CQV Engineer m / f / w
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3930 Visp, Switzerland |
Temporary Employment
We are seeking a highly skilled CQV Engineer to support the validation of equipment, systems, and facilities in accordance with cGMP standards. The role involves drafting and executing IQ/OQ/PQ protocols, coordinating equipment installation, and preparing comprehensive validation documentation.
Project title: CQV Engineer m / f / w
Type of employment: Payroll
Industry: Biotech
Skills: commissioning and qualification,Validation (IQ/OQ/PQ)
Project start: ASAP
Project duration: 30.04.2026
Location: 3930 Visp, Switzerland - 100% onsite
Tasks:
- Coordinate commissioning and qualification activities for facilities, utilities, and equipment
- Draft and execute IQ/OQ/PQ protocols
- Prepare validation documentation including URS, DQ, FMEA, Risk Assessments, FAT, SAT
- Write detailed reports of completed validation activities
- Identify efficiencies and improvements in validation processes
- Stay updated on regulatory changes affecting equipment and facility validation
- Support Quality Systems: Document Management, Change Control, Non-Conformities, CAPAs
- Write and revise engineering procedures
- Assist in developing validation, requalification, and maintenance programs
- Perform other duties as assigned
Qualifications:
- Bachelor’s degree in a scientific or technical field
- Minimum 5 years of experience in the pharmaceutical industry
- Strong technical writing and documentation skills
- Excellent communication and organizational abilities
- Fluent in German; English is a plus
Referenznummer: 16737
Branche: Biotech
Beginn des Projekts: ASAP
Dauer: 30.04.2026
Anstellungsart: Temporary Employment
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