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Medical Devices jobs in Ontario

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    • Proficient knowledge of new product and process development, current regulatory issues and regulations in Canada and the U.S. for NHPs/dietary supplements,…
    • Experience providing patient instruction on the use and care of medical devices or therapeutic products.
    • Prepare and submit Assistive Devices Program (ADP)…
    • Responsible for decontamination, reprocessing and sterilization of equipment, supplies and instrumentation.
    • Contributing to a safe, inclusive environment for…
    • Produce safe, high-quality medical devices that provide a better healthcare experience for our customers.
    • We are looking for new members to join our team and…
    • Dedicated personal device for business purposes.
    • As an interpreter supporting healthcare providers, emergency services, and public service organizations, you…
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    • Perform treatment preparation duties, including Computed Tomography (CT) Simulation and customized accessory fabrication (e.g. moulds, immobilization devices,…
    • Leads the development of a professional, service-focused culture within the nuclear operations and facilities to ensure the safe, efficient, and optimal use of…
    • 5–10 years of progressive experience in a licensed medical laboratory environment, including leadership responsibilities.
    • Accurately in the electronic medical record (EMR) system.
    • Certification and scope of practice until advanced medical assistance is available.
    • Operate energy-based devices, including skin tightening and resurfacing technologies.
    • Collaborate with the medical and operations teams to ensure exceptional…
    • Experience operating aesthetic devices and technologies.
    • Sales and retail experience in medical-grade skincare products.
    • Fast-paced, client-focused environment.
    • In this rehabilitative and complex care setting, you’ll have the time and resources to achieve meaningful progress with patients who need long-term, functional…
    • Offer personalized consultations and guide customers through device fittings and demonstrations.
    • In this role, you will manage the customer journey by…
    • We offer a robust benefits package to support your health, well-being, and growth, including medical, dental, and vision coverage, life & AD&D insurance, short-…
    • Provide statistical consultation to medical and clinical trial personnel for the publication of trial results, and participate in the writing of abstracts,…
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Job Post Details

Regulatory Affairs Associate - job post

Nutrasource
120 Research Lane, Guelph, ON
$46,563.40–$60,000.00 a year - Full-time

Job details

Pay

  • $46,563.40–$60,000.00 a year

Job type

  • Full-time

Location

120 Research Lane, Guelph, ON

Full job description

The Regulatory Affairs Associate works in a cross-functional project environment to support assessment of products against regulatory frameworks and registration of products in North America.

Primary Responsibilities

· Compiles regulatory applications (primarily for Health Canada and the FDA) to achieve departmental and organizational objectives.

· Prepares regulatory documentation as appropriate in accordance with product classification and associated regulatory pathways (e.g., OTC/Pharmaceutical Drugs, Food Ingredients, Natural Health Products (NHPs)/Dietary Supplements, Veterinary Health Products, Cosmetics, Medical Devices).

· Supports literature reviews and drafting of safety and efficacy data.

· Supports reviews of product and manufacturing changes for compliance with applicable regulations.

· Keeps abreast of domestic and global regulatory trends, laws, and movements

Core Competencies

· Proficient knowledge of new product and process development, current regulatory issues and regulations in Canada and the U.S. for NHPs/dietary supplements, prescription and non-prescription drugs, biologics, and medical devices preferred;

· Excellent oral and written communication, including technical writing skills and the ability to review and critique regulatory documents

· Ability to work well within a team and as an individual contributor.

· Computer literacy with MS Office Suite

Qualifications

· Bachelor’s Degree in a scientific discipline

· Minimum of 1-2 years industry experience, within the regulatory affairs function of a CRO/CPG/Pharmaceutical/Nutraceutical/Medical Device company

Pay: $46,563.40-$60,000.00 per year

Work Location: In person

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