Are you an experienced quality compliance specialist in analytical chemistry looking to make a direct impact on life-saving biopharmaceutical products? Join the Quality Control team in Basel to drive critical laboratory compliance, deviation investigations, and root-cause analyses. This is a fully site-based role, supporting close, real-time collaboration and technical precision needed to manufacture medicines to the highest quality and safety standards.
Start date: As soon as possible
Contract duration: 12 months
Location: Basel, Switzerland
Hours: 41 hours per week
Tasks
- Drive compliance and operational excellence within Quality Control analytical laboratories supporting biopharmaceutical manufacturing.
- Lead end-to-end deviation investigations, root-cause analysis (RCA), and author comprehensive Corrective and Preventive Action (CAPA) plans.
- Write, review, and manage Quality Change Requests and associated quality-relevant documentation to meet tight submission timelines.
- Act as a key compliance bridge between Quality Control (QC) analytical teams and central Quality Assurance (QA) stakeholders.
- Partner directly with lab technicians, conducting interviews and gathering analytical data across physico-chemical and bioanalytical workflows.
- Support compliance activities related to sample management processes and analytical instrument qualification protocols.
- Foster continuous process improvement within the QC track systems and mentor lab staff on data integrity standards.
Requirements
- Minimum 5 years of practical experience within analytical chemistry, bioanalytics, or a GMP laboratory environment.
- Proven expertise in authoring quality-relevant records, managing deviations, OOX investigations, and CAPA implementation.
- Strong practical knowledge of GMP principles, analytical methods, data integrity, instrument qualification, and sample management.
- Demonstrated hands-on experience performing structured root-cause analysis techniques in a laboratory setting.
- Bachelor's degree (BSc required; MSc or PhD preferred) in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related discipline.
- Professional business fluency in English (written and spoken) is required; basic German language skills are an advantage.
- Excellent interpersonal and communication skills to effectively collaborate with lab personnel and align with QA decision-makers.
Benefits
- An agile career and dynamic working culture.
- An inclusive and ethical workplace.
- Competitive hourly rate.
- Compensation for this role will be determined by the candidate’s qualifications, skills, experience, and relevant knowledge.
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