Job Summary
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This is a leadership role that involves managing and optimizing day-to-day team performance and workflow. You will oversee validation activities, starting from user definition in collaboration with business partners to the final handover of laboratory equipment to the business.
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The ideal candidate will have strong experience in cleaning, process equipment, and delivering solutions in a pharmaceutical setting. They will also have excellent understanding of GxP regulations, 21 CFR Part 11, Eudralex Annex 11 or other international requirements.
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Main Responsibilities
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* Lead and oversee validation activities for GIO
* Coach, train, and mentor team members on project-related topics
* Monitor team workload and ensure deadlines and quality are met
* Plan and prioritize workloads, resources, and timelines to ensure efficient project execution
* Continuously assess and adapt workflows to enhance performance and quality of deliverables
* Ensure compliance with international regulations and internal procedures
* Perform technical review of validation documentation (if needed)
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Requirements
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* Bachelor's or master's degree related to Life Sciences, Computer Science, Automation, Bioengineering, or related study
* Strong experience in cleaning, process equipment
* At least 5 years of experience in a pharmaceutical with a focus on delivering solutions
* Excellent understanding of GxP regulations, 21 CFR Part 11, Eudralex Annex 11 or other international requirements
* Proficiency in French and English, both written and spoken
* Proven experience as Project and/or Team Coordinator
* Excellent leadership and team management abilities
* Strong communication skills to engage and align with stakeholders at all levels
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About Us
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We are a dynamic organization that values innovation, teamwork, and excellence. We offer a supportive environment where you can grow and develop your skills and career.
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