Manager, Regulatory Affairs

Found in: Whatjobs CA C2 - 2 weeks ago

Ottawa, 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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