QA Lot-Review Specialist II (GMP)

A global life sciences company is looking for a QA Specialist II to ensure accurate review of manufacturing batch records and documentation compliance. Role requires attention to detail and experience in GMP environments. The ideal candidate has 3-5 years in Quality Assurance, strong organizational skills, and familiarity with Good Documentation Practices. This position offers a competitive benefits package including bonuses, insurance, and 401(k) matching. Join a dedicated team at the forefront of life sciences innovation. #J-18808-Ljbffr