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

Medical Writer jobs

Sort by: -
    • Medical Devices (Class I–II).
    • Natural Health Products (NHPs/NPNs).
    • The RAS plans, authors, files and maintains regulatory submissions and dossiers, and ensures…
    • Research professional, scientific, medical, academic, and industry associations that may require conference management or association management services.
    • Medical degree (MD or equivalent) from a recognized medical school.
    • Act as a medical consultant for the establishment and annual review of 811 clinical…
    • Senior Scientific Content Writer and Editor (Remote)*.
    • Collaborate with content strategists, editors, project managers, designers, and channel strategists to…
    • Proficient knowledge of new product and process development, current regulatory issues and regulations in Canada and the U.S. for NHPs/dietary supplements,…
    • Work-related/industry experience - reviewing medical assessment files, communicating with assessors, QA, and Adjusters is an asset but not required.
    • As a peer reviewer, further enhance the learning of the medical writer, providing feedback on the document and peer review findings.
    • Editing medical presentations to validate content against citations.
    • You would be responsible for, content development, editing and designing medical…
    • C’est pourquoi les gens aiment travailler chez nous.
    • Les possibilités de changer les choses dans le cadre d’initiatives client intéressantes sont illimitées…
  • View similar jobs with this employer
    • Accenture Song accélère la croissance et l'atteinte de la valeur ajoutée pour ses clients en leur assurant une pertinence durable auprès de leur clientèle.
    • About Lockwood: Lockwood collaborates with clients in the pharmaceutical, biotech, and medical device industries to identify effective, holistic, science-based…
    • About Lockwood: Lockwood collaborates with clients in the pharmaceutical, biotech, and medical device industries to identify effective, holistic, science-based…
    • The Publishing Officer will support regulatory submission publishing activities for global markets as part Publishing project.
    • Le rôle du représentant médical est d’évaluer la validité des protocoles de recherche d’un point de vue scientifique et médical et d’assurer que les projets de…
    • Direct collaboration with clinicians, medical directors, and health policy professionals.
    • Currently enrolled in or recently graduated from medical school, PA,…
Get e-mail updates for the latest Medical Writer 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.

People also searched:

medical writing
remote medical writer
scientific writer
scientific writing
remote pharmacist
medical office assistant
medical receptionist
writing
medical assistant
medical office

Career Resources:

Job Post Details

Pharmaceutical Regulatory Affairs Specialist - job post

CRL Synergy
Calgary, AB T2S 1W3
$68,000–$100,000 a year - Full-time

Job details

Pay

  • $68,000–$100,000 a year

Job type

  • Full-time

Location

Calgary, AB T2S 1W3

Benefits

Pulled from the full job description

  • Paid time off
  • Vision care
  • Dental care
  • Life insurance
  • Disability insurance
  • On-site gym
  • Extended health care

Full job description

Job Overview
CRL Synergy, one of Canada’s largest and fastest-growing suppliers of control label products, is seeking a detail-oriented and proactive Regulatory Affairs (RAS) Specialist.CRL Synergy is seeking a Regulatory Affairs (RAS) Specialist who can thrive in a fast-paced environment that involves working in an office team environment.

The Regulatory Affairs Specialist is the site lead for all Health Canada submissions and post-market activities covering four product categories sold across Canada:

  • Drugs (DIN-assigned OTC)
  • Cosmetics
  • Medical Devices (Class I–II)
  • Natural Health Products (NHPs/NPNs)

The RAS plans, authors, files and maintains regulatory submissions and dossiers, and ensures compliant labelling/advertising.

This role will also provide quality assurance support through maintenance of the RA SOPs, ensuring they are current and implemented, perform data collection, and subsequent analysis.

The successful candidate will provide support for new product development, ensuring Health Canada and customer requirements are being met, including labelling accuracy for new and modified product.

Responsibilities

  • Oversight of Pharmacovigilance program

· Collaborate with cross-functional teams to implement corrective and preventive actions (CAPA) related to customer complaints.

· Participate in risk management activities and contribute to the development of risk assessment strategies.

  • Ensuring accurate record keeping and filing as per organizational procedures.
  • Handle clerical and administrative activities.
  • Review and assess customer complaints for adverse reactions and reportable incidents. Perform surveillance activities for ongoing product quality and safety.
  • Complete Annual Summary Reports and perform screening of scientific literature for product safety information.
  • Assisting in updating methods and procedures (SOPs) related to the Quality Management System with a focus on the customer complaint and pharmacovigilance program.

Qualifications

  • Bachelor’s degree in a relevant field; advanced degree preferred.
  • Proven experience in regulatory affairs or a related field, with a strong understanding of compliance requirements.
  • Demonstrated skills in project management, including the ability to manage multiple projects simultaneously.
  • Strong leadership abilities with experience in supervising teams or mentoring staff.
  • Excellent analytical skills with a focus on process improvement methodologies.
  • Familiarity with sales or business development processes is a plus.
  • Exceptional communication skills, both written and verbal, with the ability to effectively convey complex information to diverse audiences. Join us in making a difference through compliance excellence!

Job Type: Full-time

Pay: $68,000.00-$100,000.00 per year

Benefits:

  • Company events
  • Dental care
  • Disability insurance
  • Extended health care
  • Life insurance
  • On-site gym
  • On-site parking
  • Paid time off
  • Vision care

Education:

  • Bachelor's Degree (preferred)

Experience:

  • Regulatory Affairs: 2 years (preferred)

Work Location: In person

Let Employers Find YouUpload Your Resume