Associate Commissioning Engineer II, GMP Life Sciences

Novo Nordisk; West Lebanon (NH); On-site; USD 85,000 - 115,000; Full time

Benefits offered by this job

Annual bonus

Paid time off

Health/Dental/Vision

401(k) match

Parental leave

Product access

Job summary

Novo Nordisk's West Lebanon, NH site seeks a Facilities Engineer to support commissioning of new and existing equipment, processes and instrumentation in line with SRV and regulatory requirements. You will develop and execute commissioning protocols, assist in supplier selection, and ensure records meet cGMP standards.

This role works with Validation, Manufacturing, and Quality teams to drive successful SAT/FAT activities and ensure compliance, with on-site work Monday through Friday at the West

Qualifications

• Experience with data analysis and report writing.
• Entry level understanding of Validation and commissioning.
• Change control processes and cGMP documentation practices preferred.
• Excellent written and verbal communication skills.

Responsibilities

• Maintains proficiency of facilities, utilities, systems and equipment operations.
• Author and participate in commissioning protocols and execution; include SAT/FAT.
• Support creation and review of documentation in line with regulatory requirements.
• Collaborate with Validation and other teams to ensure timely deliverables.
• Provide SME input for commissioning activities and site validations.
• Support deviations and change requests related to commissioning activities.

Skills

Data analysis

Report writing

Validation concepts

cGMP documentation

Communication skills

Teamwork

Education

Associate's degree in life science or engineering

Bachelor's degree in life science or engineering

Job description

Novo Nordisk's West Lebanon, NH site seeks a Facilities Engineer to support commissioning of new and existing equipment, processes and instrumentation in line with SRV and regulatory requirements. You will develop and execute commissioning protocols, assist in supplier selection, and ensure records meet cGMP standards.

This role works with Validation, Manufacturing, and Quality teams to drive successful SAT/FAT activities and ensure compliance, with on-site work Monday through Friday at the West