Quality Assurance Specialist

vor 4 Wochen


BaselStadt, Schweiz nemensis ag Vollzeit
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  • 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



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