Elevate quality control practices as a Quality Assurance Specialist with Nualtis in Saint-Laurent, QC. Engage in compliance and continuous improvement within a pioneering pharmaceutical environment. As part of the Quality Operations team at Nualtis, you will ensure adherence to quality systems and regulatory requirements in both developmental and commercial phases.

Your collaboration with various departments will help maintain compliance with Health Canada, FDA, and cGMP standards. This role emphasizes your proactive approach and detail-oriented mindset, vital for achieving regulatory success. Key Responsibilities:

- Implement and maintain quality systems across all departments
- Write and review quality documentation including SOPs and reports




- Manage supplier/vendor audits and qualifications
- Conduct internal audits and facilitate regulatory inspections
- Prepare quality compliance metrics and reports for management Requirements:
- Bachelor’s or Master’s in a Scientific Discipline
- 2-5 years of quality assurance experience
- Robust GMP/cGMP knowledge and documentation skills
- Proficient in Microsoft Office applications
- Bilingualism in English and French is preferred Contribute to pharmaceutical quality assurance and compliance at Nualtis, supporting the future of drug delivery innovations.

📌 Quality Assurance Specialist at Nualtis (Montreal)
🏢 Nualtis
📍 Montreal