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Manufacturing Associate Upstream | Manufacturing Associate in Job Job at Quality Consulting Group 1

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Manufacturing Associate Upstream

Location:
Thousand Oaks, CA
Description:

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.Responsibilities: Work in a dynamic production environment at site supporting development, clinical, and launch activities. Work within the Cell Banking group and will perform operations for cell bank production. Hands on operations in support of Cell Bank production in a clean room environment. A bulk of the operations occur in a Grade 5 hood and requires additional gowning and strict adherence to aseptic practices. Prepare media per defined manufacturing procedures (MPs) and standard operating procedures (SOPs) Follow GMP documents (SOPs, MPs) with strict adherence to safety and compliance Perform and monitor critical processes and able to interpret data to understand process performance Perform in process sampling of cell culture flasks and operate analytical equipment Work in a clean room environment wearing full clean room gowning, hairnet and latex gloves when performing all work. Initiate quality deviation records Draft and revise documents (SOPs, MPs) Identify, recommend, and implement improvements related to routine functions Assist in the review of paper and electronic documentation for assigned functions (equipment logs, batch records) Qualifications: Bachelor’s degree in Science or Engineering 4 years of related experience Able to follow all applicable SOPs and documentation as dictated in a safe manner Effectively work in teams and communicates and escalates issues as necessary Adept at learning technical processes regarding Cell Culture, equipment, documentation, and more Knowledge in Aseptic technique in Cell Culture, Positive attitudes/social skills, Strong work ethic. Mechanically inclined Sterile GMP Manufacturing for buffer/media preparation. Day shift 8am-4:30pm Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity,, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law. Powered by JazzHR
Company:
Quality Consulting Group
Industry:
Manufacturing
Posted:
June 18 on The Resumator
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