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
- Strong 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 in Montréal employer: Nualtis
Nualtis is an exceptional employer located in Saint-Laurent, QC, offering a dynamic and collaborative work environment where you can make a meaningful impact on product quality and patient safety. With a focus on employee growth, Nualtis provides opportunities for professional advancement within a tight-knit team of experts dedicated to innovation in drug delivery. Enjoy competitive compensation and a comprehensive benefits package while contributing to the success of a pioneering company in the pharmaceutical industry.
