In this role, you'll focus on validating equipment and facilities to ensure compliant, reliable operations. You will manage CQV activities across facilities, utilities, and systems, and maintain documentation for regulatory review. You’ll collaborate with cross-functional teams to drive QA activities and continuous process improvements.

Start Date: ASAP

Duration: 6 Months

Place of Work: Visp

Key Responsibilities

  • Prepare validation documents
  • Execute IQ/OQ and PQ for equipment, systems and utilities
  • Write reports of completed validation activities
  • Work to identify efficiencies in the validation program approach
  • Apply lessons learned and stay informed of regulatory changes as it applies to equipment/facility validation
  • Perform assigned Quality Systems activities (Document Management, Change Control, Non-Conformities, CAPAs)
  • Write and/or revise procedures related to Engineering activities
  • Support the Engineering group to prepare the validation, requalification, and maintenance program
  • Perform other duties as assigned

Candidate Profile

  • Bachelor’s Degree in Science or Technical field
  • Work Experience: Advanced level in the pharmaceutical industry, 5–10 years
  • Excellent technical writing
  • Thorough and timely documentation
  • Proficiency in English and German, strong written and oral communication
  • Ability to work effectively across departments

  • Excellent organization and time management

     

Job ID 41181220