Senior GMP Manufacturing & AI Advisor (remote)
Company: Coopers Group AG Agency
- Location: Zurich, Switzerland
- Work mode: Remote
- Seniority: Senior
- Posted: 4 days ago
- Offer language: English
Job description
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For our client in Zurich, we are looking for an experienced Senior GMP Manufacturing & AI Advisor (remote).
We are looking for an professional who combines deep GMP manufacturing expertise with hands-on experience in Artificial Intelligence within regulated pharmaceutical environments. The ideal candidate will act as a trusted advisor, helping to identify, assess, and implement AI-driven improvements across manufacturing and quality processes.
Your Tasks:
- Analyze the end-to-end autogenous vaccine development process and identify operational bottlenecks, inefficiencies, and decision-making challenges
- Assess opportunities for AI-driven solutions, including predictive analytics, document automation, workflow optimization, and decision support systems
- Develop and prioritize AI initiatives based on feasibility, business value, and implementation potential
- Support the establishment of a regulatory-compliant organization aligned with current and emerging AI regulations
- Evaluate manufacturing sites and recommend pilot locations based on maturity assessments and operational readiness
- Conduct stakeholder interviews and present executive-level recommendations and roadmaps
- Contribute to the development of pilot programs and scalable AI deployment strategies within GMP-regulated environments
Your Profile:
- 12+ years of hands-on GMP manufacturing experience within the pharmaceutical, biotech, or animal health industry
- Proven operational experience in Production, Quality Assurance, MS&T, or Engineering, including batch execution, deviation management, and regulatory inspections
- Demonstrated experience delivering AI or advanced analytics use cases within GMP environments during the last 24 months
- Expertise in Generative AI or AI agent solutions within GxP-regulated processes
- Strong knowledge of AI/ML validation, data integrity, and compliance frameworks including GAMP 5, CSA, 21 CFR Part 11, EU Annex 11, and ALCOA+
- Experience conducting manufacturing site assessments and advising senior leadership teams
- Up-to-date knowledge of evolving AI-related pharmaceutical regulations and GMP requirements
- Excellent communication and stakeholder management skills, with the ability to present complex topics to executive audiences
- Fluent in English
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