Validation & Data Integrity Specialist

Validation & Data Integrity Specialist – Contract

Location: Visp, Switzerland (Hybrid – 3 days onsite, 2 days remote)

Contract: Initial 6 months

Hours: Full-time

Start Date: ASAP

About the Opportunity

Meet Life Sciences is currently supporting a pharmaceutical client based in Visp, Switzerland, who is looking for an experienced Validation & Data Integrity Specialist to join an ongoing GMP inspection readiness programme.

This is an initial 6-month contract opportunity, supporting validation activities, data integrity compliance and the preparation of manufacturing systems and processes for regulatory inspections.

Key Responsibilities

• Support GMP validation and qualification activities across manufacturing equipment, facilities, utilities and systems.
• Review and execute validation documentation, including IQ, OQ and PQ protocols.
• Assess data integrity compliance in line with GMP requirements and ALCOA+ principles.
• Identify validation and compliance gaps, supporting remediation activities ahead of regulatory inspections.
• Review deviations, CAPAs and change controls related to validation activities.
• Support inspection readiness activities, ensuring validation documentation is accurate, complete and compliant.
• Collaborate with Quality Assurance, Manufacturing, Engineering and Validation teams to address compliance risks.
• Support the review of computerised systems and associated validation documentation where required.

Requirements

• Previous experience in validation or qualification within a GMP pharmaceutical or biotechnology manufacturing environment.
• Strong understanding of GMP regulations and validation principles.
• Hands-on experience with IQ, OQ and PQ documentation and execution.
• Knowledge of data integrity requirements and ALCOA+ principles.
• Experience supporting GMP inspections, audits or remediation projects.
• Familiarity with deviations, CAPAs, risk assessments and change control.
• Experience with computerised system validation (CSV) would be advantageous.
• Ability to work independently in a fast-paced GMP manufacturing environment.

Contract Details

• Initial 6-month contract
• Full-time engagement
• 3 days onsite in Visp, Switzerland, with 2 days remote
• ASAP start

Interested?

If you have experience in GMP validation, qualification or data integrity within pharmaceutical or biotechnology manufacturing, I'd be happy to discuss the opportunity further.

Please reach out directly or send your CV to learn more.