B. Braun US Pharmaceutical Manufacturing LLC

B. Braun Medical, Inc. Company: B. Braun US Pharmaceutical Manufacturing LLC Job Posting Location: Irvine, California, United States Functional Area: Other Areas Working Model: Onsite Days of Work: Thursday, Wednesday, Friday, Saturday Shift: 3/4 X 12 Relocation Available: No Requisition ID: 11785 B. Braun Medical Inc., a leader in infusion therapy and pain management, develops, manufactures, and markets innovative medical products and services to the healthcare industry. Other key product areas include nutrition, pharmacy admixture and compounding, ostomy and wound care, and dialysis. The company is committed to eliminating preventable treatment errors and enhancing patient, clinician and environmental safety. B. Braun Medical is headquartered in Bethlehem, Pa., and is part of the B. Braun Group of Companies in the U.S., which includes B. Braun Interventional Systems, Aesculap and CAPS . Globally, the B. Braun Group of Companies employs more than 64,000 employees in 64 countries. Guided by its Sharing Expertise philosophy, B. Braun continuously exchanges knowledge with customers, partners and clinicians to address the critical issues of improving care and lowering costs. To learn more about B. Braun Medical, visit Position Summary The Craftsperson - Electrician helps keep our plant running safely and reliably by installing, maintaining, and repairing electrical distribution systems that power manufacturing equipment, machinery, lighting, and facility infrastructure. In this hands-on role, you will perform preventive maintenance, troubleshoot electrical and equipment failures, and recommend corrective actions that reduce downtime and improve system performance. This position is ideal for an experienced industrial electrician with advanced technical knowledge, strong problem-solving skills, and experience working with electrical systems from 24 volts up to 4kV. In this role, you will have the chance to: • Install, connect, energize, test, adjust, and calibrate electrical components, wiring harnesses, terminals, chassis, and panels to support safe and reliable operation. • Perform scheduled preventive maintenance and troubleshoot electrical malfunctions involving manufacturing equipment, facility systems, and auxiliary equipment. • Inspect machinery and electrical systems for faults or signs of potential failure to help prevent downtime and production interruptions. • Use appropriate PPE and electrical testing equipment, including multimeters, amp probes, power recording devices, and power quality meters. • Recommend corrective actions and equipment improvements that enhance system safety, reliability, functionality, and efficiency. • Document maintenance and repair activities and communicate effectively with supervisors, peers, contractors, and vendors. • Periodically assist with orienting, training, assigning, or checking the work of peers and help ensure assigned work meets established targets. Essential Requirements • High school diploma or GED. • 8+ years of related electrical maintenance experience in an industrial, manufacturing, or facilities environment. • Advanced working knowledge of industrial electrical systems, including experience with voltages ranging from 24 volts up to 4kV. • Demonstrated ability to troubleshoot, repair, maintain, test, adjust, and calibrate electrical equipment and systems. • Working knowledge of applicable electrical codes, regulations, safety practices, PPE requirements, and field procedures. • Ability to evaluate critical situations, consult with supervisory staff, and recommend appropriate corrective action. • Ability to work the assigned 12-hour night schedule and non-standard hours as business needs require. • Ability to meet the physical requirements of the position, including exerting up to 40 pounds of force occasionally, up to 20 pounds frequently, and up to 10 pounds constantly; frequently standing, walking, reaching, pushing, and pulling; and occasionally climbing stairs or ladders, kneeling, crawling, stooping, or squatting. Preferred Experience includes: • Associate or technical degree in electrical technology, industrial maintenance, or a related field. • Electrical license or certification. • Experience maintaining electrical distribution systems and production equipment in a manufacturing environment. • Experience supporting or guiding peers, contractors, or vendors on technical work. Work Environment This position works primarily in a production/manufacturing environment and may occasionally support office, warehouse, and laboratory areas. The role frequently works near moving mechanical parts and in moderate noise conditions. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions. Compensation The targeted hourly range for this role is $33.44 - $38.58 , plus a 7.5% shift differential for the end-of-week night shift. The targeted range for this role takes into account a range of factors that are considered when making compensation and hiring decisions; included but not limited to: skill sets; experience and training; licensure and certifications; and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. Compensation decisions are dependent on the facts and circumstances of each case. The range provided is a reasonable estimate. B. Braun offers an excellent benefits package, which includes healthcare, a 401(k) plan, and tuition reimbursement. To learn more about B. Braun and our safety healthcare products or view a listing of our employment opportunities, please visit us on the internet at . Through its "Sharing Expertise " initiative, B. Braun promotes best practices for continuous improvement of healthcare products and services. We are an equal opportunity employer. We evaluate applications 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 characteristic. Know Your Rights: Workplace Discrimination is Illegal, click here . All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or other legally protected status. Compensation details: 33.44-38.58 Hourly Wage PIe04e-5227

B. Braun Medical, Inc. Company: B. Braun US Pharmaceutical Manufacturing LLC Job Posting Location: Irvine, California, United States Functional Area: Quality Working Model: Onsite Days of Work: Friday, Thursday, Wednesday, Tuesday, Monday Shift: 5X8 Relocation Available: No Requisition ID: 14755 B. Braun Medical Inc., a leader in infusion therapy and pain management, develops, manufactures, and markets innovative medical products and services to the healthcare industry. Other key product areas include nutrition, pharmacy admixture and compounding, ostomy and wound care, and dialysis. The company is committed to eliminating preventable treatment errors and enhancing patient, clinician and environmental safety. B. Braun Medical is headquartered in Bethlehem, Pa., and is part of the B. Braun Group of Companies in the U.S., which includes B. Braun Interventional Systems, Aesculap and CAPS . Globally, the B. Braun Group of Companies employs more than 64,000 employees in 64 countries. Guided by its Sharing Expertise philosophy, B. Braun continuously exchanges knowledge with customers, partners and clinicians to address the critical issues of improving care and lowering costs. To learn more about B. Braun Medical, visit Ready to lead where science, quality, and patient safety come together? Join B. Braun and shape the future of laboratory excellence while driving the strategy, compliance, and innovation behind critical healthcare products. Why this role matters: The Director, Lab Quality Control serves as the senior site authority for Quality Control Chemistry and Microbiology, providing the scientific and operational leadership needed to protect product quality and maintain regulatory compliance. This role establishes the site's laboratory strategy, leads critical quality initiatives, and ensures that laboratory operations remain scientifically sound, inspection-ready, and aligned with business and product portfolio requirements. How you will make an impact: Develop, maintain, and execute the site Quality Control strategy in alignment with business objectives, product portfolio requirements, and regulatory expectations. Provide strategic oversight for QC Chemistry and QC Microbiology operations, including release, stability, raw material, in-process, microbiological, and sterility-related testing activities. Establish and govern laboratory standards for testing compliance, data integrity, investigations, sample management, analytical methods, specifications, and laboratory workflows. Serve as the primary site subject matter expert during regulatory inspections and customer audits involving laboratory operations and quality systems. Partner with Quality Assurance, Manufacturing, Sterility Assurance, Engineering, Validation, Technical Services, Supply Chain, and Regulatory Affairs to support site operations and timely product release. Lead laboratory optimization, method modernization, automation, Lean deployment, and quality system improvement initiatives. Foster a culture of quality, accountability, scientific rigor, collaboration, safety, and continuous improvement. What sets you up for success: Bachelor's degree in a STEM discipline required; master's degree or doctorate preferred. 10+ years of related experience, including significant leadership responsibility within laboratory quality control or pharmaceutical manufacturing. Demonstrated expertise in QC Chemistry and/or QC Microbiology operations within a sterile drug product manufacturing environment. Significant experience with laboratory compliance, data integrity, out-of-specification and out-of-trend investigations, analytical methods, and pharmaceutical quality systems. Proven experience supporting regulatory inspections, customer audits, and interactions with senior internal and external stakeholders. Ability to resolve complex scientific, operational, and compliance issues using sound judgment, technical expertise, and risk-based decision-making. Lean Six Sigma certification or demonstrated experience applying Lean and continuous-improvement methodologies preferred. What you will enjoy along the way: The opportunity to shape the laboratory quality strategy for a regulated sterile pharmaceutical manufacturing site. A highly visible leadership role with influence across Quality, Manufacturing, Technical Operations, Supply Chain, and Regulatory Affairs. The ability to modernize analytical capabilities through automation, method lifecycle management, Lean principles, and emerging technologies. Responsibility for developing laboratory leaders, building organizational capability, and determining the effective allocation of people and resources. Meaningful work that directly supports product quality, regulatory compliance, operational reliability, and patient safety. A collaborative environment built on scientific rigor, accountability, diverse perspectives, and continuous improvement. Salary Range: $184,000 - $261,000 At B. Braun, together means better. We believe that diversity makes us stronger. That is why we are committed to creating an inclusive workplace where everyone feels respected, valued, and empowered to make a meaningful impact. We welcome applications from people of all identities, backgrounds, and perspectives. Join us. Apply now! Check us out on Social Media! B. Braun Group LinkedIn Join us and let's drive advancements in health care! Apply now! The targeted range for this role takes into account a range of factors that are considered when making compensation and hiring decisions; included but not limited to: skill sets; experience and training; licensure and certifications; and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. Compensation decisions are dependent on the facts and circumstances of each case. The range provided is a reasonable estimate. B. Braun offers an excellent benefits package, which includes healthcare, a 401(k) plan, and tuition reimbursement. To learn more about B. Braun and our safety healthcare products or view a listing of our employment opportunities, please visit us on the internet at . Through its "Sharing Expertise " initiative, B. Braun promotes best practices for continuous improvement of healthcare products and services. We are an equal opportunity employer. We evaluate applications 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 characteristic. Know Your Rights: Workplace Discrimination is Illegal, click here . All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or other legally protected status. Compensation details: 00 Yearly Salary PIef78ff78ad7f-0021

B. Braun Medical, Inc. Company: B. Braun US Pharmaceutical Manufacturing LLC Job Posting Location: Irvine, California, United States Functional Area: Quality Working Model: Onsite Days of Work: Friday, Thursday, Wednesday, Tuesday, Monday Shift: 5X8 Relocation Available: No Requisition ID: 14034 B. Braun Medical Inc., a leader in infusion therapy and pain management, develops, manufactures, and markets innovative medical products and services to the healthcare industry. Other key product areas include nutrition, pharmacy admixture and compounding, ostomy and wound care, and dialysis. The company is committed to eliminating preventable treatment errors and enhancing patient, clinician and environmental safety. B. Braun Medical is headquartered in Bethlehem, Pa., and is part of the B. Braun Group of Companies in the U.S., which includes B. Braun Interventional Systems, Aesculap and CAPS . Globally, the B. Braun Group of Companies employs more than 64,000 employees in 64 countries. Guided by its Sharing Expertise philosophy, B. Braun continuously exchanges knowledge with customers, partners and clinicians to address the critical issues of improving care and lowering costs. To learn more about B. Braun Medical, visit Position Summary B. Braun Medical Inc. is seeking a QA Associate, Sterilization Assurance to support quality oversight of sterilization and product release activities within a GMP-regulated manufacturing environment. This role is responsible for reviewing sterilization records, batch documentation, and quality system records to ensure compliance with regulatory requirements, Good Documentation Practices (GDP), and data integrity standards. The QA Associate partners closely with Manufacturing, Engineering, Facilities, and Quality teams to support product disposition, release activities, and resolution of quality events. In This Role, You Will Have the Chance To: Review sterilization records, batch documentation, and quality records for accuracy, completeness, and compliance with GMP, GDP, and data integrity requirements. Utilize electronic systems including LIMS, MES, Wonderware, and Electronic Batch Records (EBR) to support sterilization review and release activities. Identify, document, and escalate deviations, nonconformances, and documentation discrepancies in accordance with established procedures. Verify sterilization documentation and traceability records to support product release decisions. Collaborate with Manufacturing, Quality, Engineering, and Facilities teams to resolve quality and documentation issues. Support product disposition and release activities while maintaining audit-ready records. Participate in continuous improvement initiatives to enhance compliance and operational efficiency. Essential Requirements High School Diploma or GED required. Minimum one (1) year of experience in manufacturing, quality, laboratory, or FDA-regulated environments. Experience reviewing documentation for accuracy, completeness, and compliance. Working knowledge of GMPs, GDP, and quality system requirements. Strong attention to detail and commitment to data integrity. Proficiency with Microsoft Office and electronic quality systems. Strong organizational, analytical, and problem-solving skills. Ability to work non-standard hours as business needs require. Regular and predictable onsite attendance required. Preferred Qualifications Associate or Bachelor's degree in Biology, Microbiology, Chemistry, Biomedical Sciences, Engineering, Quality Management, or a related scientific discipline. Experience working in pharmaceutical, medical device, biotechnology, or other regulated manufacturing environments. Familiarity with sterilization processes, validation principles, CAPA, deviation investigations, and nonconformance management. Experience with LIMS, MES, Wonderware, Electronic Batch Records, or similar quality systems. Knowledge of FDA regulations, including 21 CFR Part 11 and cGMP requirements. Knowledge & Skills Ability to interpret procedures, specifications, and quality documentation. Strong written and verbal communication skills with the ability to collaborate cross-functionally. Ability to manage multiple priorities in a fast-paced environment. Sound judgment in identifying, escalating, and resolving quality-related issues. Commitment to quality, compliance, and continuous improvement. Physical Demands & Work Environment Ability to sit, stand, walk, and perform computer-based work throughout the workday. Ability to lift up to 20 pounds occasionally. Requires visual acuity and attention to detail for review of electronic and paper records. Work is performed in office, laboratory, and GMP-regulated manufacturing environments. Regular interaction with production operations and manufacturing equipment. Moderate noise levels may be present in manufacturing areas. Pay Range- $24.00 - $28.00/hour The targeted range for this role takes into account a range of factors that are considered when making compensation and hiring decisions; included but not limited to: skill sets; experience and training; licensure and certifications; and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. Compensation decisions are dependent on the facts and circumstances of each case. The range provided is a reasonable estimate. B. Braun offers an excellent benefits package, which includes healthcare, a 401(k) plan, and tuition reimbursement. To learn more about B. Braun and our safety healthcare products or view a listing of our employment opportunities, please visit us on the internet at . Through its "Sharing Expertise " initiative, B. Braun promotes best practices for continuous improvement of healthcare products and services. We are an equal opportunity employer. We evaluate applications 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 characteristic. Know Your Rights: Workplace Discrimination is Illegal, click here . All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or other legally protected status. Compensation details: 24-28 Hourly Wage PI713dc0c7e5-