Perrigo Posted October 10, 2026

Formulation Scientist - Nutrition (Eau Claire, WI, US, 54703)

Eau Claire, 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

Prepare nutritional formulations that meet technical and applicable regulatory legal requirements.

Complete data tabulation, stability assessment and technical reports to support new and revised formulations and shelf life extensions.

Prepare formula-related documentation required for registration of powdered and liquid Infant products.

Provide nutritional technical support to the Pilot Plant and factories to meet operational requirements not limited to manufacturing documentation, theoretical calculations, and change management.

This is an onsite position located at our Eau Claire, WI facility.

Scope of the Role

Prepare prototype and/or master formulas and associated technical documentation that comply with nutritional, regulatory, and legal requirements and meet commercial objectives.

Prepare Pilot Plant and/or Plant Trial technical documentation for any necessary trial work.

Complete periodic data review of new and existing finished products to ensure compliance with nutritional requirements throughout shelf life. Use established statistical principles to conduct assessments and make recommendations for shelf life and shelf life extensions. Provide concise written reports summarizing information.

Provide nutritional technical support to the factories including change management, formula fits, theoretical assessments, batch adjustments, and inventory management of raw materials to minimize waste.

Prepare new ingredients such as vitamin and/or mineral premixes and their associated specifications for new and/or existing formulas. Periodically review existing raw material data to monitor for changes.

Provide timely responses to retailer and customer requests. Support formulation Organic audit requirements for factories.

Participate in cross functional team(s) to establish and provide accountability for project timelines, roadblocks, and critical steps.

Experience Required

Typically these skills are acquired with a BS in Science with a strong foundation in nutrition, manufacturing, algebra, and chemistry.  Preferred:  BS in Food Science, Nutrition, or related degree.

Typically 4 yrs or relevant professional experience. Previous formulation experience preferred.

Strong working knowledge in Nutrition, Algebra, Statistics and Chemistry.

Advanced proficiency in Microsoft Excel and competency in other Office applications. Experience in SAP, SLIM, Ensur, Open Text, DOE and statistical applications preferred but not required.

Ability to review and comprehend implications of regulations for different markets (FDA, CODEX, EFSA, HC, etc.).

Highly focused, superior accuracy and attention to detail, and excellent written and verbal communication skills.

Good problem solving and analytical skills.

Knowledge of product development processes from prototype to commercialization.

Ability to work independently in a result driven, high-paced dynamic environment. A willingness to switch gears and align quickly on emerging priorities.

Ability to handle multiple complex projects with high fidelity.

Ability to work cross functionally with Quality, Operations, Marketing, Sales and Regulatory.

General understanding of nutritional manufacturing unit processes and the underlying food chemistry and technology principles preferred but not required.

Exhibit curiosity and a willingness to learn, consumer focus and Perrigo’s core values in day-to-day work life.

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

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Job details

Seniority
Not listed
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Eau Claire, United States
Employment type
Not listed

How this role compares

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

We currently track 2619 comparable Manufacturing & CMC roles across 166 biopharma companies.

2619Comparable roles tracked
2402Currently active
166Companies hiring similar roles
53Countries represented

Salary context

669 of 2619 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
Highest disclosed · Executive Director, CMC Regulatory Science · ModernaTX, Inc. $224,900/yr – $404,600/yr
Peer group range $0 – $314,750 (median $122,400)

Where these roles are based

Top locations among the 2619 comparable roles

United States1260
India167
Germany135
France118
Ireland89
Netherlands78

+ 47 more countries

Seniority mix

1230 of 2619 peers have a known seniority level

Senior349
Manager265
Intern/Fellow/Postdoc166
Associate150
Principal96
Associate Director85
Director74
Senior Director38
Executive/VP7

Therapeutic area mix

17 of 2619 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease10
Oncology3
Rare Disease2
Respiratory1
Dermatology & Aesthetics1

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
AstraZeneca New Haven, Connecticut, United States of America
Same function Same country
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Same function Same country
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Lilly Indianapolis, Indiana, United States of America Director
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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.

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%
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Function Therapeutic area Seniority Country
40%
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Lilly · Indianapolis, Indiana, United States of America · Director
Function Therapeutic area Seniority Country
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Function Therapeutic area Seniority Country
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Senior Scientist, Conjugation Process Development
Seagen Inc · Washington – Bothell, 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.