Associate Director, RA Canada

Posted Yesterday
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4 Locations
In-Office
124K-213K Annually
Senior level
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Role
The Associate Director leads regulatory affairs for Canada, ensuring compliance with local laws, guiding product registrations, and managing regulatory risks while collaborating with various stakeholders.
Summary Generated by Built In

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:

Regulatory Affairs Group

Job Sub Function:

Regulatory Affairs

Job Category:

People Leader

All Job Posting Locations:

Palm Beach Gardens, Florida, United States of America, Raynham, Massachusetts, United States of America, Toronto, Ontario, Canada, West Chester, Pennsylvania, 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.​

DePuy Synthes is recruiting for a(n) Associate Director, RA Canada, located in Toronto, Ontario or US locations of Raynham, MA, Warsaw, IN or West Chester, PA 

Job Overview 

The Associate Director, RA Canada provides regulatory leadership for the Canadian market, ensuring compliance with local regulatory requirements while enabling timely and sustainable market access for DePuy Synthes products. This role plays a critical leadership position within the Regulatory organization, partnering with commercial, quality, and global regulatory teams to shape regulatory strategy, manage risk, and support business growth in a highly regulated environment. 

 

Key Responsibilities 

  • Lead and oversee regulatory affairs strategy and execution for the Canada local market in alignment with global regulatory objectives. 

  • Ensure compliance with Health Canada requirements, internal policies, and quality system standards. 

  • Provide strategic regulatory guidance to support product registrations, renewals, variations, and lifecycle management. 

  • Serve as the senior regulatory point of contact and escalation lead for Canada Local Market Support. 

  • Partner with cross‑functional stakeholders including Commercial, Quality, Supply Chain, Legal, and Global Regulatory Affairs. 

  • Monitor regulatory changes in Canada and assess potential impacts to products, portfolios, and operations. 

  • Support regulatory inspections, audits, and health authority interactions as required. 

  • Lead, coach, and develop regulatory talent, fostering strong compliance, accountability, and performance. 

  • Ensuring proactive engagement and shaping of regional policy initiatives that are critical to business strategy, continuity, and growth. 

 

Qualifications 

Education: 

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

  • Advanced degree or professional certification in Regulatory Affairs (preferred). 

Experience and Skills: 

Required: 

  • Typically 8–10 years of progressive experience in Regulatory Affairs within the medical device or other regulated industries. 

  • Strong knowledge of Canadian regulatory requirements and Health Canada processes. 

  • Demonstrated experience leading regulatory strategy and execution at the country level. 

  • Proven ability to manage regulatory risk and complex stakeholder environments. 

  • Strong leadership, communication, and decision‑making skills. 

  • Ability to operate effectively in a global, matrixed organization. 

Preferred: 

  • Experience supporting US or global regulatory operating models. 

  • Experience working in multinational medical device or healthcare organizations. 

  • Exposure to regulatory inspections, audits, and authority negotiations. 

  • Demonstrated success driving regulatory transformation or process improvement initiatives. 

  • Regulatory Affairs Certification (RAC) or equivalent. 

Other: 

  • Language: English required; French proficiency preferred. 

  • Travel: Moderate national travel; occasional international travel. If based in a US location, 50% travel could be expected 

  • Certifications: RAC or equivalent preferred but not required. 

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:

Business Writing, Compliance Risk, Developing Others, Fact-Based Decision Making, Inclusive Leadership, Industry Analysis, Innovation, Leadership, Legal Support, Managing Managers, Operations Management, Policy Development, Product Licensing, Public Policies, Regulatory Affairs Management, Regulatory Compliance, Regulatory Development, Regulatory Environment, Strategic Thinking

The anticipated base pay range for this position is :

$124,000.00 - $212,750.00

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)).
This position is eligible to participate in the Company’s long-term incentive program.
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

Skills Required

  • Bachelor's degree in Regulatory Affairs, Life Sciences, Engineering, or a related discipline
  • Typically 8-10 years of progressive experience in Regulatory Affairs within regulated industries
  • Strong knowledge of Canadian regulatory requirements and Health Canada processes
  • Demonstrated experience leading regulatory strategy and execution
  • Strong leadership and decision-making skills
  • English required; French proficiency preferred
  • Regulatory Affairs Certification (RAC) or equivalent preferred

Johnson & Johnson Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Johnson & Johnson and has not been reviewed or approved by Johnson & Johnson.

  • Healthcare Strength Healthcare coverage is characterized as comprehensive across medical, dental, and vision, with added supports like onsite clinics, fitness centers, and Employee Assistance resources. Mental-health services and wellbeing reimbursements are also described as meaningful components of the overall package.
  • Retirement Support Retirement offerings are portrayed as a major differentiator, combining a 401(k) with employer matching and an employer-funded pension plan. Stock options and other long-term financial supports are also positioned as part of the broader rewards mix.
  • Parental & Family Support Family-related benefits are presented as notably strong, including paid parental leave for all new parents and additional leave types for caregiving and bereavement. Financial assistance for adoption, fertility treatment, and surrogacy is highlighted as a significant support.

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The Company
HQ: New Brunswick, NJ
143,612 Employees
Year Founded: 1886

What We Do

Profound Change Requires Boldness. Johnson & Johnson is the largest and most broadly based healthcare company in the world. We’re producing life-changing breakthroughs every day, and have been for the last 130 years. The combination of new technologies and your expertise enables amazing things to happen. Teams from J&J’s consumer business are creating digital tools to help people track the health of their skin. Those working in medical devices are 3-D printing artificial joints personalized for each patient, while researchers in pharmaceuticals use AI to discover lifesaving drugs. Imagine what the rest of our team of 134,000 people at 260 companies in more than 60 countries across the world is accomplishing. We redefine what it means to be a big company in today’s world. Social Media Community Guidelines: http://www.jnj.com/social-media-community-guidelines

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