We are looking for a Compliance Manufacturing Specialist for our client based in Corsier-sur-Vevey, for a 5-month assignment.
Your role:
As a Compliance Manufacturing Specialist, you will play a key role in supporting Manufacturing Operations on all quality and compliance aspects.
You will lead and support compliance activities across Dispensing, Media/Buffer, USP, and DSP areas, ensuring operational excellence and adherence to GMP standards.
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You will contribute to deviation management, CAPA definition and implementation, and compliance process improvements.
You will support Batch Record review using MES, as well as the introduction and evaluation of new raw materials and consumables.
You will participate in HACCP and risk analyses, ensuring that manufacturing operations meet internal and external quality expectations.
You will also define and maintain material specifications in close collaboration with Quality Assurance and Manufacturing teams.
Your contribution will directly support product quality, process robustness, and regulatory compliance within a dynamic biotech environment.
Your profile:
- Technical diploma, Bachelor’s, or Engineering degree in Biotechnology, Biochemistry, or related field.
- 2–5 years of experience in a biotech or pharmaceutical manufacturing environment.
- Good knowledge of USP/DSP processes and GMP requirements.
- Ideally, prior experience in Quality Assurance or a compliance-related role.
- Familiarity with IT tools such as MS Office, Trackwise, SAP, MES, and LIMS.
- Fluent in French and English (written and spoken).
- Excellent teamwork and communication skills, able to work effectively with diverse stakeholders.
- Strong commitment to quality, continuous improvement, and a culture of feedback.
