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MSP Lead | MSP Partnering at Aristo Group | Empowering Life Science with the Perfect Match
As a Senior QA Specialist, you will support the implementation of a new Fill & Finish and Visual Inspection area and contribute to routine GMP operations. You'll ensure compliance with cGMP standards, manage deviations, and maintain high-quality documentation.
Type of employment: Payroll
Skills: Quality Assurance,Fill and Finish
Project start: 01.08.2025
Key Responsibilities
- QA support for new Fill & Finish/Visual Inspection setup
- Oversight of routine GMP activities in sterile production
- Review and approval of GMP documents (SOPs, protocols)
- Deviation and CAPA management in TrackWise
- Ensure data integrity and compliance with regulatory standards
- Support audits, batch reviews, GMP tours, and process improvements
- Maintain training compliance and system access rights
Qualifications
- Master’s degree (or equivalent) in a scientific field
- 2–3 years' QA experience in GMP sterile manufacturing
- Strong knowledge of production processes and quality systems
- Proficient in French and English (written and spoken)
Seniority level
Employment type
Job function
Job function
Quality Assurance
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