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    • Medical Devices (Class I–II).
    • Natural Health Products (NHPs/NPNs).
    • The RAS plans, authors, files and maintains regulatory submissions and dossiers, and ensures…
    • Recommend and promote medical-grade skincare products when appropriate.
    • Minimum 2 years of experience in a medical aesthetics environment preferred.
    • MANAGER OPERATING ROOM/MEDICAL DEVICE REPROCESSING DEPARTMENT Pre Op Clinic.
    • About The Opportunity Reporting to the Vice President of Clinical Services/Chief…
    • Experience in the medical or pharmaceutical field industry is an asset.
    • Status: Full time permanent (40 h/week).
    • Maintain a clean and orderly workstation.
    • We offer a competitive salary/benefits package, an annual Remote Retention Allowance and Relocation Allowance as applicable.
    • *Length of Shift in weeks: *2.
    • Assemble small, high-precision medical devices following detailed work instructions.
    • This role involves the precise assembly and soldering of small electronic…
    • Strong background in B2B sales, ideally within healthcare, medical devices, medical supplies, or related distribution environments.
    • Provide informed guidance on medical supplies, mobility devices, bracing, compression therapy, wound-care products, and home-health equipment.
    • Conduct preoperative patient assessments, review medical histories, verify informed consent, confirm surgical site and procedure details, and ensure patient…
    • Model data flows and makes architectural decisions based on product requirements, schedule, device limitations, bandwidth, latency, and system-level constraints…
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    • Manage and maintain first aid supplies, emergency response equipment, medical cabinets, and field safety kits.
    • Technical Leadership and Execution (5%)*.
    • Ability to push wheelchairs and safely secure mobility devices.
    • Safely secure wheelchairs and mobility devices according to training, vehicle requirements, and…
  • View similar jobs with this employer
    • Manage and maintain first aid supplies, emergency response equipment, medical cabinets, and field safety kits.
    • Technical Leadership and Execution (5%)*.
  • View similar jobs with this employer
    • Manage and maintain first aid supplies, emergency response equipment, medical cabinets, and field safety kits.
    • Technical Leadership and Execution (5%)*.
  • View similar jobs with this employer
    • Manage and maintain first aid supplies, emergency response equipment, medical cabinets, and field safety kits.
    • Technical Leadership and Execution (5%)*.
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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

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