Biotech Process Support Associate I - cGMP Manufacturing

BioSpace; West Lebanon (NH); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Annual performance bonus

36 Paid days off

Health Insurance

Dental Insurance

Vision Insurance

8% 401K match

14 weeks Paid Parental Leave

Free access to Novo Nordisk products

Job summary

Novo Nordisk in West Lebanon, NH, is seeking a Process Support specialist to help coordinate improvements, maintain quality records, and train technicians in GMP-compliant procedures. The role requires strong cGMP knowledge, attention to detail, and cross-functional collaboration within the site manufacturing team.

This is an on-site, Monday–Friday position at the bioproduction facility. The candidate should have a high school diploma with manufacturing experience or a science/engineering degree

Qualifications

• Education: High School diploma or equivalent required
• Bachelor's degree in science or engineering preferred
• Six years manufacturing experience with HS; two years with Bachelor's preferred

Responsibilities

• Coordinate process/equipment improvements with Production Support and Manufacturing
• Review and approve completed process documentation
• Train others on manufacturing processes and QMS systems
• Revise and create documentation (SOPs, batch records, FT’s) for product manufacture
• Investigate deviations and perform root cause analysis
• Incorporate pre-planned process improvements and cost-reduction projects
• Support hands-on manufacturing as needed to cover production
• Assist with health authority inspections

Skills

cGMP knowledge

Quality systems

Lean manufacturing

Analytical thinking

Communication skills

On-call support

Education

High School diploma or equivalent

Bachelor's degree in science or engineering preferred

Tools

QMS systems

Documentation systems

Job description

Novo Nordisk in West Lebanon, NH, is seeking a Process Support specialist to help coordinate improvements, maintain quality records, and train technicians in GMP-compliant procedures. The role requires strong cGMP knowledge, attention to detail, and cross-functional collaboration within the site manufacturing team.

This is an on-site, Monday–Friday position at the bioproduction facility. The candidate should have a high school diploma with manufacturing experience or a science/engineering degree