Our client is a globally leading company in the development and manufacturing of biological pharmaceuticals. At the Lucerne site, innovative biotechnological processes are developed and implemented for clinical and commercial manufacturing.

To support the Process Engineering team, our client is looking for a senior-level professional who thrives in a GMP-regulated environment, is technology-driven, and enjoys collaborating in an international setting.

Key Responsibilities

• Lead and coordinate technical innovation projects in a GMP-compliant biotech environment
• Evaluate and implement new technologies, systems, and equipment for biologics manufacturing
• Prepare technical documentation such as user requirement specifications (URS) and CAPEX requests
• Support harmonization of batch and continuous manufacturing processes
• Contribute to GMP documentation including SOPs, risk assessments, qualification protocols, etc.
• Collaborate closely with local and global teams (e.g. US, Ireland)
• Act as a change agent, driving digitalization and improved ways of working

Profile

• Degree in a technical or life sciences field (e.g. bioengineering, process engineering, biotechnology)
• Minimum 5 years of experience in the biotech or pharmaceutical industry
• Proven experience in project management with cross-functional and global teams
• Solid understanding of Upstream and Downstream processes and GMP compliance
• Fluent in English (C1); German skills (B1) are advantageous
• Proactive, independent, and solution-oriented working style

What We Offer

• Work in a highly modern and innovation-driven GMP manufacturing environment
• Collaborate with global experts and contribute to next-generation biotechnological solutions
• Independent role with strong technical impact and visibility
• Competitive salary, structured onboarding, and long-term development opportunities