Onsite Process Engineer I — Biopharma GMP

Initial Therapeutics, Inc.; West Lebanon (NH); On-site; USD 95,000 - 125,000; Full time

Benefits offered by this job

Annual bonus

Health insurance

Dental insurance

Vision insurance

401K with match

Parental leave 14 weeks

Product samples

Job summary

Novo Nordisk in West Lebanon, NH is seeking a Process Engineer to support production on the shop floor, ensuring cGMP compliance and accurate documentation. The role includes training technicians, participating in CAPAs and investigations, and coordinating process improvements across multiple teams.

The ideal candidate has a bachelor’s degree in engineering and 3+ years in biopharma processes, with strong communication skills and the ability to work alternating on-call hours.

Qualifications

• Bachelor’s degree in engineering or related discipline required.
• 3+ years related experience in pharmaceutical/biotech process preferred.
• Knowledge of GMPs and regulatory requirements (FDA/EU) preferred.
• Excellent written and verbal communication skills.
• Ability to work in a high-paced team-oriented environment and on-call support.

Responsibilities

• Assist with SOPs, JIs, DVs and other production documentation for shopfloor.
• Participate in development and implementation of procedural or automation improvements.
• Support day-to-day shopfloor issues and equipment troubleshooting.
• Write/review protocols, summaries and trend reports for ongoing production, verification, and validations.
• Coordinate scheduling of improvements within area and with outside vendors as needed.
• Represent Manufacturing in cross-functional teams and present material during audits.
• Participate in on-call rotations, including weekends.

Skills

cGMP knowledge

Documentation

Cross-functional collaboration

On-floor manufacturing support

Training and SOP development

Education

Bachelor’s degree in engineering

Tools

Automation systems

Job description

Novo Nordisk in West Lebanon, NH is seeking a Process Engineer to support production on the shop floor, ensuring cGMP compliance and accurate documentation. The role includes training technicians, participating in CAPAs and investigations, and coordinating process improvements across multiple teams.

The ideal candidate has a bachelor’s degree in engineering and 3+ years in biopharma processes, with strong communication skills and the ability to work alternating on-call hours.