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    • 3+ years of experience in regulatory affairs, compliance, or a related field.
    • Knowledge of international regulatory requirements.
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    • Minimum 5 years in quality and regulatory affairs management within the medical device sector.
    • Ensure appropriate training on quality and regulatory topics…
    • Compile, publish, and validate regulatory submissions in line with health authority requirements.
    • The Publishing Officer will support regulatory submission…
    • 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…
    • Understanding relevant legislation and guidelines of international, national and provincial regulatory bodies is a strong asset.
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    • Support internal and regulatory audits.
    • This role is responsible for creating and managing GMP-compliant technical documentation, ensuring regulatory adherence,…
    • 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;…
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    • Department: Production Strategy and Projects (DS).
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    • Our Medical Strategy team, part of our Medical Craft, shapes how scientific insights inform brand and business decisions.
    • Applicants must have an earned doctorate or equivalent degree in physiology or a related field in biomedical sciences.
    • Research plan (max 5 pages).
    • Abundant opportunities exist for faculty members in the department to collaborate across the wider biomedical science research community on campus, including…
    • Assistant, Associate, or Professor - Geographic Full-Time Contingent Position.
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    • In depth knowledge of ICH- Good Clinical Practice (GCP) and all relevant regulatory requirements.
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    • Advanced digital technologies (including artificial intelligence, quantum technologies, and cybersecurity).
    • These Impact+ Chairs are consistent with the Canada…
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Job Post Details

Product Compliance & Regulatory Affairs Specialist - job post

Frontier Dental Supply
3.7 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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