QC Analyst II 0708

Portsmouth, NH

Posted: 11/09/2020 Job Number: JN -122020-12301

Job Description

QC Analyst II

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.

QC Analyst II
Location: Portsmouth, NH
Industry: Pharmaceutical
Shift Hours: 8am - 5pm - Mon - Fri
Salary: $29.85 Based on Experience
Employment Type: 12 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 QC Analyst II will act as a team member of the Quality Control department to support production of in-process and final product drug lots for customers. Also participate in quality testing for ongoing customer stability studies. Provide on-time, high quality results to meet Manufacturing demands.

A QC Analyst II: Applies job skills and company's policies and procedures to complete a variety of tasks. Works on assignments that are semi-routine in nature where ability to recognize deviation from accepted practice is required. Works on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors.

Running test samples for In-Process, Lot Release and Stability studies
Reviewing assays
Writing- Quality Records (Deviations, CAPA, Change Control) and Test Methods
Adherence to cGMPs is required at all times during the manufacture of APIs. All personnel own the quality of what they deliver and are responsible for notifying responsible management in a timely manner of regulatory inspections, serious GMP deficiencies, process deviations, product defects and related actions.

Bachelor or Associates Degree

Preferred area of study: Microbiology, Biochemistry or Related Science

2-4+ years industry experience, preferably in a cGMP environment
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