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QA Specialist

Key information

  • Publication date:13 January 2025
  • Workload:100%
  • Contract type:Unlimited employment
  • Language:English (Intermediate)
  • Place of work:Upper Valais
On behalf of our client, we are seeking a detail-oriented Quality Assurance Specialist to join their team in Visp.
This role is critical in managing and optimizing Quality Systems within a GMP-regulated environment, ensuring compliance with regulatory requirements and internal standards.

Location: Visp, Switzerland
Contract Type: Contract
Duration: ASAP until 31/07/2025
Start Date: ASAP
Workload: 100%

Your Responsibilities:
* Collaborate with cross-functional teams to manage and execute Quality System-related projects within defined timelines.
* Draft, review, and finalize new procedures to ensure clarity, consistency, and alignment with organizational and regulatory requirements.

Your Background:
* Bachelor's (B.Sc.) or Master's (M.Sc.) degree in natural sciences or a related field.
* Significant work experience in a GMP-regulated environment, preferably within a Quality System unit.
* Proven ability to manage multiple tasks and interact effectively with diverse stakeholders.
* Strong proficiency in written and spoken English; German is an advantage.
* Expertise with Microsoft tools, particularly Excel and PowerPoint.

What's on Offer:
* An opportunity to contribute to the development and execution of Quality Systems within a renowned pharmaceutical organization.
* A collaborative and supportive work environment in Visp, a hub for cutting-edge pharmaceutical and biotech projects.
* Potential for professional growth and career development.
If you are passionate about Quality Systems and GMP compliance and meet the above requirements, we would love to hear from you!

For more information, please contact:
Veronika von Mentzer, Recruiter
Email: Write an email

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Contact

  • Swisslinx