Associate Manager, Regulatory Affairs
Top Benefits
About the role
Kenvue Is Currently Recruiting For a Associate Manager, Regulatory Affairs
What We Do At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent.
Who We Are Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here.
Role Reports To Regulatory Affairs Manager
Location: North America, Canada, Ontario, Markham
Work Location: Hybrid
What You Will Do The Associate Manager, Regulatory Affairs is responsible for ensuring compliance with regulatory requirements, preparing and submitting regulatory documentation, and providing expert advice to project teams. You will coordinate submission timelines, respond to agency inquiries, and manage pre- and post-market product lifecycle submissions:
Key Responsibilities
- Lead cross-functional initiatives to streamline regulatory submission processes, ensuring timely approvals while maintaining compliance with evolving Health Canada standards.
- Develop and implement innovative strategies to anticipate regulatory changes, proactively advising cross-functional teams to mitigate risks and capitalize on opportunities.
- Collaborate with R&D, quality assurance, legal and marketing teams to integrate regulatory considerations early in product development, enhancing market readiness and compliance.
- Ensure full compliance with regulatory agency regulations and interpretative guidance throughout the submission process and post-market life cycle.
- Prepare detailed and accurate responses to inquiries and correspondence from regulatory agencies in a timely manner.
- Collect, organize, and assemble all necessary documentation and data for regulatory submissions in strict adherence to applicable guidelines.
- Review advertising, promotional and artwork in compliance with Health Canada guidelines and regulations.
- Develop and manage submission timelines under the guidance of senior regulatory affairs personnel to ensure on-time delivery.
- Analyze complex regulatory challenges involving intangible variables and provide innovative, data-driven solutions utilizing data to monitor regulatory trends and performance metrics.
- Advise project teams on regulatory strategies and potential impacts to facilitate informed decision-making.
- Mentor junior regulatory specialists, fostering a culture of continuous learning and regulatory excellence within the team.
- Shape the regulatory environment through participation in industry associations and Health Canada consultations
Required Qualifications What we are looking for
- Bachelor’s degree or equivalent in Life Sciences, Pharmacy, or a related scientific or regulatory field.
- Minimum 6 years of progressive experience in Canadian regulatory affairs, preferably with expertise in cosmetics, natural health products or drugs.
- Demonstrated expertise in interpreting and applying Health Canada regulations and guidelines including preparing, submitting and maintaining regulatory submissions.
- Excellent communication skills, including the preparation of regulatory correspondence and regulatory strategies and articulation to cross-functional teams.
- Ability to manage multiple projects and timelines concurrently under minimal supervision.
Desired Qualifications
- Exceptional ability to interpret and apply Health Canada regulatory guidelines creatively to support innovative product development.
- Strong analytical mindset with proficiency in leveraging regulatory intelligence tools and data to monitor and forecast industry trends.
- Experience working collaboratively with senior regulatory staff and project teams to develop robust regulatory strategies.
- Excellent communication and leadership skills, capable of influencing cross-functional teams and mentoring emerging regulatory professionals.
- Strong analytical skills with the ability to evaluate complex data and intangible variables to solve regulatory challenges.
- Knowledge of the evolving regulatory landscape and participation in industry associations and Health Canada consultations
- Proficiency with regulatory systems and tools (e.g. eCTD, Veeva, RIMs)
What’s In It For You Annual base salary for new hires in this position ranges:$107,550.00 - $157,550.00
This takes into account a number of factors including work location, the candidate’s skills, experience, education level & other job-related factors.
- Competitive Benefit Package*
- Paid Company Holidays, Paid Vacation, Volunteer Time & More!
- Learning & Development Opportunities
- Kenvuer Impact Networks
- This list could vary based on location/region
- Note: Total Rewards at Kenvue include salary, bonus (if applicable) and benefits. Your Talent Access Partner will be able to share more about our total rewards offerings and the specific salary range for the relevant location(s) during the recruitment & hiring process.
Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on merit without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.
Kenvue incorporates Artificial Intelligence into our recruitment process to enhance job postings and streamline the sorting and screening of applications, helping attract a qualified candidate pool. Our experienced team will review and select the top applicants, ensuring that human judgment guides our hiring decisions. For more information, please refer to our Careers Privacy Policy.
Non-Vacancy: This posting does not correspond to an existing vacancy but is part of our proactive recruitment efforts.
Not the right fit? Search for Associate Manager, Regulatory Affairs jobs in Markham, Ontario
About Kenvue
Kenvue is the world’s largest pure-play consumer health company by revenue. Built on more than a century of heritage and propelled forward by science, our iconic brands — including Aveeno®, BAND-AID® Brand Adhesive Bandages, Johnson’s®, Listerine®, Neutrogena®, Tylenol® and Zyrtec® — are recommended by health care professionals and can be trusted by consumers who use our products to improve their daily lives. Our team members share a digital-first mindset, with an approach to innovation grounded in deep human insights and work every day to earn a place for our products in consumers’ hearts and homes. At Kenvue, we believe everyday care can not only make people well; it can make them whole.
Beware of recruitment scams: https://www.kenvue.com/media/recruitment-scams-alert
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Associate Manager, Regulatory Affairs
Top Benefits
About the role
Kenvue Is Currently Recruiting For a Associate Manager, Regulatory Affairs
What We Do At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent.
Who We Are Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here.
Role Reports To Regulatory Affairs Manager
Location: North America, Canada, Ontario, Markham
Work Location: Hybrid
What You Will Do The Associate Manager, Regulatory Affairs is responsible for ensuring compliance with regulatory requirements, preparing and submitting regulatory documentation, and providing expert advice to project teams. You will coordinate submission timelines, respond to agency inquiries, and manage pre- and post-market product lifecycle submissions:
Key Responsibilities
- Lead cross-functional initiatives to streamline regulatory submission processes, ensuring timely approvals while maintaining compliance with evolving Health Canada standards.
- Develop and implement innovative strategies to anticipate regulatory changes, proactively advising cross-functional teams to mitigate risks and capitalize on opportunities.
- Collaborate with R&D, quality assurance, legal and marketing teams to integrate regulatory considerations early in product development, enhancing market readiness and compliance.
- Ensure full compliance with regulatory agency regulations and interpretative guidance throughout the submission process and post-market life cycle.
- Prepare detailed and accurate responses to inquiries and correspondence from regulatory agencies in a timely manner.
- Collect, organize, and assemble all necessary documentation and data for regulatory submissions in strict adherence to applicable guidelines.
- Review advertising, promotional and artwork in compliance with Health Canada guidelines and regulations.
- Develop and manage submission timelines under the guidance of senior regulatory affairs personnel to ensure on-time delivery.
- Analyze complex regulatory challenges involving intangible variables and provide innovative, data-driven solutions utilizing data to monitor regulatory trends and performance metrics.
- Advise project teams on regulatory strategies and potential impacts to facilitate informed decision-making.
- Mentor junior regulatory specialists, fostering a culture of continuous learning and regulatory excellence within the team.
- Shape the regulatory environment through participation in industry associations and Health Canada consultations
Required Qualifications What we are looking for
- Bachelor’s degree or equivalent in Life Sciences, Pharmacy, or a related scientific or regulatory field.
- Minimum 6 years of progressive experience in Canadian regulatory affairs, preferably with expertise in cosmetics, natural health products or drugs.
- Demonstrated expertise in interpreting and applying Health Canada regulations and guidelines including preparing, submitting and maintaining regulatory submissions.
- Excellent communication skills, including the preparation of regulatory correspondence and regulatory strategies and articulation to cross-functional teams.
- Ability to manage multiple projects and timelines concurrently under minimal supervision.
Desired Qualifications
- Exceptional ability to interpret and apply Health Canada regulatory guidelines creatively to support innovative product development.
- Strong analytical mindset with proficiency in leveraging regulatory intelligence tools and data to monitor and forecast industry trends.
- Experience working collaboratively with senior regulatory staff and project teams to develop robust regulatory strategies.
- Excellent communication and leadership skills, capable of influencing cross-functional teams and mentoring emerging regulatory professionals.
- Strong analytical skills with the ability to evaluate complex data and intangible variables to solve regulatory challenges.
- Knowledge of the evolving regulatory landscape and participation in industry associations and Health Canada consultations
- Proficiency with regulatory systems and tools (e.g. eCTD, Veeva, RIMs)
What’s In It For You Annual base salary for new hires in this position ranges:$107,550.00 - $157,550.00
This takes into account a number of factors including work location, the candidate’s skills, experience, education level & other job-related factors.
- Competitive Benefit Package*
- Paid Company Holidays, Paid Vacation, Volunteer Time & More!
- Learning & Development Opportunities
- Kenvuer Impact Networks
- This list could vary based on location/region
- Note: Total Rewards at Kenvue include salary, bonus (if applicable) and benefits. Your Talent Access Partner will be able to share more about our total rewards offerings and the specific salary range for the relevant location(s) during the recruitment & hiring process.
Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on merit without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.
Kenvue incorporates Artificial Intelligence into our recruitment process to enhance job postings and streamline the sorting and screening of applications, helping attract a qualified candidate pool. Our experienced team will review and select the top applicants, ensuring that human judgment guides our hiring decisions. For more information, please refer to our Careers Privacy Policy.
Non-Vacancy: This posting does not correspond to an existing vacancy but is part of our proactive recruitment efforts.
Not the right fit? Search for Associate Manager, Regulatory Affairs jobs in Markham, Ontario
About Kenvue
Kenvue is the world’s largest pure-play consumer health company by revenue. Built on more than a century of heritage and propelled forward by science, our iconic brands — including Aveeno®, BAND-AID® Brand Adhesive Bandages, Johnson’s®, Listerine®, Neutrogena®, Tylenol® and Zyrtec® — are recommended by health care professionals and can be trusted by consumers who use our products to improve their daily lives. Our team members share a digital-first mindset, with an approach to innovation grounded in deep human insights and work every day to earn a place for our products in consumers’ hearts and homes. At Kenvue, we believe everyday care can not only make people well; it can make them whole.
Beware of recruitment scams: https://www.kenvue.com/media/recruitment-scams-alert