Deviation Investigation Level 2 - Day Shift

Lonza Group

Portsmouth, NH, US
Not specified; performance-related bonus available...
Day shift (12-hour rotating schedule)
Lead deviation investigations in cgmp environment
Apply root cause analysis tools like 5 whys
Develop corrective and preventive actions capas
Lonza Group is seeking a Deviation Investigator Level 2 for their Portsmouth, NH office, focusing on leading deviation investigations in a cGMP environment. The role involves mentoring junior investigators and utilizing root cause analysis tools to ensure compliance and effective corrective actions

Job Summary

  • The Deviation Investigator II is responsible for leading and executing deviation investigations within a cGMP environment to identify root causes.
  • This role offers a comprehensive benefits package including performance-related bonuses, medical insurance, and a 401(k) matching plan.
  • Candidates will mentor Level I investigators while managing a moderate workload of concurrent investigations with a target of over 80% Right First Time completion.

Matching Summary

Match Score: 85

Lonza Group is seeking a Deviation Investigator Level 2 for their Portsmouth, NH office, focusing on leading deviation investigations in a cGMP environment. The role involves mentoring junior investigators and utilizing root cause analysis tools to ensure compliance and effective corrective actions.

Salary

Not specified; Performance-related bonus available; Medical, dental, vision, 401(k), life, disability, PTO included

Skills & Requirements

Must-have

  • Lead deviation investigations in cGMP environment
  • Apply root cause analysis tools like 5 Whys
  • Develop corrective and preventive actions CAPAs
  • Maintain data integrity and Good Documentation Practices
  • Mentor junior investigators on investigation quality

Nice-to-have

  • Experience with biologics or mammalian processes
  • Strong cross-functional collaboration skills
  • Proactive solution-oriented mindset
  • Ability to navigate conflict effectively
  • Proficiency in Microsoft Office suite

Key Requirements

  • Bachelor's degree in Life Sciences or Engineering
  • 3-5+ years experience in GMP-regulated environment
  • Proven experience leading deviation investigations
  • Strong technical writing and documentation skills

Work Rights

Not specified

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