Biotech Project Engineer — GMP Systems (Onsite NH)

Novo Nordisk; West Lebanon (NH); On-site; USD 90,000 - 120,000; Full time

Job summary

Novo Nordisk in West Lebanon, NH, seeks a Project Engineer to support GMP manufacturing projects and capital and process improvements. You will work with the Project Engineering team and cross-functional colleagues, coordinating with vendors and contractors to drive safe, compliant project execution.

On-site role 5 days a week, you will develop ideas, write protocols, lead troubleshooting, and participate in risk assessments while ensuring alignment with FDA/EU requirements and Novo Nordisk

Qualifications

• Knowledge of Automation, GMPs, Compliance and Regulatory requirements is essential.
• Excellent communication skills and ability to work in a high-paced team environment.
• Employee must remain accessible during on-call period and respond within sixty (60) minutes.

Responsibilities

• Lead process and equipment troubleshooting to support deviations and corrective actions.
• Ensure systems and processes are validated in accordance with FDA, EU and NN requirements.
• Participate in development and implementation of procedural or automation improvement changes.
• Participate in design and hazard reviews of plant expansions or process changes and serve as the technical point of contact for contractor services.
• Plan and execute activities according to timeline and in a compliant manner.

Skills

Automation knowledge

GMPs & regulatory knowledge

Communication skills

On-call availability

Education

Bachelor’s degree in engineering

Master’s degree in engineering

Job description

Novo Nordisk in West Lebanon, NH, seeks a Project Engineer to support GMP manufacturing projects and capital and process improvements. You will work with the Project Engineering team and cross-functional colleagues, coordinating with vendors and contractors to drive safe, compliant project execution.

On-site role 5 days a week, you will develop ideas, write protocols, lead troubleshooting, and participate in risk assessments while ensuring alignment with FDA/EU requirements and Novo Nordisk