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Open nowPosted 7 days ago

Senior Quality Assurance Specialist

Coopers Group AG

Where
Wallis, Switzerland
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Your applicationOpen nowSenior Quality Assurance SpecialistCoopers Group AG · Wallis, Switzerland

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  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

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The clock on this job

Early applications get read.

14.0% of postings close within 7 days. Measured by our own scanner across the market. Coopers Group AG postings stay open a median of 4 days.

Share of postings closed within
  1. 2.3%1 day
  2. 4.7%3 days
  3. 14.0%7 days
  4. 22.5%14 days
  5. 38.3%30 days
  6. 59.0%60 days
This job: posted 7 days ago

Coopers Group AG median: 4 days open

The posting

  • Life Sciences - Quality Management
  • Wallis
  • Contracting
  • Teilzeit
  • Immediately - 31.05.2027
  • Quality Assurance, cleanroom, Quality Control

Location: Visp

Contract start date: immediately

Contract end date: 31 May 2027

Responsibilities

  • Provide Quality oversight for environmental monitoring, with a particular focus on EM PQ as part of cleanroom qualification.
  • Support the preparation and review of environmental risk assessments, qualification protocols, reports, and trend reports.
  • Review environmental monitoring results, identify adverse trends, and ensure appropriate follow-up of alert and action limit excursions.
  • Support investigations into monitoring excursions and contamination incidents, including root cause assessment and corrective and preventive actions.
  • Support cleanroom hygiene practices, including cleaning and disinfection, gowning, personnel behavior, and material transfers.
  • Collaborate with Manufacturing, Quality Control, Engineering, and Quality Assurance to address contamination risks and improve cleanroom control.
  • Contribute to procedures, change assessments, and continuous improvement activities related to environmental monitoring and cleanroom hygiene.
  • Support regulatory inspections and customer audits within your area of expertise.

Requirements

  • Bachelor-s degree in microbiology, biology, biotechnology, or a related scientific discipline, or an equivalent relevant qualification.
  • 6+ years of Experience of relevant experience in Quality Assurance, Quality Control Microbiology, environmental monitoring, or cleanroom manufacturing in a pharmaceutical or biotechnology environment.
  • Practical understanding of environmental monitoring, microbiological contamination control, and cleanroom hygiene.
  • Working knowledge of Good Manufacturing Practice (GMP) requirements.
  • Ability to review and interpret data, investigate issues, and develop practical solutions.

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