For our client Merck based in Aubonne, we are looking for a QA Engineering Expert for a duration of 9 months (until 31.12.2024).
Your role:
Ensure that equipment & automated systems implemented are in accordance with internal procedures and current guidelines/regulations (including procedures related to change, risk and deviation management)
Support Equipment and Automated Systems deviation management.
Support, review and approve change control proposal (CCP) as QA engineering for projects
Participate to risk assessments
Review and approve quality documents (design documents, validation plans & summary reports, procedures, protocols, data reviews, reports and procedural documents)
Ensure that validation, calibration and preventive maintenance programs are in place and are respected
Routine activities:
Review and approve quality documents (operational documents, procedures, forms, intervention report for automation activities) for equipment and automated systems activities
Ensure support for deviations related to equipment and automated systems including QA assessment, investigation and CAPA review / approval and closure
Ensure that periodical technical interventions programs are in place and respected.
Participate to annual reviews as required.
Ensure QA activities in SAP-PM system: equipment/system and maintenance plans creation /modification/removal
Support department to guarantee that equipment and automated systems procedures and forms are understandable and easy to complete and review.
Participate to seminars and training sessions on equipment and automated systems qualifications best practices to maintain "state-of-the-art" in-house expertise.
Ensure backup of the QA engineer for project and routine activities
For our client Merck based in Aubonne, we are looking for a QA Engineering Expert for a duration of 9 months (until 31.12.2024).
Your role:
Ensure that equipment & automated systems implemented are in accordance with internal procedures and current guidelines/regulations (including procedures related to change, risk and deviation management)
Support Equipment and Automated Systems deviation management.
Support, review and approve change control proposal (CCP) as QA engineering for projects
Participate to risk assessments
Review and approve quality documents (design documents, validation plans & summary reports, procedures, protocols, data reviews, reports and procedural documents)
Ensure that validation, calibration and preventive maintenance programs are in place and are respected
Routine activities:
Review and approve quality documents (operational documents, procedures, forms, intervention report for automation activities) for equipment and automated systems activities
Ensure support for deviations related to equipment and automated systems including QA assessment, investigation and CAPA review / approval and closure
Ensure that periodical technical interventions programs are in place and respected.
Participate to annual reviews as required.
Ensure QA activities in SAP-PM system: equipment/system and maintenance plans creation /modification/removal
Support department to guarantee that equipment and automated systems procedures and forms are understandable and easy to complete and review.
Participate to seminars and training sessions on equipment and automated systems qualifications best practices to maintain "state-of-the-art" in-house expertise.
Ensure backup of the QA engineer for project and routine activities
See what comes ahead in the application process. Find out how we help you land that job.
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apply with randstad.
Applying with us is easy. We will review your application and see if you are a good fit for the job and the company.
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we'll contact you.
Our consultant will call you at a suitable time to discuss your application and further career aspirations.
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getting you registered.
If you’ve never worked with us before, we’ll need some basic additional pieces of information to confirm your eligibility to work in Switzerland.
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compliance, reference and background check.
Next, we just need to verify a few things - we’ll make the relevant compliance checks and and in ensuring you’re perfect for the role, we’ll make contact with any relevant references you’ve provided and will keep you posted.
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the perfect job for you.
Our expert team will either arrange an interview for the role you’ve applied for, or if they believe there’s a better opportunity, they’ll suggest alternative options too.
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the interview.
We’ll ensure that you’re fully prepared ahead of your interview and know exactly what to expect - good luck!
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start your new job.
Congratulations, you’re ready to begin your new job. The team will ensure that you’re fully prepared for your first day.
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ongoing support.
After starting your new mission, we will contact you to check how you are doing and make sure you have our support in your new role.
Within the scope of a challenging, ambitious and future-oriented project driven by a dynamic team in an inspiring environment, we look for a QA laboratory equipment/system specialist.Your Role :· Define the laboratory equipment/systems quality strategy including data integrity aspects· Review and approval of GxP documents, including URS, traceability matrix, risk assessments, systems drawings, procedures, qualification documents…· Collabo
Within the scope of a challenging, ambitious and future-oriented project driven by a dynamic team in an inspiring environment, we look for a QA laboratory equipment/system specialist.Your Role :· Define the laboratory equipment/systems quality strategy including data integrity aspects· Review and approval of GxP documents, including URS, traceability matrix, risk assessments, systems drawings, procedures, qualification documents…· Collabo
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