Environmental Materials and EPR Program Compliance Manager

Johnson & Johnson MedTech; Raynham (MA); On-site; USD 117,000 - 201,000; Full time

Benefits offered by this job

Travel up to 10%

RAC preferred

Job summary

Johnson & Johnson MedTech in Raynham, MA is seeking a global SME for materials compliance and EPR responsibilities within Regulatory Affairs. You'll monitor global requirements, lead data governance, and coordinate with affiliates to meet registrations and reporting obligations.

The role emphasizes cross-functional collaboration, program management, and continuous improvement across compliance processes. Candidate should have 6–8 years in regulatory affairs or product stewardship, with strong

Qualifications

• Bachelor’s degree in Environmental Science, Engineering, EHS, Regulatory Affairs, Life Sciences, Data Science, or related discipline is required.
• Advanced degree or relevant professional certification is preferred.

Responsibilities

• Serve as the global SME for materials compliance and EPR requirements, including but not limited to EEE, WEEE, e-waste, batteries, packaging, plastics, reporting, registrations, fees, and take-back schemes.
• Monitor and interpret emerging global requirements; lead impact assessments and translate findings into actionable business plans and clear stakeholder guidance.
• Maintain regulatory trackers, compliance dashboards, metrics, inventories, and leadership updates.
• Identify data gaps and lead the collection, validation, governance, reporting, and retention of materials and EPR data, including improvements to supporting technology.
• Coordinate with regional affiliates and business partners to complete registrations, reports, fees, and other compliance obligations on time.
• Lead Materials and EPR Communities of Practice, training, action tracking, and representation in enterprise or industry working groups.
• Partner with Government Affairs & Policy, trade associations, and industry groups on advocacy and company positions.
• Develop and maintain policies, procedures, work instructions, and best practices.
• Support audits, inspections, assessments, information requests, corrective actions, customer inquiries, acquisitions, divestitures, and integrations.
• Provide practical SME support and drive continuous improvement across compliance processes.

Skills

Materials compliance

Regulatory affairs

Data reporting

Project management

English proficiency

Education

Bachelor's degree

Advanced degree preferred

Tools

Regulatory data systems

Compliance dashboards

Job description

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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

Regulatory Affairs Group

Job Sub Function

Regulatory Affairs

Job Category

People Leader

All Job Posting Locations

Raynham, Massachusetts, United States of America

Job Description

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.

Key Responsibilities

• Serve as the global SME for materials compliance and EPR requirements, including but not limited to EEE, WEEE, e-waste, batteries, packaging, plastics, reporting, registrations, fees, and take-back schemes.
• Monitor and interpret emerging global requirements; lead impact assessments and translate findings into actionable business plans and clear stakeholder guidance.
• Maintain regulatory trackers, compliance dashboards, metrics, inventories, and leadership updates.
• Identify data gaps and lead the collection, validation, governance, reporting, and retention of materials and EPR data, including improvements to supporting technology.
• Coordinate with regional affiliates and business partners to complete registrations, reports, fees, and other compliance obligations on time.
• Lead Materials and EPR Communities of Practice, training, action tracking, and representation in enterprise or industry working groups.
• Partner with Government Affairs & Policy, trade associations, and industry groups on advocacy and company positions.
• Develop and maintain policies, procedures, work instructions, and best practices.
• Support audits, inspections, assessments, information requests, corrective actions, customer inquiries, acquisitions, divestitures, and integrations.
• Provide practical SME support and drive continuous improvement across compliance processes.

Qualifications And Education

• Bachelor’s degree in Environmental Science, Engineering, EHS, Regulatory Affairs, Life Sciences, Data Science, or a related discipline is required.
• Advanced degree or relevant professional certification is preferred.

Required

Experience and Skills:

• 6–8 years of progressive experience in Product Stewardship, environmental compliance, regulatory affairs, or a related field.
• Strong knowledge of global materials compliance and EPR requirements, with experience implementing regulatory programs in industry.
• Ability to interpret emerging regulations, assess business impact, and translate technical requirements into executable plans and clear communications.
• Experience with regulatory data, reporting, dashboards, documentation, and technology-enabled compliance solutions.
• Strong project and program management skills, including governance, metrics, and action tracking.
• Ability to work independently, exercise sound judgment, manage priorities, solve problems, and maintain attention to detail.
• Strong influencing, facilitation, collaboration, writing, and presentation skills in a global matrixed organization.
• English proficiency.

Preferred

• Experience in healthcare, medical devices, pharmaceuticals, or another highly regulated industry.
• Experience with advocacy, trade associations, audits, inspections, compliance assessments, or corrective actions.
• Familiarity with sustainability, circular economy, and environmental reporting.
• Experience supporting global portfolios, acquisitions, or divestitures.

Other

• Travel: Up to 10%, including occasional international collaboration.
• Certifications: RAC, environmental compliance, or sustainability certification preferred.

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 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 applicants’ needs. Individuals who would like to request an accommodation should use the applicable external applicant or internal employee accommodation resource.

The anticipated base pay range for this position is :

$117,000.00 - $201,250.00