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Job content

Job Title:

QC Specialist

Job Description:

Mission:

Provide direct support to the team for the QC batch disposition in due time with the right level of quality and compliance. Ensure the daily management of QC deviation and investigation for the chemical team

Your responsibilities will be:

  • Supervises the daily work for lab event, deviation and phase I investigation. This include support for the investigation, record in the defined system, evaluation and closure with QA

  • Reviews and approves analytical test results for completeness and accuracy using LIMS

  • Changes lot status using LIMS/ERP

  • Monitors results for trends; and implement Change Control, CAPAs as needed using QA Track

  • Develops and maintains applicable laboratory procedures, test methods, specifications, documentation and records

  • Support for the training of Team members

  • Applies Lean techniques with Team members. Ensure and control the respect to the defined standard

  • Participates in Lab Audits and Inspections

  • Ensures the laboratory is kept in a safe working environment and in compliance with OSHA and other requirements and other laboratory safety standards

Required profile:

  • Preferably with 5-10 years of laboratory experience in Pharmaceutical or Chemical industry

  • Pharmacist, Chemist/Biochemist/Engineer or equivalent with 5+ years’ relevant experience within pharmaceutical industry with experience in Medical Device and Microbiology

  • Preferably Experience with GMP documents and guidelines

  • Advanced knowledge of analytical methods and testing required

  • Demonstrated knowledge of GMPs, FDA and other regulatory requirements is required

  • Be familiar with electronic systems

  • Language: French

  • English is a must

Location:

Switzerland SMP - St Prex
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Deadline: 04-05-2024

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