Quality Assurance Engineer - Pharma Manufacturing

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View: 138

Update day: 10-04-2024

Location: Zug Zug ZG

Category: High Technology Mechanical / Technical Electrical / Electronics IT - Software

Industry: Staffing Recruiting

Position: Entry level

Job type: Contract

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Job content

Quality Assurance Engineer - Pharma Manufacturing - 5197 URAOur client, a dynamic global bio-pharmaceutical company headquartered in Switzerland, covering multiple therapeutic areas, is looking for a German speaking Quality Assurance Engineer on a contract based in the Schaffhaussenarea .Main Responsibilities
  • Represent QA Engineering in assigned qualification projects in the company.
  • Assure projects on qualification aspects in Pharma-/Chemical- and Solids-Manufacturing, in Optical Inspection, Device Assembly Packaging and Warehouses, all including Utilities, Monitoring systems and HVAC systems are compliable to internal and external requirements/guidelines.
  • Support QA Engineering in all aspects where needed depending on individual qualification.
  • Adherence to the above mentioned Adherence to all quality systems
  • Compliance with the GMP, EHS and SOX requirements and guidelines, which are connected to the respective function.
  • Support the qualification aspects of technical projects, assosiated with the entire life cycle of the system, implementation, testing/qualification and ongoing support, such as conducting appropriate event impact assessments, evaluating changes, up to the final retention period of records in the areas as mentioned in chapter 1
  • Assure review for compliance and approval of all critical qualification deliverables / documents (e.g. QP, URS, eFMEA, DQ, IQ, OQ, PQ, QSR & PM-Plans) in all areas mentioned above.
  • Provide input and supervision for appropriate qualification projects according to the current training status.
  • Provide input and support to measuring device qualification and their life cycle
  • Provide input and support to risk management system, such as eFMEA
  • Continuously observe, communicate and implement pro-actively possible areas for improvement
  • Attend trainings relevant to the successful execution of the function
  • Keep up to date of the current international industrial standards and new developments
Qualifications And Experience
  • Relevant working/residency permit or Swiss/EU-Citizenship required.
  • MSc (ideally) or BSc in a related field
  • At least five years of experience in a similar role in the pharmaceutical industry are a mandatory requirement
  • Fluent German is mandatory for the position
  • Flex model of work: 3 days at site, 2 home office (if the project allows it and upon agreement with the line manager)
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Deadline: 25-05-2024

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