Process Engineer I - API (Clayton, NC, US)

NCBiotech; Clayton (NC); On-site; USD 70,000 - 95,000; Full time

Benefits offered by this job

Health Insurance

Paid time off

401K with company match

Tuition Assistance

Life & Disability Insurance

Job summary

Novo Nordisk in Clayton, NC is seeking an engineer to provide routine support and troubleshooting for the manufacturing facility. The role focuses on improving system and equipment reliability to meet customer, business, and regulatory requirements.

You will collaborate with cross-functional teams, participate in validation activities, and help drive continuous improvement while upholding safety and GMP standards.

Qualifications

• Bachelor’s degree in engineering, science, or related field with minimum 1 year of engineering/technical experience (GMP preferred).
• Associate's degree with minimum 3 years of engineering/technical experience (GMP preferred).
• High school diploma with minimum 5 years of engineering/technical experience (GMP preferred).
• Experience with design of requirements documents a plus.
• Knowledge of regulatory expectations (FDA) is a plus.
• Experience with Process Control Systems is a plus.
• Ability to work in a team and cross-functional environment.
• Ability to support a 24/7 operations business.

Responsibilities

• Support validation & verification within area.
• Ensure quality of equipment and processes.
• Support process improvement projects for assigned area.
• Support manufacturing operations and provide technical support to operating facilities to meet business goals.
• Generate ideas and support implementation for improvement within area.
• Own self development and partner with manager for development needs and career path.
• Follow safety & environmental requirements.
• Other duties as assigned.

Skills

Team collaboration

Regulatory knowledge

Process control systems

Requirements documents

GMP environment experience

24/7 operations support

Networking & knowledge sharing

Engineering/technical background

Education

Bachelor’s Degree in Engineering, Science, or relevant technical field

Associate’s Degree in Engineering, Science, or relevant technical field

High School Diploma or equivalent

Job description

About the Department

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 14 weeks 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 with a minimum of one (1) year of engineering or technical experience required, preferably in a GMP regulated environment
• May consider an Associate’s Degree in Engineering, Science, or relevant technical field of study from an accredited university with a minimum of three (3) years of engineering or technical experience required, preferably in a GMP regulated environment
• May consider High School Diploma or equivalent with a minimum of five (5) years 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 regulatory authorities e.g. FDA a plus
• Experience with Process Control Systems a plus
• Proven ability to establish & maintain networks & facilitate processes that encourage cross organizational knowledge sharing a plus
• Ability to provide support for a 24/7 operational business required

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

At Novo Nordisk, we're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and defeating diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.

Novo Nordisk is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, protected veteran status or any other characteristic protected by local, state or federal laws, rules or regulations.

If you are interested in applying to Novo Nordisk and need special assistance or an accommodation to apply, please call us at 1-855-411-5290. This contact is for accommodation requests only and cannot be used to inquire about the status of applications.