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Medical Writing jobs in Ontario

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    • Excellent oral and written communication, including technical writing skills and the ability to review and critique regulatory documents.
    • Excellent writing and editing skills in preparing concise, clearly written scientific and medical content to different target audiences, including use of…
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    • Minimum of 3 years of medical copy development expertise, with success in crafting persuasive content for diverse healthcare audiences (HCPs, patients,…
    • 3+ years of experience in proposal writing, technical writing, marketing communications, or a related role, preferably in a consulting, engineering, utility,…
    • You possess excellent written and verbal communication skills and the ability to explain complex issues in plain language, both verbally and in writing.
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    • Experience with proposal writing and/or project management.
    • Depending on your employment status, AECOM benefits may include medical, dental, vision, life, AD&D,…
    • Strong English communication skills (speaking, listening, reading, and writing).
    • Comprehensive benefit package specific to your work status (including extended…
    • Strong technical writing and communication skills.
    • At Parsons, we offer a robust Employee Assistance Program as well as comprehensive medical, dental and vision…
    • Nous vous acceptons comme vous êtes.
    • En tant qu’employeur soucieux de l’égalité des chances, Dialogue s’engage à créer un lieu de travail diversifié et inclusif…
    • Strong writing and storytelling skills you can translate complex information into clear, compelling content.
    • To ensure an efficient and fair review process, we…
    • In addition, we offer an attractive groups benefits package, that includes coverage for dental, drug and medical.
    • Create graphics of neuroimaging results;
    • Sault Area Hospital does not use artificial intelligence (AI) to screen, assess or select applicants for a position.
    • All requests are handled confidentially. ×.
    • Fluent in English, with excellent writing and proofreading skills.
    • Group Health Insurance Plan (medical, dental, health care spending account).
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    • You are comfortable working with both qualitative and quantitative inputs, including conversations, interviews, survey data, partner insights, and performance…
    • Competitive medical and dental benefits.
    • Strong communication skills, especially with writing, proofreading, and editing.
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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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