Novo Nordisk

Senior IT Compliance Analyst - IT & OT - GMP (Petersburg, VA, US)

Petersburg, United States Type not listed
Quality Senior

Novo Nordisk is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

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.

Our new Petersburg, Virginia site marks a strategic move to advance our capabilities in Emerging Technologies (ET) within Chemical API development and production. The highly experienced site is designed to strengthen and accelerate our Small Molecule (SMOL) strategy while amplifying our operational capacity. This is to safeguard and support ET´s SMOL projects in the coming years, aligning with our vision and strengthening our potential for growth and innovation.

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 subject matter expertise in IT compliance, process improvement, and IT compliance service delivery management across the site. Ensures that IT solutions are compliant with relevant regulations and standards and facilitates the seamless transition and handover of projects to service operations with key stakeholders. Ensures governance and continuous improvement as an enabler supporting product quality, patient safety, and data integrity, and contributes to the organization's goals of improving the lives of people with chronic diseases.

Relationships

Reports to Manager.

Essential Functions

Develop and maintain validation and qualification documentation

Conduct risk assessments and impact analyses to identify potential compliance issues and develop mitigation strategies

Provide guidance and support to project teams on validation and qualification requirements

Continuously monitor and improve documentation and processes to ensure compliance with regulatory requirements and Novo Nordisk standards

Facilitate the seamless transition and handover of projects to service operations with key stakeholders

Maintain system documentation and process according to Novo Nordisk standards and in compliance with regulatory requirements

Participate as an IT SME in audits and inspections and provide needed documentation to demonstrate validated state and proper management of IT solutions throughout the life cycle

Collaborate with cross-functional teams to ensure that all IT solutions meet business needs, are delivered on time & within budget, are properly documented, and managed throughout their life cycle

Ensure that all IT solutions, documentation, and processes are following regulatory requirements and Novo Nordisk standards

Provide leadership and expertise in IT compliance, process improvement, and project coordination

Coach and mentor personnel, and provide guidance as needed

Participate in process group meetings and contribute to process group activities

Follow all safety & environmental requirements in the performance of duties

Other duties as assigned

Physical Requirements

May move equipment &/or supplies weighing up to 33 pounds within the facility using various body positions. May be required 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. May require the ability to work in loud noise environments with hearing protections. Ability to work in an open office environment with the possibility of frequent distraction. Ability to travel up to 10% of the time. % can change on a case-by-case basis based on the role.

Qualifications

Bachelor’s Degree in IT, Engineering, Science, or relevant field of study from an accredited university with a minimum of seven (7) years of experience in IT compliance and five (5) years of experience in Validation and Testing of IT Solutions required, preferably within the pharmaceutical industry

Master’s degree in IT, Engineering, Science, or relevant field of study from an accredited university preferred with a minimum of five (5) years of experience in IT compliance and three (3) years of experience in Validation & Testing of IT solutions, required; preferable within the pharmaceutical industry

Excellent written and verbal communication skills in English

Strong customer service skills and ability to collaborate effectively in a team environment

Excellent problem solving, negotiation, conflict management, and interpersonal skills

Excellent planning, organizing, decision making and deal with complexity and ambiguity

Strong computer skills and expert-level proficiency in Microsoft Office (MS Office)

Preferred Qualifications: Certified Information Systems Auditor (CISA)

Lean Six Sigma (Green Belt or Black Belt)

Experience serving as an SME supporting Audits and Inspections

Experience in GxP, change management, and deviation handling

Experience with Incident, Problem, and Change Management in IT

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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Job details

Seniority
Senior
Function
Quality
Therapeutic area
Not listed
Location
Petersburg, United States
Employment type
Not listed

How this role compares

Computed from every other active Quality role in our database, not just this employer's listings.

We currently track 136 comparable Senior Quality roles across 36 biopharma companies.

136Comparable roles tracked
125Currently active
36Companies hiring similar roles
21Countries represented

Salary context

34 of 136 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Peer group range $98,050 – $219,500 (median $147,075)

Where these roles are based

Top locations among the 136 comparable roles

United States72
India15
Ireland13
Singapore10
United Kingdom4
China's Mainland3

+ 15 more countries

Seniority mix

136 of 136 peers have a known seniority level

Senior96
Associate Director26
Principal14

Therapeutic area mix

0 of 136 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

No peers with a known therapeutic area yet.

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
AbbVie Irvine, CA Senior
Same function Same seniority Same country
60%similar
AbbVie San Francisco, CA Senior
Same function Same seniority Same country
60%similar
Gilead Sciences, Inc. La Verne, United States Senior
Same function Same seniority Same country
60%similar
Regeneron Pharmaceuticals, Inc (USA) Renss, United States Senior
Same function Same seniority Same country
60%similar
Regeneron Pharmaceuticals, Inc (USA) Renss, United States Senior
Same function Same seniority Same country
60%similar
Regeneron Pharmaceuticals, Inc (USA) Rensselaer, United States Senior
Same function Same seniority Same country

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
Senior R&D Quality Officer, Product Development Quality Assurance
AbbVie · Irvine, CA · Senior
Function Therapeutic area Seniority Country
60%
Sr QA Validation Specialist (Oversight)
Regeneron Pharmaceuticals, Inc (USA) · Renss, United States · Senior
Function Therapeutic area Seniority Country
60%
Senior Specialist, Quality Assurance Lot Disposition
JuN - Seattle Dexter · Bothell, United States · Senior
Function Therapeutic area Seniority Country
60%
Senior Scientist, Drug Product Analytical Science (ASAT), Cell Therapy
JuN - Seattle Dexter · Seattle 400 Dexter, United States · Senior
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.