Quality Assurance Associate II

Job content

One of our major clients is looking to strengthen their team with a Quality Assurance Associate to manage technical lot release activities for clinical and commercial GMP Intermediates, APIs, and Drug Products to ensure that disposition timelines are met.

Main Responsibilities

Coordinate release activities with the other team members

Review and assess the impact of deviations during batch record review related to manufacturing process as needed

Review executed batch production records to ensure compliance with approved procedures, quality agreements and GMP expectations

Perform activities connected with the CMO independent Batch Record Review certification program

Required Qualifications

Minimum of Bachelor’s degree in a scientific discipline (Chemistry, Microbiology, etc.) and 3 years’ experience in the pharmaceutical industry

Ability to travel domestically and internationally 5% of time

5 to 6+ years relevant GMP Experience

Knowledge and experience with US/EU GMPs, ICH and other applicable international regulations

Experience Working With CMOs (Contract Manufacturing Organizations) Preferred

If this sounds like you or someone in your network, please reach out to me.

Job Title: Quality Assurance Associate II

Location: Zug, Switzerland

Job Type: Contract

Aerotek and Actalent Services, an Allegis Group company. Allegis Group AG, Aeschengraben 20, CH-4051 Basel, Switzerland. Registration No. CHE-101.865.121. Aerotek and Actalent Services are companies within the Allegis Group network of companies (collectively referred to as "Allegis Group"). Aerotek, Actalent Services, Aston Carter, EASi, TEKsystems, Stamford Consultants and The Stamford Group are Allegis Group brands. If you apply, your personal data will be processed as described in the Allegis Group Online Privacy Notice available on our website.

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