Hybrid Regulatory Affairs at Purity

Position: Hybrid Regulatory Affairs Role at Purity Life
Impact product compliance and quality at Purity Life as a Regulatory Affairs and Quality Assurance Specialist, located in Acton with hybrid work options. This position is integral to ensuring products meet regulatory standards across Canada.

As a full-time specialist working under the Regulatory Affairs Manager, you will engage in compliance tasks for Natural Health Products and Medical Devices.

Your role includes regulatory submissions, maintaining documentation, and enhancing quality management systems. Join a team committed to excellence in health and wellness regulatory compliance.

Key Responsibilities:

• Ensure adherence to Health Canada and CFIA standards

• Maintain thorough regulatory documentation and records

• Monitor and report on product quality and safety

• Assist with supplier qualification and product label reviews

• Support training initiatives for GMP practices

Requirements:

• Bachelor’s degree in a relevant scientific discipline

• Working knowledge of quality assurance frameworks

• Experience in compliance within Food and Health sectors

• Strong detail-oriented and multitasking capabilities

• Bilingual in French and English is an asset

Your expertise can help elevate the product quality landscape at Purity Life across all warehouses in Canada.
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