Job Description
Piper Companies is looking for a Sr. Associate, QA who is responsible for performing QA activities in support of the quality system for a Therapeutic Manufacturer in Philadelphia, PA.
Responsibilities for the Sr. Associate, QA include:
• Initial review of SOPs, Work Instructions, Qualification, Validation and other reports and controlled documents
• Evaluate and investigate deviation reports
• Assist with implementation and validation of electronic QMS
• Review and approve executed batch records
Qualifications for the Sr. Associate, QA include:
• Bachelor's of Science Degree in a scientific/technical field (Chemistry, Biology, Microbiology, Engineering, etc.)
• 5+ years of GMP related experience, preferably in the early phase biologics or cell therapy
• Experience reviewing/revising GMP related documents including SOPs, Batch Records, Validation/Qualification reports, etc.
• Full understanding of regulatory requirements and QMS
• Experience with electronic system implementation and validation is a plus
Compensation for the Sr. Associate, QA include:
• Hourly Rate - Commensurate with experience
• Full benefits package:
o Medical, Dental, & Vision (Starts the 1 st of the month after start date)
o 2 weeks PTO, 6 Paid Holidays, 401k
o Subsidized Benefits through Piper Companies
Please send resume to Derek Herbine: - provided by Dice