QA Area Specialist III - Finished Production (Validation Focus) (Clayton, NC, US)

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

This role supports our Finished Production area with a focus on review of validation activities. Ensures plant systems batch release, and/or relevant quality processes are compliant with regulations. Has product release authority if role is in batch release. Quality oversight, review & approval of validation activities and documents associated with projects, new systems, changes to existing systems & maintaining validated state of equipment, processes, and systems. Presentation, support & coaching for audits & inspections. Review & approval of complex Change Requests (CR's), Deviations (DVs), CAPAs & other documentation. Performs Self Audits (in conjunction with line of business (LoB)); Quality Assurance (QA) presence & process confirmation on shop floor. Site Clayton Process Representative, as assigned. Able to support all processes & functions in Department. Trends and reports data as applicable. This role requires prior experience in a GMP environment. This is an onsite based role Monday-Friday.

Relationships

Reports to: Associate Director, QA Finished Production.

Essential Functions

Make decisions on quality & compliance issues with little guidance

Participate in process group activities as assigned & leads local implementations

Ensure site compliance with Regulations, ISOISP standards, corporate & local standard operating procedures (SOPs)

Lead improvement activities/improvement of standards within the assigned process

Review & approves change control documentation, SOPs & other current good manufacturing practice (cGMP) documentation

Provide coaching to Site regarding quality & compliance related activities

Supports, reviews & approves complex cross-functional investigations & root-cause analysis

Facilitates sharing of regulatory & compliance expectations

Reviews & approves complex DVs, CRs, (SOPs), trend & report data for CAPA, Quality Management Reviews (QMRs) & Annual Product Review (APR) reports

Eliminates non-value-added practices

Follow all safety & environmental requirements in the performance of duties

Other accountabilities, as assigned

Qualifications

High School Diploma or equivalent (GED) required

Bachelor’s degree in Life Sciences or a relevant field of study from an accredited university preferred. ***If hired as a AQP, Bachelor’s degree in Life Sciences or a relevant field of study from an accredited university required

Minimum of seven (7) years of QA and/or related quality experience in manufacturing, utility and/or packaging systems, preferably in the pharmaceutical or medical device field required

Demonstrated expertise in Regulations & quality systems in one or more of the following: product disposition, DV/CAPA, Change Control, Audits, Supplier Management, Project Management, Validation, laboratory method and equipment validation, warehouse/logistics, and IT preferred

Quality Risk Management experience required

Experience with regulatory requirements computer system, such as 21 CFR Part 11, GAMP5, ISO, Data Integrity required

Experience in use of Risk Assessment & Vendor Assessments during evaluation of change controls, deviation and validation activities required

Expert in cGMP documentation practices. Requires a minimum of four (4) years of experience in reviewing GMP documents for compliance purposes for approval of quality documentation preferred

Excellent troubleshooting skills; able to identify root cause of problem required

Demonstrated knowledge of critical controls & input/output requirements for processes in these areas: semi-finished manufacturing, finished manufacturing QC, IT & process utilities preferred

Excellent written & verbal communication skills required

Auditing experience with certification preferred (internal/external) required

Experience with LEAN, Six Sigma & other continuous improvement methodologies required

Expert competence in one or more core validation areas (sterilization, packaging, cleaning, utilities, process or computer validation) preferred

Knowledge of statistical methods (hypothesis testing, sampling, trending, CpK, etc.) required

Expert in utilizing appropriate root-cause analysis tools & techniques preferred

Experience with Risk Assessment & Risk Management required

Demonstrated excellence with time management, organizational & project management skills required

Physical Requirements

Moves equipment &/or supplies weighing up to 33 pounds within the facility using various body positions. Ability to do close precision work with their hands. Must be able to remain in a stationary position (sitting and standing) 50% of the time. May required corrected vision to 20/20 or 20/25 based on role. May require color vision based on role. May require the ability to work in loud noise environments with hearing protections.

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.

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