Johnson & Johnson Posted September 23, 2026

Supplier Quality Manager

Raynham, United States Full time
Quality Manager
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Johnson & Johnson 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 Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world.  We provide an inclusive work environment where each person is considered as an individual.  At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Quality

Job Sub Function:

Supplier Quality

Job Category:

People Leader

All Job Posting Locations:

Palm Beach Gardens, Florida, United States of America, Raynham, Massachusetts, United States of America, Warsaw, Indiana, United States of America, West Chester, Pennsylvania, United States of America

Job Description:

About MedTech

Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.

Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech

We are searching for the best talent for a Supplier Quality Manager to be located at a Raynham, MA; Warsaw, IN; Palm Beach Gardens, FL or West Chester, PA.

The Supplier Quality Manager is accountable for establishing and monitoring robust quality assurance programs to ensure external manufacturers consistently meet DePuy Synthes quality, regulatory, and business requirements. This includes oversight of supplier quality systems, manufacturing process controls, product quality performance, risk management activities, and compliance with applicable global regulations and standards. The Source Quality Manager drives continuous improvement initiatives, strengthens supplier capabilities, and fosters a culture of quality excellence to ensure the reliable delivery of safe, effective, and compliant products.

Key Responsibilities:

Lead Source Quality and Purchasing Controls for external manufacturers, ensuring supplier quality systems, process controls, and product quality requirements consistently meet DePuy Synthes, regulatory, and industry standards.

Drive Supplier Performance and Compliance through supplier qualification, quality metrics, risk management, quality agreements, audits, and ongoing performance monitoring to ensure a compliant and reliable supply base.

Champion Continuous Improvement and Digital Transformation by simplifying, standardizing, and digitizing Supplier Quality processes, systems, and reporting to improve efficiency, effectiveness, and compliance.

Provide Technical Quality Leadership for supplier-related quality activities including nonconformance management, investigations, CAPA, change management, verification and validation, and manufacturing process controls.

Partner Cross-Functionally and with External Manufacturers to resolve quality issues, mitigate supply and compliance risks, support product lifecycle activities, and achieve business objectives.

Develop and Lead a High-Performing Team by recruiting, coaching, and developing talent, establishing effective training programs, and fostering a culture of quality, accountability, and continuous improvement.

Support Business and Regulatory Objectives through leadership during internal audits, supplier assessments, and regulatory inspections while ensuring financial, GMP, Health, Safety, and Environmental commitments are met

Qualifications

Education:

University/Bachelor’s degree or equivalent in Engineering/Scientific or associated relevant Technical / Engineering discipline is required.

An Advanced degree in engineering/scientific or discipline is preferred.

Experience and Skills

Required:

A minimum of 6 years progressive experience in a regulated industry.

A minimum of 2 years of experience in a managerial capacity.

Previous work experience with Suppliers.

Demonstrated knowledge of business impact of compliance issues and risk management.

Experience in leadership roles involving project management, problem solving and technical projects.

This individual is expected to possess high performing skills in negotiating and influencing decision makers, decision making skills, communication skills, judgement, tact and leadership skills.

Preferred:

Relevant experience in medical devices and/or pharmaceutical industry.

Experience in Supply Chain and/or R&D.

Experience with Six Sigma/Process Excellence tools, training and certification.

Other:

This position may require up to 20% travel, both domestic and international.

Johnson & Johnson announced plans to separate our Orthopedics business to establish a standalone orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals.

Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers , internal employees contact AskGS to be directed to your accommodation resource.

Required Skills:

Preferred Skills:

Coaching, Consistency, Controls Compliance, Critical Thinking, Data Savvy, Engineering, Financial Competence, Good Automated Manufacturing Practice (GAMP), ISO 9001, Lean Supply Chain Management, Leverages Information, Process Improvements, Quality Control Testing, Quality Standards, Quality Systems Documentation, Quality Validation, Science, Technology, Engineering, and Math (STEM) Application, Technologically Savvy

The anticipated base pay range for this position is :

$102,000.00 - $177,100.00

Additional Description for Pay Transparency:

Subject to the terms of their respective plans, employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).

Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:

Vacation –120 hours per calendar year

Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year

Holiday pay, including Floating Holidays –13 days per calendar year

Work, Personal and Family Time - up to 40 hours per calendar year

Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child

Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year

Caregiver Leave – 80 hours in a 52-week rolling period10 days

Volunteer Leave – 32 hours per calendar year

Military Spouse Time-Off – 80 hours per calendar year

For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits

Job details

Seniority
Manager
Function
Quality
Therapeutic area
Not listed
Location
Raynham, 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 243 comparable Manager Quality roles across 71 biopharma companies.

243Comparable roles tracked
227Currently active
71Companies hiring similar roles
32Countries represented

Salary context

66 of 243 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 $102,000/yr – $177,100/yr
Lowest disclosed · Associate Quality Control Chemist (Laboratory) - 2nd Shift · Merck KGaA $27/hr – $46/hr (≈ $56,160–$95,680/yr)
Peer group range $75,920 – $208,845 (median $167,375)

Where these roles are based

Top locations among the 243 comparable roles

United States106
China24
Ireland13
Netherlands11
Germany10
India9

+ 26 more countries

Seniority mix

243 of 243 peers have a known seniority level

Manager160
Associate Director45
Associate38

Therapeutic area mix

0 of 243 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
Novartis Carlsbad, United States 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

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, Medical Device (Sustaining)
Regeneron Pharmaceuticals, Inc (USA) · Renss, United States · Manager
Function Therapeutic area Seniority Country
60%
Quality Systems & Data Manager
GlaxoSmithKline LLC · Zebulon, United States · Manager
Function Therapeutic area Seniority Country
60%
Senior Manager Quality Assurance – Major Deviations Lifecycle Team
Amgen Manufacturing Limited LLC · Juncos, 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.