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QC Analyst

Portsmouth, NH

Posted: 10/18/2020 Job Number: JN -102020-12095

Job Description

QC ANALYST 1

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: QC ANALYST 1
Location: Portsmouth, NH
Industry: Pharmaceutical
Shift Hours: Monday-Friday 8-4:30 (some flexibility with the start time)
Salary: $24.13 Based on Experience
Employment Type: Long Term 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.

Job Summary:
The QC Analyst I will act as a team member of the Quality Control department to support production of in-process and final product drug lots for customers and ongoing stability studies. Provide on-time, high quality results to meet manufacturing demands. Testing includes pH, osmolality, UV-Vis, and conductivity. In addition to testing, routine responsibilities include but are not limited to reagent preparation, cleaning glassware, and cleaning and organization of the lab

Minimum Required Qualifications/Skills
  • Running test samples for In-process, Lot Release, and Stability studies.
  • Reviewing assays
  • Writing- Quality Records (Deviations, CAPA, Change Control) and Test Methods
  • Training others
  • 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 field
  • 0-2+ years industry experience, preferably in a cGMP environment

EOE/ADA

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