Ready for your next role in QC in the biopharmaceutical industry?
About the Client
Our client is a global leader in life sciences, operating in a modern, fast-paced hub in Basel, Switzerland. Known for their cutting-edge research and high-quality standards, they provide a collaborative environment where professionals can contribute to the development of innovative biologics and therapeutic solutions. The company's strong commitment to excellence and continuous improvement makes them a sought-after employer for those looking to grow their careers in the biotechnology, pharmaceutical, food, or chemical industries.
Job Description
Our client is looking for an experienced QC Analyst to join their team in Basel. In this role, you will be responsible for performing analytical testing of biologics and large molecules in compliance with cGMP standards. Your work will include executing phys-chem assays, maintaining lab equipment, and contributing to quality and process improvements. This is a hands-on position where accuracy, attention to detail, and the ability to work independently are essential.
Responsibilities
- Perform analytical testing on biologics and related products, including identity, purity, and content assays
- Follow cGMP and Good Documentation Practices (GDP) when conducting tests and recording results
- Prepare and maintain laboratory solutions and materials (e.g., mobile phases, pH meter calibration)
- Troubleshoot and support resolution of equipment and testing issues, proposing solutions
- Contribute to lab organization by managing inventory, consumables, and maintaining a clean workspace
- Support drafting and updating of equipment and instrument SOPs
- Participate in process improvements and lab optimization projects
- Assist with on-site audits and ensure the lab meets inspection readiness standards
Requirements
- Minimum 5 years of experience in analytical quality testing (QC) within the pharmaceutical or chemical industries
- In-depth knowledge of physico-chemical analytics and working under GMP regulations
- Proficient in Empower 3.7 software
- Strong skills in scientific reporting, data interpretation, and documentation
- Ability to work independently while contributing to a team environment
- Good communication skills and fluency in written and spoken English
- Experience supporting audits and maintaining compliance standards
Benefits
- 1 year contract through Oxford Global Resources.
- Work at a pharmaceutical leader in a state of the art facility.
- Competitive salary.
