Operations Compliance​/Quality Specialist; m​/f

Your expertise is in demand: univativ connects you with companies that rely on professional competence and solid know-how. Whether you want to enrich your career with exciting projects, contribute your knowledge in responsible positions, or develop yourself in a new environment.

For an internationally operating company in a regulated environment, we are looking for two experienced professionals in the area of Operations Compliance / Quality. In this role, you will support the laboratory organization in quality-related processes and actively contribute to ensuring GMP-compliant operations.

• Manage QC-related deviations, root cause investigations, CAPAs, and change controls
• Maintain and revise QC-specific controlled documents (e.g., test methods, SOPs, forms, 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

• 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

• 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
• Very structured, reliable, and detail-oriented working style
• Experience with electronic quality systems and LIMS is an advantage
• Strong documentation and communication skills
• Fluent English (written and spoken);
  German or French is an advantage