Regulatory Affairs Specialist, Intermediate

Regulatory Affairs Specialist, IntermediateJob DescriptionPosted Tuesday, October 21, 2025 at 4:00 AMAbout UsSynaptive Medical is a Canadian medical device company, based in the Greater Toronto Area (Mississauga, Ontario), providing advanced precision imaging and intervention technology for improved diagnosis and treatment. Synaptive’s suite of products include Magnetic Resonance Imaging (MRI) systems, surgical planning, navigation, and robotic visualization. These products can be seamlessly combined or used independently in the operating room to improve detection and treatment for oncology, stroke and neurogenerative patients. The company has a global footprint of high-profile customers operating 24-7 for the betterment of all patients.The company has several opportunities for passionate and innovative people to join the team and share in the development of technologies to solve surgical and imaging challenges in patient care.The OpportunityThe Regulatory Affairs Specialist, Intermediate role is a vital role at Synaptive Medical Inc. (SMI) where you will work with various regulatory authorities globally and other departments in the company. You will bring vast medical device regulatory knowledge and in-depth technical and product development knowledge to this team. You will lead the development of regulatory submissions in multiple jurisdictions and contribute majority of the content while utilizing the Engineering and QA/RA teams as necessary. You will also participate in the regulatory review process with the authorities and ensure that the timing of regulatory filing and licenses are maintained. Your experience in development of regulatory strategy for various medical devices and strategically using this insight to influence the product development pathway will be critical.What You’ll DoYou will own regulatory filing strategy and submission for SMI’s products AND the develop content for regulatory filing for products that are manufactured by Synaptive.Must have a good understanding of regulations in the EU, USA, Canada and other jurisdictions, specifically MDR, FDA and Health CanadaProven experience having worked with Notified Bodies, Foreign Agents, Distributors and having a solid understanding of MDSAP, ISO 13485, ISO 14971, ISO 60601 and other relevant standards.Must have experience creating Technical Files/Checklist, Clinical Evaluation Reports and Post Market ReportsRepresents the regulatory department on product development teams and on project teams ensuring that regulatory requirements are clearly communicatedOversees and prepares submissions to be filed with the Regulatory Authorities in multiple jurisdictions for surgical, diagnostic imaging and consumable productsSeek out new regulatory requirements and ensure that they are reviewed and that proper risk assessments are performed to ensure ongoing compliance to existing and new regulationsProvides oversight for promotional material/trade shows, marketing collateral, of regulated products ensuring that compliance with all regulatory requirements are met.Regular cadence with key stakeholders to ensure ongoing alignment of regulatory strategy/plan with stakeholdersEnsure records are current and maintained, including timely renewal of licenses with regulatorsParticipate in internal/notified body, customer audits both scheduled and unannouncedKey participant in the management of regulatory recalls, including timely internal response and timely communication to customers, regulators, notified bodies, agents, distributors and other partiesEmpower employees to take responsibility for their jobs and goals. Delegate responsibility and expect accountability and regular feedback.Appropriately communicate through department meetings, one-on-one meeting and appropriate email, IM, regular interpersonal communicationWhat You’ll NeedBachelor’s Degree in science or related field. MSc preferred.Certification in a regulatory or quality discipline preferred, such as RAC.Minimum 4 years’ experience working in medical devices in an RA leadership roleKnowledge of FDA, MDR, Health Canada Regulations, ISO 13485 and ISO 14971Experience working directly with the FDA, Health Canada, Notified Bodies on regulatory filings/strategy is required. Similar experience with Health Canada is an asset.Experience with electronic submissions/the electronic submission process and how regulatory agencies operateExperience using software platform, such as Fusion, Trackwise or MasterControlKnowledge of 21 CFR 820, ISO13485:2016, MDSAP, MDR and ISO 14971About YouExcellent problem-solving, technical proficiency, and analytical abilitiesExcellent communication skills and knowledge in technical writingAble to adapt and drive change in a product development and manufacturing settingAbility to identify potential problems and take appropriate actionStrong organizational and time management skillsMust be able to work with others in different disciplinesMust be able to work in a team setting and on individual basisCOVID-19 ConsiderationsSynaptive has a special duty to take a leadership role in protecting the health and wellbeing of its employees and the public. The COVID-19 vaccines are an important public health measure for mitigating the spread of COVID-19 in the workplace and society. As a condition of employment, the successful candidate will be asked to provide proof of vaccination or a reason protected by legislation why they cannot be vaccinated against COVID-19.Diversity & InclusivitySynaptive is based out of one of the most diverse countries in the world. This includes differences related to race, ethnicity, national origin, gender, gender expression and presentation, sexual orientation, religion, age, ability and socioeconomic status. To us, diversity is one our strongest assets to our organization. We commit ourselves to promoting the recognition and appreciation of our diverse and rich culture. We believe that it is critical to our success to promote freedom of thought and opinion in a respectful environment. The decisions we make are rooted by respectfully considering each other’s thoughts and opinions and by working towards a greater common goal, saving lives.AccommodationSynaptive Medical is an equal opportunity employer and welcomes applications from all qualified individuals, including visible minorities, Indigenous People, and persons with disabilities. We welcome and encourage applications from people with disabilities. If as a qualified job applicant, you request accommodation, Synaptive will consult with you to provide reasonable accommodations according to your specific needs. If you wish to make a request, you will be provided an opportunity if your application is selected to proceed in our hiring process.How to ApplyUnless otherwise stated, applications will only be considered from candidates eligible to work in Canada, or the country in which they’re applying to, without sponsorship.If you are interested in this position and can demonstrate that you meet or exceed the requirements defined in the job description, please include #GOBRAIN in the top right corner of your resume and then complete your online application by clicking “Apply Now” and following the prompts.The successful candidate to this role will be asked to complete background checks, which may include criminal, credit, employment and/or educational checks. All offers of employment are conditional on the receipt of satisfactory results of any applicable background check.We would like to thank everyone who submits an application. Due to the volume that we receive, only those candidates selected for interviews will be contacted. #J-18808-Ljbffr