Process Professional I (Durham, NC, US)

Biopharma Careers

North Carolina

On-site

USD 85,000 - 110,000

Full time

2 days ago
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Benefits offered by this job

Leading pay
Annual bonus
Paid time off
Health insurance from day one
Dental insurance
Vision insurance
401K with company match
Parental leave
Life & Disability Insurance
Tuition Assistance
Employee referral rewards

Job summary

Novo Nordisk in North Carolina seeks a manufacturing professional to support people, equipment and processes in our operations areas to meet business and regulatory requirements. You will provide process solutions for routine to moderate complexity issues and support training for junior team members.

Based in Durham at our Emerging Technologies - SDF US facility, the role emphasizes continuous improvement, data collection for reviews, and adherence to GMP.

Qualifications

  • Bachelor’s degree in engineering, technology or related field.
  • Manufacturing experience preferred, pharmaceutical environment ideal.
  • Excellent written communication skills required.
  • GMP knowledge required.

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

Skills

GMP knowledge
Problem solving
Written communication

Education

Bachelor’s degree in engineering/technology
Associate’s degree with manufacturing experience
High School Diploma with manufacturing experience

Tools

SAP
PAS-X

Job description

About the Department

For more than 100 years, Novo Nordisk has been tackling the unmet medical needs of people living with serious chronic diseases, such as diabetes & obesity. 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 Emerging Technologies -Solid Dosage Forms US facility in Durham, NC is a 194,000 square foot tableting and packaging facility that supports the production of our innovative oral treatments for patients with type 2 diabetes. SDF maintains a curious and pioneering spirit, harmonious with our growing pipeline of new products and emerging technologies.

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
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 reporting
  • Follow all safety & environmental requirements in the performance of duties
  • Other accountabilities, as 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).

Minimum 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
Preferred Qualifications
  • 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.

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