Senior Validation Specialist
2 weeks ago
About the Role
We are seeking a highly skilled Senior Validation Specialist to join our team at AtkinsRéalis. As a key member of our CQV group, you will provide technical and project leadership in the pharmaceutical industry, with a focus on design/build/validation processes and cGMP regulation requirements.
Your Responsibilities
- Develop and review technical documentation for clients in regulated industries, including qualification and validation protocols and reports.
- Coordinate and execute testing of systems and processes to assess compliance against requirements.
- Analyze test data and collect samples, where required.
- Operate testing equipment and troubleshoot issues of diverse scope.
- Provide recommendations on equipment/process operation/optimization.
- Support the CQV group to meet department goals and objectives.
Why Choose AtkinsRéalis?
We offer a dynamic work environment, competitive pay, flexible benefits, an employee share plan, and a defined contribution pension plan. Our team is committed to health and safety, and we prioritize work-life balance.
Requirements
- Bachelor's degree in chemical or mechanical Engineering or a related Science program.
- Thorough knowledge of cGMP and regulatory requirements for validation.
- Minimum of 8 years relevant work experience, demonstrating knowledge of validation principles, including validation planning, user requirement and functional specifications, commissioning, IQ, OQ, PQ.
- Strong knowledge of utilities and general production systems used in pharmaceutical manufacturing.
- Excellent verbal and written communication skills.
- Proficient in English (oral/written), French knowledge (an asset).
What We Offer
We are committed to diversity and inclusion, and we seek individuals with diverse characteristics, backgrounds, and perspectives. If you are a motivated and experienced professional looking for a new challenge, please apply today.
AtkinsRéalis is an equal opportunities employer.
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