MES Project Manager - Pharmaceutical Industry
About Us: Inova is a premier consulting firm based in Switzerland, known for delivering cutting-edge solutions in the pharma industry. Our team of experts specializes in guiding pharma companies through complex regulatory landscapes and ensuring the highest standards of product quality and safety.
Job Description: The Project Manager – MES Implementation is responsible for leading the deployment of a Manufacturing Execution System (MES) within a regulated pharmaceutical environment. This role involves end-to-end project management, ensuring that the MES solution is implemented efficiently, on time, and in compliance with GMP standards. The Project Manager will coordinate cross-functional teams, manage stakeholders, and oversee system integration, ensuring seamless alignment with manufacturing operations.
Key Responsibilities:
1. Lead the planning, execution, and delivery of the MES implementation project, ensuring adherence to scope, budget, and timelines.
2. Define project objectives, milestones, and risk mitigation strategies in collaboration with IT, Manufacturing, and Quality teams.
3. Coordinate internal and external stakeholders, including MES vendors, system integrators, and validation teams.
4. Ensure compliance with GMP, GxP, and data integrity requirements throughout the project lifecycle.
5. Oversee system configuration, validation, and user training to facilitate a smooth transition to the new MES.
6. Drive project governance, ensuring alignment with global IT and manufacturing standards.
7. Identify and resolve potential project risks, ensuring proactive mitigation strategies.
8. Foster effective communication between technical and operational teams, ensuring seamless system adoption.
Qualifications & Experience:
1. Minimum 5 years of experience in MES implementation within the pharmaceutical or biotech industry.
2. Strong knowledge of GMP, GxP, and regulatory requirements for computerized systems.
3. Experience with leading MES platforms (e.g., Werum PAS-X, Rockwell PharmaSuite, Emerson Syncade).
4. Proven ability to manage cross-functional teams, including IT, manufacturing, and validation experts.
5. Expertise in project management methodologies (e.g., Agile, Waterfall, PMI standards).
6. Excellent problem-solving, risk management, and stakeholder engagement skills.
7. Fluent in English and French.
We Offer:
1. A dynamic work environment with opportunities to collaborate on high-impact projects in the pharmaceutical industry.
2. A commitment to professional growth and a supportive, multicultural team.
How to Apply: Interested candidates are invited to submit their CV through this form. Please include references and any relevant project details in your application.
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