Deviation Investigation Level 3 - Night Shift

Lonza Group

Portsmouth, NH, US
Not specified; performance-related bonus available...
3rd shift (night shift)
Bachelor's degree in life sciences or engineering
5-7 years gmp regulated environment experience
Advanced root cause analysis tools proficiency
Lonza Group is seeking a Deviation Investigation Level 3 professional for a night shift position in Portsmouth, NH. This role requires leading complex investigations in a cGMP environment, providing technical guidance and mentorship, while offering a competitive benefits package

Job Summary

  • The Deviation Investigator III leads complex deviation investigations and drives high-quality, compliant outcomes within a cGMP environment.
  • This role provides strategic guidance to teams, mentors Level I and II investigators, and ensures strict adherence to data integrity standards.
  • Candidates receive a comprehensive benefits package including performance bonuses, medical insurance, 401(k) matching, and paid time off.

Matching Summary

Match Score: 85

Lonza Group is seeking a Deviation Investigation Level 3 professional for a night shift position in Portsmouth, NH. This role requires leading complex investigations in a cGMP environment, providing technical guidance and mentorship, while offering a competitive benefits package.

Salary

Not specified; Performance-related bonus available; Benefits include medical, dental, vision, 401(k), life, disability, and PTO

Skills & Requirements

Must-have

  • Bachelor's degree in Life Sciences or Engineering
  • 5-7 years GMP regulated environment experience
  • Advanced root cause analysis tools proficiency
  • cGMP and data integrity standards adherence
  • Strong technical writing skills for compliance

Nice-to-have

  • Experience with biologics manufacturing processes
  • Mammalian manufacturing process knowledge
  • Cross-functional collaboration and influencing skills
  • Continuous improvement mindset
  • Ability to manage high volume concurrent investigations

Key Requirements

  • Bachelor's degree required
  • 5-7+ years QA/GMP experience
  • Expertise in CAPA development
  • Proficiency in Microsoft Office suite

Work Rights

Not specified

Tailored Resume

Cover Letter