Responsible Person Dir Quality Assurance (m/f/d)

MSD (Merck)

Lucerne, Switzerland
Quality role in sterile manufacturing
Experience in regulatory inspections
Strong project management skills
The Biologics drug substance manufacturing facility at Schachen is a premier, state-of-the-art facility that enables and advances our best work

Job Summary

  • The Biologics drug substance manufacturing facility at Schachen is a premier, state-of-the-art facility that enables and advances our best work.
  • The Site RP is a key member of the Quality Leadership Team, ensuring compliance with Swissmedic expectations.
  • This role requires strong collaboration and communication skills to develop a strong working relationship across functional areas.

Matching Summary

The Biologics drug substance manufacturing facility at Schachen is a premier, state-of-the-art facility that enables and advances our best work.

Skills & Requirements

Must-have

  • Quality Role in Sterile Manufacturing
  • Experience in Regulatory Inspections
  • Strong Project Management Skills

Nice-to-have

  • Cross-Functional Team Collaboration
  • Mentoring and Coaching Skills
  • Creativity in Problem Solving

Key Requirements

  • Bachelor’s degree in Life Science
  • 10+ Years Experience in Quality Role
  • Eligible as Responsible Person as per I-SMI.TI.17

Work Rights

Not specified

Tailored Resume

Cover Letter