CQV Engineer
vor 4 Wochen
About Capgemini Engineering
We value excellence, diligence, responsibility, dynamism, and innovation. Our diverse workplace offers training, tools, and foundations for professional and personal growth. We are seeking an experienced CQV Engineer to join our team.
Job Responsibilities
- Commissioning preparation, execution, and approval, including vendor supervision on testing scope and quality.
- Writing qualification documents, such as VP, IQ, OQ, PQ, and PPQ protocols and reports, risk assessments, and development protocols for utilities, facilities, and process equipment.
- Execution of DQ, IQ, OQ, PQ, including protocol deviations, investigation, and corrective action activities for utilities, facilities, and process equipment.
- Coordination and execution of FAT/SAT, commissioning activities for new GMP systems in collaboration with internal and external partners.
Requirements
- BSc/MSc Degree in Engineering or Science, preferably in Chemical, Mechanical, or Pharmaceutical Engineering or any related field.
- Minimum 3 years of experience in Commissioning and/or Qualification and/or Validation in the Pharmaceutical industry (Clean Utilities, Process Equipment, Systems).
- Excellent written and verbal communication skills, with the ability to prepare clear and concise documentation.
- Demonstrated ability to manage multiple projects and priorities in a fast-paced environment.
- Ability to work collaboratively in a cross-functional team environment.
- Fluency in English is a must.
Benefits
- Between 30% and 70% remote work in agreement with your manager and client needs.
- Options to order ergonomically proven equipment for your home-office premises.
- Support for trainings, formation upon agreement with the manager.
- Contribution on gym subscription.
- Trust-based managerial culture.
- Team rituals and get-togethers.
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