Johnson & Johnson Posted August 20, 2026

Manager, Technical Regulatory Compliance

Warsaw, United States Full time
Quality Manager

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:

Quality & Compliance Audit

Job Category:

Professional

All Job Posting Locations:

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

Job Description:

DePuy Synthes is recruiting for a Manager, Technical Regulatory Compliance,   located   in Raynham MA or Palm Beach Gardens FL or West Chester PA.

Job Overview

The Manager, Technical Regulatory   Compliance   is responsible for   leading compliance activities related to technical, system, and process regulatory requirements. This role ensures that technical operations, systems, and documentation   comply with   applicable regulations, quality system standards, and internal policies. The position plays a critical role in managing compliance risk, supporting audit and inspection readiness, and enabling compliant execution of technical initiatives by partnering closely with Quality, Regulatory Affairs, Engineering, Manufacturing, and IT teams.

Key Responsibilities

Lead and manage technical regulatory compliance activities in alignment with global and regional compliance strategies.

Provide compliance oversight for technical processes, systems, and documentation supporting regulated activities.

Interpret regulatory and technical standards and translate them into actionable compliance requirements.

Partner with Quality, Regulatory Affairs, Engineering, Manufacturing, and IT teams to support compliant   system   and process implementation.

Support internal audits, external audits, and health authority inspections related to technical compliance.

Monitor compliance risks, trends, and performance metrics and drive corrective and preventive actions.

Ensure consistent application of global and site‑specific compliance policies, procedures, and controls.

Drive continuous improvement initiatives to strengthen technical   compliance   governance and effectiveness.

Qualifications

Education :

Bachelor’s degree in Regulatory Affairs, Quality, Engineering, Life Sciences, Information Systems, or   a related   discipline (required).

Advanced degree in a scientific, regulatory, or technical field (preferred).

Experience and Skills :

Required :

Typically   6-8   years of progressive experience in Regulatory Compliance, Quality Systems, Engineering, or related roles within a regulated industry.

Strong working knowledge of regulatory and technical requirements   impacting   quality systems and manufacturing processes.

Experience supporting audits, inspections, and regulatory assessments.

Ability to manage complex technical compliance topics across cross‑functional stakeholder groups.

Strong analytical, risk‑management, and problem‑solving skills.

Effective written and verbal communication skills.

Preferred :

Experience in medical devices, healthcare, or other highly regulated industries.

Familiarity with U.S. regulatory and technical compliance frameworks.

Experience working in a global or matrixed organization.

Exposure to regulatory inspections involving technical or system compliance.

Quality or Regulatory certifications (e.g., RAC, ASQ).

Other :

Language: English   required .

Travel: Limited; occasional domestic travel.

Certifications: Quality or Regulatory certifications preferred but not   required .

For more information on how we support the whole health of our employees throughout their wellness,   career   and life journey, please visit   www.careers.jnj.com .

Johnson & Johnson announced plans to separate our Orthopaedics 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.

#LI-Hybrid

#DePuySynthesCareers

Required Skills:

Preferred Skills:

Agile Internal Audit, Analytical Reasoning, Audit and Compliance Trends, Compliance Frameworks, Compliance Management, Compliance Policies, Compliance Risk, Controls Compliance, Critical Thinking, Developing Others, Inclusive Leadership, Leadership, Problem Solving, Quality Auditing, Quality Control (QC), Quality Standards, Regulatory Compliance, Regulatory Environment, Risk Management, Supervision, Third-Party Auditing

Job details

Seniority
Manager
Function
Quality
Therapeutic area
Not listed
Location
Warsaw, 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 236 comparable Manager Quality roles across 65 biopharma companies.

236Comparable roles tracked
216Currently active
65Companies hiring similar roles
28Countries represented

Salary context

70 of 236 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 Metrologist · Merck KGaA $27/hr – $46/hr (≈ $56,160–$95,680/yr)
Peer group range $75,920 – $219,500 (median $165,300)

Where these roles are based

Top locations among the 236 comparable roles

United States107
China23
India17
Ireland15
Japan13
Belgium7

+ 22 more countries

Seniority mix

236 of 236 peers have a known seniority level

Manager161
Associate Director46
Associate29

Therapeutic area mix

0 of 236 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
Gilead Sciences, Inc. La Verne, 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
Gilead Sciences, Inc. Foster City, 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 Control
Gilead Sciences, Inc. · La Verne, United States · 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%
Senior Manager Quality Assurance, Drug Product (Filling)
Regeneron Pharmaceuticals, Inc (USA) · Renss, 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.