... drug safety, case processing, and regulatory compliance (FDA/Health Canada) , along with the ... Support audits and regulatory inspections * Perform trend analysis and signal detection reporting ...
... drug safety, case processing, and regulatory compliance (FDA/Health Canada) , along with the ... Support audits and regulatory inspections * Perform trend analysis and signal detection reporting ...
... IMPDs/Health Canada). * Collaborate with Technical Development, Manufacturing, Quality Control, Quality Assurance, and Regulatory Affairs to ensure continuity of drug supply for early clinical ...
... IMPDs/Health Canada). * Collaborate with Technical Development, Manufacturing, Quality Control, Quality Assurance, and Regulatory Affairs to ensure continuity of drug supply for early clinical ...
Quality Assurance Manager
Cincinnati, OH · On-site
Ensure regulatory compliance and inspection readiness for FDA, Health Canada, customer, supplier ... OTC drug manufacturing * Quality Management Systems * Investigations and CAPA processes
Quick apply
Quality Assurance Manager
Cincinnati, OH · On-site
Ensure regulatory compliance and inspection readiness for FDA, Health Canada, customer, supplier ... OTC drug manufacturing * Quality Management Systems * Investigations and CAPA processes
Quality Assurance Manager
Cincinnati, OH · On-site
Ensure regulatory compliance and inspection readiness for FDA, Health Canada, customer, supplier ... OTC drug manufacturing * Quality Management Systems * Investigations and CAPA processes
Quality Assurance Manager
Cincinnati, OH · On-site
Ensure regulatory compliance and inspection readiness for FDA, Health Canada, customer, supplier ... OTC drug manufacturing * Quality Management Systems * Investigations and CAPA processes
Quality Assurance Manager
Cincinnati, OH · On-site
Ensure regulatory compliance and inspection readiness for FDA, Health Canada, customer, supplier ... OTC drug manufacturing * Quality Management Systems * Investigations and CAPA processes
Quality Assurance Manager
Cincinnati, OH · On-site
Ensure regulatory compliance and inspection readiness for FDA, Health Canada, customer, supplier ... OTC drug manufacturing * Quality Management Systems * Investigations and CAPA processes
Associate Director, Formulation and Drug Product Development
Waltham, MA · On-site
$159K - $195K/yr
... IMPDs/Health Canada). * Collaborate with Technical Development, Manufacturing, Quality Control, Quality Assurance, and Regulatory Affairs to ensure continuity of drug supply for early clinical ...
Associate Director, Formulation and Drug Product Development
Waltham, MA · On-site
$159K - $195K/yr
... IMPDs/Health Canada). * Collaborate with Technical Development, Manufacturing, Quality Control, Quality Assurance, and Regulatory Affairs to ensure continuity of drug supply for early clinical ...
Lead customer audits, FDA inspections, Health Canada inspections, accreditation surveys, Board of Pharmacy inspections, and other regulatory reviews * Verify corrective-action effectiveness and close ...
Lead customer audits, FDA inspections, Health Canada inspections, accreditation surveys, Board of Pharmacy inspections, and other regulatory reviews * Verify corrective-action effectiveness and close ...
Vice President, Quality & Regulatory Affairs
Irvine, CA · On-site
$160K - $211K/yr
Serves as the primary company representative for FDA inspections, Health Canada assessments, and BSI ISO 13485 surveillance and recertification audits. * Maintains inspection and audit readiness ...
Quick apply
Vice President, Quality & Regulatory Affairs
Irvine, CA · On-site
$160K - $211K/yr
Serves as the primary company representative for FDA inspections, Health Canada assessments, and BSI ISO 13485 surveillance and recertification audits. * Maintains inspection and audit readiness ...
Vice President, Quality & Regulatory Affairs
Irvine, CA · On-site
$161K - $212K/yr
Serves as the primary company representative for FDA inspections, Health Canada assessments, and BSI ISO 13485 surveillance and recertification audits. * Maintains inspection and audit readiness ...
Vice President, Quality & Regulatory Affairs
Irvine, CA · On-site
$161K - $212K/yr
Serves as the primary company representative for FDA inspections, Health Canada assessments, and BSI ISO 13485 surveillance and recertification audits. * Maintains inspection and audit readiness ...
Vice President, Quality & Regulatory Affairs
Irvine, CA · On-site
$161K - $212K/yr
Serves as the primary company representative for FDA inspections, Health Canada assessments, and BSI ISO 13485 surveillance and recertification audits. * Maintains inspection and audit readiness ...
Vice President, Quality & Regulatory Affairs
Irvine, CA · On-site
$161K - $212K/yr
Serves as the primary company representative for FDA inspections, Health Canada assessments, and BSI ISO 13485 surveillance and recertification audits. * Maintains inspection and audit readiness ...
Vice President, Quality & Regulatory Affairs
$161K - $212K/yr
Serves as the primary company representative for FDA inspections, Health Canada assessments, and BSI ISO 13485 surveillance and recertification audits. * Maintains inspection and audit readiness ...
Vice President, Quality & Regulatory Affairs
$161K - $212K/yr
Serves as the primary company representative for FDA inspections, Health Canada assessments, and BSI ISO 13485 surveillance and recertification audits. * Maintains inspection and audit readiness ...
Vice President, Quality & Regulatory Affairs
Irvine, CA · On-site
$161K - $212K/yr
Serves as the primary company representative for FDA inspections, Health Canada assessments, and BSI ISO 13485 surveillance and recertification audits. * Maintains inspection and audit readiness ...
Vice President, Quality & Regulatory Affairs
Irvine, CA · On-site
$161K - $212K/yr
Serves as the primary company representative for FDA inspections, Health Canada assessments, and BSI ISO 13485 surveillance and recertification audits. * Maintains inspection and audit readiness ...
Basic knowledge of cGMPs (USFDA, Health Canada, PIC/S and/or Eudralex). * Demonstrated decision ... Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate ...
Basic knowledge of cGMPs (USFDA, Health Canada, PIC/S and/or Eudralex). * Demonstrated decision ... Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate ...
Support audits and inspections from FDA, Health Canada, and other regulators Cross-Functional Leadership * Work closely with R&D, product, legal, and support teams to ensure regulatory alignment
Quick apply
Support audits and inspections from FDA, Health Canada, and other regulators Cross-Functional Leadership * Work closely with R&D, product, legal, and support teams to ensure regulatory alignment
Experience interacting directly with FDA, Notified Bodies, Health Canada, and other global ... Experience supporting audits, inspections, technical documentation, labeling review, design ...
Experience interacting directly with FDA, Notified Bodies, Health Canada, and other global ... Experience supporting audits, inspections, technical documentation, labeling review, design ...
Regulatory Affairs Specialist
Ottawa, IL · On-site
$70K - $100K/yr
Maintain regulatory files and documentation supporting audits, inspections, customer inquiries, and ... FDA OTC drug regulations * cGMP requirements * Health Canada regulations * EU Cosmetic Regulation
Quick apply
Regulatory Affairs Specialist
Ottawa, IL · On-site
$70K - $100K/yr
Maintain regulatory files and documentation supporting audits, inspections, customer inquiries, and ... FDA OTC drug regulations * cGMP requirements * Health Canada regulations * EU Cosmetic Regulation
Lead engagement with FDA and Health Canada. * Collaborate with regional commercial, medical ... Lead inspection readiness and regulatory response; primary escalation point for regulatory risks.
Lead engagement with FDA and Health Canada. * Collaborate with regional commercial, medical ... Lead inspection readiness and regulatory response; primary escalation point for regulatory risks.
... Health Canada, TGA, etc.). Advise on the appropriate regulatory pathways (e.g., 510(k), PMA, CE ... Act as a liaison with regulatory authorities during inspections, responding to queries and ...
... Health Canada, TGA, etc.). Advise on the appropriate regulatory pathways (e.g., 510(k), PMA, CE ... Act as a liaison with regulatory authorities during inspections, responding to queries and ...
... Health Canada, TGA, etc.). Advise on the appropriate regulatory pathways (e.g., 510(k), PMA, CE ... Act as a liaison with regulatory authorities during inspections, responding to queries and ...
... Health Canada, TGA, etc.). Advise on the appropriate regulatory pathways (e.g., 510(k), PMA, CE ... Act as a liaison with regulatory authorities during inspections, responding to queries and ...
... Health Canada, TGA, etc.). Advise on the appropriate regulatory pathways (e.g., 510(k), PMA, CE ... and Inspections: Assist in preparing for and supporting regulatory inspections and audits by ...
... Health Canada, TGA, etc.). Advise on the appropriate regulatory pathways (e.g., 510(k), PMA, CE ... and Inspections: Assist in preparing for and supporting regulatory inspections and audits by ...
Health Canada Drug Inspector information
See salary details
$24.5K - $31.3K
3% of jobs
$31.3K - $38K
16% of jobs
$39.7K is the 25th percentile. Wages below this are outliers.
$38K - $44.8K
23% of jobs
The median wage is $46.9K / yr.
$44.8K - $51.6K
27% of jobs
$55.9K is the 75th percentile. Wages above this are outliers.
$51.6K - $58.4K
10% of jobs
$58.4K - $65.1K
4% of jobs
$65.1K - $71.9K
5% of jobs
$71.9K - $78.7K
2% of jobs
$78.7K - $85.5K
2% of jobs
$85.5K - $92.2K
2% of jobs
$92.2K - $99K
5% of jobs
$24.5K
$54.9K
$99K
How much do health canada drug inspector jobs pay per year?
As of Sep 15, 2026, the average yearly pay for health canada drug inspector in the United States is $54,939.00, according to ZipRecruiter salary data. Most workers in this role earn between $38,500.00 and $63,500.00 per year, depending on experience, location, and employer.
What is a Health Canada Drug Inspector?
Health Canada Drug Inspectors are professionals responsible for ensuring that drugs sold in Canada comply with the Food and Drugs Act and its regulations. They conduct inspections of pharmaceutical manufacturers, importers, distributors, and retailers to verify that drugs are safe, effective, and properly labeled. Their work helps protect public health by identifying and addressing non-compliance, conducting investigations, and sometimes overseeing recalls of unsafe products. Drug Inspectors may also provide guidance to industry stakeholders to help them meet federal requirements.
What are some common challenges faced by Health Canada Drug Inspectors during site inspections?
Health Canada Drug Inspectors often face challenges such as ensuring compliance in facilities with varying levels of regulatory knowledge, navigating complex manufacturing processes, and addressing language barriers or documentation inconsistencies. Inspectors must stay up to date with evolving regulations and be prepared to handle situations where immediate corrective actions are necessary. Collaboration with facility staff and effective communication are critical in overcoming these challenges and ensuring public health and safety.
What are the key skills and qualifications needed to thrive as a Health Canada Drug Inspector, and why are they important?
To thrive as a Health Canada Drug Inspector, you need a solid background in pharmaceutical sciences, chemistry, or a related field, along with knowledge of regulatory compliance and health product safety. Familiarity with inspection protocols, laboratory analysis tools, and regulatory databases such as the Drug Submission Tracking System (DSTS) is essential. Strong attention to detail, analytical thinking, and effective communication skills help inspectors navigate complex regulations and liaise with industry stakeholders. These skills ensure that drug products meet safety and quality standards, protecting public health and maintaining regulatory compliance.
What is the difference between Health Canada Drug Inspector vs Health Canada Food Inspector?
| Aspect | Health Canada Drug Inspector | Health Canada Food Inspector |
|---|---|---|
| Required Credentials | Post-secondary education in sciences, certifications in regulatory compliance | Post-secondary education in food science, certifications in food safety |
| Work Environment | Inspecting pharmaceutical manufacturing, laboratories, and distribution facilities | Inspecting food processing plants, warehouses, and retail outlets |
| Employer & Industry | Health Canada, pharmaceutical industry | Health Canada, food industry |
| Common Search/Comparison | Yes | Yes |
Health Canada Drug Inspectors focus on ensuring the safety and compliance of pharmaceuticals, while Food Inspectors oversee food safety standards. Both roles require regulatory knowledge, inspections, and certifications, but they specialize in different sectors within health regulation.
Are drug inspectors in demand?
Drug inspectors, including those working for agencies like Health Canada, are in steady demand due to ongoing needs for regulatory oversight of pharmaceuticals and compliance with safety standards. Employment opportunities depend on government budgets, regulatory changes, and industry growth, with positions often requiring relevant certifications and experience in drug regulation or inspection.
How much do health Canada drug inspectors make in Canada?
Health Canada drug inspectors typically earn a salary ranging from CAD 70,000 to CAD 100,000 annually, depending on experience and level of responsibility. They often work in government offices, requiring knowledge of regulatory standards and inspection procedures.
How to become a health Canada drug inspector in Canada?
To become a Health Canada drug inspector, candidates typically need a university degree in pharmacy, chemistry, biology, or a related field, along with relevant work experience in pharmaceutical regulation or quality control. Applicants must pass written exams and interviews, and often require knowledge of Good Manufacturing Practices (GMP) and regulatory standards. Certification or training in inspection procedures may also be necessary for this role.
What are popular job titles related to Health Canada Drug Inspector jobs?
For Health Canada Drug Inspector jobs, the most frequently searched job titles are:
Pharmacovigilance Specialist / Assistant
Boston, MA • On-site
Kaav Inc.
Other
Re-posted 13 days ago
Job description
Job Title: Pharmacovigilance Specialist / Assistant
Location: Remote (Candidates in Fort Worth, TX or Boston, MA preferred for future hybrid)
Job Summary:
seeking a Pharmacovigilance Specialist to support adverse event case processing and safety reporting. This role is highly interactive and requires working closely with patients, healthcare professionals (HCPs), vendors, and internal teams.
The ideal candidate will have strong experience in drug safety, case processing, and regulatory compliance (FDA/Health Canada), along with the ability to operate in a fast-paced, high-volume environment.
Key Responsibilities:
Adverse Event Case Management (50%)
Location: Remote (Candidates in Fort Worth, TX or Boston, MA preferred for future hybrid)
Job Summary:
seeking a Pharmacovigilance Specialist to support adverse event case processing and safety reporting. This role is highly interactive and requires working closely with patients, healthcare professionals (HCPs), vendors, and internal teams.
The ideal candidate will have strong experience in drug safety, case processing, and regulatory compliance (FDA/Health Canada), along with the ability to operate in a fast-paced, high-volume environment.
Key Responsibilities:
Adverse Event Case Management (50%)
- Review and evaluate incoming communications (phone, email, fax, etc.) for adverse event (AE) reporting
- Perform medical evaluation of AE cases for seriousness and reporting requirements
- Process and manage cases in safety databases (e.g., ARGUS)
- Conduct follow-ups to gather missing or additional case information
- Prepare and submit expedited and periodic safety reports to FDA and Health Canada
- Ensure AE intake from marketing programs and social media platforms
- Support audits and regulatory inspections
- Perform trend analysis and signal detection reporting
- Maintain knowledge of FDA & Health Canada pharmacovigilance regulations
- Understand company SOPs, drug safety processes, and compliance requirements
- Develop knowledge of Galderma products and dermatology-related conditions
- Maintain and update case tracking systems and databases
- Perform reconciliation with Medical Information, Quality, and external partners
- Develop and deliver training on adverse event reporting
- Support onboarding of new employees and vendors
- Assist in SOP creation and process documentation
- Bachelor's degree in Life Sciences, Healthcare, or related field
- 5+ years of Pharmacovigilance / Drug Safety experience
- Strong experience in case processing and adverse event reporting
- Knowledge of FDA and Health Canada safety regulations
- Hands-on experience with ARGUS or similar safety databases
- Strong understanding of medical terminology and drug safety concepts
- Ability to handle patient and HCP interactions (including sensitive discussions)
- RN, PharmD, or other healthcare certification
- Experience with biologics, drugs, or combination products
- Background in CROs or Pharma/Biotech companies
- Experience in SOP writing and training delivery
- Exposure to global pharmacovigilance environments
- Pharmacovigilance & Adverse Event Case Processing
- FDA / Health Canada Regulations
- ARGUS Safety Database
- Strong communication with patients & HCPs
- Critical thinking & escalation judgment
- Self-driven and able to work independently in remote setup
- Strong communication and collaboration skills
- Ability to handle high-volume workload and prioritize effectively
- Comfortable in externally facing, high-visibility role
- CROs: IQVIA, Parexel, ICON, Syneos, PPD, Labcorp
- Pharma/Biotech: Pfizer, Amgen, Novartis, AbbVie, Merck
- Round 1: Hiring Manager (Nancy Dubois)
- Round 2: Senior Pharmacovigilance Team
- Immediate need due to high case volume and understaffing
- Role is highly visible and interactive, not just backend processing
- Potential for future conversion (must be open to hybrid in TX or MA)