Process Engineer - Biotech Manufacturing

Role:
Process Engineer supporting downstream bioproduction in a GMP environment at Novo Nordisk's West Lebanon facility. Primary focus is on maintaining efficient manufacturing operations for biologics such as hemophilia and growth hormone products. The role emphasizes documentation, process troubleshooting, continuous improvement initiatives, and regulatory compliance, supporting the manufacturing of life-saving biologic therapies.

• on-floor process support
• documentation
• SOP and deviation management
• equipment troubleshooting
• process improvements
• validation activities
• participation in audits and investigations
• cross-functional collaboration with manufacturing, engineering, quality, and technical teams

• Bachelor’s degree in engineering or related field
• 3+ years of experience in pharmaceutical or biotech manufacturing, preferably in large-scale biologics production
• knowledge of GMP compliance, process validation, automation, and good engineering practices
• excellent communication
• the ability to support on-call troubleshooting

• Onsite position in sterile bioprocessing
• some cross-functional and external vendor coordination
• physical ability for GMP environment duties
• travel up to 10%