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QA Lot Review Specialist

Portsmouth, NH

Posted: 11/09/2020 Job Number: JN -112020-12186

Job Description

QA Lot Review Specialist

SRG offers flexible staffing solutions with a national presence. We provide contract, contract-to-hire, direct hire and executive search services. SRG utilizes an innovative approach to identify and qualify talent that is unique to the Staffing industry, featuring a cutting-edge platform that allows us to rapidly and precisely match professionals to client requirements. We have a proprietary database of over one million candidates and maintain continuous contact with our qualified talent.

Title: QA Lot Review Specialist
Location: Portsmouth, NH
Industry: Pharmaceutical
Shift Hours: 8am - 5pm - Mon - Fri
Salary: $21.00 Based on Experience
Employment Type: 6 month Contract (Benefits Available)

Environment: A global leader and trusted supplier in the pharma, biotech and specialty ingredients markets. Headquartered in Basel, Switzerland, the company is focused on advanced manufacturing, high-quality control systems, regulatory expertise, and research and development (R&D) capabilities. The company s products and services include active pharmaceutical ingredients (API), stem cell therapies, drinking water sanitizers, vitamin B compounds, organic personal care ingredients, industrial preservatives and microbial control solution to combat viruses, bacteria and other dangerous pathogens.

Key Accountabilities and Duties:
  • The primary responsibility of the Quality Assurance Lot Review Specialist I is to review and closeout of all production batch documentation prior to release.
  • Documentation includes manufacturing batch records and ancillary documentation such as Lot Genealogy Reports, and QC assays used in the production of Active Pharmaceutical Ingredients (API).
  • The Quality Lot Review Specialist I makes decisions regarding routine tasks that arise during review of records and escalates to senior members of the team for complex issues; develops a skill set appropriate to the level that includes understanding quality systems, manufacturing practices, Good Documentation Practices, as well as effective communication and listening

EOE/ADA
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