Top Benefits
About the role
Job Description Vaughan, Ontario (On-Site) | Reports to President | Full-Time
Our client is a fast-growing health supplements and PPE manufacturer and distributor seeking a hands-on Quality Assurance/Regulatory Affairs Manager to lead compliance, quality, and regulatory initiatives. Reports to the President. This role offers direct impact , cross-functional influence , and a clear path to QA/RA Director as they expand.
What Youll Do Lead regulatory submissions (Health Canada, NSF, FDA) and product/site licensing.
Develop & maintain SOPs and oversee regulatory compliance monitoring .
Plan and execute internal/external audits and manage CAPA programs .
Partner with R&D, Manufacturing, and Supply Chain to embed compliance in daily operations.
Monitor regulatory changes and update processes accordingly.
Build their QMS from the ground up.
Qualifications What You Bring 5+ years in combined QA/RA roles in natural health products, nutraceuticals, food manufacturing, PPE, medical devices, or pharmaceuticals.
Proven success in regulatory submissions to Health Canada, NSF, or FDA.
Strong knowledge of GMP, NSF standards, and QMS implementation .
Bonus: Familiarity with ISO 13485 and/or Health Canada Medical Device Regulations .
Leadership style: Proactive, organized, and able to take ownership.
Excellent communication, problem-solving, and stakeholder management skills.
Why Is This a Great Opportunity Why Join Them? High-impact role with visible results.
Career growth to QA/RA Director.
Collaborative and entrepreneurial environment.
Competitive salary and benefits.
About NPAworldwide
NPAworldwide connects premier independent recruiting firms located throughout Europe, Asia, Australia, Africa and the Americas to facilitate cooperative, split-fee placements. Working with an NPAworldwide member ensures:
- Global reach with timely response
- Industry/occupational specialties
- Cultural sensitivity
- Unparalleled integrity
Top Benefits
About the role
Job Description Vaughan, Ontario (On-Site) | Reports to President | Full-Time
Our client is a fast-growing health supplements and PPE manufacturer and distributor seeking a hands-on Quality Assurance/Regulatory Affairs Manager to lead compliance, quality, and regulatory initiatives. Reports to the President. This role offers direct impact , cross-functional influence , and a clear path to QA/RA Director as they expand.
What Youll Do Lead regulatory submissions (Health Canada, NSF, FDA) and product/site licensing.
Develop & maintain SOPs and oversee regulatory compliance monitoring .
Plan and execute internal/external audits and manage CAPA programs .
Partner with R&D, Manufacturing, and Supply Chain to embed compliance in daily operations.
Monitor regulatory changes and update processes accordingly.
Build their QMS from the ground up.
Qualifications What You Bring 5+ years in combined QA/RA roles in natural health products, nutraceuticals, food manufacturing, PPE, medical devices, or pharmaceuticals.
Proven success in regulatory submissions to Health Canada, NSF, or FDA.
Strong knowledge of GMP, NSF standards, and QMS implementation .
Bonus: Familiarity with ISO 13485 and/or Health Canada Medical Device Regulations .
Leadership style: Proactive, organized, and able to take ownership.
Excellent communication, problem-solving, and stakeholder management skills.
Why Is This a Great Opportunity Why Join Them? High-impact role with visible results.
Career growth to QA/RA Director.
Collaborative and entrepreneurial environment.
Competitive salary and benefits.
About NPAworldwide
NPAworldwide connects premier independent recruiting firms located throughout Europe, Asia, Australia, Africa and the Americas to facilitate cooperative, split-fee placements. Working with an NPAworldwide member ensures:
- Global reach with timely response
- Industry/occupational specialties
- Cultural sensitivity
- Unparalleled integrity