Commissioning Qualification Validation Specialist
vor 1 Monat
Our client in Visp is seeking a Commissioning Qualification Validation (CQV) Engineer to support their CAPEX project on a temporary contract, with a minimum duration of 6 months and potential for extension or transition into a permanent role.
Key Responsibilities:- Coordinate equipment installation and validate facilities and utilities.
- Develop and execute IQ/OQ/PQ protocols in accordance with cGMP requirements.
- Generate validation documentation, including URS, DQ, FMEA, Risk Assessments, FAT, SAT, and various protocols.
- Write comprehensive reports detailing validation activities.
- Identify opportunities to improve validation processes and implement efficiencies.
- Participate in Quality Systems activities, such as Document Management, Change Control, Non-Conformities, and CAPA's.
- Support the Engineering team in preparing validation, requalification, and maintenance programs.
- Bachelor's Degree in a Science or Technical field.
- 3-6 years of experience in an advanced level within the Pharma industry.
- Proficient in technical writing with a keen attention to detail.
***Please only apply if you are eligible to work in Switzerland and the EU.***
***Please forward your application should you meet the requirements above – applications which do not meet these requirements will not be considered.***
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