QC Expert

Reference Number: 895722-W
Type of placement: Contract, 12 Months
Location: Switzerland, North West

Introduction:

One of our clients, a global pharmaceutical company, is currently looking for a QC Expert.

Main Responsibilities:

  • Maintains and builds contacts with external experts, e.g. Global Quality Organization, Technical Research and Development, RegCMC, Supply Chain Management, Health Safety & Environment etc. and ensures fast and direct communication channels
  • Provides scientific and technical expertise on QA/QC procedures within other organizations
  • Maintains and adheres to cGMP, SOPs, CAPA
  • Prepares, participates in and conducts authority inspections and audits
  • Ensure uniform GMP standards through regular exchange with central QA function
  • Initiate revision, validation and improvement of GMP documents e.g. testing monographs, SOP's, qualification and validation documents
  • Provide input to health authority requests
  • Manage investigations regarding product quality (e.g. OOS/OOE, deviations, customer complaints)
  • Procures validation support; supports launches
  • Local and global project participation or lead
  • Maintains state-of-the-art knowledge of Health Authority requirements, trends, technologies, processes and systems
  • Implementation of business process improvements with impact on time, quality and costs 
  • Keep timelines (e.g. availability of documentation, qualification, validation, batch release, investigations) 
  • Successful implementation of cross-functional projects

Qualifications and Experience:

  • University or academic degree in Chemistry, Biology, Pharmacy or equivalent
  • At least 5 years of experience in chemical/pharmaceutical industry
  • Solid knowledge of GMP guidelines and working knowledge of safety and environmental regulations
  • Fluent in both German and English required (adequate knowledge oral & written)
  • Relevant working/residency permit or Swiss/EU-Citizenship required

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