Position: Entry level

Job type: Full-time

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Job content

Do you have some years of experience in Quality Assurance in pharmaceutical environments? Do you have knowledge in validation/qualification, deviation, and CAPA management? Then you should read the following lines!

One of our clients, an international pharmaceutical company, is looking for a:

Quality Assurance Officer

Contact type: permanent

Location: Neuchatel Canton

Your Tasks

  • Monitoring data and key performances indicators in order to insure continuous improvement of the quality system
  • Complaints and Deviation management
  • Quality investigations and definition of CAPAs
  • Supplier qualification for finished and semi-finished products, materials, raw materials and their periodic requalification
  • Issuance of Master Batch Records, and validation and qualification protocols and reports
  • Definition of standard operating procedures and GMP-related documentation along with other involved units/ department Managers
  • Execution of batch record review, validation, and qualification of equipment utilities and machines
  • Involvement in self- and third parties’ inspections
  • Issuance of GMP related documents (risk analysis, technical reports, etc.)
  • Change Control

Your Profile

  • Bachelor/Master degree in related technical science (Chemistry, Pharmacy, Engineering, or equivalent)
  • Already experience in the Pharmaceutical field, Production or Quality Assurance. Experience gained preferably in small-medium Pharmaceuticals with marketing authorization (GMP certificated) released by the local health authorities.
  • Knowledge of the pharmaceutical industry
  • Expertise in injectables production both aseptic and terminally sterilized processes advantageous
  • French and English Fluent
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Deadline: 25-05-2024

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