Perrigo Posted October 27, 2026

Regulatory Affairs Art Auditor (Allegan, MI, US, 49010)

Allegan, United States Type not listed
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Perrigo 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

At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All . We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone , we are the people behind the brands you trust. We are Opill®, Compeed®, Solpadeine®, NiQuitin®, and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.

Join us on our One Perrigo journey as we evolve to win in self-care.

Description Overview

We're growing our Regulatory Affairs team and are seeking an Art Auditor to help drive accuracy, compliance, and quality throughout the artwork review process.

Scope of the Role

Ensure product labeling components are 100% accurate and error free prior to sending to print vendors.

Ability to read labeling fine print and to identify differences in text, placement and color when compared to side-by-side copy

Must possess exceptional attention to detail skills and accuracy in order to ensure required regulatory compliance standards are met.

Demonstrates excellent judgement, planning skills and ability to organize work effectively to meet daily deadlines

Must be able to work collaboratively as part of team as well as deliver results working independently

Experience Required

Minimum two years of experience in reading, understanding and interpreting regulatory and/or scientific terminology used in the pharmaceutical industry is required.

Prior experience in an FDA regulated environment, preferred

Prior experience in an auditing position or quality systems position is preferred.

Strong oral and written communications skills.

Benefits

We believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally.

Find out more about  Total Rewards  at Perrigo.

Hybrid Working Approach

We love our offices and the setting they provide for in-person collaboration and celebration. But we also appreciate the opportunity to work remotely can energise you too, so we promote flexibility with the ability to work two days a week from home in many roles.

We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more  here

Applicants please note: To apply to this position please click the APPLY button at the bottom of the application.  (The SAVE button will only save your profile information but not submit an application for this open position.) All application materials, including resumes and CVs, must be submitted in English. Thank you.

We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law.  #weareperrigo

Job details

Seniority
Not listed
Function
Regulatory Affairs
Therapeutic area
Not listed
Location
Allegan, United States
Employment type
Not listed

How this role compares

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

We currently track 571 comparable Regulatory Affairs roles across 113 biopharma companies.

571Comparable roles tracked
501Currently active
113Companies hiring similar roles
48Countries represented

Salary context

144 of 571 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Lowest disclosed · Associate Consultant, Regulatory Science and Strategy · IQVIA $58,700/yr – $146,800/yr
Highest disclosed · Executive Director, Medical Writing · Regeneron Pharmaceuticals, Inc (USA) $285,600/yr – $475,900/yr
Peer group range $102,750 – $380,750 (median $205,000)

Where these roles are based

Top locations among the 571 comparable roles

United States232
India42
United Kingdom40
Japan34
Poland24
Ireland21

+ 42 more countries

Seniority mix

461 of 571 peers have a known seniority level

Manager178
Director83
Associate Director57
Senior56
Senior Director30
Intern/Fellow/Postdoc22
Associate16
Principal13
Executive/VP6

Therapeutic area mix

50 of 571 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Immunology17
Oncology13
Rare Disease6
Dermatology & Aesthetics5
Vaccines & Infectious Disease3
Neuroscience3
Cardiovascular / CVRM2
Respiratory1

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.

40%similar
AbbVie Director
Same function Same country

Open in 2 locations

North Chicago, United StatesFlorham Park, United States
40%similar
Mylan Inc. Washington, United States Manager
Same function Same country
40%similar
Mylan Pharmaceuticals Inc. Washington, United States
Same function Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

Or follow a whole field: get every new Regulatory Affairs job in the United States, and choose locations and companies.

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.

40%
Director, RA Global Regulatory Strategy
AbbVie · North Chicago, IL · Director
Function Therapeutic area Seniority Country
40%
Director, RA Global Regulatory Strategy
AbbVie · Florham Park, NJ · Director
Function Therapeutic area Seniority Country
40%
Senior Manager, Core Labeling Strategy
Mylan Inc. · Washington, United States · Manager
Function Therapeutic area Seniority Country
40%
Head of US Regulatory Affairs Advertising and Promotion, Global Regulatory Affairs
Mylan Pharmaceuticals Inc. · Washington, United States · Seniority not listed
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.