Associate Commissioning Engineer, Life Sciences (GMP)

BioSpace

West Lebanon (NH)

On-site

USD 90,000 - 130,000

Full time

6 days ago
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Benefits offered by this job

Competitive pay + annual bonus
36 paid days off
Health, dental, vision insurance
8% 401K match
Paid parental leave
Product access

Job summary

Novo Nordisk is seeking a Facilities Engineering specialist at the West Lebanon, NH bioproduction site. The role focuses on commissioning activities, SRV-driven validation, and collaboration with production, validation, and quality teams to ensure compliant protocols and successful project delivery.

The position emphasizes experience in GMP environments, data analysis, and documentation, with opportunities for career growth and mentorship within NN’s global manufacturing network.

Qualifications

  • Associate degree with two years of related experience required.
  • Bachelor's degree with one year related experience preferred.
  • Pharmaceutical process or biotechnology experience preferred.
  • Knowledge of data analysis and cGMP documentation practices.

Responsibilities

  • Author and participate in commissioning protocols and execution for utilities, equipment and instrumentation.
  • Support development of SRV-based validation activities and site acceptance/testing where applicable.
  • Ensure compliance of commissioning records and documentation with FDA, EMA, and NN requirements.
  • Collaborate with cross-functional teams (Validation, Manufacturing, Engineering, Facilities and Quality).
  • Provide SME input and data for change controls and protocol reviews.

Skills

Data analysis
Report writing
Communication skills
Team collaboration

Education

Associate's degree in life science or engineering
Bachelor's degree in life science or engineering

Job description

Novo Nordisk is seeking a Facilities Engineering specialist at the West Lebanon, NH bioproduction site. The role focuses on commissioning activities, SRV-driven validation, and collaboration with production, validation, and quality teams to ensure compliant protocols and successful project delivery.

The position emphasizes experience in GMP environments, data analysis, and documentation, with opportunities for career growth and mentorship within NN’s global manufacturing network.

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