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Regulatory Affairs Associate

CanPrev Natural Health Products Ltd.
North York, ON

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Détails du poste

Permanent | Temps plein
Il y a 11 jours

Avantages

Réductions Tarifaires
Assurance Dentaire
Congés payés
Assurance Vision
Heures d'arrivée et de départ flexibles

Compétences

Bilingue
Français
Compétences rédactionnelles
Études postsecondaires
Classement
Anglais
Recherche
Microsoft Office
Bases de données
Expérience administrative
Esprit d'analyse
Assurance qualité
Baccalauréat
Saisie de données
Intelligence artificielle
Terminologie médicale
Compétences en communication
Gestion du temps

Description complète du poste

About Us:

CanPrev Natural Health is a dynamic and innovative company dedicated to providing exceptional products in the natural health industry. We grew out of the desire to make natural medicine safe, effective and accessible to everyone. And for close to two decades, we continue to believe and strive to help empower and inspire Canadians to take charge of their health.

Position Overview:

The Regulatory Affairs Associate supports the development, maintenance, and compliance of product licenses and labeling for Natural Health Products (NHPs) in Canada and dietary supplements in the United States. This role is responsible for accurate label text creation and updates in accordance with applicable regulations, as well as providing administrative and clerical support to ensure timely submissions, license maintenance, and regulatory compliance across the product portfolio.

Key Responsibilities:

Labeling & Compliance

Create, review, and update product label text to ensure compliance with Canadian Natural Health Product Regulations and U.S. dietary supplement requirements.
Maintain accuracy and consistency of Product Licence Applications (PLAs), Natural Product Numbers (NPNs), and Supplement Facts/Drug Facts panels.
Ensure label claims, ingredient listings, and formatting meet regulatory and internal standards.
Support label revisions related to formulation changes, regulatory updates, and marketing initiatives.

Regulatory Submissions & License Maintenance

Assist in the preparation, submission, and tracking of regulatory applications and amendments (e.g., amendments, product licenses, notifications).
Maintain regulatory databases and documentation for licensed products.
Monitor license status, renewal timelines, and submission deadlines to ensure ongoing compliance.
Support responses to regulatory authority requests and deficiency notices.

Administrative & Clerical Support

Perform departmental administrative tasks including document management, filing, and record-keeping.
Coordinate internal approvals and version control for regulatory documents and labeling.
Track and organize product information, specifications, and supporting documentation.
Assist in maintaining standard operating procedures (SOPs) and regulatory templates.

Cross-Functional Collaboration

Liaise with internal teams including Quality Assurance, Product Development, Marketing, and Operations to support regulatory requirements.
Communicate labeling and compliance requirements clearly to non-regulatory stakeholders.

Key Qualifications:

Bachelor’s degree in a relevant field (e.g., life sciences, regulatory affairs, nutrition, or related discipline).
1–3 years of experience in regulatory affairs, preferably within Natural Health Products, dietary supplements, or a related industry.
Familiarity with Canadian NHP regulations and U.S. dietary supplement frameworks.

Key Skills:

Strong attention to detail with a high degree of accuracy in data entry and document review.
Working knowledge of labeling requirements, including ingredient nomenclature and claim compliance.
Excellent organizational and time management skills with the ability to manage multiple priorities.
Proficiency in Microsoft Office and regulatory database systems.
Strong written and verbal communication skills.
AI proficiency an asset.

Preferred Qualifications

Experience with NHP labeling, PLA submissions, and U.S. label compliance reviews.
Understanding of bilingual (English/French) labeling requirements in Canada.
Exposure to GMP requirements for NHPs and dietary supplements.

Schedule

Monday to Friday
Work Location: North York Hybrid – 4 days on site

We thank all applicants for their interest in CanPrev Natural Health; however, only chosen applicants will be contacted. We regret that we are unable to respond to individual inquiries about application status. CanPrev Natural Health is an equal opportunity employer that fosters an inclusive, equitable, and accessible environment. Please notify us if you require accommodation at any time during the recruitment process.

Job Types: Full-time, Permanent

Pay: $55,000.00-$60,000.00 per year

Benefits:

Dental care
Flexible schedule
Paid time off
Store discount
Vision care

Application question(s):

Do you have post-secondary education in Life Sciences, Regulatory Affairs, or a related field?
How many years of experience do you have in a regulatory, quality assurance (QA), or compliance role?
Are you familiar with Health Canada’s Natural Health Product (NHP) regulations and databases (e.g., LNHPD, NHPID)? If yes, briefly describe how you've used them in past roles.
Do you have any experience entering or managing adverse reaction (AR) reports in a safety database? If yes, please list the database(s) or tools you've used.

Work Location: Hybrid remote in North York, ON

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