Msat Process Engineering Lead

Institutehumanbiology

Unknown
Process engineering in biomanufacturing
Single-use technology implementation
Cgmp compliance and validation
The MSAT PE Lead/Subject Matter Expert is a pivotal technical role designed for talented individuals who bring unparalleled expertise in developing and integrating advanced biomanufacturing processes

Job Summary

  • The MSAT PE Lead/Subject Matter Expert is a pivotal technical role designed for talented individuals who bring unparalleled expertise in developing and integrating advanced biomanufacturing processes.
  • This role drives end-to-end process engineering projects across greenfield projects and routine operations, reducing time-to-market, improving efficiency, and ensuring excellence throughout the product lifecycle.
  • Roche fosters a culture of personal expression, open dialogue, and genuine connections, valuing and respecting each individual to thrive both personally and professionally.

Matching Summary

The MSAT PE Lead/Subject Matter Expert is a pivotal technical role designed for talented individuals who bring unparalleled expertise in developing and integrating advanced biomanufacturing processes.

Skills & Requirements

Must-have

  • Process engineering in biomanufacturing
  • Single-use technology implementation
  • cGMP compliance and validation
  • Process monitoring and troubleshooting
  • Facility design and qualification
  • Cross-functional collaboration
  • Operational efficiency improvements

Nice-to-have

  • Strategic project leadership
  • Continuous improvement mindset
  • Global team collaboration
  • Strong communication skills
  • Creative leadership abilities
  • Agile methodologies

Key Requirements

  • Bachelor’s Degree in Pharmaceutical or Biological sciences preferred
  • Minimum 5 years process engineering experience
  • At least 8 years MSAT/technical or operational experience in injection pharmaceutical industry
  • Experience in aseptic filling facility design and qualification
  • Hands-on new facility startup and operational ramp-up experience
  • Comprehensive knowledge of cGMP and pharmaceutical regulations
  • Fluent English communication skills

Work Rights

Not specified

Tailored Resume

Cover Letter