CQV Engineer

Company : Headcount Ag

Job Type : Full Time

Kanton Wallis

Number of Applicants

:

000+

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Job Description - CQV Engineer

Commissioning Qualification Validation Engineer Our client in Visp is seeking a Commissioning Qualification Validation (CQV) Engineer to join their team on a temporary contract to support their CAPEX project.

This role involves a diverse array of tasks centered around validating equipment and facilities, ensuring compliance with cGMP standards. As a CQV Engineer, you will oversee the installation of equipment, develop validation protocols, execute validation procedures, and meticulously document results. 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.
Requirements:
Bachelor’s Degree in a Science or Technical field.
5-10 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*** headcount AG