Jobs

    CQV Engineer - Visp, Schweiz - headcount AG

    headcount AG
    headcount AG Visp, Schweiz

    vor 4 Stunden

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    Ganztags
    Beschreibung
    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
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