Skip to main content
Post your resume and find your next job on Indeed!

Medical Device Clinical Consultant jobs

Sort by: -
    • We are seeking a Product Compliance & Regulatory Affairs Specialist to ensure our products meet all necessary regulatory and compliance requirements across…
    • Educate medical staff including one-on-one teaching during surgical procedures utilizing our medical devices.
    • Develop in-depth clinical knowledge of anatomy and…
    • Experience with sterile products, complex generics, biosimilars, and drug–device combination products.
    • The Regulatory Affairs Manager leads Canadian regulatory…
    • Experience in running clinical activities according to ICH-GCP as well as Canadian regulatory clinical trial regulations and IMC guidelines.
    • Volume varies based on specialty and we consistently check in to make sure we are respecting your bandwidth.
    • Contract (payment on per-consult basis).
    • Medical Devices (Class I–II).
    • Natural Health Products (NHPs/NPNs).
    • The RAS plans, authors, files and maintains regulatory submissions and dossiers, and ensures…
    • Strong background in B2B sales, ideally within healthcare, medical devices, medical supplies, or related distribution environments.
    • This position may require onsite consultant engagements with in the pharmaceutical industry.
    • This pharmaceutical consultant role focuses on applying your GMP…
    • 10+ years of experience in healthcare strategy, digital transformation, or management consulting.
    • Strong knowledge of Ontario healthcare and digital health…
    • Leading or contributing to clinical and applied health research and quality aligned with Bruyère Health priorities.
    • Working knowledge of GCP/ICH guidelines and the clinical development process.
    • In depth proven experience in pharmaceutical and/or device research required.
    • Understanding of Pharmaceutical development and manufacturing processes; analytical, labelling clinical and non-clinical knowledge.
  • View similar jobs with this employer
    • We offer medical, dental, vision, and prescription drug coverage for employees and their eligible family members.
    • Thorough understanding of regulated clinical trial environment and in depth knowledge of drug development process.
    • Mentor and coach colleagues as required.
    • Minimum 4 years of experience working with medical devices under ISO 13485, MDSAP, MDD and/or MDR compliant QMS.
    • Must be able to travel to both US and Canada.
Get e-mail updates for the latest Medical Device Clinical Consultant jobs

By creating a job alert, you agree to our Terms . You can change your consent settings at any time by unsubscribing or as detailed in our terms.

Career Resources:

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
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

Let Employers Find YouUpload Your Resume