Process Professional I

Novo Nordisk; Clayton (NC); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Generous PTO

Health insurance

Dental insurance

Vision insurance

401K with match

Parental leave

Tuition assistance

Life & disability insurance

Employee referral awards

Job summary

Novo Nordisk in Clayton, NC is seeking a Manufacturing Process Specialist to support operations, equipment, and processes to meet business and regulatory requirements. You will provide solution for routine to moderate issues and train junior team members.

You will collaborate with production and QA, conduct deviation investigations, and drive continuous improvement using Lean tools while adhering to safety and environmental standards. This role reports to the Manager.

Qualifications

• Bachelor’s degree in engineering/technology or related field required.
• Associate’s degree + 2 years manufacturing experience may be considered.
• High School diploma + 4 years manufacturing experience may be considered.
• Minimum 1 year manufacturing experience preferred, preferably in a pharmaceutical manufacturing environment.
• Excellent written communication skills required.
• GMP knowledge required.
• Basic investigation and problem-solving experience required.
• Exposure to regulatory audits a plus.
• General knowledge of change control and QMS systems preferred.
• Relevant electronic manufacturing system experience (SAP, PAS-X) preferred.

Responsibilities

• Work with production and QA to provide in depth deviation investigations and root cause analysis.
• Drive continuous improvements via Lean tools.
• Provide training on process and procedure changes.
• Identify and implement process needs and improvement opportunities for routine to moderate complexity issues.
• Responsible for collection of data for periodic reviews and reporting.

Skills

Excellent written communication

GMP knowledge

Basic investigation & problem-solving

Adult learning methodologies training

Education

Bachelor’s degree in engineering/technology or related field

Associate’s degree + 2 years manufacturing experience

High School Diploma + 4 years manufacturing experience

Tools

SAP

PAS-X

QMS systems

Job description

About The Department

At Novo Nordisk, we want to make a difference. 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.

About The Department

At Novo Nordisk, we want to make a difference. 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 Product Supply Aseptic Manufacturing (PS AM) facility in Clayton, NC is a 457,000 square foot aseptic “fill and finish” site that is responsible for producing innovative, injectable diabetes and obesity treatments. At PS AM, 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

Support people, equipment and processes for our operations areas to meet business and regulatory requirements. Provide process solutions for routine to moderate complexity issues. Support training for junior team members.

Relationships

Reports to Manager.

Essential Functions

• Work with production and QA to provide in depth deviation investigations and root cause analysis
• Drive continuous improvements via Lean tools
• Provide training on process and procedure changes
• Identify and implement process needs and improvement opportunities for routine to moderate complexity issues
• Responsible for collection of data for periodic reviews and reportingFollow all safety & environmental requirements in the performance of duties
• Other accountabilities, assigned

Physical Requirements

Ability to work in an open office environment with the possibility of frequent distraction. Ability to travel up to 20% of the time (% can change on a case-by-case basis based on the role).

Qualifications

• Bachelor’s degree (engineering, technology or related field of study preferred) from an accredited university required
  • May consider an Associate’s degree from an accredited university with a minimum of two (2) years of manufacturing experience required
  • May consider a High School Diploma (GED) with a minimum four (4) years of manufacturing experience required
• Minimum of one (1) year of manufacturing experience preferred, preferably in a pharmaceutical manufacturing environment
• Excellent written communication skills required
• GMP knowledge required
• Basic investigation and systematic problem-solving experience required
• Manufacturing experience preferred
• General knowledge of change control and Quality Management System (QMS) systems preferred
• Relevant electronic manufacturing system experience preferred (ex: SAP, PAS-X, etc)
• Demonstrated knowledge of adult learning methodologies and ability to use multiple methods to train others preferred
• Exposure to regulatory audits/inspections a plus

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.