Technical QA Manager managing QA across programs/projects at RDG, focusing on technical capabilities and automation delivery. Collaborating with stakeholders and internal teams to ensure successful QA services.
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
Job type
Experience level
Salary
Not specified
Degree requirement
No Education Requirement
Location requirements
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