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Medical Device jobs in Calgary, AB

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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…
    • Be willing to learn and use technology tools, including mobile devices, apps, and registers, used in day-to-day operations.
    • Be at least 16 years of age.
    • Manage device security policies using MDM software (Kandji) to protect company assets.
    • Oversee endpoint security, identity and access management, privileged…
    • Extended health benefits (medical, dental, vision, paramedical).
    • Manage the control of monitoring and measuring (inspection and test) devices in accordance with…
    • Be able to select the right Protection and Automation devices complying with customer requirements.
    • Aware of protection philosophy, concepts, standards and…
    • Students at Christine Meikle School have complex learning, medical, and emotional needs.
    • Christine Meikle School offers highly specialized programming for…
    • Offer personalized consultations and guide customers through device fittings and demonstrations.
    • In this role, you will manage the customer journey by…
    • Offer personalized consultations and guide customers through device fittings and demonstrations.
    • In this role, you will manage the customer journey by…
    • Perform Preventive and predictive maintenance on automation and instrumentation devices.
    • Integrate field devices including sensors, actuators, and…
    • The primary role of a Protection & Control Technologist is to perform programming, testing and verification of protection & control devices in the field.
    • Deliver interpretation services via video and expediently type data on a company- provided device, such as a laptop, in order to perform the essential functions…
    • The primary role of a Protection & Control Technologist is to perform programming, testing and verification of protection & control devices in the field.
    • Exposure to regulated industries such as medical devices, industrial controls, oil and gas, or similarly technical environments.
    • Dedicated personal device (desktop, laptop, or tablet).
    • As an interpreter supporting healthcare providers, emergency services, insurance organizations,…
    • The work entails inspection and repair of hoists, pullers, crane systems and other lifting devices.
    • Lifting Equipment offers competitive wages based on work…
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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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