Specialist Quality Assurance Position Available In Beaver, Pennsylvania

Aliquippa, PA
4 DAYS AGO
21516955
Summary
Aliquippa, PA
Competitive Salary
1 Years Experience
Bachelor’s degree
No Commisssion
40.00 hours per week / Day Shift /Full-Time
Description Innova Solutions has a client that is immediately hiring Specialist Quality Assurance Position type:

Full-time- Contract Duration:

18

Months Location:

Easton, PA 18045 (ONSITE) As Specialist Quality Assurance, you will:

Job Description:

The candidate will physically work on-site at a third-party GMP-compliant warehouse in Pennsylvania.

Expected hours:

8:00 AM to 5:00 PM, Monday-Friday. The ideal candidate will have 5+ years of QA experience specifically involving raw materials in a GMP-regulated environment such as pharmaceutical, biotech, or other life sciences industries. A bachelor’s degree is strongly preferred; master’s candidates may be considered, Strong attention to detail, comfort in a warehouse environment, and GMP compliance experience are essential.

Responsibilities:

Ensure operations align with applicable regulations and Client’s requirements relating to Good Manufacturing Practices, Good Distribution Practices, Good Documentation Practices, and Safety Collaborate with the LSP to ensure adherence to service levels, identifying performance improvement opportunities in alignment with the Operations READ framework (reliability, efficiency, agility, differentiation) Implement business continuity for services and processes Partner with key internal customer groups and/or outside vendors to ensure successful operations Participate / Conduct quarterly Client’s Business / Quality reviews and address service failures with the LSP Ensure metric targets are achieved and establish standardized mechanisms to measure progress against targets Understand and incorporate risk management strategy into overall supply chain strategy Ensure compliance with required training for staff supporting Client’s business Provide leadership, guidance, mentorship, and training to staff and partner groups Perform receipt, storage, and distribution documentation review to ensure alignment with procedures, current Good Manufacturing Practices (cGMP), Good Distribution Practices (GDP) and other applicable regulations Perform cGMP process, procedure, document and record review, and approval, including but not limited to deviations, CAPAs, change controls, risk assessment, and validation records Perform incoming raw material inspection, environmental monitoring, and documentation review Provide leadership updates regarding the health and initiatives relating to the QMS at site management reviews Preferred Qualific To view the full job description please use the link below.

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