Beschreibung

An exciting new 6-month opportunity has arisen to join us as Quality Assurance Process Validation for our Biotech drug substance plant in Corsier-sur-Vevey.

Your role: 

• Coach and assure quality systems are applied in a consistent manner
• Approve Quality Plans and Validation Master Plan and periodic reviews
• Assure correct implementation of CCPs and adequate handling of deviations and CAPAs in order to ensure the validated status
• Assure that GMP documentation is up to date and well applied
• Review, approve and maintain risk analysis
• Define, develop and support implementation and control compliance with corporate an MSSA Vevey standards
• Assure QA presence on regular project meetings
• Develop the execution strategy including rules & procedures for commissioning, qualification or validation of projects
• Develop the execution strategy including rules & procedures validation/qualification, review and approve protocols and reports
• Ensure that general procedures MSSA-Vevey are in line with GMP/Merck Serono guidelines
• Ensure and maintain an adequate level of qualification and validation for all systems and products through the validation master plan
• Review and approved protocols and reports from BPS/MFG related to process development and validation
• Follow deviations and change control linked to validation/qualification projects 

  Who you are:

  • University postgrade degree in Science or Engineering
  • Knowledge of cGMP regulations
  • At least 2 years’ experience in a quality environment in pharmaceutical industry or equivalent, ideally in biotechnology
  • Good interpersonal skills, with a positive attitude and the ability to support his colleagues in a context of growth and changes
  • Good writing skills.
  • French & English written & spoken.