Manager, Regulatory Affairs

2 weeks ago

Ahuntsic North QC HB, Montréal, Canada Options Consulting Solutions Full time
MANAGER, REGULATORY AFFAIRS
FULL-TIME
OTTAWA OR TORONTO

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
Competitive salary
Incentive bonus
Comprehensive benefits
Paid sick/personal days
3 weeks’ vacation
Professional development
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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