Manager, Regulatory Affairs
2 weeks ago
Are you in expert in health products regulations and submissions?
The Company
Our client is a national trade association renowned for the fantastic everyday products they offer. They are looking for an expert in regulatory affairs with a learning mindset and determination to be a top contributor to take the lead in regulatory activities with a consultative approach. If you are analytical, detail-oriented, strategic, and keen to make a positive impact, this could be the next step in your career
What’s in it for you
- Incentive bonus
- Hybrid work model-2 days in office
- Summer hours
- And more
The Job
Reporting to the Vice President of Health Policy and Regulatory Affairs, you are a leader within the department and tasked with ensuring compliance to consumer health product guidelines and ensuring regulatory initiatives are current and effective. Specifically, you will:
- Manage submissions and projects directed by the VP in collaboration with other teams and members.
- Conduct analyses and assessments of regulations (current, potential, and emerging) and related activities.
- Prepare and review regulatory proposals, guidance, and other policy materials with insight into impact for manufacturers and members.
- Develop and present technical submissions on behalf of the organization, aligned with regulations and guidelines.
- Provide technical expertise on documents and initiatives, ensuring compliance with regulations as well as company goals and objectives.
- Draft member consensus position such as responses to government and other stakeholders on health product regulation.
- Manage assigned member share groups and act as liaison for company staff and members on regulations.
- Represent the organization in external activities, meetings, and workshops.
- Communicate with external stakeholders, organizations, partnerships, etc.
- Perform other duties and tasks as required to support the department.
What you bring to the job
You are a strong leader and team player with expertise in regulatory affairs and a commitment to continuous learning. You are results-oriented, meticulous, and analytical, and take a consultative approach. You always maintain professionalism and strive to ensure the success of your team and the organization. You also have:
- A bachelor’s degree in a relevant field, such as science, biomedical studies, etc.
- Education in regulatory affairs (diploma or program) is strongly preferred.
- At least 8 years of experience in health sector regulations.
- Experience with consumer health products is highly preferred.
- Sound ability to understand and interpret both technical and regulatory documents.
- Able to communicate information quickly, clearly, and rationally – both written and verbal.
- Exceptional written communication skills to compile technical information for presentation and submission.
- Strong ability to perform effectively as an individual contributor as well as a collaborator and within a team.
- Proficiency with MS Office for document creation, as well as video conferencing platforms and technology for meetings and presentations.
- Bilingualism in English and French is a strong asset.
- Able to travel to Ottawa for events and team activities.
I really look forward to hearing from you, but please understand that I will only be contacting those that are applicable for the role
Options Consulting Solutions is an equal opportunity employer and welcomes applications from all individuals. Applicants selected for an in-person interview will be asked whether specific accommodations are needed to support a personal disability.
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Options Consulting Solutions in Toronto, Ontario, Canada
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