CQV Engineer: GMP Validation in Life Sciences (Switzerland)

EFOR; Basel; Vor Ort; CHF 110.000 - 140.000; Vollzeit

Zusammenfassung

EFOR Group in Switzerland seeks a CQV Engineer to support pharma/biotech projects. You will oversee commissioning, qualification and validation for GMP facilities, equipment, utilities and laboratory systems, collaborating with Engineering, Quality, Manufacturing, Automation and vendors.

The on-site role requires a degree in Engineering or life sciences, CQV experience with IQ/OQ/PQ, and GMP lifecycle knowledge. Fluent English is required; German is an advantage.

Qualifikationen

• Experience in CQV, Qualification, Validation within a regulated environment.
• Knowledge of GMP requirements and validation lifecycle.
• Experience with IQ, OQ, and PQ protocol execution.
• Strong problem-solving and organizational skills.
• Excellent communication and teamwork; fluent English; German a plus.

Aufgaben

• Plan, execute, and document qualification activities for GMP systems.
• Develop, review, and execute IQ/OQ/PQ protocols.
• Support FAT and SAT activities.
• Collaborate with cross-functional teams and external vendors.
• Ensure GMP compliance and participate in audits.
• Identify opportunities for process improvements.

Kenntnisse

CQV

IQ/OQ/PQ

GMP knowledge

Documentation & Compliance

Ausbildung

Bachelor's or Master's degree in Engineering/ Biotechnology/ Pharmaceutical Sciences

Jobbeschreibung

EFOR Group in Switzerland seeks a CQV Engineer to support pharma/biotech projects. You will oversee commissioning, qualification and validation for GMP facilities, equipment, utilities and laboratory systems, collaborating with Engineering, Quality, Manufacturing, Automation and vendors.

The on-site role requires a degree in Engineering or life sciences, CQV experience with IQ/OQ/PQ, and GMP lifecycle knowledge. Fluent English is required; German is an advantage.