3 Patient Monitoring jobs in Canada
Medical Devices Marketing Manager
Posted today
Job Viewed
Job Description
Job Description
ABOUT THE COMPANY
This Canadian-owned healthcare manufacturer and distributor develops innovative, clinically effective medical products that support patient care across the continuum of acute and long-term care. You’ll join a collaborative and growing marketing team that works closely with national sales, operations, and product development teams to deliver value-driven solutions to hospitals, clinics, and care providers across Canada in the areas of digestive health and pain management.
WHAT ARE THE PRIMARY RESPONSIBILITIES OF THE JOB?
- Lead the creation and execution of strategic marketing plans and product roadmaps.
- Manage full P&L accountability for assigned product platforms.
- Strengthen brand identity while launching new products and growing existing lines.
- Analyze business intelligence data to optimize pricing and margin performance.
- Support RFP submissions with sales and contracts teams.
- Collaborate with Business Operations to enhance the customer experience.
- Develop field-ready tools and programs to support the national sales team.
- Mentor and coach sales reps, marketing associates, and distributors.
Requirements
WHAT DOES THE IDEAL CANDIDATE OFFER?
Education & Training
- Bachelor’s degree in Business, Marketing, or Life Sciences.
Work Experience & Accomplishments
- 4+ years of experience in life sciences or healthcare marketing.
- Proven ability to lead product marketing, vendor partnerships, and strategic planning.
- Strong track record of working cross-functionally across Sales, Operations, and Product Development.
- Experience in contract negotiations and marketing through distribution channels.
- Demonstrated success in technical marketing environments.
Skills & Competencies
- Strong analytical and financial acumen (pricing, margin, forecasting).
- Skilled communicator, capable of presenting to internal and external stakeholders.
- Proficiency with MS Office and business intelligence tools.
- Ability to lead marketing efforts across multiple projects and product lines.
- Comfortable navigating both office and production/warehouse environments.
Benefits
WHAT DOES THE COMPANY OFFER IN RETURN?
- Competitive salary, bonus potential and benefits.
- Stable, Canadian-owned company with a growing national presence.
- Opportunity to make a direct impact on the healthcare sector.
- Collaborative, values-based work culture.
- Professional development and advancement opportunities.
- Hybrid work environment (3 days in-office, 2 days WFH)
Are you ready to lead marketing strategy for a trusted Canadian medical brand? Apply now to take the next step in your healthcare marketing career.
Quality Assurance & Regulatory Affairs Associate – Pharmaceuticals & Medical Devices
Posted today
Job Viewed
Job Description
Quality Assurance & Regulatory Affairs Associate Position –
Pharmaceuticals & Medical Devices
Our company is a specialty medical device, cell-tissue-organs, and pharmaceutical importer and distributor. We are committed to providing exceptional service and brand awareness to thousands of hospitals, dental and oral surgery clinics that we serve in Canada, the United States and around the world. Our company represents leading brands in their respective categories.
p>We are importer and distributor of drugs including: narcotics, prescriptions, ethical and OTC drugs, medical devices (MD), cell-tissue-organs (CTO) and natural health products (NHP) in Canada. Our company is also an importer and distributor of medical devices (MD), and human-cell-tissue products (HCTP) in the USA. Furthermore, our company is the owner of a health Canada drug license for dental anesthetics. p>The QA & RA associate position is a GMP role responsible for a wide variety of Quality Assurance and Regulatory Affairs activities related to Drugs, MDs, CTOs and NHPs. In addition, the QA & RA Associate will communicate with vendors, prepare documentation and processes, contribute to drugs or MD submissions, and maintain all documentation and records.Compensation: 60K to 70K
Location: Mississauga, ON
Essential Job Functions and Responsibilities
General
- Support and maintain a process that ensures all requirements from Health Canada and FDA are met
- Maintain all documentation and necessary records for Drugs, MDs, CTOs and NHPs activity
Quality Assurance
- As approved AQPIC, perform all the duties related to narcotics activity onsite (e.g. product receiving, inspection, distribution, monthly reporting etc.)
- Maintain the Quality Management Systems (QMS) for drugs, MDs, CTOs , and HCTPs
- Write new SOPs. Review and update of SOPs and standard forms.
- Documentation review and drug inspection for batch release, including narcotics
- Full process for Quality Product Complaints for drugs, MDs, CTOs, and NHPs
- Review and documentation of all returned products
- Review and documentation of starting materials, and emergency kits
- Review of imported NHP finished products
- Participate in Health Canada GMP inspection
- Participate in Health Canada, and FDA inspections for MDs, and CTOs /HCTPs
- Participate in annual self-inspection and corrective /preventive actions
- Support on ISO-13485 certification and recertification for MD Quality Management System
- Documentation of change controls and deviations
- Prepare, review and maintain all documentation from DIN manufacturers
- Preparation, review and maintenance of any logs, spreadsheet, or records
- Support with staff GMP and QMS training
- Perform quality inspection of facilities
Regulatory Affairs
- Review and document all ADRs, and forward to respective authorities, when needed
- Support and records on drug pharmaco-vigilance process, and MD problem reporting
- Support on renewing all drug and MD licenses, and updating all licenses: DEL, MDEL, CTO, NHP SL, wholesale/ distributor, tissue bank, and FDA registrations
- Participate to comply with recall procedure for drugs, MDs in Canada, and MDs and HCTPs in USA
- Participate in Health Canada pharmaco-vigilance inspection
- Support submission process for existing and new products, drugs, MDs, and NHPs
- Support any regulatory change submission for drugs in eCTD format /software
- Support and review final submission documents, keep submission copies, and e-file
- Support international regulatory documentation requests
- Maintain and submit monthly narcotics report to Health Canada
Requirements
- Bachelor’s degree in science or a related field (e.g., Biology, Chemistry, Biochemistry, Biotechnology, Kinesiology, Pharmacology, Pharmacy, Biomedical Sciences, etc.) < i>4+ years of experience in pharmaceuticals and/or medical devices (MD) in an associate or above role
- Meet all Health Canada requirements to be approved as AQPIC (Narcotics activity)
- Skilled on writing GMP technical documents
- Experience on regulatory of drugs and MDs
- Strong knowledge of Health Canada (HC) Drug regulations, as well as HC and US FDA MD regulations.
- Specialized degree in Quality Assurance/ Regulatory Affairs and/ or Regulatory Affairs Certification (RAC) is considered an asset
- Able to be on-site for a minimum of 4 days a week
- Strong knowledge of Health Canada requirements for Good Manufacturing Practices (GMP) for drugs
- Strong knowledge of Health Canada requirements for Quality Management Systems (QMS) for MDs
- Experience in narcotics handling (e.g., AQPIC) is an asset
- Knowledgeable in FDA requirements for Quality Management Systems for MDs and HCTPs
- Experience in preparation of drug submission is an asset
- Knowledgeable, thru education and /or professional experience in Drugs Pharmacovigilance and MDs Problem Reporting
- SAP experience is an asset
- Knowledge and experience in Health Canada requirements for NHPs activities preferred
- Excellent writing and communication skills
- Strong computer knowledge, including MS office (Word, Excel), Adobe, and network environments
- Self-management and organizational skills
- Strong problem-solving skills
What's in it for you
- Salary range $60,000 - $0,000
- Bonuses 1,500 to 2,000 annually based on performance
- Full benefits package
- RRSP plan
- 15 PTO days to start
Be The First To Know
About the latest Patient monitoring Jobs in Canada !