Biopharma Process Support Specialist I

Novo Nordisk; West Lebanon (NH); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Competitive pay

Annual bonus

Paid time off

Health insurance

Dental insurance

Vision insurance

401K match

Paid parental leave

Product access

Job summary

Novo Nordisk in West Lebanon, NH seeks a manufacturing operations support specialist to assist downstream processes, drive deviations investigations, changes, and training while ensuring QMS documentation aligns with cGMP standards.

You will work on-site, coordinating with multiple teams to sustain production efficiency and quality. Strong written and verbal communication, problem-solving, and Lean principles are essential.

Qualifications

• Requires high school diploma or equivalent; six years manufacturing experience.
• Bachelor’s degree or equivalent with two years of experience preferred.
• Pharmaceutical or biotechnology experience strongly preferred.
• Knowledge of cGMPs and quality regulations.
• Ability to follow written instructions; attention to detail.
• Demonstrate lean manufacturing principles.
• Excellent communication skills.
• On-call availability within 60 minutes.

Responsibilities

• Liaison between Production Support and Manufacturing for process/equipment improvements.
• Review/approve completed process documentation.
• Train others on manufacturing processes and QMS systems.
• Revise/create SOPs and batch records for production.
• Investigate Deviation events using Root Cause Analysis.
• Support process improvements and cost-reduction projects.
• Manage multi-disciplinary projects with minimal supervision.
• Support Health Authority inspections.

Skills

Communication

Problem solving

Lean manufacturing

Analytical thinking

Organization

On-call responsiveness

Education

High School diploma or equivalent

Bachelor’s degree in science or engineering preferred

Job description

Novo Nordisk in West Lebanon, NH seeks a manufacturing operations support specialist to assist downstream processes, drive deviations investigations, changes, and training while ensuring QMS documentation aligns with cGMP standards.

You will work on-site, coordinating with multiple teams to sustain production efficiency and quality. Strong written and verbal communication, problem-solving, and Lean principles are essential.