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

Medical Biotechnology 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…
    • Assemble small, high-precision medical devices following detailed work instructions.
    • This role involves the precise assembly and soldering of small electronic…
  • View similar jobs with this employer
    • Knowledge of regulations governing medical information exchange with healthcare professionals within the Canadian pharmaceutical environment.
    • API offers a generous paid time off (PTO) policy that includes vacation days, medical/personal days, and holidays.
    • Maintain documents within QMS systems.
    • A Clinical Lab Technician, Microbiologist or Analytical Chemist / Biochemist with extensive experience on running clinical analytical assays on various clinical…
    • Microbiology (biotechnology/pharmaceutical ): 10 years (required).
    • Supported by 5 or more years of microbiology laboratory experience within a biotechnology/…
    • Maintain documentation, including lab notebooks, equipment logbooks and microbiological data.
    • Perform all activities in compliance with GLP/GMP guidelines &…
  • View similar jobs with this employer
    • 10+ years, direct experience in pharmaceutical/biotechnology manufacturing, and quality environments/organizations.
    • We are seeking a Part-Time Quality Director (remote) to provide oversight of GMP and regulatory quality activities over a 16-month contract term.
    • HyperMabs Inc. *is a fast-growing biotechnology company focussed on research and development of novel treatments for diseases with high unmet medical need.
    • We are looking for a reliable, hands-on Technician with general mechanical or handyman experience.
    • This role is ideal for someone comfortable working with tools…
    • This pharmaceutical consultant role focuses on applying your GMP knowledge and experience to various projects, such that the client is confident in the approach…
    • Proficient knowledge of new product and process development, current regulatory issues and regulations in Canada and the U.S. for NHPs/dietary supplements,…
    • To support the execution of GxP audit and inspection activities across GCP, GLP, and GVP, ensuring compliance with applicable global regulations and internal…
    • Experience: Previous exposure to administrative environments (medical, clinic, or corporate office setting) is highly preferred.
Get e-mail updates for the latest Medical Biotechnology 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:

napanee
laboratory technician
medical assistant
medical office
medical office assistant
medical receptionist
microbiology
molecular biology
pharmaceutical
science

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