• 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