodology Effective verbal and written communication skills Ability to make effective decisions and presentations on complex manufacturing and inspection topics to technicians, engineers, managers, customers & suppliers. Working Environment While performing the duties of this job, work is performed primarily in an adequately lit, well ventilated, climate controlled general office environment. Close computer work is regularly required. The work usually involves minimal physical exertion. The noise level in the general office environment is usually moderate. This job may require occasional or more frequent interaction with employees on the manufacturing shop floor. While on the shop floor, the employee may be exposed to fumes, airborne particles, toxic or caustic chemicals, risks of moving equipment and parts, and other risks associated with a manufacturing environment. Because of this environment and associated risks, coordination with shop floor managers/employees may be necessary before entering the shop floor and use of job appropriate personal protective equipment and clothing is required on the shop floor. The noise level on the shop floor is often loud. Employment at Wagstaff is dependent on successfully passing a company-paid drug screening and background check upon hire. Benefits eligibility is subject to the terms and conditions of the applicable policies, plans and programs of Wagstaff. Wagstaff is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, pregnancy, genetic information, disability, status as a protected veteran, or any other protected category under applicable federal, state, and local laws. PM22 PIf-3760
09/08/2025
Full time
Wagstaff Description: Wagstaff manufactures equipment for aluminum producers, who process formed aluminum into parts and products you use every day. Pay: $26-$35 per hour, depending on experience As an employee of Wagstaff, you'll enjoy: Paid non-working holidays Monthly, site-wide BBQs Up to 8% retirement contribution Annual bonus program 1200 Sqft onsite gym, accessible 24/hrs a day Family friendly, company-wide events To review our full benefits summary, please visit Want to learn more about Wagstaff? Join us for a virtual tour! Job Summary Assists with the development, implementation and consistent application of Wagstaff's metrology program in collaboration with other departments throughout the production stream from design through manufacturing and inspection. Administers the consistent application of metrological concepts as defined in the ASME Y14.5 Dimension and Tolerancing standard. Work as a member of the Manufacturing Engineering team and in collaboration with Quality Assurance to develop design, manufacturing, inspection & calibration standards and methods associated with geometric form specifications (GD&T). Primary Job Responsibilities Assists with the development and maintenance of Wagstaff's metrology program Administers the implementation of the metrology program through the entire production stream including design, manufacturing, and inspection. Identifies sources of error contributing to uncertainty of results to determine reliability of measurement processes in quantitative terms. Redesigns or adjusts measurement processes as needed to minimize errors. Specifies measurement instrumentation needed to ensure effective inspections. Assists with developing calibration methods and techniques based on principles of measurement science, technical analysis of measurement problems, and accuracy and precision requirements. Mentors and trains other employees to enhance CMM skills Communicates with engineering, manufacturing, quality assurance, and laboratory personnel in design, implementation, evaluation, and revision of geometric dimensions and tolerances. Advises others on methods of resolving measurement problems Responsible for writing, maintaining, and updating calibration documentation and inspection records. Abide by company policies In order to achieve business objectives, work weeks in excess of 40 hours may be required Assist in developing and providing training for Quality Assurance programs and processes Assist in statistical studies and analysis Other duties as assigned Requirements: Associate's Degree in Quality, Engineering, Mathematics, or equivalent experience Minimum of 4 years of experience in using CMM or PCMM equipment Preferred experience with Laser Tracker or Laser Scanning equipment Thorough understanding of Dimension and Tolerancing standard ASME Y14.5 Experience with PolyWorks inspection software Formal training, or equivalent knowledge and skills, in gauging and inspection methodology Effective verbal and written communication skills Ability to make effective decisions and presentations on complex manufacturing and inspection topics to technicians, engineers, managers, customers & suppliers. Working Environment While performing the duties of this job, work is performed primarily in an adequately lit, well ventilated, climate controlled general office environment. Close computer work is regularly required. The work usually involves minimal physical exertion. The noise level in the general office environment is usually moderate. This job may require occasional or more frequent interaction with employees on the manufacturing shop floor. While on the shop floor, the employee may be exposed to fumes, airborne particles, toxic or caustic chemicals, risks of moving equipment and parts, and other risks associated with a manufacturing environment. Because of this environment and associated risks, coordination with shop floor managers/employees may be necessary before entering the shop floor and use of job appropriate personal protective equipment and clothing is required on the shop floor. The noise level on the shop floor is often loud. Employment at Wagstaff is dependent on successfully passing a company-paid drug screening and background check upon hire. Benefits eligibility is subject to the terms and conditions of the applicable policies, plans and programs of Wagstaff. Wagstaff is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, pregnancy, genetic information, disability, status as a protected veteran, or any other protected category under applicable federal, state, and local laws. PM22 PIf-3760
QA Technician / Weld Inspector
WAGSTAFF INC Spokane, Washington
Wagstaff Description: Wagstaff manufactures equipment for aluminum producers, who process formed aluminum into parts and products you use every day. Pay: $30- $39.98 per hour, depending on experience As an employee of Wagstaff, you'll enjoy: Paid non-working holidays Monthly, site-wide BBQs Up to 8% retirement contribution Annual bonus program 1200 Sqft onsite gym, accessible 24/hrs a day Family-friendly, company-wide events To view our full benefits summary, please visit Want to learn more about Wagstaff AT? Visit Job Summary As a Quality Professional on Wagstaff's Quality Assurance team, you will play a crucial role in upholding our reputation for precision and quality. If you are experienced in conducting dimensional, weld and NDE inspections and you are ready to take your career to the next level, join Wagstaff's growing team of Quality Assurance Technicians! In this role, you'll use your experience and skill set to conduct inspections using a variety of precision tools and technologies that have a direct impact on project success at Wagstaff. Your attention to detail and excellent communication skills will contribute to your interactions with co-workers, auditors, customers, suppliers, and visitors, as well as continuous improvement and problem-solving activities. Primary Job Responsibilities Perform weld and NDE (VT/PT/MT/UT) inspections on various stainless steel weldments and fabricated equipement Inspect and report on materials, services, processes, and products using measuring instruments and techniques to ensure conformance with the company's quality standards Enter data and maintain paper and electronic quality records where required Participates in problem solving and continuous improvement projects Represent Wagstaff when interacting with auditors, customers, suppliers and visitors Communicate with customers and suppliers on quality-related issues as directed by the Quality Assurance Manager Prepare inspection sheets Collect, monitor, organize, report, and distribute data as it relates to quality functions of Wagstaff Prepare and present reports Assist with specialized inspections as it correlates with individual certifications. Abide by company policies In order to achieve business objectives, work weeks in excess of 40 hours may be required Other duties as assigned Requirements: High school diploma or GED required Candidates must have at least 2 years of dimensional and weld inspection experience or 4 years of trade experience in fabrication, welding, or machining. Ability to read blueprints and mechanical inspection skills, experience/training in Geometric Dimensioning and Tolerance (GD&T) Candidates must have vision capable of reading a Jaeger Number 1 or equivalent type and size letter at no less than 12 inches (natural or corrected vision). Candidates cannot be color blind Candidates must be physically able to perform inspections in a manufacturing environment, including the operation of overhead cranes, jibs, and forklifts, after undergoing company training Proficient in the use of Microsoft Office business software Detail-oriented, accurate, and thorough Preferred candidate qualifications: Current AWS Certified Weld Inspector (CWI) with NDE Level II credentials (VT/PT/MT/UT) or the ability to quickly acquire NDE Level II credentials with company-provided training. Experience with AWS D1.1 & 1.6 and ASME Section VIII & B31.3 weld inspections highly desirable. Experience with stainless fabrication highly desirable. Working Environment While performing the duties of this job, work is performed primarily in an adequately lit, well ventilated, climate controlled general office environment. Close computer work is regularly required. The work usually involves minimal physical exertion. The noise level in the general office environment is usually moderate. This job may require occasional or more frequent interaction with employees on the manufacturing shop floor. While on the shop floor, the employee may be exposed to fumes, airborne particles, toxic or caustic chemicals, risks of moving equipment and parts, and other risks associated with a manufacturing environment. Because of this environment and associated risks, coordination with shop floor managers/employees may be necessary before entering the shop floor, and use of job appropriate personal protective equipment and clothing is required on the shop floor. The noise level on the shop floor is often loud. Employment at Wagstaff is dependent on successfully passing a company-paid drug screening and background check upon hire. Benefits eligibility is subject to the terms and conditions of the applicable policies, plans and programs of Wagstaff. Wagstaff is an Equal Opportunity Employer . All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, pregnancy, genetic information, disability, status as a protected veteran, or any other protected category under applicable federal, state, and local laws. PM22 PI10bb4beff46a-0068
09/05/2025
Full time
Wagstaff Description: Wagstaff manufactures equipment for aluminum producers, who process formed aluminum into parts and products you use every day. Pay: $30- $39.98 per hour, depending on experience As an employee of Wagstaff, you'll enjoy: Paid non-working holidays Monthly, site-wide BBQs Up to 8% retirement contribution Annual bonus program 1200 Sqft onsite gym, accessible 24/hrs a day Family-friendly, company-wide events To view our full benefits summary, please visit Want to learn more about Wagstaff AT? Visit Job Summary As a Quality Professional on Wagstaff's Quality Assurance team, you will play a crucial role in upholding our reputation for precision and quality. If you are experienced in conducting dimensional, weld and NDE inspections and you are ready to take your career to the next level, join Wagstaff's growing team of Quality Assurance Technicians! In this role, you'll use your experience and skill set to conduct inspections using a variety of precision tools and technologies that have a direct impact on project success at Wagstaff. Your attention to detail and excellent communication skills will contribute to your interactions with co-workers, auditors, customers, suppliers, and visitors, as well as continuous improvement and problem-solving activities. Primary Job Responsibilities Perform weld and NDE (VT/PT/MT/UT) inspections on various stainless steel weldments and fabricated equipement Inspect and report on materials, services, processes, and products using measuring instruments and techniques to ensure conformance with the company's quality standards Enter data and maintain paper and electronic quality records where required Participates in problem solving and continuous improvement projects Represent Wagstaff when interacting with auditors, customers, suppliers and visitors Communicate with customers and suppliers on quality-related issues as directed by the Quality Assurance Manager Prepare inspection sheets Collect, monitor, organize, report, and distribute data as it relates to quality functions of Wagstaff Prepare and present reports Assist with specialized inspections as it correlates with individual certifications. Abide by company policies In order to achieve business objectives, work weeks in excess of 40 hours may be required Other duties as assigned Requirements: High school diploma or GED required Candidates must have at least 2 years of dimensional and weld inspection experience or 4 years of trade experience in fabrication, welding, or machining. Ability to read blueprints and mechanical inspection skills, experience/training in Geometric Dimensioning and Tolerance (GD&T) Candidates must have vision capable of reading a Jaeger Number 1 or equivalent type and size letter at no less than 12 inches (natural or corrected vision). Candidates cannot be color blind Candidates must be physically able to perform inspections in a manufacturing environment, including the operation of overhead cranes, jibs, and forklifts, after undergoing company training Proficient in the use of Microsoft Office business software Detail-oriented, accurate, and thorough Preferred candidate qualifications: Current AWS Certified Weld Inspector (CWI) with NDE Level II credentials (VT/PT/MT/UT) or the ability to quickly acquire NDE Level II credentials with company-provided training. Experience with AWS D1.1 & 1.6 and ASME Section VIII & B31.3 weld inspections highly desirable. Experience with stainless fabrication highly desirable. Working Environment While performing the duties of this job, work is performed primarily in an adequately lit, well ventilated, climate controlled general office environment. Close computer work is regularly required. The work usually involves minimal physical exertion. The noise level in the general office environment is usually moderate. This job may require occasional or more frequent interaction with employees on the manufacturing shop floor. While on the shop floor, the employee may be exposed to fumes, airborne particles, toxic or caustic chemicals, risks of moving equipment and parts, and other risks associated with a manufacturing environment. Because of this environment and associated risks, coordination with shop floor managers/employees may be necessary before entering the shop floor, and use of job appropriate personal protective equipment and clothing is required on the shop floor. The noise level on the shop floor is often loud. Employment at Wagstaff is dependent on successfully passing a company-paid drug screening and background check upon hire. Benefits eligibility is subject to the terms and conditions of the applicable policies, plans and programs of Wagstaff. Wagstaff is an Equal Opportunity Employer . All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, pregnancy, genetic information, disability, status as a protected veteran, or any other protected category under applicable federal, state, and local laws. PM22 PI10bb4beff46a-0068
Catapult Staffing
Test Technician III with Security Clearance
Catapult Staffing Lynnwood, Washington
Test Technician III - Production Test Technician Department: Manufacturing Location: Lynnwood, WA - Onsite (7:00AM-3:30PM) Role Type: Contract Clearance: Secret About Our Client Our client develops, integrates, and deploys advanced technology solutions that address existing and emerging missions for a range of customers across the Department of Defense (DoD). Their Lynnwood, WA facility is expanding operations based on significant business growth and is building a production capability from the ground up for a diverse range of innovative products that support critical defense missions. Job Description As a Production Test Technician, you will work closely with manufacturing engineers and technicians to assemble and test electro-mechanical devices, improve production processes, and ensure a clean and organized manufacturing floor. Your primary responsibilities include factory acceptance testing of complex electro-mechanical devices using Linux systems, test and data collection using various lab equipment, and operation of industrial environmental chambers. You'll work in a pilot production line environment with a team of 8 manufacturing engineers and technicians, focusing on learning assembly processes rapidly and contributing to continuous improvement initiatives. The ideal candidate brings a background in sophisticated electro-mechanical products for DoD customers, experience with CCA and Piezo electric testing, 2+ years of Linux experience, and the ability to obtain SECRET clearance. Duties and Responsibilities Perform factory acceptance testing of complex electro-mechanical devices using Linux systems. Conduct test and data collection using various lab equipment including oscilloscopes, digital multimeters, and impedance analyzers. Operate and maintain industrial environmental chambers performing Highly Accelerated Stress Screens. Perform inspection and test of CCAs and Piezo electrics for conformance to test specifications. Lead process improvement projects in work cells and on the manufacturing floor. Suggest redlines to work instructions and test procedures to document improvements. Ensure an organized and clean workspace (5S) including total preventive maintenance of equipment, tooling, and fixtures. Foster an environment of continuous improvement using industry's best practices such as Root Cause Analysis and Kaizen. Read, interpret, and understand assembly drawings and technical documentation. Rapidly understand test procedures and their requirements. Use hand tools, power tools, adhesives, and scales competently. Maintain compliance with ESD, FOD, and EH&S requirements. Document test results and maintain accurate records using Microsoft Office applications. Required Experience/Skills Background in development, production, delivery, and ongoing support of sophisticated electro-mechanical products that serve DoD customer requirements. Experience with inspection and test of CCAs and Piezo electrics for conformance to test specifications. 2 years of experience operating Linux computers. Experience with ESD, FOD, and EH&S requirements. Ability to read, interpret, and understand assembly drawings. Ability to rapidly understand test procedures and their requirements. Competent in using hand tools, power tools, adhesives, and scales. Competent in the use of Microsoft Office (Word, Excel, PowerPoint, Visio). Ability to lead process improvement projects. Experience suggesting improvements to work instructions and test procedures. HIGH SCHOOL diploma or equivalent and 3+ years of prior relevant experience. SECRET security clearance or ability to rapidly attain one. Nice-to-Haves Experience operating Qualmark Typhoon 3.0 Chamber or equivalent. Experience troubleshooting electrical systems. J-STD-001 and/or IPC-A-610 Certification. Competent in using crimpers, wire strippers, and soldering irons. Knowledge and experience with ISO 9001:2015 Quality Management Standards. Experience in world-class lean manufacturing. Education High school diploma or equivalent required. 3+ years of prior relevant experience required. Join Our Manufacturing Team! If you're an experienced production technician with a background in electro-mechanical products and DoD customer requirements, we invite you to apply. This role offers the opportunity to work on cutting-edge defense systems while contributing to the growth of our expanding Lynnwood facility.
08/31/2025
Full time
Test Technician III - Production Test Technician Department: Manufacturing Location: Lynnwood, WA - Onsite (7:00AM-3:30PM) Role Type: Contract Clearance: Secret About Our Client Our client develops, integrates, and deploys advanced technology solutions that address existing and emerging missions for a range of customers across the Department of Defense (DoD). Their Lynnwood, WA facility is expanding operations based on significant business growth and is building a production capability from the ground up for a diverse range of innovative products that support critical defense missions. Job Description As a Production Test Technician, you will work closely with manufacturing engineers and technicians to assemble and test electro-mechanical devices, improve production processes, and ensure a clean and organized manufacturing floor. Your primary responsibilities include factory acceptance testing of complex electro-mechanical devices using Linux systems, test and data collection using various lab equipment, and operation of industrial environmental chambers. You'll work in a pilot production line environment with a team of 8 manufacturing engineers and technicians, focusing on learning assembly processes rapidly and contributing to continuous improvement initiatives. The ideal candidate brings a background in sophisticated electro-mechanical products for DoD customers, experience with CCA and Piezo electric testing, 2+ years of Linux experience, and the ability to obtain SECRET clearance. Duties and Responsibilities Perform factory acceptance testing of complex electro-mechanical devices using Linux systems. Conduct test and data collection using various lab equipment including oscilloscopes, digital multimeters, and impedance analyzers. Operate and maintain industrial environmental chambers performing Highly Accelerated Stress Screens. Perform inspection and test of CCAs and Piezo electrics for conformance to test specifications. Lead process improvement projects in work cells and on the manufacturing floor. Suggest redlines to work instructions and test procedures to document improvements. Ensure an organized and clean workspace (5S) including total preventive maintenance of equipment, tooling, and fixtures. Foster an environment of continuous improvement using industry's best practices such as Root Cause Analysis and Kaizen. Read, interpret, and understand assembly drawings and technical documentation. Rapidly understand test procedures and their requirements. Use hand tools, power tools, adhesives, and scales competently. Maintain compliance with ESD, FOD, and EH&S requirements. Document test results and maintain accurate records using Microsoft Office applications. Required Experience/Skills Background in development, production, delivery, and ongoing support of sophisticated electro-mechanical products that serve DoD customer requirements. Experience with inspection and test of CCAs and Piezo electrics for conformance to test specifications. 2 years of experience operating Linux computers. Experience with ESD, FOD, and EH&S requirements. Ability to read, interpret, and understand assembly drawings. Ability to rapidly understand test procedures and their requirements. Competent in using hand tools, power tools, adhesives, and scales. Competent in the use of Microsoft Office (Word, Excel, PowerPoint, Visio). Ability to lead process improvement projects. Experience suggesting improvements to work instructions and test procedures. HIGH SCHOOL diploma or equivalent and 3+ years of prior relevant experience. SECRET security clearance or ability to rapidly attain one. Nice-to-Haves Experience operating Qualmark Typhoon 3.0 Chamber or equivalent. Experience troubleshooting electrical systems. J-STD-001 and/or IPC-A-610 Certification. Competent in using crimpers, wire strippers, and soldering irons. Knowledge and experience with ISO 9001:2015 Quality Management Standards. Experience in world-class lean manufacturing. Education High school diploma or equivalent required. 3+ years of prior relevant experience required. Join Our Manufacturing Team! If you're an experienced production technician with a background in electro-mechanical products and DoD customer requirements, we invite you to apply. This role offers the opportunity to work on cutting-edge defense systems while contributing to the growth of our expanding Lynnwood facility.
Catapult Staffing
Electro-Mechanical Production Technician with Security Clearance
Catapult Staffing Lynnwood, Washington
Mech Assembler III - Electro-Mechanical Production Technician Department: Manufacturing Location: Lynnwood, WA - Onsite Role Type: Contract Clearance: Secret About Our Client Our client develops, integrates, and deploys advanced technology solutions that address existing and emerging missions for a range of customers across the Department of Defense (DoD). Job Description As an Electro-Mechanical Production Technician, you will work closely with manufacturing engineers and technicians to assemble and test electro-mechanical devices, improve production processes, and ensure a clean and organized manufacturing floor. Your primary responsibilities include assembly of complex electro-mechanical systems and sub-systems, test and data collection using various lab equipment, and fostering an environment of continuous improvement. You'll work in a pilot production line environment with a team of 8 manufacturing engineers and technicians, focusing on learning assembly processes rapidly while contributing to process improvements. The ideal candidate brings a background in sophisticated electro-mechanical products for DoD customers, experience with CCA and Piezo electric testing, and expertise in lean manufacturing principles with the ability to lead process improvement initiatives. Duties and Responsibilities Assemble complex electro-mechanical systems and sub-systems including experience with polyurethane encapsulation and soldering. Perform test and data collection using various lab equipment including oscilloscopes, digital multimeters, and impedance analyzers. Inspect and test CCAs and Piezo electrics for conformance to drawings and specifications. Lead process improvement projects in work cells and on the manufacturing floor. Write or redline work instructions for new production processes to document improvements. Ensure an organized and clean workspace (5S) including total preventive maintenance of equipment, tooling, and fixtures. Foster an environment of continuous improvement using industry best practices such as Root Cause Analysis and Kaizen. Value the importance of following precise Standard Work instructions while empowering team members to contribute to improvements. Read, interpret, and understand assembly drawings and technical documentation. Rapidly understand work instructions and their requirements. Assemble small components into space-restricted subsystems with precision. Use crimpers, wire strippers, and soldering irons competently. Operate hand tools, power tools, adhesives, and scales effectively. Maintain compliance with ESD, FOD, and EH&S requirements. Document processes and improvements using Microsoft Office applications. Required Experience/Skills Background in development, production, delivery, and ongoing support of sophisticated electro-mechanical products that serve DoD customer requirements. Experience with inspection and test of CCAs and Piezo electrics for conformance to drawings. Ability to lead process improvement projects in work cells and manufacturing floor. Capability to write or redline work instructions for new production processes. Ability to read, interpret, and understand assembly drawings. Ability to rapidly understand work instructions and their requirements. Experience assembling small components into space-restricted subsystems. Competent in using crimpers, wire strippers, and soldering irons. Competent in using hand tools, power tools, adhesives, and scales. Competent in the use of Microsoft Office (Word, Excel, PowerPoint, Visio). Experience with ESD, FOD, and EH&S requirements. Experience in world-class lean manufacturing principles. High school diploma or equivalent and 3+ years of prior relevant experience. SECRET security clearance. Nice-to-Haves Handling experience with Hazmat materials. J-STD-001 and/or IPC-A-610 Certification. Kitting experience in manufacturing environments. Knowledge and experience with ISO 9001:2015 Quality Management Standards. Additional lean manufacturing certifications or training. Education High school diploma or equivalent required. 3+ years of prior relevant experience required. Pay & Benefits Summary Hourly rate: $35.06 6-month contract with possibility of conversion to full-time employee (FTE) Growth and development opportunities within the role and greater team Professional development in lean manufacturing environment Join Our Manufacturing Excellence Team! If you're an experienced electro-mechanical production technician with DoD background and lean manufacturing expertise, we invite you to apply. This role offers the opportunity to work on cutting-edge defense systems while contributing to the growth of our expanding Lynnwood facility and leading process improvement initiatives.
08/31/2025
Full time
Mech Assembler III - Electro-Mechanical Production Technician Department: Manufacturing Location: Lynnwood, WA - Onsite Role Type: Contract Clearance: Secret About Our Client Our client develops, integrates, and deploys advanced technology solutions that address existing and emerging missions for a range of customers across the Department of Defense (DoD). Job Description As an Electro-Mechanical Production Technician, you will work closely with manufacturing engineers and technicians to assemble and test electro-mechanical devices, improve production processes, and ensure a clean and organized manufacturing floor. Your primary responsibilities include assembly of complex electro-mechanical systems and sub-systems, test and data collection using various lab equipment, and fostering an environment of continuous improvement. You'll work in a pilot production line environment with a team of 8 manufacturing engineers and technicians, focusing on learning assembly processes rapidly while contributing to process improvements. The ideal candidate brings a background in sophisticated electro-mechanical products for DoD customers, experience with CCA and Piezo electric testing, and expertise in lean manufacturing principles with the ability to lead process improvement initiatives. Duties and Responsibilities Assemble complex electro-mechanical systems and sub-systems including experience with polyurethane encapsulation and soldering. Perform test and data collection using various lab equipment including oscilloscopes, digital multimeters, and impedance analyzers. Inspect and test CCAs and Piezo electrics for conformance to drawings and specifications. Lead process improvement projects in work cells and on the manufacturing floor. Write or redline work instructions for new production processes to document improvements. Ensure an organized and clean workspace (5S) including total preventive maintenance of equipment, tooling, and fixtures. Foster an environment of continuous improvement using industry best practices such as Root Cause Analysis and Kaizen. Value the importance of following precise Standard Work instructions while empowering team members to contribute to improvements. Read, interpret, and understand assembly drawings and technical documentation. Rapidly understand work instructions and their requirements. Assemble small components into space-restricted subsystems with precision. Use crimpers, wire strippers, and soldering irons competently. Operate hand tools, power tools, adhesives, and scales effectively. Maintain compliance with ESD, FOD, and EH&S requirements. Document processes and improvements using Microsoft Office applications. Required Experience/Skills Background in development, production, delivery, and ongoing support of sophisticated electro-mechanical products that serve DoD customer requirements. Experience with inspection and test of CCAs and Piezo electrics for conformance to drawings. Ability to lead process improvement projects in work cells and manufacturing floor. Capability to write or redline work instructions for new production processes. Ability to read, interpret, and understand assembly drawings. Ability to rapidly understand work instructions and their requirements. Experience assembling small components into space-restricted subsystems. Competent in using crimpers, wire strippers, and soldering irons. Competent in using hand tools, power tools, adhesives, and scales. Competent in the use of Microsoft Office (Word, Excel, PowerPoint, Visio). Experience with ESD, FOD, and EH&S requirements. Experience in world-class lean manufacturing principles. High school diploma or equivalent and 3+ years of prior relevant experience. SECRET security clearance. Nice-to-Haves Handling experience with Hazmat materials. J-STD-001 and/or IPC-A-610 Certification. Kitting experience in manufacturing environments. Knowledge and experience with ISO 9001:2015 Quality Management Standards. Additional lean manufacturing certifications or training. Education High school diploma or equivalent required. 3+ years of prior relevant experience required. Pay & Benefits Summary Hourly rate: $35.06 6-month contract with possibility of conversion to full-time employee (FTE) Growth and development opportunities within the role and greater team Professional development in lean manufacturing environment Join Our Manufacturing Excellence Team! If you're an experienced electro-mechanical production technician with DoD background and lean manufacturing expertise, we invite you to apply. This role offers the opportunity to work on cutting-edge defense systems while contributing to the growth of our expanding Lynnwood facility and leading process improvement initiatives.
Tech 3, Bakery-Maintenance - 2nd Shift
Aspire Bakeries Hazleton, Pennsylvania
Aspire Bakeries is a North American baking company with a leadership position in specialty frozen baked goods. Formed from leading bakery companies, its innovative food portfolio includes breads, artisan breads, buns, cookies, donuts, muffins and pastries from beloved brands like La Brea Bakery , Otis Spunkmeyer , and Oakrun Farm Bakery . With 13 bakeries in North America, we are committed to driving innovation, predicting upcoming consumer trends and flavors, and exceeding our customers' expectations. Aspire Bakeries champions the values of Integrity, Ownership, Customer Focus, Creativity and Care to help us deliver on People Safety, Food Safety, Quality and Collaboration. The Maintenance Technician III provides complex technical repairs and preventive maintenance on Bakery equipment including mechanical, electrical, pneumatic, hydraulic, and computerized systems to minimize downtime. This role troubleshoots issues, performs repairs, installs new parts, executes equipment overhauls, tests repaired equipment, and maintains records in the computerized maintenance system. Responsibilities: Provides technical repairs to complex electronic, mechanical, and Programmable Logic Controllers (PLCs). Troubleshoots, repairs, fabricates, and/or installs electronic systems, complex gauges, instrumentation repairs, and new parts including mechanical and electronic interfaces Troubleshoots, repairs, adjusts, installs, and programs electronic, electric, and pneumatic controls and instrumentation used to control and measure equipment performance, access to buildings, building automation systems, fire protection systems, material handling systems (elevators, etc.), and energy measurement systems. Assists production workers in diagnosing malfunctions in systems and equipment. Executes major equipment overhauls. Tests equipment after repairs, changeovers, or extended downtime. Maintains production equipment while operating on a defined production schedule. Operates general machinery and tools including saws, drills, power tools, scissor lifts, forklifts, etc. Interacts with and maintains records in accordance with Maintenance Management System requirements and job assignments and communicates via email, all with the use of computer systems Completes duties in accordance with quality assurance, GMPs, safety, and other company programs and procedures, and in compliance with government code and regulations. Maintains clean, organized, and safe work area, including wiping and washing equipment and tools, sweeping and mopping floors, and trash removal. Confers with and coordinates activities with Bakery personnel and other departments to minimize disruptions to production and maintenance schedules. Performs other duties as assigned or required. Qualifications: High school diploma with a minimum of 4 years of experience in instrumentation, measurement, and control systems, electronics, mechanical and/or electrical experience in industrial and manufacturing machinery or 6 years of experience in instrumentation, measurement, and control systems, electronics, mechanical and/or electrical experience in industrial and manufacturing machinery. A Bachelor's degree in Engineering or a related field is preferred. 4 or more years experience in industrial maintenance environment troubleshooting PLC software, I/O, and field devices and working with mechanical, pneumatic, or hydraulic systems preferred Experience in three of the following skills: refrigeration, plumbing, electrical, mechanical, and food manufacturing process controls. Knowledge of equipment set-up, functionality, operating procedures, and preventative maintenance techniques. Able to handle multiple tasks with the capability of prioritizing and planning work activities. Must have the ability to read and interpret electrical, mechanical, instrumentation, and control systems design documentation and vendor-supplied documents including Process & Instrument Drawings (PID), electrical single line drawings, instrument loop drawings, electrical cable, routing and termination, mechanical diagrams and machine layout drawings. Must be able to work in a fast-paced environment and must also adapt to frequent changes that occur on the production line. Shift: 2nd (1:30p-9:45p) Aspire Bakeries is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.
08/30/2025
Full time
Aspire Bakeries is a North American baking company with a leadership position in specialty frozen baked goods. Formed from leading bakery companies, its innovative food portfolio includes breads, artisan breads, buns, cookies, donuts, muffins and pastries from beloved brands like La Brea Bakery , Otis Spunkmeyer , and Oakrun Farm Bakery . With 13 bakeries in North America, we are committed to driving innovation, predicting upcoming consumer trends and flavors, and exceeding our customers' expectations. Aspire Bakeries champions the values of Integrity, Ownership, Customer Focus, Creativity and Care to help us deliver on People Safety, Food Safety, Quality and Collaboration. The Maintenance Technician III provides complex technical repairs and preventive maintenance on Bakery equipment including mechanical, electrical, pneumatic, hydraulic, and computerized systems to minimize downtime. This role troubleshoots issues, performs repairs, installs new parts, executes equipment overhauls, tests repaired equipment, and maintains records in the computerized maintenance system. Responsibilities: Provides technical repairs to complex electronic, mechanical, and Programmable Logic Controllers (PLCs). Troubleshoots, repairs, fabricates, and/or installs electronic systems, complex gauges, instrumentation repairs, and new parts including mechanical and electronic interfaces Troubleshoots, repairs, adjusts, installs, and programs electronic, electric, and pneumatic controls and instrumentation used to control and measure equipment performance, access to buildings, building automation systems, fire protection systems, material handling systems (elevators, etc.), and energy measurement systems. Assists production workers in diagnosing malfunctions in systems and equipment. Executes major equipment overhauls. Tests equipment after repairs, changeovers, or extended downtime. Maintains production equipment while operating on a defined production schedule. Operates general machinery and tools including saws, drills, power tools, scissor lifts, forklifts, etc. Interacts with and maintains records in accordance with Maintenance Management System requirements and job assignments and communicates via email, all with the use of computer systems Completes duties in accordance with quality assurance, GMPs, safety, and other company programs and procedures, and in compliance with government code and regulations. Maintains clean, organized, and safe work area, including wiping and washing equipment and tools, sweeping and mopping floors, and trash removal. Confers with and coordinates activities with Bakery personnel and other departments to minimize disruptions to production and maintenance schedules. Performs other duties as assigned or required. Qualifications: High school diploma with a minimum of 4 years of experience in instrumentation, measurement, and control systems, electronics, mechanical and/or electrical experience in industrial and manufacturing machinery or 6 years of experience in instrumentation, measurement, and control systems, electronics, mechanical and/or electrical experience in industrial and manufacturing machinery. A Bachelor's degree in Engineering or a related field is preferred. 4 or more years experience in industrial maintenance environment troubleshooting PLC software, I/O, and field devices and working with mechanical, pneumatic, or hydraulic systems preferred Experience in three of the following skills: refrigeration, plumbing, electrical, mechanical, and food manufacturing process controls. Knowledge of equipment set-up, functionality, operating procedures, and preventative maintenance techniques. Able to handle multiple tasks with the capability of prioritizing and planning work activities. Must have the ability to read and interpret electrical, mechanical, instrumentation, and control systems design documentation and vendor-supplied documents including Process & Instrument Drawings (PID), electrical single line drawings, instrument loop drawings, electrical cable, routing and termination, mechanical diagrams and machine layout drawings. Must be able to work in a fast-paced environment and must also adapt to frequent changes that occur on the production line. Shift: 2nd (1:30p-9:45p) Aspire Bakeries is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.
Mechanic I/II/III, Maintenance (Nights)
CSL Behring Holly Springs, North Carolina
With operations in 35+ nations and ~27,000 employees worldwide, CSL is driven to develop and deliver a broad range of lifesaving therapies to treat disorders such as hemophilia and primary immune deficiencies, and vaccines to prevent influenza. Our therapies are also used in cardiac surgery, organ transplantation and burn treatment. CSL is the parent company of CSL Behring and Seqirus. CSL Behring is a global leader in the protein biotherapeutics industry, focused on bringing to market biotherapies used to treat serious and often rare conditions. CSL Behring operates CSL Plasma, one of the world's largest collectors of human plasma, which is used to create CSL's therapies. Seqirus is one of the largest influenza vaccine companies in the world and is a transcontinental partner in pandemic preparedness and a major contributor to the prevention and control of influenza globally. We invite you to take a look at the many career possibilities available around the globe and consider building your promising future at CSL by becoming a member of our team! Job Description Job Purpose: Reporting to a Maintenance Manager / Supervisor, incumbent will be responsible for the maintenance of aseptic and non-aseptic process equipment (GMP & non-GMP) in the Bulk and Fill Finish, Packaging, labeling, and cartoning areas. Incumbent will engage in supporting manufacturing and the execution of maintenance tasks, with minimal supervision. Shift - Nights Hours- 6PM-6AM Follows the 2,2, 3 schedule - off every other weekend Level will be determined based on years of experience Major Accountabilities: Works closely with Quality, Engineering and Operations groups to ensure strict compliance with GMP guidelines at all times, specifically to ensure that the equipment is maintained in GMP compliance. Maintains and performs corrective, preventative maintenance on aseptic and non-aseptic manufacturing equipment for in GMP & non-GMP systems. Maintains and provides recommendations for spare parts and PM procedures for equipment. Supports other departments/areas to troubleshoot, test, repair, and optimize, equipment. Participates in the continuous improvement efforts within the site Maintenance Program (including reliability). Responsible to respond to alarms for assigned equipment/areas. Executes maintenance work for various customers with minimal interruptions. Works with contract service providers and support contractors executing maintenance activities. Provides support for start-up, commissioning and turnover of new systems in assigned area. Uses tools and software (CMMS, PAS, Pi, PLCs, ETOPS, SAP) required to resolve equipment and process issues within all technical competencies. Assists other technicians and associates. Minimum Requirements: High school diploma or Equivalent required. Minimum of 1 year relevant industry experience or an associate's degree in relevant technical discipline with 2+ years of experience OR equivalent. Strong desire experience with trouble-shooting pharmaceutical manufacturing process problems (e.g., centrifuges, pressure test failures, electrical, autoclaves, utilities, clean steam, filling/packaging) Experience and knowledge of maintenance principles within a cGMP Biotechnology / Pharmaceutical manufacturing environment. Knowledge of DCS, PLC, and/or Building Automation Systems (BAS) control systems. Proven knowledge of a Computerized Maintenance Management System (CMMS). Ability to problem solve and troubleshoot systems in an industrial environment required Ability to plan and organize tasks. Interpersonal effectiveness and communication skills (written and oral) are required in order to interface across management levels and departments.
09/09/2021
Full time
With operations in 35+ nations and ~27,000 employees worldwide, CSL is driven to develop and deliver a broad range of lifesaving therapies to treat disorders such as hemophilia and primary immune deficiencies, and vaccines to prevent influenza. Our therapies are also used in cardiac surgery, organ transplantation and burn treatment. CSL is the parent company of CSL Behring and Seqirus. CSL Behring is a global leader in the protein biotherapeutics industry, focused on bringing to market biotherapies used to treat serious and often rare conditions. CSL Behring operates CSL Plasma, one of the world's largest collectors of human plasma, which is used to create CSL's therapies. Seqirus is one of the largest influenza vaccine companies in the world and is a transcontinental partner in pandemic preparedness and a major contributor to the prevention and control of influenza globally. We invite you to take a look at the many career possibilities available around the globe and consider building your promising future at CSL by becoming a member of our team! Job Description Job Purpose: Reporting to a Maintenance Manager / Supervisor, incumbent will be responsible for the maintenance of aseptic and non-aseptic process equipment (GMP & non-GMP) in the Bulk and Fill Finish, Packaging, labeling, and cartoning areas. Incumbent will engage in supporting manufacturing and the execution of maintenance tasks, with minimal supervision. Shift - Nights Hours- 6PM-6AM Follows the 2,2, 3 schedule - off every other weekend Level will be determined based on years of experience Major Accountabilities: Works closely with Quality, Engineering and Operations groups to ensure strict compliance with GMP guidelines at all times, specifically to ensure that the equipment is maintained in GMP compliance. Maintains and performs corrective, preventative maintenance on aseptic and non-aseptic manufacturing equipment for in GMP & non-GMP systems. Maintains and provides recommendations for spare parts and PM procedures for equipment. Supports other departments/areas to troubleshoot, test, repair, and optimize, equipment. Participates in the continuous improvement efforts within the site Maintenance Program (including reliability). Responsible to respond to alarms for assigned equipment/areas. Executes maintenance work for various customers with minimal interruptions. Works with contract service providers and support contractors executing maintenance activities. Provides support for start-up, commissioning and turnover of new systems in assigned area. Uses tools and software (CMMS, PAS, Pi, PLCs, ETOPS, SAP) required to resolve equipment and process issues within all technical competencies. Assists other technicians and associates. Minimum Requirements: High school diploma or Equivalent required. Minimum of 1 year relevant industry experience or an associate's degree in relevant technical discipline with 2+ years of experience OR equivalent. Strong desire experience with trouble-shooting pharmaceutical manufacturing process problems (e.g., centrifuges, pressure test failures, electrical, autoclaves, utilities, clean steam, filling/packaging) Experience and knowledge of maintenance principles within a cGMP Biotechnology / Pharmaceutical manufacturing environment. Knowledge of DCS, PLC, and/or Building Automation Systems (BAS) control systems. Proven knowledge of a Computerized Maintenance Management System (CMMS). Ability to problem solve and troubleshoot systems in an industrial environment required Ability to plan and organize tasks. Interpersonal effectiveness and communication skills (written and oral) are required in order to interface across management levels and departments.
Product Engineering Specialist - Plastics
ABB Group Senatobia, Mississippi
Join ABB and work in a team that is dedicated to creating a future where innovative digital technologies allow greater access to cleaner energy. ABB Smart Power is a global technology leader, with solutions that make power supplies smart, connected and protected. Its intelligent solutions make power more competitive by improving the energy efficiency, productivity and reliability of almost any operation. Manufacturing at ABB ranges from assembly of customized industrial robots to advanced production of electrical switches and breakers. The innovative products we make, drive the world's largest ships, connect remote renewable power sources with consumers, and automate complex industrial processes. The role reports to Engineering Manager III and is located in Senatobia, Mississippi. As a Product Engineering Specialist - Plastics, need to execute engineering activities focused on plastic components localization, optimizing production cost, quality and on time delivery of products. Serve as the main technical reference for the suppliers and internal functions. Your responsibilities Technical Specifications Develops technical specifications in order to provide all the information's useful to quote and design plastic molds, thermosetting and thermoplastic both. Design Evaluation of the mold design proposed by the suppliers and final approver for the green light. Perform capacity analysis and life cycle studies. Supply Chain Technical reference for the evaluation and definition of the suppliers and the quotations of the components. Suppliers Establishes contacts with suppliers for technical support, to improve material quality and/or to decrease costs. Obtains prototype product and support during the certification of the product. Provide responsible support for directional production of line stop situations by reducing the risk of failure of product shipments. Maintenance Responsible for the maintenance schedule for all the molds owned by ABB and for the management of the standard and non/standard maintenance. Cost Responsible for the verification of the product life cycle and the definition of the product cost. Production Lead validation activities of both thermoplastic and thermosetting molds working with all stakeholders including Production and Quality. Training Provide training support to technicians. Capex Responsible for capital equipment and tooling purchases including justifications, quotes, and selection process. Your background Bachelor's Degree required with 3-5 years of experience in a plastic mold manufacturing, engineering or related setting. Candidates must already have a work authorization that would permit them to work for ABB in the US. Bachelor's Degree in Engineering with 5 years of experience in a plastic mold manufacturing, engineering or related setting is preferred. More about us Bring your very own sense of pride and purpose as you help us drive forward the Fourth Industrial Revolution - creating a sustainable future for our planet, and your career. Join ABB and harness the power of our diverse global network, as you collaborate with and learn from our world-class teams. Above all, challenge yourself every day. Let's write the future, together. Equal Employment Opportunity and Affirmative Action at ABB ABB is an Equal Employment Opportunity (EEO) and Affirmative Action Employer encouraging diversity in the workplace. All qualified applicants will receive consideration for employment without regard to their race, creed, color, ancestry, religion, sex, national origin, citizen status, age, sexual orientation, gender identity, disability, marital status, family medical leave status, or protected veterans status. For more information regarding your (EEO) rights as an applicant, please visit the following websites: . As an Equal Employment Opportunity and Affirmative Action Employer, applicants may request to review the Affirmative Action Plan of a particular ABB facility between the hours of 9:00 A.M. - 5:00 P.M. EST Monday through Friday by contacting an ABB HR Representative at 1-. Protected veterans and qualified individuals with a disability may request a reasonable accommodation if you are unable or limited in your ability to use or access ABB's career site as a result of your disability. You may request reasonable accommodations by calling an ABB HR Representative at 1- or by sending an email to . Resumes and applications will not be accepted in this manner.
01/30/2021
Full time
Join ABB and work in a team that is dedicated to creating a future where innovative digital technologies allow greater access to cleaner energy. ABB Smart Power is a global technology leader, with solutions that make power supplies smart, connected and protected. Its intelligent solutions make power more competitive by improving the energy efficiency, productivity and reliability of almost any operation. Manufacturing at ABB ranges from assembly of customized industrial robots to advanced production of electrical switches and breakers. The innovative products we make, drive the world's largest ships, connect remote renewable power sources with consumers, and automate complex industrial processes. The role reports to Engineering Manager III and is located in Senatobia, Mississippi. As a Product Engineering Specialist - Plastics, need to execute engineering activities focused on plastic components localization, optimizing production cost, quality and on time delivery of products. Serve as the main technical reference for the suppliers and internal functions. Your responsibilities Technical Specifications Develops technical specifications in order to provide all the information's useful to quote and design plastic molds, thermosetting and thermoplastic both. Design Evaluation of the mold design proposed by the suppliers and final approver for the green light. Perform capacity analysis and life cycle studies. Supply Chain Technical reference for the evaluation and definition of the suppliers and the quotations of the components. Suppliers Establishes contacts with suppliers for technical support, to improve material quality and/or to decrease costs. Obtains prototype product and support during the certification of the product. Provide responsible support for directional production of line stop situations by reducing the risk of failure of product shipments. Maintenance Responsible for the maintenance schedule for all the molds owned by ABB and for the management of the standard and non/standard maintenance. Cost Responsible for the verification of the product life cycle and the definition of the product cost. Production Lead validation activities of both thermoplastic and thermosetting molds working with all stakeholders including Production and Quality. Training Provide training support to technicians. Capex Responsible for capital equipment and tooling purchases including justifications, quotes, and selection process. Your background Bachelor's Degree required with 3-5 years of experience in a plastic mold manufacturing, engineering or related setting. Candidates must already have a work authorization that would permit them to work for ABB in the US. Bachelor's Degree in Engineering with 5 years of experience in a plastic mold manufacturing, engineering or related setting is preferred. More about us Bring your very own sense of pride and purpose as you help us drive forward the Fourth Industrial Revolution - creating a sustainable future for our planet, and your career. Join ABB and harness the power of our diverse global network, as you collaborate with and learn from our world-class teams. Above all, challenge yourself every day. Let's write the future, together. Equal Employment Opportunity and Affirmative Action at ABB ABB is an Equal Employment Opportunity (EEO) and Affirmative Action Employer encouraging diversity in the workplace. All qualified applicants will receive consideration for employment without regard to their race, creed, color, ancestry, religion, sex, national origin, citizen status, age, sexual orientation, gender identity, disability, marital status, family medical leave status, or protected veterans status. For more information regarding your (EEO) rights as an applicant, please visit the following websites: . As an Equal Employment Opportunity and Affirmative Action Employer, applicants may request to review the Affirmative Action Plan of a particular ABB facility between the hours of 9:00 A.M. - 5:00 P.M. EST Monday through Friday by contacting an ABB HR Representative at 1-. Protected veterans and qualified individuals with a disability may request a reasonable accommodation if you are unable or limited in your ability to use or access ABB's career site as a result of your disability. You may request reasonable accommodations by calling an ABB HR Representative at 1- or by sending an email to . Resumes and applications will not be accepted in this manner.
Manufacturing Technician III, Compounding, B2 shift
AbbVie Waco, Texas
About AbbVie AbbVie's mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women's health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at . on Twitter , Facebook , Instagram , YouTube and LinkedIn . Responsible for compounding high-quality solutions, semi-solids, emulsions, and suspensions in accordance with Good Manufacturing Practices (GMP) and department Standard Operating Procedures (SOP). This position is responsible for the following: Accurate formulation of products. Stage, load, operate, and monitor all equipment for product formulations. Weighing and mixing chemicals according to specific formulas. Calibrate, operate, and monitor all formulation-related equipment (e.g., mixers, scales, meters, etc.). Perform operations necessary to adjust the pH of product for in-process testing. Clean, steam, and sanitizes all tanks, lines, facilities, equipment and chemical containers used in the product formulation process in accordance with current SOP's and cGMP's. Ensure sterile product transfer to filling departments. Accurately complete documents and record production volumes (batches) in compliance with current GDP standards. Assumes other duties and responsibilities, as necessary, within the Compounding department, in an effort to provide the required support to ensure adherence to the production schedule. Qualifications Essential Knowledge, Skills & Abilities: Ability to perform detailed tasks and document activities completely and accurately. Ability to think and plan in a logical sequential order. Able to work in a controlled environment that includes surgical mask and goggles. Ability to comply with gowning validation and subsequent gowning verifications. Ability to work any shift (up to 12-hours) as required dependent on business needs. Capable of standing for long periods of time. Capable of using hands to feel objects, use tools or controls and reach with hands and arms. Ability to read, comprehend, write, and communicate effectively in English. Ability to carry out detailed written or verbal instructions. Ability to work and communicate with others in a professional and effective manner, within a team-oriented environment. Basic user knowledge and understanding of Windows-based computer systems such as Microsoft Office, with an ability to learn other computer-based systems. Physically able to continuously stand and walk. Physically able to lift up to 40 lbs. for men and 35 lbs. for women. Physically able to bend, climb, lift, squat, stoop, and stretch to reach frequently. Education & Experience: High School Diploma or GED equivalent and/or Associate's Degree with five (5) years regulated Compounding experience, OR B.S. in the Sciences preferred. At least two (2) years of related work experience, preferably in a high-speed production or manufacturing environment. Experience working in a GMP regulated environment preferred. Basic user knowledge of Microsoft Office, SAP experience preferred. Experience working in an Aseptic Production environment preferred. Significant Work Activities Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day) Travel No Job Type Experienced Schedule Full-time Job Level Code IC Equal Employment Opportunity At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic.
01/23/2021
Full time
About AbbVie AbbVie's mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women's health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at . on Twitter , Facebook , Instagram , YouTube and LinkedIn . Responsible for compounding high-quality solutions, semi-solids, emulsions, and suspensions in accordance with Good Manufacturing Practices (GMP) and department Standard Operating Procedures (SOP). This position is responsible for the following: Accurate formulation of products. Stage, load, operate, and monitor all equipment for product formulations. Weighing and mixing chemicals according to specific formulas. Calibrate, operate, and monitor all formulation-related equipment (e.g., mixers, scales, meters, etc.). Perform operations necessary to adjust the pH of product for in-process testing. Clean, steam, and sanitizes all tanks, lines, facilities, equipment and chemical containers used in the product formulation process in accordance with current SOP's and cGMP's. Ensure sterile product transfer to filling departments. Accurately complete documents and record production volumes (batches) in compliance with current GDP standards. Assumes other duties and responsibilities, as necessary, within the Compounding department, in an effort to provide the required support to ensure adherence to the production schedule. Qualifications Essential Knowledge, Skills & Abilities: Ability to perform detailed tasks and document activities completely and accurately. Ability to think and plan in a logical sequential order. Able to work in a controlled environment that includes surgical mask and goggles. Ability to comply with gowning validation and subsequent gowning verifications. Ability to work any shift (up to 12-hours) as required dependent on business needs. Capable of standing for long periods of time. Capable of using hands to feel objects, use tools or controls and reach with hands and arms. Ability to read, comprehend, write, and communicate effectively in English. Ability to carry out detailed written or verbal instructions. Ability to work and communicate with others in a professional and effective manner, within a team-oriented environment. Basic user knowledge and understanding of Windows-based computer systems such as Microsoft Office, with an ability to learn other computer-based systems. Physically able to continuously stand and walk. Physically able to lift up to 40 lbs. for men and 35 lbs. for women. Physically able to bend, climb, lift, squat, stoop, and stretch to reach frequently. Education & Experience: High School Diploma or GED equivalent and/or Associate's Degree with five (5) years regulated Compounding experience, OR B.S. in the Sciences preferred. At least two (2) years of related work experience, preferably in a high-speed production or manufacturing environment. Experience working in a GMP regulated environment preferred. Basic user knowledge of Microsoft Office, SAP experience preferred. Experience working in an Aseptic Production environment preferred. Significant Work Activities Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day) Travel No Job Type Experienced Schedule Full-time Job Level Code IC Equal Employment Opportunity At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic.
Manufacturing Technician III - Downstream
Gilead Sciences, Inc. Oceanside, California
Manufacturing Technician III - Downstream United States - California - Oceanside Gilead Sciences, Inc. is a research-based bio-pharmaceutical company that discovers, develops and commercializes innovative medicines in areas of unmet medical need. With each new discovery and investigational drug candidate, we seek to improve the care of patients living with life-threatening diseases around the world. Gilead's therapeutic areas of focus include HIV/AIDS, liver diseases, cancer and inflammation, and serious respiratory and cardiovascular conditions. Making an impact on a global scale Inclusion is one of the company's five core values. That's because we know that we are stronger and more innovative at Gilead when we are informed by a diverse set of backgrounds, experiences and points of view. Gilead Sciences is a biopharmaceutical company that discovers, develops and commercializes innovative therapeutics in areas of unmet medical need. The company's mission is to advance the care of patients suffering from life-threatening diseases worldwide. When you join Gilead, you join our mission to change the world by enabling people to live healthier and more fulfilling lives. Come join a mission-driven bio-pharmaceutical organization that values inclusion and diversity, has a strong portfolio of products, and is constantly #CreatingPossible Manufacturing Technician III- Downstream Gilead Sciences, Inc. is a research-based biopharmaceutical company founded in 1987. Together we deliver life-saving therapies to patients in need. With the commitment and drive you bring to the workplace every day, you will be part of a team that is changing the world and helping millions of people live healthier, more fulfilling lives. Our worldwide staff is a close community where you can see the tangible results of your contributions, where every individual matters, and everyone has a chance to enhance their skills through ongoing development. Our scientific focus has resulted in marketed products that are benefiting hundreds of thousands of people, a pipeline of late-stage drug candidates, and unmatched patient access programs to ensure medications are available to those who could otherwise not afford them. By joining Gilead, you will further our mission to address unmet medical needs and improve life by advancing the care of patients with life-threatening diseases. Department: Downstream Manufacturing, Oceanside Job Responsibilities The Manufacturing Technician III is responsible for the operation of large and small scale chromatography columns and skids, viral filtration and ultrafiltration/diafiltration skids, as well as all related equipment and systems necessary to clean, configure, sanitize/sterilize and maintain said equipment. Operation and practical knowledge of glass washers, autoclaves, filters, pumps and analytical equipment to support and monitor the process is expected. Safety and Compliance are the two primary objectives of manufacturing operations. Reports to Team Lead on a regular basis on line performance and reports any issues that need to be resolved. Expected duties also include planning and executing the safe and efficient operation of assigned processes, Good Documentation Practices, timely communication of deviations, incidents and/or safety concerns and all relevant housekeeping duties to ensure the work areas are kept to a high level of cleanliness and inspection readiness. Involvement in planning and full execution/proper documentation of all operations associated with: Buffer preparation Protein Purification by means of column chromatography, Viral Filtration and UFDF Clean in Place (CIP) and Steam in Place (SIP) of fixed tanks/vessels and portable equipment and Clean out of Place (COP)/Glasswash of misc. parts and equipment Proficiency and routine maintenance of analytical equipment including but not limited to: pH/conductivity meters, bioanalyzers, osmometers, benchtop centrifuges, cell counters and microscopes Experience with DeltaV Automation Systems and Unicorn System Control or equivalent Aseptic Processing experience and knowledge required. Knowledge of quality systems, validation principles, regulatory and ICH guidelines and multi-product controls required Background or understanding of Lean concepts (Kaizen, 5S, KanBan) desired Works under demanding production schedules and strict compliance/quality requirements Coordination with support groups including, but not limited to: Process Development, Quality Assurance and Control, Calibration, Maintenance, Validation, and Materials Management as a Manufacturing representative Ability to work independently and in teams, proactive and self-managing, proven problem solving as well as a detailed and organized approach are key components to the success of this candidate. Must be flexible to work day, swing, or night shifts, and/or weekends Knowledge, Experience, and Skills: Knowledge of written Standard Operating Procedures (SOPs) and Master Batch Records Good verbal, written, and interpersonal communication skills are required. Working knowledge in Microsoft Office applications and administrative policies Ability to follow direction and work under minimal supervision Demonstrates capability in organizing more complex activities in a manufacturing process Minimum Qualifications: A minimum 3 years of relevant experience, HS Diploma and a Certificate to FETAC level 6 (GSL) 0 - 2 years of relevant experience with a Bachelors degree in engineering or scientific discipline Prior experience in a Biologics cGMP related industry is required. For jobs in the United States: As an equal opportunity employer, Gilead Sciences Inc. is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact for assistance. For more information about equal employment opportunity protections, please view the 'EEO is the Law' poster. NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT PAY TRANSPARENCY NONDISCRIMINATION PROVISION Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team. Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion. For Current Gilead Employees and Contractors: Please log onto your Internal Career Site to apply for this job. Copyright ©2017 Jobelephant.com Inc. All rights reserved. Posted by the FREE value-added recruitment advertising agency jeid-6edd147bdecad9a929eb094c
01/21/2021
Full time
Manufacturing Technician III - Downstream United States - California - Oceanside Gilead Sciences, Inc. is a research-based bio-pharmaceutical company that discovers, develops and commercializes innovative medicines in areas of unmet medical need. With each new discovery and investigational drug candidate, we seek to improve the care of patients living with life-threatening diseases around the world. Gilead's therapeutic areas of focus include HIV/AIDS, liver diseases, cancer and inflammation, and serious respiratory and cardiovascular conditions. Making an impact on a global scale Inclusion is one of the company's five core values. That's because we know that we are stronger and more innovative at Gilead when we are informed by a diverse set of backgrounds, experiences and points of view. Gilead Sciences is a biopharmaceutical company that discovers, develops and commercializes innovative therapeutics in areas of unmet medical need. The company's mission is to advance the care of patients suffering from life-threatening diseases worldwide. When you join Gilead, you join our mission to change the world by enabling people to live healthier and more fulfilling lives. Come join a mission-driven bio-pharmaceutical organization that values inclusion and diversity, has a strong portfolio of products, and is constantly #CreatingPossible Manufacturing Technician III- Downstream Gilead Sciences, Inc. is a research-based biopharmaceutical company founded in 1987. Together we deliver life-saving therapies to patients in need. With the commitment and drive you bring to the workplace every day, you will be part of a team that is changing the world and helping millions of people live healthier, more fulfilling lives. Our worldwide staff is a close community where you can see the tangible results of your contributions, where every individual matters, and everyone has a chance to enhance their skills through ongoing development. Our scientific focus has resulted in marketed products that are benefiting hundreds of thousands of people, a pipeline of late-stage drug candidates, and unmatched patient access programs to ensure medications are available to those who could otherwise not afford them. By joining Gilead, you will further our mission to address unmet medical needs and improve life by advancing the care of patients with life-threatening diseases. Department: Downstream Manufacturing, Oceanside Job Responsibilities The Manufacturing Technician III is responsible for the operation of large and small scale chromatography columns and skids, viral filtration and ultrafiltration/diafiltration skids, as well as all related equipment and systems necessary to clean, configure, sanitize/sterilize and maintain said equipment. Operation and practical knowledge of glass washers, autoclaves, filters, pumps and analytical equipment to support and monitor the process is expected. Safety and Compliance are the two primary objectives of manufacturing operations. Reports to Team Lead on a regular basis on line performance and reports any issues that need to be resolved. Expected duties also include planning and executing the safe and efficient operation of assigned processes, Good Documentation Practices, timely communication of deviations, incidents and/or safety concerns and all relevant housekeeping duties to ensure the work areas are kept to a high level of cleanliness and inspection readiness. Involvement in planning and full execution/proper documentation of all operations associated with: Buffer preparation Protein Purification by means of column chromatography, Viral Filtration and UFDF Clean in Place (CIP) and Steam in Place (SIP) of fixed tanks/vessels and portable equipment and Clean out of Place (COP)/Glasswash of misc. parts and equipment Proficiency and routine maintenance of analytical equipment including but not limited to: pH/conductivity meters, bioanalyzers, osmometers, benchtop centrifuges, cell counters and microscopes Experience with DeltaV Automation Systems and Unicorn System Control or equivalent Aseptic Processing experience and knowledge required. Knowledge of quality systems, validation principles, regulatory and ICH guidelines and multi-product controls required Background or understanding of Lean concepts (Kaizen, 5S, KanBan) desired Works under demanding production schedules and strict compliance/quality requirements Coordination with support groups including, but not limited to: Process Development, Quality Assurance and Control, Calibration, Maintenance, Validation, and Materials Management as a Manufacturing representative Ability to work independently and in teams, proactive and self-managing, proven problem solving as well as a detailed and organized approach are key components to the success of this candidate. Must be flexible to work day, swing, or night shifts, and/or weekends Knowledge, Experience, and Skills: Knowledge of written Standard Operating Procedures (SOPs) and Master Batch Records Good verbal, written, and interpersonal communication skills are required. Working knowledge in Microsoft Office applications and administrative policies Ability to follow direction and work under minimal supervision Demonstrates capability in organizing more complex activities in a manufacturing process Minimum Qualifications: A minimum 3 years of relevant experience, HS Diploma and a Certificate to FETAC level 6 (GSL) 0 - 2 years of relevant experience with a Bachelors degree in engineering or scientific discipline Prior experience in a Biologics cGMP related industry is required. For jobs in the United States: As an equal opportunity employer, Gilead Sciences Inc. is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact for assistance. For more information about equal employment opportunity protections, please view the 'EEO is the Law' poster. NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT PAY TRANSPARENCY NONDISCRIMINATION PROVISION Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team. Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion. For Current Gilead Employees and Contractors: Please log onto your Internal Career Site to apply for this job. Copyright ©2017 Jobelephant.com Inc. All rights reserved. Posted by the FREE value-added recruitment advertising agency jeid-6edd147bdecad9a929eb094c
NEED - Biomedical Technician III
Infobahn Softworld Inc. Westborough, Massachusetts
Title : Biomedical Technician III Duration : 6+ Months We are looking for a Sr R&D Lab Technician Disposables to work with our expert Cell and Gene Therapy Disposables Kit R&D team based in Marlborough, MA. Do you have a passion for cell therapy? Then we would love to hear from you. What you'll do Participate in the design and organization of experiments in conjunction with the Tech Lead and or R&D Team members. Serve as a resource to R&D Team. Perform hands-on tests of new products in development. Prepare samples and execute tests, collaborating with colleagues as necessary to gain access and training. Record test data in accordance with GLP. In addition to executing existing tests, you will also be expected to propose, design, improve, develop and/or implement new tests procedures for evaluating new product's specifications within the verification and validation activities framework. Contribute to the generation of work instructions, tests protocols, and reports. Follow departmental work instructions, SOP's, OSHA safety regulations and cGMPs & cGLPs to perform assigned tasks. Monitor and oversee lab supply inventory, generate expense purchase requisitions, if applicable, and maintain documentation in accordance with established procedures. Interface with internal groups to assure laboratory equipment maintenance, calibration and documents conform with established practices. Who you are Formal Training/ Education: Minimum (required): Associates Degree in Technology or Engineering Equivalent combination of education and work experience Job-related Experience: Minimum (required): ? 8-10 years relevant work experience in medical device and/or life science industry (FDA 21CFR820, ISO13485) Typical previous positions: o Quality Control/Test Sr Lab Tech o Sr R&D Product Development Tech o Sr Manufacturing Engineering Tech (Production support, Mfg Process Development) Knowledge, Skill or Ability: Deep knowledge in medical device disposables (Class II), with relevant experience in developing tests methods, writing test protocols, and verifying product design specifications of new products. Backgrounds in manufacturing process development related to medical device, disposables an asset (IQ, OQ, PQ, Process FMEA) Basic knowledge of mechanical design of fixtures (CAD Design - SolidWorks) Familiarity with the mechanical testing of plastic parts and sub-assemblies (e.g. tensile/shear/compression test, hardness measurement, pressure decay measurement, burst test) and product reliability tests (e.g. any tear/wear/aging test) Ability to work under cGMP/cGLP guidelines Strong communication, interpersonal skills and the ability to work in a team environment are required. Demonstrate strong ethical behavior Detail-oriented, and able to work independently as well as part of a team Possess good computer skills (Microsoft Office is required. Word, Excel) - provided by Dice
10/01/2020
Full time
Title : Biomedical Technician III Duration : 6+ Months We are looking for a Sr R&D Lab Technician Disposables to work with our expert Cell and Gene Therapy Disposables Kit R&D team based in Marlborough, MA. Do you have a passion for cell therapy? Then we would love to hear from you. What you'll do Participate in the design and organization of experiments in conjunction with the Tech Lead and or R&D Team members. Serve as a resource to R&D Team. Perform hands-on tests of new products in development. Prepare samples and execute tests, collaborating with colleagues as necessary to gain access and training. Record test data in accordance with GLP. In addition to executing existing tests, you will also be expected to propose, design, improve, develop and/or implement new tests procedures for evaluating new product's specifications within the verification and validation activities framework. Contribute to the generation of work instructions, tests protocols, and reports. Follow departmental work instructions, SOP's, OSHA safety regulations and cGMPs & cGLPs to perform assigned tasks. Monitor and oversee lab supply inventory, generate expense purchase requisitions, if applicable, and maintain documentation in accordance with established procedures. Interface with internal groups to assure laboratory equipment maintenance, calibration and documents conform with established practices. Who you are Formal Training/ Education: Minimum (required): Associates Degree in Technology or Engineering Equivalent combination of education and work experience Job-related Experience: Minimum (required): ? 8-10 years relevant work experience in medical device and/or life science industry (FDA 21CFR820, ISO13485) Typical previous positions: o Quality Control/Test Sr Lab Tech o Sr R&D Product Development Tech o Sr Manufacturing Engineering Tech (Production support, Mfg Process Development) Knowledge, Skill or Ability: Deep knowledge in medical device disposables (Class II), with relevant experience in developing tests methods, writing test protocols, and verifying product design specifications of new products. Backgrounds in manufacturing process development related to medical device, disposables an asset (IQ, OQ, PQ, Process FMEA) Basic knowledge of mechanical design of fixtures (CAD Design - SolidWorks) Familiarity with the mechanical testing of plastic parts and sub-assemblies (e.g. tensile/shear/compression test, hardness measurement, pressure decay measurement, burst test) and product reliability tests (e.g. any tear/wear/aging test) Ability to work under cGMP/cGLP guidelines Strong communication, interpersonal skills and the ability to work in a team environment are required. Demonstrate strong ethical behavior Detail-oriented, and able to work independently as well as part of a team Possess good computer skills (Microsoft Office is required. Word, Excel) - provided by Dice

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