Job Opportunity: Operations Compliance / Quality Professionals
We are seeking two experienced professionals to join our internationally operating company in a regulated environment. In this pivotal role, you will support the laboratory organization in quality-related processes and actively contribute to ensuring GMP-compliant operations.
Job Description
- Manage QC-related deviations, root cause investigations, CAPAs, and change controls.
- Maintain and revise QC-specific controlled documents (e.g., test methods, SOPs, logbooks).
- Implement CAPA within agreed timelines and support training on procedures.
- Support data integrity activities and ensure correct, complete, and consistent documentation.
- Conduct or support QC-related risk assessments and mitigation activities.
- Monitor QC quality metrics (e.g., deviation trends, cycle times, data integrity observations).
- Collaborate with laboratory team leaders and QA to resolve quality issues promptly.
- Ensure proper implementation of changes impacting QC workflows, systems, or methods.
Qualifications
- Several years of experience in a pharmaceutical QC environment or in a regulated laboratory.
- Solid GMP knowledge.
- Experience in conducting investigations and root cause analyses.
- Structured, reliable, and detail-oriented working style.
- Experience with electronic quality systems and LIMS is an advantage.
- Strong documentation and communication skills.
- Fluent in English (written and spoken); proficiency in German or French is a plus.
Benefits
- Responsible and varied role.
- Short decision-making paths and direct communication.
- Collaborative environment with cross-functional teamwork.
- Opportunity to actively shape and further develop processes.
Apply online using the form below. Please note that only applications matching the job profile will be considered.