Biomedical Regulatory Affairs jobs
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Product Compliance & Regulatory Affairs Specialist
NewOften replies in 2 daysFrontier Dental SupplyMarkham, ON- $75,000–$80,000 a year
- Full-time
- Tuition reimbursement
- Vision care
- Dental care
- Life insurance
- Company events
- Extended health care
- 3+ years of experience in regulatory affairs, compliance, or a related field.
- Knowledge of international regulatory requirements.
View similar jobs with this employerDraeger Medical Canada, Inc.Mississauga, ON- $114,000–$136,800 a year
- Permanent
- Tuition reimbursement
- Vision care
- Dental care
- Paid vacation
- RRSP match
- Minimum 5 years in quality and regulatory affairs management within the medical device sector.
- Ensure appropriate training on quality and regulatory topics…
- ProductLife GroupRemote
- Fixed term contract
- Compile, publish, and validate regulatory submissions in line with health authority requirements.
- The Publishing Officer will support regulatory submission…
- View all ProductLife Group jobs - Remote jobs - Publisher jobs in Remote
- Salary Search: Publishing Officer – VAF salaries in Remote
- University of ManitobaWinnipeg, MB
- Full-time +1
- DPT currently has 16 full-time faculty and has a rich history of excellence in research and education in biomedical and clinical pharmacology and is committed…
- University of ManitobaWinnipeg, MB
- $32.25–$45.94 an hour
- Full-time +1
- Monday to Friday
- Understanding relevant legislation and guidelines of international, national and provincial regulatory bodies is a strong asset.
- University of ManitobaWinnipeg, MB
- $32.25–$45.94 an hour
- Full-time +1
- Monday to Friday
- Understanding relevant legislation and guidelines of international, national and provincial regulatory bodies is a strong asset.
- NeuroRx ResearchMontréal, QC
- $46,624.54–$85,733.87 a year
- Full-time
- Monday to Friday
- Extended health care
- NeuroRx est un chef de file dans l'analyse avancée d'images cérébrales et la gestion de projets au service de l'industrie pharmaceutique et biotechnologique.
- Applied Pharmaceutical InnovationEdmonton, AB T6N 1H1
- $74,750–$97,750 a year
- Full-time +1
- Paid time off
- Vision care
- Dental care
- Employee assistance program
- RRSP match
- Work from home
- Support internal and regulatory audits.
- This role is responsible for creating and managing GMP-compliant technical documentation, ensuring regulatory adherence,…
Project Manager, Regulatory Sciences
Easily applyNutrasourceGuelph, ON- $60,000–$70,000 a year
- Full-time
- Contribute to regulatory dossier writing with a high standard of accuracy and clarity.
- 3–5+ years of regulatory experience in dietary supplements and/or foods;…
View similar jobs with this employerSanofi EUToronto, ON M5R 3V5- $69,200–$100,000 a year
- Extended health care
- Department: Production Strategy and Projects (DS).
- The B100 Bulk Compliance Professional will manage projects affecting B100 Bulk Manufacturing in relation to…
Assistant Medical Strategist
Easily applyKlick HealthToronto, ON- $90,000–$110,000 a year
- Full-time
- Our Medical Strategy team, part of our Medical Craft, shapes how scientific insights inform brand and business decisions.
- View all Klick Health jobs - Toronto jobs - Medical Assistant jobs in Toronto, ON
- Salary Search: Assistant Medical Strategist salaries in Toronto, ON
- University of ManitobaWinnipeg, MB
- Full-time
- Applicants must have an earned doctorate or equivalent degree in physiology or a related field in biomedical sciences.
- Research plan (max 5 pages).
- University of ManitobaWinnipeg, MB
- Abundant opportunities exist for faculty members in the department to collaborate across the wider biomedical science research community on campus, including…
- University of ManitobaWinnipeg, MB
- Full-time
- Assistant, Associate, or Professor - Geographic Full-Time Contingent Position.
- Major areas of research include: i) Population health, outcomes research, and…
- CalianHalifax, NS
- $95,000–$115,000 a year
- Full-time
- In depth knowledge of ICH- Good Clinical Practice (GCP) and all relevant regulatory requirements.
- In-depth knowledge of ICH – Good Clinical Practice (GCP) and…
- View all Calian jobs - Halifax jobs
- Salary Search: Clinical Project Manager salaries in Halifax, NS
Canada Impact+ Research Chairs (Impact+)
Easily applyUniversity of AlbertaEdmonton, AB T6G 2B7- Full-time
- Advanced digital technologies (including artificial intelligence, quantum technologies, and cybersecurity).
- These Impact+ Chairs are consistent with the Canada…
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Product Compliance & Regulatory Affairs Specialist - job post
3.73.7 out of 5 stars
Markham, ON
$75,000–$80,000 a year - Full-time
Responded to 51-74% of applications in the past 30 days, typically within 2 days.
You must create an Indeed account before continuing to the company website to apply
Job details
Pay
- $75,000–$80,000 a year
Job type
- Full-time
Location
Markham, ON
Benefits
Pulled from the full job description
- Tuition reimbursement
- Vision care
- Dental care
- Life insurance
- Extended health care
- Company events
- On-site parking
Full job description
**Must be willing to work on-site in Markham office 5 days/week**
We are seeking a Product Compliance & Regulatory Affairs Specialist to ensure our products meet all necessary regulatory and compliance requirements across Canada and the USA.
Key Responsibilities:
- Regulatory Compliance & Documentation Ensure all products comply with applicable regulations (e.g., FDA, Health Canada, CE, ISO, RoHS, REACH). Prepare and maintain regulatory filings, product registrations, and technical documentation. Manage certifications and liaise with regulatory agencies as needed.
- Labeling & Safety Compliance Review product labels, packaging, and marketing materials for regulatory accuracy. Ensure proper documentation and distribution of Safety Data Sheets (SDS/MSDS).
- Cross-functional Collaboration Work closely with Procurement, Legal, and Marketing teams to integrate compliance requirements into product development. Provide regulatory guidance for new product launches and market expansions.
- Audits & Risk Management Support internal and external audits, inspections, and regulatory submissions. Develop and implement corrective action plans to address compliance risks.
- Monitoring & Reporting Stay updated on changes in regulations and industry standards. Assess and communicate regulatory risks and requirements to leadership.
Qualifications & Experience:
- Bachelor's degree in Regulatory Affairs, Life Sciences, Engineering, or a related field.
- 3+ years of experience in regulatory affairs, compliance, or a related field.
- Strong knowledge of regulatory frameworks (e.g., FDA, Health Canada, CE, ISO 13485, RoHS, REACH).
- Experience with technical documentation, audits, and risk management.
- Strong attention to detail, problem-solving skills, and ability to work cross-functionally.
- Experience in the dental industry, an asset.
- Familiarity with regulatory submission software and compliance databases.
- Knowledge of international regulatory requirements.
Pay: $75,000.00-$80,000.00 per year
Benefits:
- Company events
- Dental care
- Extended health care
- Life insurance
- On-site parking
- Tuition reimbursement
- Vision care
Work Location: In person
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