Quality Assurance Operations Specialist

vor 22 Stunden


Visp, Schweiz Actalent Vollzeit

We are currently looking for a Quality Assurance Operations specialist that will be responsible for Drug Product QA-related inquiries and issues in manufacturing operations.

Key Responsibilities:

  • Serve as the primary contact for Drug Product QA-related inquiries and issues in manufacturing operations.
  • Maintain regular QA oversight on the shop floor.
  • Evaluate, review, and approve GMP documents and quality records, including SOPs, risk assessments, deviations, investigations, CAPAs, change controls, protocols, and executed MBRs.
  • Represent QA during internal, customer, and regulatory inspections and audits.
  • Provide GMP-related training to Operations personnel.

Key Requirements:

  • Master's degree in biotechnology or a related field.
  • 3-5 years of significant work experience in a GMP-regulated environment, particularly in aseptic manufacturing activities, preferably within a Quality Unit.
  • Proven experience collaborating with stakeholders across various departments and management levels.
  • Fluent in English; knowledge of German is an advantage.

Location: Visp

Duration: 12 months

If you are interested, apply directly or send me your CV at mbertrand@actalentservices.com.

*While we appreciate every application, please note that due to the high volume of responses, we may only be able to contact shortlisted candidates.

Seniority level

Associate

Employment type

Full-time

Job function

Quality Assurance

Industries

Pharmaceutical Manufacturing

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