The Specialist QC Compliance acts as a Subject Matter Expert (SME) responsible for ensuring that Quality Control (QC) processes adhere to regulatory requirements, cGMP expectations, and site procedures. The role focuses on driving continuous improvement, maintaining data integrity, and managing quality events within a fast-paced biotechnology or pharmaceutical environment.
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Job details
Summary
- Yverdon-les-Bains, Vaud
- Temporary
Posted 28. may 2026
- Reference number
- 25208
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Margot Ferraton
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Job details
Role Overview: Specialist QC Compliance
Key Responsibilities
Quality Systems Management: Oversee, document, investigate, and close quality events. Ensure the timely execution of deviations, root cause analyses, CAPAs, change controls, and periodic reviews.
Data Integrity: Coordinate the QC Data Integrity Plan, conduct risk assessments, implement mitigations, and deliver data integrity training to the team.
Equipment & Validation: Support the qualification and validation of QC equipment and related software (URS, protocols, risk assessments, reports). Track equipment work orders, maintenance, and calibration records.
Operational Support: Assist with QC sample management (reception, aliquoting, LIMS entry), material release, and monthly reviews of environmental monitoring system (EMS) alarms.
Documentation & Audits: Author, review, and maintain SOPs and related quality documents. Participate in audit/inspection readiness and address any observations.
Regulatory Watch: Monitor and coordinate the implementation of regulatory and pharmacopoeial updates.
Candidate Requirements
Education: MSc in Biotechnology, Pharmaceuticals, Engineering, or equivalent industry experience.
Experience: Minimum 5 years in a GMP environment, with at least 3-5 years specifically in Quality Control.
Technical Skills: Deep expertise in quality systems (Deviations, CAPA, Change Controls), hands-on equipment software qualification, and strong troubleshooting abilities.
Soft Skills: Proactive, rigorous, and team-oriented with a proven ability to build trust and work in highly regulated environments.
Languages: Fluent in both French and English (C1 level or equivalent).
Role Overview: Specialist QC Compliance
The Specialist QC Compliance acts as a Subject Matter Expert (SME) responsible for ensuring that Quality Control (QC) processes adhere to regulatory requirements, cGMP expectations, and site procedures. The role focuses on driving continuous improvement, maintaining data integrity, and managing quality events within a fast-paced biotechnology or pharmaceutical environment.
Key Responsibilities
Quality Systems Management: Oversee, document, investigate, and close quality events. Ensure the timely execution of deviations, root cause analyses, CAPAs, change controls, and periodic reviews.
Data Integrity: Coordinate the QC Data Integrity Plan, conduct risk assessments, implement mitigations, and deliver data integrity training to the team.
Equipment & Validation: Support the qualification and validation of QC equipment and related software (URS, protocols, risk assessments, reports). Track equipment work orders, maintenance, and calibration records.
Operational Support: Assist with QC sample management (reception, aliquoting, LIMS entry), material release, and monthly reviews of environmental monitoring system (EMS) alarms.
Documentation & Audits: Author, review, and maintain SOPs and related quality documents. Participate in audit/inspection readiness and address any observations.
Regulatory Watch: Monitor and coordinate the implementation of regulatory and pharmacopoeial updates.
...
Candidate Requirements
Education: MSc in Biotechnology, Pharmaceuticals, Engineering, or equivalent industry experience.
Experience: Minimum 5 years in a GMP environment, with at least 3-5 years specifically in Quality Control.
Technical Skills: Deep expertise in quality systems (Deviations, CAPA, Change Controls), hands-on equipment software qualification, and strong troubleshooting abilities.
Soft Skills: Proactive, rigorous, and team-oriented with a proven ability to build trust and work in highly regulated environments.
Languages: Fluent in both French and English (C1 level or equivalent).
