13 Financial Regulations jobs in Toronto

Who We Are

At Momentum Financial Services Group, we help people move forward by reimagining how money works for those who need it most. With more than 40 years of experience, we're the team behind Money Mart-Canada's largest non-

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 Function:**
Regulatory Affairs Group
**Job Sub** **Function:**
Regulatory Affairs
**Job Category:**
Professional
**All Job Posting Locations:**
Toronto, Ontario, Canada
**Job Description:**
We are searching for the best talent for our Manager, Regulatory Affairs position to be located in Toronto, Ontario under the flexible working model (at least 3 days in office).
**About Innovative Medicine**
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at Regulatory Affairs Manager is responsible for managing and leading the regulatory activities to obtain and maintain drug product registration status in compliance with Canadian drug laws and regulations, as well as corporate policies and procedures. As a subject matter expert and leader for Regulatory Affairs, the individual will provide guidance to local and global business partners. This role may have direct report(s).
**You will be responsible for:**
+ Developing and implementing regulatory strategic plans for product registration and lifecycle management.
+ Leading the preparation of regulatory submissions including New Drug Submissions (NDSs), Supplemental New Drug Submissions (SNDSs), and ad hoc reports to Health Canada, and maintain the life cycle of currently marketed products. The focus of this role is on the clinical/therapeutic claims and not the Chemistry, Manufacturing and Controls.
+ Leading the development and review of responses to Health Canada queries in relation to clinical efficacy and safety, clinical pharmacology, biopharmaceutics and preclinical subject matter (e.g. Clarifax, Notice of Non-Compliance (NON), and Notice of Deficiency (NOD)).
+ Leading interactions with Health Canada throughout the submission review cycle to ensure timely regulatory approval and optimal labelling.
+ Collaborating with global cross-functional teams and the Global Regulatory Affairs (GRA) function/teams to facilitate regulatory activities.
+ Collaborating with internal partners to ensure alignment of regulatory affairs strategy with business priorities, and to meet strategic business objectives and stretch goals.
+ Developing effective working relationships with business partners and the authorities to support regulatory strategies.
+ Managing emerging issues (e.g. new safety finding) and the associated risk communications.
+ Providing regulatory guidance and input to internal partners on messaging, promotional material review, and PAAB responses.
+ Monitoring the regulatory environment, interpreting changes, analyzing gaps and conducting impact assessment, and participating/leading implementation into systems/processes.
+ Actively contributing to the improvement of departmental processes and initiatives to enhance the internal work environment.
+ Mentoring and developing interns and/or directing reports as applicable.
**Qualifications/ Requirements:**
+ A minimum B.Sc. in Biological or related sciences is required. MSc/PhD preferred.
+ Minimum 5 years of pharmaceutical Regulatory Affairs or related experience is required.
+ Experience with the preparation and approval of regulatory submissions for brand name prescription drugs to a major Regulatory Authority (e.g. Health Canada, FDA, EMA, MHRA, TGA, SwissMedic) is required.
+ Must have experience in clinical and therapeutic aspects of submissions is required.
+ Strong working knowledge of the drug development process is required.
+ Knowledge of Canadian drug laws, regulations, guidelines and policies, and the Health Authority organizational structure and processes for the review and approval of drug submissions is required.
+ Ability to interpret and understand Regulations in the context of the scientific and commercial environment is required.
+ Strong scientific writing skills is required.
+ Ability to interpret and summarize clinical data is required.
+ Strong problem solving and analytical skills is required.
+ Ability to interpret basic biostatistics and observational research methodologies is preferred.
Diversity and inclusion are central elements of the shared culture across the Johnson & Johnson Family of Companies. Attracting, developing and retaining a workforce that reflects the diversity of our customers and communities is essential to our success. We are committed to providing a respectful, inclusive and accessible work environment where all employees have the opportunity to achieve their potential.
**#LI-Hybrid**

Please note: This is a paid co-op opportunity for students currently enrolled in an academic program, available for the Winter term (January to April).

The Crump Group Inc. is a family-owned and operated premium pet treat manufacturer. Started in 2006, we have successfully established 3 market leading brands (Caledon Farms, Crumps Naturals AND Dog Delights) distributed throughout Canada and the United States. The Crump Group Inc., a large & rapidly growing pet food manufacturer based in Mississauga Ontario and Nashville North Carolina is seeking a dynamic, results Regulatory Affairs Assistant Job Overview

We are looking for a qualified Regulatory Affairs Assistant. In the position of Regulatory Affairs Assistant, provide assistance and reporting to the Director of Quality and Regulatory Affairs in all aspects of day-to-day duties to include the following:

Key Responsibilities:

• Assist in preparing, reviewing, and submitting regulatory documents for product approvals.
• Research and analyze regulatory requirements specific to (industry/region).
• Maintain and update regulatory databases and filing systems.
• Support cross-functional teams in ensuring compliance with applicable standards.
• Monitor updates to local and international regulations and communicate key changes.
• Participate in audits, inspections, and quality assurance initiatives as required.
• Provide administrative support to the Regulatory Affairs team.

Qualifications:

• Currently enrolled in a (Bachelor's/Master's) program in (Life Sciences, Pharmacy, Engineering, or related field).
• Strong interest in regulatory affairs and compliance.
• Excellent organizational skills and attention to detail.
• Strong written and verbal communication skills.
• Ability to work collaboratively in a team environment.
• Research and analyze regulatory requirements specific to the pet / animal feed industry
• Proficiency in Microsoft Office

What You’ll Gain:

• Hands-on experience with regulatory processes and documentation.
• Exposure to cross-functional collaboration in a professional setting.
• Professional development opportunities and mentorship.

The Crump Group is committed to equity in employment and diversity. The Crump Group will provide an inclusive and barrier free recruitment process to applicants with accessibility needs in accordance with the Ontario Human Rights Code and the Accessibility for Ontarians with Disabilities Act (AODA). If you require a disability-related accommodation during this process, please inform The Crump’s Group of your requirements.

In compliance with Ontario's Bill 190, we confirm that this posting represents a current, existing vacancy. This job description may be amended at any time.

Please note: This is a paid co-op opportunity for students currently enrolled in an academic program, available for the Winter term (January to April).

The Crump Group Inc. is a family-owned and operated premium pet treat manufacturer. Started in 2006, we have successfully established 3 market leading brands (Caledon Farms, Crumps Naturals AND Dog Delights) distributed throughout Canada and the United States. The Crump Group Inc., a large & rapidly growing pet food manufacturer based in Mississauga Ontario and Nashville North Carolina is seeking a dynamic, results Regulatory Affairs Assistant Job Overview

We are looking for a qualified Regulatory Affairs Assistant. In the position of Regulatory Affairs Assistant, provide assistance and reporting to the Director of Quality and Regulatory Affairs in all aspects of day-to-day duties to include the following:

Key Responsibilities:

• Assist in preparing, reviewing, and submitting regulatory documents for product approvals.
• Research and analyze regulatory requirements specific to (industry/region).
• Maintain and update regulatory databases and filing systems.
• Support cross-functional teams in ensuring compliance with applicable standards.
• Monitor updates to local and international regulations and communicate key changes.
• Participate in audits, inspections, and quality assurance initiatives as required.
• Provide administrative support to the Regulatory Affairs team.

Qualifications:

• Currently enrolled in a (Bachelor's/Master's) program in (Life Sciences, Pharmacy, Engineering, or related field).
• Strong interest in regulatory affairs and compliance.
• Excellent organizational skills and attention to detail.
• Strong written and verbal communication skills.
• Ability to work collaboratively in a team environment.
• Research and analyze regulatory requirements specific to the pet / animal feed industry
• Proficiency in Microsoft Office

What You’ll Gain:

• Hands-on experience with regulatory processes and documentation.
• Exposure to cross-functional collaboration in a professional setting.
• Professional development opportunities and mentorship.

The Crump Group is committed to equity in employment and diversity. The Crump Group will provide an inclusive and barrier free recruitment process to applicants with accessibility needs in accordance with the Ontario Human Rights Code and the Accessibility for Ontarians with Disabilities Act (AODA). If you require a disability-related accommodation during this process, please inform The Crump’s Group of your requirements.

In compliance with Ontario's Bill 190, we confirm that this posting represents a current, existing vacancy. This job description may be amended at any time.

Please note: This is a paid co-op opportunity for students currently enrolled in an academic program, available for the Winter term (January to April).

The Crump Group Inc. is a family-owned and operated premium pet treat manufacturer. Started in 2006, we have successfully established 3 market leading brands (Caledon Farms, Crumps Naturals AND Dog Delights) distributed throughout Canada and the United States. The Crump Group Inc., a large & rapidly growing pet food manufacturer based in Mississauga Ontario and Nashville North Carolina is seeking a dynamic, results Regulatory Affairs Assistant Job Overview

We are looking for a qualified Regulatory Affairs Assistant. In the position of Regulatory Affairs Assistant, provide assistance and reporting to the Director of Quality and Regulatory Affairs in all aspects of day-to-day duties to include the following:

Key Responsibilities:

• Assist in preparing, reviewing, and submitting regulatory documents for product approvals.
• Research and analyze regulatory requirements specific to (industry/region).
• Maintain and update regulatory databases and filing systems.
• Support cross-functional teams in ensuring compliance with applicable standards.
• Monitor updates to local and international regulations and communicate key changes.
• Participate in audits, inspections, and quality assurance initiatives as required.
• Provide administrative support to the Regulatory Affairs team.

Qualifications:

• Currently enrolled in a (Bachelor's/Master's) program in (Life Sciences, Pharmacy, Engineering, or related field).
• Strong interest in regulatory affairs and compliance.
• Excellent organizational skills and attention to detail.
• Strong written and verbal communication skills.
• Ability to work collaboratively in a team environment.
• Research and analyze regulatory requirements specific to the pet / animal feed industry
• Proficiency in Microsoft Office

What You’ll Gain:

• Hands-on experience with regulatory processes and documentation.
• Exposure to cross-functional collaboration in a professional setting.
• Professional development opportunities and mentorship.

The Crump Group is committed to equity in employment and diversity. The Crump Group will provide an inclusive and barrier free recruitment process to applicants with accessibility needs in accordance with the Ontario Human Rights Code and the Accessibility for Ontarians with Disabilities Act (AODA). If you require a disability-related accommodation during this process, please inform The Crump’s Group of your requirements.

In compliance with Ontario's Bill 190, we confirm that this posting represents a current, existing vacancy. This job description may be amended at any time.

**Reference No** .R
**Position Title:** Head, Regulatory Affairs, General Medicine and Vaccines
**Department:** Regulatory Affairs
**Location:** Toronto, ON
**Posting Date:** Friday, August 15, 2025
**Closing Date:** Monday, September 1, 2025
**About the Job**
Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate progress.
The primary purpose of this position is to provide leadership to a team of regulatory professionals for regulatory affairs activities including early approvals and regulatory compliance activities throughout the entire product lifecycle for a portfolio of development and marketed prescription products, as defined by Head, Regulatory Affairs.
This position may also be a designated back-up to the Head, Regulatory Affairs
We are an innovative global healthcare company that helps the world stay ahead of infectious diseases by delivering more than 500 million vaccine doses a year. Across different countries, our talented teams are exploring new technologies to protect people and promote healthy communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world.
**Main Responsibilities:**
**Regulatory Activities and Resources (60%)**
+ Provide leadership and managerial support to submissions teams to ensure quality decisions and timely preparation of submissions to Health Canada in order to achieve the shortest time to approval and the best possible labelling. The portfolio supports products in the General Medicine and Vaccines Business units.
+ Ensure team maintains compliance (as per Global Regulatory Affairs performance timelines) to provision of current and accurate data in internal database systems
+ Evaluate business development opportunities in order to assess optimal regulatory strategy
+ Provide strategic direction and leadership in the management of clinical trial regulatory activities for defined portfolio
+ Participate in Business Unit (as assigned by Head, Regulatory Affairs) cross-functional leadership team(s) to ensure strategic leadership and contribution from regulatory affairs to core business activities
+ As part of RA Leadership team, assist Head, Regulatory Affairs in setting strategic direction for team and ensuring smooth daily operations
Regulatory Resources:
+ Ensure and maintain visibility and excellence of the team within business units by developing good scientific skills in the core therapeutic areas
+ Maintain awareness and knowledge of new and emerging local and international (EU and US) regulatory trends as well as on basic regulatory quality Canadian requirements
+ Review and provide comments on Health Canada draft guidelines and policies.
**Development of Human Capital (20-30%):**
Direct Reports:
+ Ensure implementation of departmental vision and strategies into individual priorities and goals
+ Provide constructive feedback and coaching to all direct reports on an ongoing basis to facilitate and enable the attainment of employees' development plans
+ Complete performance review activities for all direct reports as per the established corporate guidelines and practices
Self-Development:
+ Elaborate and implement a personal development plan that will allow for the attainment of personal goals and required competencies aligned to the corporate values and priorities
**Networking (10-20%):**
+ Establish and maintain a network with the key corporate regulatory sites and business units to assure the successful execution and alignment of Canadian-specific strategies within an international corporate context
+ Develop, optimize and maintain a network with key partners including the Canadian regulatory authority and key opinion leaders and seize opportunities to negotiate improved regulatory processes with the Canadian authority
+ Act as Sanofi liaison to industry advocacy external groups such as BIOTECanada or Innovative Medicines Canada (IMC), as required
**About You:**
**Education:**
+ Minimum Bachelor's degree in science or a degree in a health-related field
**Experience:**
+ At least 5 years of experience in regulatory affairs, as a project leader or in another related position and extensive knowledge of the regulatory environment
**Specific skills and/or competencies:**
+ Leadership and managerial skills (strong decision-making, communication, project management and risk analysis skills)
+ Building effective teams
+ Developed change leadership skills (i.e., ability to cope with and adapt to change, effectively prioritize, and deal with ambiguity)
+ Strong strategic and operational thinking (i.e., able to think big picture balanced with strong analytical skills)
+ Excellent negotiation skills with demonstrated ability to manage and influence key stakeholders
+ Fosters innovation (i.e., embraces new insights, concepts, trends & processes)
**Languages**
+ English (written and spoken)
+ French is an asset
**Computer knowledge**
+ MS Outlook, PowerPoint, Word, Excel, Adobe Acrobat, Veeva Vault database familiarity is an asset
**Travel**
+ Occasional
**Why Choose Us?**
+ Bring the miracles of science to life alongside a supportive, future-focused team.
+ Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally.
+ Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
+ Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs
Applications received after the official close date will be reviewed on an individual basis. This position is for a new vacant role that we are actively hiring for.
Sanofi is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. We welcome and encourage applications from all qualified applicants. Accommodations for persons with disabilities required during the recruitment process are available upon request.
#GD-SG
#LI-GZ
#LI-Onsite
**Pursue** **_progress_** **, discover** **_extraordinary_**
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
_North America Applicants Only_
The salary range for this position is:
$125,300.00 - $80,966.66
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the LINK ( .
La fourchette salariale pour ce poste est la suivante:
125,300.00 - 180,966.66
Toute compensation sera déterminée en fonction de l'expérience démontrée. Les employés peuvent être admissibles à participer aux programmes d'avantages sociau de l'enterprise. Des informations supplémentaires sur les avantages sont disponibles via le lien ( .
Global Terms & Conditions and Data Privacy Statement ( is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.
With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting or via our movie We are Sanofi ( an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live.
All in for Diversity, Equity and Inclusion at Sanofi - YouTube (