Quality Assurance Specialist (m/f/d)
- ID: 11625
- Temporary via nemensis ag, 100%
- Duration: 13/05/2024 bis 12/11/2025 (Verlängerung möglich)
- Salary: CHF 33 - 50.-/h
Responsibilities:
- Review manufacturing and analytical batch records for batches from the CHAD department (internal/external).
- Assist the Technical Regulatory Department and the New Chemical Entities Department with paper archiving.
- Oversee the timely release of documents and batches compliant with Good Manufacturing Practices (GMP).
- Contribute to departmental projects and objectives according to agreed timelines and standards.
- Maintain compliance with GMP in the Technical Regulatory Department.
Requirements:
- Technician with at least 5 years of experience or Bachelor's degree with at least 3 years of experience.
- Fluent in German and English (sufficient knowledge both oral and written).
- Communication skills to adequately address GMP and logistics-related questions with line unit experts.
- Scientific, technical, and regulatory knowledge in a specific area.
- Basic knowledge of drug development.
- Detailed knowledge of Good Manufacturing Practices, working knowledge of safety and environmental regulations and guidelines.
Benefits at nemensis ag:
- Nemensis ag is your specialized recruitment agency in the Life Sciences sector based in Basel.
- Comprehensive advice and support during the application process by our consultants.
- Access to a large customer network and exciting positions in Northwest Switzerland.
- Quick and straightforward entry through individual guidance and advice during the application process.
Are you passionate about making a difference in the life sciences? Reach out today and discover a range of opportunities that leverage your unique skills and advance your career!
Contact:
Jannis Reis
Junior Consultant
Write an email
Address
nemensis ag