黑料传送门

QC Analyst (junior)

Highly Competitive
  1. Contract
  2. Good Manufacturing Practice (GMP)
  3. Switzerland
Neuchâtel, Switzerland
Posting date: 27 Oct 2025
67468

Step into the heart of Swiss pharma as a Junior QC Analyst-where your precision, French fluency, and GMP expertise ensure quality from sample to solution.

黑料传送门 is seeking a QC Analyst (Junior) for a contract role based in Switzerland. In this role, you will act as the primary point of contact for QC laboratories, ensuring the timely provision of samples, stabilities, and articles required for analysis. This position involves variable working hours, including occasional weekend shifts and on-call periods. Proficiency in French is essential for this role.

Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.

Responsibilities:

  • Manage and process samples for analysis, including control, aliquoting, identification, recording, distribution, storage, or destruction, adhering to operational procedures and Good Manufacturing Practices (GMP).
  • Ensure proper reception, processing, and distribution practices as outlined in protocols and procedures.
  • Document and report any deviations observed during sample receipt to relevant departments.
  • Accurately record and complete attributes for each sample in the appropriate system within defined deadlines.
  • Handle backup samples, including receiving, recording, transferring, outputting, and destruction as per requests and procedures.
  • Coordinate the shipment of samples to external sites or regulatory authorities following established schedules and guidelines.
  • Prepare cryotubes for production area sampling when required.
  • Participate in validation protocols and stability studies, managing samples from reception to analysis or stabilization and destruction.
  • Manage laboratory consumables and reagents, ensuring timely orders and stock replenishment.
  • Perform regular maintenance and calibration of equipment, monitor temperature alarms, and ensure proper documentation in logbooks.
  • Support QC teams with non-testing tasks such as solution preparation, freezer transfers, and autoclaving activities.
  • Adhere to and promote EHS (Environmental, Health, and Safety) rules, addressing any observed deviations.

Key Skills and Requirements:

  • Fluency in French is mandatory.
  • Strong understanding of Good Manufacturing Practices (GMP).
  • Ability to manage and process samples accurately and efficiently.
  • Experience with laboratory equipment maintenance and calibration.
  • Organizational skills to manage consumables and reagents inventory.
  • Flexibility to work variable hours, including one weekend per month and on-call periods.
  • Commitment to maintaining high-quality standards and adherence to EHS regulations.


If you are having difficulty in applying or if you have any questions, please contact Molly Colclough at m.colclough@proclinical.com.



Apply Now:

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