Description

On behalf of our client, we are looking for a QA Validation Expert to support validation activities in a GMP-compliant pharmaceutical environment. The selected candidate will play a key role in ensuring regulatory compliance and quality oversight of processes and equipment, working in close collaboration with technical departments to support ongoing and upcoming validation projects.

 

Location: Neuchâtel, Switzerland

Contract Duration: 07/04/2025 – 31/05/2025 (Temporary contract via Randstad, with possible extension)

Work Mode: 100% Onsite

Position: QA Validation Expert

 

On behalf of our client, we are looking for a QA Validation Expert to support validation activities in a GMP-compliant pharmaceutical environment. The selected candidate will play a key role in ensuring regulatory compliance and quality oversight of processes and equipment, working in close collaboration with technical departments to support ongoing and upcoming validation projects.

 

Main Responsibilities:

• Review of Validation Protocols
• Assess protocols related to equipment, processes, CIP, SIP, computerized systems, and HVAC/Utilities
• Ensure alignment with GMP standards, internal quality procedures, and international regulations (FDA, EMA, etc.)
• Validation Report Review
• Evaluate test results to confirm all protocol requirements are met
• Identify deviations and propose appropriate corrective actions
• Quality Support
• Collaborate with cross-functional teams (Production, Engineering, Validation) to ensure quality integration
• Provide quality input during project meetings

   

  Required Profile:

  • Education:
  • Degree in Pharmacy, Biotechnology, Chemistry, or another scientific discipline
  • Experience:
  • Minimum 2 years in a similar role within the pharmaceutical industry
  • Hands-on experience in validation of process, equipment, CIP/SIP, computerized systems
  • Experience with filling lines and freeze-dryers is a strong asset
  • Technical Skills:
  • Solid knowledge of GMP and regulatory guidelines (FDA, EMA, ICH)
  • Familiarity with IQ/OQ/PQ protocols and risk assessment methodologies
  • Soft Skills:
  • Excellent attention to detail and strong analytical skills
  • Effective communicator, able to interact with cross-functional stakeholders
  • Solution-oriented mindset with the ability to manage several priorities under pressure
  • Fluency in English and French is a strong advantage

     

    What’s in it for you:

    • Contribute to high-impact validation projects in a reputable pharmaceutical company
    • Gain valuable experience in GMP and regulatory-driven environments