QC Analyst (m/f/d)

Start date: asap
Reference number: 762054/1
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Your responsibilities

  • Sample storage and management
  • Analytical testing and documentation of API / drug substance / drug product / finished product / Complaints / stability / packaging material samples
  • Ensure all activities in compliance with cGxP, incl. data integrity
  • Stability (when not centralized)
  • Testing/Sample storage and management
  • Analytical documentation of stability samples to cGxP standards
  • Perform and document lab analysis (standard and more complex techniques)
  • Support analytical investigations and OOx
  • Implementation of innovative DP/DS methods from development
  • Participation in co-validation activities or analytical transfers

Your profile

  • Bachelor (or Master) in Biology or molecular Biology (no PHD needed)
  • Experience in GMP 
  • Comitted to work in 6/4 shift model

Your benefits

  • A very renowned company

About Hays

With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – completely free of charge. Register with us and reap the benefits of interesting job offers that match your skills and experience.

Staffing process for freelance specialists

  1. Analysis of qualifications
  2. Telephone or personal interview
  3. Contact with customers
  4. Contract with Hays
  1. 1    
  2. 1. Analysis of qualifications

    We carry out a detailed analysis of your technical qualifications on the basis of your CV, your application documents and your profile.

  3. 2
  4. 3
  5. 4

Your contact at Hays

+41 44 225 50 00
Reference number : 762054/1
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