About the role

  • Quality Engineer for the Pharmaceutical Industry at Capgemini Engineering. Responsible for ensuring compliance and quality standards in pharmaceutical asset management processes.

Responsibilities

  • Responsible to integrate quality standards to mitigate failure mode risks during risk-based assessments
  • Responsible to ensure compliance of qualification activities
  • Responsible for review and approval of qualification documents
  • Responsible for review and approval of calibration and maintenance records
  • Responsible for review and approval of certification master data
  • Responsible for review and approval of master data E6 notifications (eStream), change controls records and quality issue/investigation records

Requirements

  • Master Engineering, Pharmacy or equivalent degree
  • Fluent in French/English
  • Experience in the Pharmaceutical industry
  • Knowledge of pharmaceutical legislation, cGMP regulations and guidelines in the area of system qualification
  • Knowledge of the different systems used during the manufacturing process
  • Strong analytical thinking, risk assessment and communication skills
  • Collaboration and teaming skills
  • Mindset for innovation and optimization

Benefits

  • Flexibility in more than one way: hybrid way of working
  • Work 70% from home
  • Flex abroad program: work up to 45 days abroad
  • array of career growth programs and diverse professions

Job title

Quality Engineer

Job type

Experience level

Mid levelSenior

Salary

Not specified

Degree requirement

No Education Requirement

Location requirements

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