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QC Specialist

Portsmouth, NH

Posted: 01/05/2021 Job Number: JN -072020-11801

Job Description

QC SPECIALIST I

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.

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 Scope:
Title: QC Specialist I
Location: Portsmouth, NH
Industry: Pharmaceutical
Hours: Sun - Wed 4x10hr shifts
Salary: $24.50hour paid weekly (Benefits Available)
Employment Type: 12-month contract


Key Responsibilities:
Running test samples for In-Process, Lot Release and Stability studies.
Provide on-time, high quality results to meet Manufacturing demands.
Reviewing and running of assays.
Writing- Quality Records (Deviations, CAPA, Change Control) and Test Methods.

Key Requirements:
Bachelor or Associates Degree. Preferred area of study in Microbiology, Biochemistry or Related Science field.
Working experience running and reviewing assays- Bioburden, endotoxin, TOC.
Some industry experience, preferably in a cGMP environment.
Use of Laboratory computer systems and Microsoft Suites (Word, Excel, Powerpoint).
Prior use of GMP Quality Systems such as: TrackWise, LIMS preferred.
Solid communication skills, both written and verbal.
Ability to work independently on assign tasks, within timeframes, as well as work within a team environment.
Working experience in process related tasks, data interpretation and independent and team problem solving.

1-3 Years Experience

EOE/ADA

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