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Talent Acquisition Specialist | Bsc(Hons) Business and Law
Contract: 01/07/2025 to 30/06/2026
Location: Basel
We are seeking an experienced QC Analyst to support drug product batch release, stability, and related testing activities in a GMP-regulated environment. The role involves independent execution of routine and validation physico-chemical assays (e.g., compendial, content, identity, purity testing) for biologics and large molecules. The successful candidate will demonstrate advanced analytical skills, operate under cGMP and GDP standards, and ensure timely, accurate data delivery. Responsibilities include lab operational support, troubleshooting equipment issues, SOP documentation, and readiness for audits. The role also contributes to lab optimization initiatives and continuous improvement efforts.
Job responsibilities:
* Experienced Analyst role for executing DP batch release/stability and related testing.
* Independently executes routine / validation phys-chem assays (e.g compendial/content/identity/purity for biologics/large molecules and related entities) in QC under cGMP following applicable SOPs and Good Documentation Practices (GDP) in a right first time and timely manner.
* Executes/reviews/approves basic operational tasks in the lab (e.g mobile phase preparations, calibration of pH meter, balance).
* Assists in investigation/troubleshooting lab equipment issues by proactively driving the investigation and proposing mitigation measures.
* Ensures lab clean/maintenance (inventory/consumables management process, 6S) to cGMP standards for audit readiness and supports onsite customer/regulatory audits.
* Supports draft/update of instrument SOPs.
* Participates and initiates as member in laboratory operational optimization and process improvement initiatives.
Key Requirements:
* EFZ, HF, CTA, BTA, PTA, BSc, Msc.
* Strong experience with Empower software v3.7 as Power user.
* +5 years working experience in a research/ technical role in the pharmaceutical or chemical industry, in analytical quality testing (QC).
* Demonstrable experience working in a cGMP-regulated environment in phys-chem analytics.
* Advanced scientific knowledge of phys-chem analytics performed in the lab.
* Experience in reporting, interpretation and documentation of scientific results.
* Good communication and inter-personal skills; Ability to work independently in a team.
* Good written and spoken English.
Seniority level
* Seniority level
Associate
Employment type
* Employment type
Contract
Job function
* Job function
Quality Assurance and Science
* Industries
Pharmaceutical Manufacturing
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