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Fermentation Process Engineer - GMP Career

Job in Powhatan, Johnston County, North Carolina, USA
Listing for: Novo Nordisk A/S
Full Time position
Listed on 2026-05-26
Job specializations:
  • Engineering
    Quality Engineering, Process Engineer, Manufacturing Engineer
  • Manufacturing / Production
    Quality Engineering, Manufacturing Engineer
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below
Position: Fermentation Process Engineer I - Start Your GMP Career
Location: Powhatan

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At Novo Nordisk, we are helping to improve the quality of life for millions of people worldwide. For more than 100 years, we have led the way in diabetes care. Being part of Novo Nordisk allows our employees to embark on the opportunity to help improve the quality of life for millions of people around the world.

In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling different steps in our injectable and oral treatment supply chains. Our newer Active Pharmaceutical Ingredients (API) facility in Clayton, NC sits on 825,000 square-feet of state-of-the-art equipment, and houses the Fermentation, Recovery and Purification in the production of ingredients for Novo Nordisk’s innovative oral products. At API, you’ll join a global network of manufacturing professionals who are passionate about what they do.

What we offer you:

  • Leading pay and annual performance bonus for all positions
  • All employees enjoy generous paid time off including 14 paid holidays
  • Health Insurance, Dental Insurance, Vision Insurance – effective day one
  • Guaranteed 8% 401K contribution plus individual company match option
  • Family Focused Benefits including 14weeks paid parental & 6 weeks paid family medical leave
  • Free access to Novo Nordisk-marketed pharmaceutical products
  • Tuition Assistance
  • Life & Disability Insurance
  • Employee Referral Awards

At Novo Nordisk, you will find opportunities, resources, and mentorship to help grow and build your career. Are you ready to realize your potential? Join Team Novo Nordisk and help us make what matters.

The Position

Provide routine support & troubleshooting for the manufacturing facility. Improve system and equipment reliability for the core processes to meet customer, business, & regulatory requirements.

Relationships

Reports to Manager or Senior Manager.

Essential Functions
  • Support validation & verification within area
  • Ensure quality of equipment and processes
  • Support process improvement project for assigned area
  • Support manufacturing operations and provide technical support to the operating facilities to meet business goals
  • Generate ideas & support implementation for improvement within area
  • Own self development and partner with manager for clear understanding of development needs for desired career path
  • Follow all safety & environmental requirements in the performance of duties
  • Other duties as assigned
Physical Requirements

Moves equipment &/or supplies weighing up to 33 pounds within the facility using various body positions. Routinely operates & inspects manufacturing equipment using hands. Strap & unstrap pallets using hands. Must be able to be on your feet for up to a 12-hour shift. May require corrected vision to 20/20 or 20/25 based on role. May require color vision based on role.

Occasionally ascends/descends a ladder. May be required to work at elevated heights. Occasionally works around odorous &/or hazardous materials. May be required to wear latex gloves. May perform critical job functions in extremely cold work environments depending on site. May position oneself within confined spaces for inspection if required of the role. Ability to work in loud noise environments with hearing protection.

May be required to secure a motorized vehicle license & operate a motorized vehicle based on the role.

Qualifications
  • Bachelor’s Degree in Engineering, Science, or relevant technical field of study from an accredited university required
  • May consider an Associate’s Degree in Engineering, Science, or relevant technical field of study from an accredited university with three (3) years of engineering or technical experience required, preferably in a GMP regulated environment
  • May consider High School Diploma or equivalent with five (5) years of engineering or technical experience required, preferably in a GMP regulated environment
  • Minimum one (1) year of engineering or technical experience required, preferably in a GMP regulated environment
  • Experience with design of requirements documents a plus
  • Functional knowledge in assigned area required
  • Ability to work in a team required
  • Knowledge about requirements/expectations of…
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