Our client is a fast-growing health supplements and PPE manufacturer and distributor seeking a hands-on Quality Assurance/Regulatory Affairs Specialist to work on initiatives related to compliance, quality, and regulatory affairs. Reports to the Quality Assurance / Regulatory Affairs Manager.  

What You’ll Do

• Work on regulatory submissions (Health Canada, NSF, FDA) and product/site licensing.

• Help the Manager develop & maintain SOPs and monitor regulatory compliance.

• Participate in planning and executing internal/external audits and CAPA programs.

• Partner with R&D, Manufacturing, and Supply Chain to help the Manager embed compliance in daily operations.

• Monitor regulatory changes and update processes accordingly.

• Help Build the QMS from the ground up as required.

What You Bring

• 3+ years in combined QA/RA roles in natural health products, nutraceuticals, food manufacturing, PPE, medical devices, or pharmaceuticals.

• Proven success in contributing to regulatory submissions to Health Canada, NSF, or FDA.

• Background in GMP, NSF standards, and QMS implementation.

• Bonus: Familiarity with ISO 13485 and/or Health Canada Medical Device Regulations.

• Strong English communication, problem-solving, and team player  skills.

• Able to work on site.

Why Join Them?

• Making a contribution with visible results.

• Career growth to QA/RA Manager.

• Collaborative and entrepreneurial environment.

• Competitive salary and benefits.