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

Medical Device Business Development jobs

Sort by: -
    • Familiarity with sales or business development processes is a plus.
    • Participate in risk management activities and contribute to the development of risk…
  • View similar jobs with this employer
    • Minimum 8 years of verifiable experience in a similar sales or business development role.
    • From automotive to medical and pharmaceutical companies, we have…
    • Strong expertise developing new business.
    • Identify and pursue new business opportunities.
    • Meet with business owners and decision makers.
    • Partner with Training to ensure onboarding, competency, and continuous development.
    • Delivers sales presentations to key clients in coordination with sales staff…
  • View similar jobs with this employer
    • Strong comfort level with daily travel and in-person, door-to-door business development, including working independently across a geographically defined…
    • Experience or interest in healthcare or medical equipment is a plus.
    • Join us in supporting the vital work of improving pediatric healthcare through quality…
    • Assist with medical device demonstrations, client education, and business development opportunities as needed.
    • On-Site | Full-Time | Greater Toronto Area*.
    • Manage integration activities involving connected clinical devices such as patient monitors, fetal monitors, dialysis, anesthesia-related devices, and other…
    • Participate in the design and development of medical devices.
    • Design, set up and perform tests to verify the viability and performance of medical devices.
    • Participate in the design and development of medical devices while following a quality system in accordance with ISO 13485.
    • Job Types: Full-time, Permanent.
    • Collaborate with internal teams to identify and advance development projects of interest.
    • Collaborate with partners to resolve issues related to regulatory…
    • We offer a challenge-rich environment where you can leverage your business development background to make a tangible impact on the bottom line.
    • La clinique ovo a comme mission de réaliser les rêves de famille grâce à des services innovateurs et une équipe passionnée.
    • La durée du contrat : 12 mois.
    • We’re Hiring in Vancouver, BC!*.
    • Dynasplint Inc. is the world leader in dynamic splinting products that aid in restoring physical function to patients with…
    • Southmedic is known globally as an innovative, high quality Canadian medical device manufacturer.
    • Strong sales and business development skills; preferred to…
Get e-mail updates for the latest Medical Device Business Development 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:

business student
development coordinator
development officer
entry level business
fundraising
innovation
medical assistant
medical office
medical office assistant
medical receptionist

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