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
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