First seen by our source: 6 hours ago
Regulatory Affairs Specialist
@ Johnson & Johnson MedTech
Markham, Ontario
SIGNALS
Overview
Johnson & Johnson MedTech is hiring a full-time Regulatory Affairs Specialist in Markham, Ontario, for its Orthopaedics business. The role develops Canadian regulatory strategies for Class III and IV medical devices and manages their lifecycle with Health Canada. The posting states a base pay range of $61,000 to $98,900 CAD and a discretionary performance bonus.
Responsibilities:
- Develop Canadian regulatory strategies for Class III and IV devices
- Manage product lifecycle regulatory aspects with Health Canada
- Maintain and improve the QMS per Health Canada and corporate requirements
- Support internal and external audits, including MDSAP inspections
- Review and approve promotional material
Requirements summary:
- Bachelor's degree in life science, engineering or physical science
- 3 to 5 years in medical device or pharmaceutical regulatory affairs preferred
- Knowledge of the Food and Drugs Act and regulations
- Experience managing regulatory submissions
- Strong written and verbal communication
Tools & skills
Regulatory affairsCommunication skillsLeadershipDocumentationTechnical writingInspectionRegulatory complianceProblem solvingQuality control systemsMedical devicesReporting
Source and dates
Source type not verified · apify-linkedin
- Employer posting date
- Not provided
- First seen by our source
- 2026-11-14
- Source record updated
- 2026-11-14
These dates describe the source record, not a live verification that the employer is still hiring. Check the original posting.
Job details
| Seniority | Mid level |
| Department | Legal & compliance |
| Experience | 3+ years |
| Hours per week | 40 (estimated) |
| Work setting | Office |
| Position | Mostly sitting |
| Physical demands | physical low · computer high |
| Languages | English |
| Licences & certifications | ISO 13485 |
| Education | Bachelor’s degree (required), Professional degree (MD, JD…) (preferred) |
| Fields of study | Life Science, Engineering, Physical Science, Quality/Regulatory Affairs |
| Perks mentioned | Performance bonus |
Summary and details written by AI from the posting; the employer’s posting is the authority.
Johnson & Johnson MedTech
| Field | Value |
|---|---|
| Open jobs on Jobsy | 4 |
Job description
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:
Professional
All Job Posting Locations:
Markham, Ontario, Canada
Job Description:
About Orthopaedics
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Are you passionate about improving and expanding the possibilities of Orthopaedics? Ready to join a team that’s reimagining how we heal? Our Orthopaedics teams help keep more than 6 million people moving each year while delivering clinical and economic value to surgeons and healthcare systems.
Our teams build solutions for joint reconstruction; trauma and craniomaxillofacial; sports, extremities, and elective foot and ankle; spine; and robotics and digital surgery.
Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech
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.
We are searching for the best talent for the Regulatory Affairs Specialist in
Markham, Ontario, Canada.
You Will Be Responsible For:
Develop and execute Canadian Regulatory strategies for complex Class III and Class IV medical devices, including combination products, to achieve and exceed business objectives.
Manage all Regulatory aspects of the product lifecycle from pre-market to post-marketing phase including reviewing and approving promotional material in alignment with corporate and Health Canada requirements.
Provide Regulatory consultation for business partners and provide expert Regulatory guidance to all internal stakeholders.
Establish and maintain strong relationships with Health Canada and business partners, driving collaboration on submission strategies, Regulatory pathways, submission status updates, recalls, and special access processes.
Maintain and continuously improve the Quality Management System (QMS) at DePuy Synthes in accordance with Health Canada regulations and corporate requirements, covering critical Regulatory and quality processes (i.e. submission management, renewal, special access, distribution, CAPA, change controls, document/records management) to enhance efficiency, compliance and overall performance.
Participate and support preparation and execution of internal and external audits, including Health Canada and MDSAP inspections.
Maintain awareness of new industry issues, trends and changes in regulation and policy and effectively communicate issues to key internal and external business partners. Coordinate comments on proposed regulations and policies.
Qualifications / Requirements:
University/Bachelor’s or equivalent degree in a Life Science, Engineering, or Physical Science is required.
Completion of post-graduate program in Quality/Regulatory Affairs is preferred.
3 - 5 years of experience in Medical Device and/or Pharmaceutical / Biologics Regulatory Affairs is preferred.
Sound knowledge of Food and Drugs Act and Regulations and relevant policies and guidelines is required.
Experience In Managing Regulatory Submission Activities Is Required.
Excellent skills in verbal and written communication are required.
Ability to develop and maintain strong working relationships with business partners and key stakeholders is required.
Demonstrated Leadership Skills Is Required.
Proven experience in successfully collaborating across functions and delivering business results is required.
Strong Documentation Skills And Technical Writing Capability Is Required.
Detail-oriented and ability to align with business objectives is required.
Experience in supporting health authority and or Notified Body inspections is an asset.
Proven ability to execute Regulatory submission strategies that align with business objectives and ensure compliance with applicable regulations is required.
Analytical and problem-solving skills, with the ability to effectively prioritize, organize, and manage multiple tasks is required.
Skills in managing change and implementation of new processes are preferred.
Experience in Quality system experience and strategic thinking in emerging and changing requirements preferred is an asset.
Experience in ISO 13485, or other Quality Systems Experience is an asset.
Experience in Canadian Regulatory Affairs for medical devices and combination products preferred.
Required Skills:
Preferred Skills:
Analytical Reasoning, Business Writing, Collaborating, Communication, Legal Support, Problem Solving, Product Licensing, Public Policies, Regulatory Affairs Management, Regulatory Compliance, Regulatory Environment, Regulatory Reporting, Risk Assessments, Strategic Thinking
The expected base pay range for this position is $61,000.00 to $98,900.00 CAD.
Under current guidelines, this position is eligible for a discretionary performance bonus.
AI Usage Disclosure
The Company uses Artificial Intelligence in its assessment of applicants.
Vacancy Disclosure
This job posting is for an existing position.
Accessibility For Ontarians With Disabilities Act
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.
Required Skills:
Preferred Skills:
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:
Professional
All Job Posting Locations:
Markham, Ontario, Canada
Job Description:
About Orthopaedics
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Are you passionate about improving and expanding the possibilities of Orthopaedics? Ready to join a team that’s reimagining how we heal? Our Orthopaedics teams help keep more than 6 million people moving each year while delivering clinical and economic value to surgeons and healthcare systems.
Our teams build solutions for joint reconstruction; trauma and craniomaxillofacial; sports, extremities, and elective foot and ankle; spine; and robotics and digital surgery.
Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech
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.
We are searching for the best talent for the Regulatory Affairs Specialist in
Markham, Ontario, Canada.
You Will Be Responsible For:
Develop and execute Canadian Regulatory strategies for complex Class III and Class IV medical devices, including combination products, to achieve and exceed business objectives.
Manage all Regulatory aspects of the product lifecycle from pre-market to post-marketing phase including reviewing and approving promotional material in alignment with corporate and Health Canada requirements.
Provide Regulatory consultation for business partners and provide expert Regulatory guidance to all internal stakeholders.
Establish and maintain strong relationships with Health Canada and business partners, driving collaboration on submission strategies, Regulatory pathways, submission status updates, recalls, and special access processes.
Maintain and continuously improve the Quality Management System (QMS) at DePuy Synthes in accordance with Health Canada regulations and corporate requirements, covering critical Regulatory and quality processes (i.e. submission management, renewal, special access, distribution, CAPA, change controls, document/records management) to enhance efficiency, compliance and overall performance.
Participate and support preparation and execution of internal and external audits, including Health Canada and MDSAP inspections.
Maintain awareness of new industry issues, trends and changes in regulation and policy and effectively communicate issues to key internal and external business partners. Coordinate comments on proposed regulations and policies.
Qualifications / Requirements:
University/Bachelor’s or equivalent degree in a Life Science, Engineering, or Physical Science is required.
Completion of post-graduate program in Quality/Regulatory Affairs is preferred.
3 - 5 years of experience in Medical Device and/or Pharmaceutical / Biologics Regulatory Affairs is preferred.
Sound knowledge of Food and Drugs Act and Regulations and relevant policies and guidelines is required.
Experience In Managing Regulatory Submission Activities Is Required.
Excellent skills in verbal and written communication are required.
Ability to develop and maintain strong working relationships with business partners and key stakeholders is required.
Demonstrated Leadership Skills Is Required.
Proven experience in successfully collaborating across functions and delivering business results is required.
Strong Documentation Skills And Technical Writing Capability Is Required.
Detail-oriented and ability to align with business objectives is required.
Experience in supporting health authority and or Notified Body inspections is an asset.
Proven ability to execute Regulatory submission strategies that align with business objectives and ensure compliance with applicable regulations is required.
Analytical and problem-solving skills, with the ability to effectively prioritize, organize, and manage multiple tasks is required.
Skills in managing change and implementation of new processes are preferred.
Experience in Quality system experience and strategic thinking in emerging and changing requirements preferred is an asset.
Experience in ISO 13485, or other Quality Systems Experience is an asset.
Experience in Canadian Regulatory Affairs for medical devices and combination products preferred.
Required Skills:
Preferred Skills:
Analytical Reasoning, Business Writing, Collaborating, Communication, Legal Support, Problem Solving, Product Licensing, Public Policies, Regulatory Affairs Management, Regulatory Compliance, Regulatory Environment, Regulatory Reporting, Risk Assessments, Strategic Thinking
The expected base pay range for this position is $61,000.00 to $98,900.00 CAD.
Under current guidelines, this position is eligible for a discretionary performance bonus.
AI Usage Disclosure
The Company uses Artificial Intelligence in its assessment of applicants.
Vacancy Disclosure
This job posting is for an existing position.
Accessibility For Ontarians With Disabilities Act
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.
Required Skills:
Preferred Skills:
Journal
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