Abbott Posted September 30, 2026

Labeling Project Manager

Plymouth, Minnesota, United States FULL_TIME
Quality Manager
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Abbott 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

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,000 colleagues serve people in more than 160 countries.

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to:

Career development with an international company where you can grow the career you dream of.

Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.

An excellent retirement savings plan with a high employer contribution

Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.

A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.

A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity

This position will work out of our Plymouth, MN location.

The Labeling Project Manager will be responsible for meeting business needs by supporting the Labeling and Universal Addendum Labeling (UAL) teams by leading/implementing projects, conducting analysis, developing managing master data, communicating with cross functional teams, and problem-solving various challenges. Top candidates will have demonstrated skills in utilizing program management methodologies, excellent organizational and problem-solving abilities, and exceptional communication skills.

What You’ll Work On

Develop, communicate, and drive detailed schedules and timelines for program deliverables across multiple organizational functions.

Create and manage labeling and UAL change processes within the document management systems.

Work cross-functionally to identify and resolve labeling and UAL inconsistencies to meet applicable requirements and project timelines.

Monitor for program risks and issues, and drive for resolution.

Ensure cross functional alignment on objectives and tasks.

Manage Labeling and UAL master data and workflow via internal IT systems.

Manages concurrent deadlines and meets deadlines for assigned work/tasks. • Analyze and interpret large data sets and identify methods of resolution.

Complies to world-wide Labeling regulations and cross-functional business requirements.

Comply with company initiatives in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), FDA & world-wide regulations, business requirements, company policies and operating procedures.

Required Qualifications

BA or BS degree in Business, Engineering, Supply Chain Management and/or Logistics, or Operations Management or equivalent combination of education and work experience.

Project management certifications preferred.

Minimum 5 years medical device industry experience preferred.

2+ years of successfully leading large-scale, multi-functional programs preferred.

Ability to manage projects and drive them to completion with attention to detail.

Requires ability to be innovative, resourceful, and work with minimal direction. • Knowledge of FDA & EU regulations, GS1 and ISO standards.

Strong written and verbal communication, at all organizational levels.

Ability to work within a team and as a leader in a fast-paced, changing environment.

Experience working in medical device industry with focuses on regulatory compliance, quality systems, labeling, or UDI preferred.

Experience working with ERP and/or PLM systems preferred. Preferably SAP and/or Windchill.

Database management and/or analytics software knowledge preferred.

Strong analytical skills with the ability to collect, organize, analyze, and disseminate significant amounts of information with attention to detail and accuracy.

Skilled in Microsoft Office specifically Excel, PowerPoint, Word, and Access.

Apply Now

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:  www.abbottbenefits.com

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

Connect with us at www.abbott.com , on Facebook at www.facebook.com/Abbott , and on Twitter @AbbottNews.

The base pay for this position is $61,300.00 – $122,700.00. In specific locations, the pay range may vary from the range posted.

Job details

Seniority
Manager
Function
Quality
Therapeutic area
Not listed
Location
Plymouth, Minnesota, United States
Employment type
FULL_TIME

How this role compares

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

We currently track 285 comparable Manager Quality roles across 80 biopharma companies.

285Comparable roles tracked
266Currently active
80Companies hiring similar roles
32Countries represented

Salary context

59 of 285 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 Quality Control Analyst (Virology) · Regeneron Pharmaceuticals, Inc (USA) $22/hr – $34/hr (≈ $45,302–$70,699/yr)
Peer group range $58,001 – $208,845 (median $159,000)

Where these roles are based

Top locations among the 285 comparable roles

United States130
China22
Ireland18
India17
Japan12
Netherlands12

+ 26 more countries

Seniority mix

285 of 285 peers have a known seniority level

Manager182
Associate68
Associate Director35

Therapeutic area mix

0 of 285 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
Corixa Corporation Marietta, United States Manager
Same function Same seniority Same country
60%similar
GlaxoSmithKline LLC Zebulon, 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.

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, Drug Product (Filling)
Regeneron Pharmaceuticals, Inc (USA) · Renss, United States · Manager
Function Therapeutic area Seniority Country
60%
Manager Quality Control (Athens, GA, United States, Georgia)
Boehringer Ingelheim · Athens, Georgia, United States · Manager
Function Therapeutic area Seniority Country
60%
Senior Manager, Clinical Study Quality Lead
Vertex Pharmaceuticals Inc (US) · Boston, 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.