Associate Specialist Upstream Operations (m/f/d)

Shape the Future of Biologics Bring Your GMP Expertise to the Next Level

Duration: ASAP – 1 year (temporary)

About Our Client

For our client, an innovative and internationally oriented biotech company in the greater Lucerne area, we are looking for an experienced Associate Specialist Upstream Operations (m/f/d). The company specialises in the GMP-compliant manufacturing of biological drug substances for early-phase clinical trials, leveraging cutting-edge technologies and a strong commitment to continuous innovation in biopharmaceutical production.

Your Responsibilities

• Hands-on execution and troubleshooting of upstream manufacturing processes in a GMP-regulated environment
• Drafting, updating, and technical review of SOPs and electronic master batch records related to process transfers and GMP manufacturing
• Active contribution to continuous improvement ...