About the Role
<p>................</p><p>For our client in Zurich, we are looking for an experienced <strong>Senior GMP Manufacturing & AI Advisor (remote).</strong></p><p>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.</p><p><strong>Your Tasks:</strong></p><ul><li>Analyze the end-to-end autogenous vaccine development process and identify operational bottlenecks, inefficiencies, and decision-making challenges</li><li>Assess opportunities for AI-driven solutions, including predictive analytics, document automation, workflow optimization, and decision support systems</li><li>Develop and prioritize AI initiatives based on feasibility, business value, and implementation potential</li><li>Support the establishment of a regulatory-compliant organization aligned with current and emerging AI regulations</li><li>Evaluate manufacturing sites and recommend pilot locations based on maturity assessments and operational readiness</li><li>Conduct stakeholder interviews and present executive-level recommendations and roadmaps</li><li>Contribute to the development of pilot programs and scalable AI deployment strategies within GMP-regulated environments</li></ul><p> </p><p><strong>Your Profile:</strong></p><ul><li>12+ years of hands-on GMP manufacturing experience within the pharmaceutical, biotech, or animal health industry</li><li>Proven operational experience in Production, Quality Assurance, MS&T, or Engineering, including batch execution, deviation management, and regulatory inspections</li><li>Demonstrated experience delivering AI or advanced analytics use cases within GMP environments during the last 24 months</li><li>Expertise in Generative AI or AI agent solutions within GxP-regulated processes</li><li>Strong knowledge of AI/ML validation, data integrity, and compliance frameworks including GAMP 5, CSA, 21 CFR Part 11, EU Annex 11, and ALCOA+</li><li>Experience conducting manufacturing site assessments and advising senior leadership teams</li><li>Up-to-date knowledge of evolving AI-related pharmaceutical regulations and GMP requirements</li><li>Excellent communication and stakeholder management skills, with the ability to present complex topics to executive audiences</li><li>Fluent in English</li></ul><p>Find more <a href="https://www.arbeitnow.ch/english-speaking-jobs">English Speaking Jobs in Switzerland</a> on Arbeitnow</a>