GMP QA Validation Specialist - Contract (Switzerland)

CTC Resourcing Solutions; Wallis; Vor Ort; CHF 105.000 - 145.000; Vollzeit

Zusammenfassung

CTC Resourcing Solutions is seeking a QA Validation Specialist for a contract role in the Valais region of Switzerland. The position focuses on ensuring GMP equipment, facilities and systems are properly qualified, validated and maintained in a compliant state.

Responsibilities include QA oversight of validation activities, change control assessments, and reviews of SOPs and validation documentation. The candidate should bring extensive CQV expertise and fluency in English with German language

Qualifikationen

• 15–20 years of experience in GMP-regulated pharmaceutical manufacturing sites.
• Experience with IQ/OQ/PQ lifecycle and validation.
• Familiar with EU GMP and FDA regulations.
• English proficiency and good German level.
• Residency permit or Swiss/EU citizenship required.
• Academic background in science or engineering preferred.

Aufgaben

• Oversee QA reviews of validation activities to ensure GMP equipment, facilities and systems remain validated.
• Maintain qualification status through change control and documentation reviews.
• Schedule tasks and coordinate with Validation Manager for Level 1 activities.
• Perform change control assessments to ensure regulatory compliance.
• Demonstrate understanding of IQ/OQ/PQ and validation procedures for equipment and facilities.
• Develop validation protocols from validation plans when applicable.
• Review SOPs, validation protocols, reports, deviations and CAPAs with rigor.
• Support audits and inspections to demonstrate facility and system compliance with EU GMP and FDA regulations.
• Assist in continuous improvement initiatives.

Kenntnisse

Quality Assurance / CQV

GMP experience

English proficiency

German language

Ausbildung

Science or technical degree (Engineering, Biotechnology, Chemistry, Biology, Pharmacy)

Jobbeschreibung

CTC Resourcing Solutions is seeking a QA Validation Specialist for a contract role in the Valais region of Switzerland. The position focuses on ensuring GMP equipment, facilities and systems are properly qualified, validated and maintained in a compliant state.

Responsibilities include QA oversight of validation activities, change control assessments, and reviews of SOPs and validation documentation. The candidate should bring extensive CQV expertise and fluency in English with German language