Perrigo Posted November 3, 2026

Validation Manager (Bronx, NY, US, 10457)

Bronx, United States Type not listed
Quality Manager
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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

The Validation Manager is responsible for the Qualification and Validation program. The Manager oversees all activities of the Validation team, leading a group of colleagues in designing, managing and executing projects. managing qualification and validation of manufacturing and packaging equipment and processes for over-the-counter semi-solid creams, ointments and gels, suppositories and nasal sprays at the Perrigo New York facility.

Scope of the Role

Oversight for a team of Validation Engineers in performing qualification and validation of manufacturing and packaging equipment and processes for over-the-counter semi-solid creams, ointments and gels, suppositories and nasal sprays at the Perrigo New York facility.

Determines validation requirements for complex operational issues

Evaluates, designs, develops and coordinates key projects, develops and writes technical documents, leads in solving complex problems to achieve goals.

Identifies and leads cross functional departments to drive compliance and continuous improvement initiatives

Provides audit and Agency inspection report related to validation requirements and activities

Experience Required

Bachelor degree in scientific field combined with five or more years of progressively responsible experience of greater breadth and/or depth.

Pharmaceutical industry experience.

Supervisory experience required.

Experience in Validation, Quality, or Operations required.

Thorough understanding of validation processes and interpretation and application of FDA and cGMP requirements.

Demonstrated ability in areas of validation (techniques, practices, precedents, theory, and principles of)

Excellent written and oral communication 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.

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
Manager
Function
Quality
Therapeutic area
Not listed
Location
Bronx, 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 338 comparable Manager Quality roles across 81 biopharma companies.

338Comparable roles tracked
299Currently active
81Companies hiring similar roles
35Countries represented

Salary context

62 of 338 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
Lowest disclosed · Associate I, Quality Control, Raw Materials · ModernaTX, Inc. $53,500/yr – $85,600/yr
Highest disclosed · Advisor, Design Validation & Learning, Biotherapeutics · Lilly $168,000/yr – $268,400/yr
Peer group range $69,550 – $218,200 (median $166,788)

Where these roles are based

Top locations among the 338 comparable roles

United States146
China24
Ireland22
India21
Germany15
Japan12

+ 29 more countries

Seniority mix

338 of 338 peers have a known seniority level

Manager219
Associate67
Associate Director52

Therapeutic area mix

0 of 338 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 North Chicago, IL Manager
Same function Same seniority Same country
60%similar
Gilead Sciences, Inc. Foster City, United States Manager
Same function Same seniority Same country
60%similar
Regeneron Pharmaceuticals, Inc (USA) Renss, United States Manager
Same function Same seniority Same country
60%similar
Regeneron Pharmaceuticals, Inc (USA) Renss, United States Manager
Same function Same seniority Same country
60%similar
RayzeBio, Inc Indianapolis, United States Manager
Same function Same seniority Same country
60%similar
Corixa Corporation Marietta, United States Manager
Same function Same seniority 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 Quality 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.

60%
Senior Manager, Clinical Quality Assurance
AbbVie · North Chicago, IL · Manager
Function Therapeutic area Seniority Country
60%
Senior Manager Quality Assurance, Medical Device (Sustaining)
Regeneron Pharmaceuticals, Inc (USA) · Renss, United States · Manager
Function Therapeutic area Seniority Country
60%
Quality Technical and Validation Manager
Corixa Corporation · Marietta, United States · Manager
Function Therapeutic area Seniority Country
60%
US_US Quality Manager External API (Columbus, United States, Ohio)
Boehringer Ingelheim · Columbus, Ohio, United States · Manager
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.