Job Description

ABOUT US

The CMO that clients rely on, people thrive in, and sets the industry standard.

Delta?Pharma, based in Montreal, Quebec, is a leading contract manufacturer and packager in the pharmaceutical, cosmetic, and natural health sector. With a GMP-certified facility licensed by Health Canada and registered with the U.S. FDA, we specialize in developing and producing high-quality creams, lotions, gels, ointments, serums, liquids, and vitamin supplements. Founded in 2000 and still independently owned, Delta?Pharma is committed to compliance, innovation, and customer-focused service.

POSITION: Manager, QA QC

Location:

Montreal (Dorval), QC

Employment Type:

Full?time, Leadership Role

Reports to:

Director, Quality and Health & Safety

POSITION PURPOSE

Drive the development, implementation, and maintenance of our Quality Systems. Guarantee compliance with Health Canada, FDA, GMP standards, and company procedures across raw material testing, in-process manufacturing, and final product release. Lead the establishment of methods, procedures, and documentation to uphold product quality and regulatory compliance.

KEY RESPONSIBILITIES

1. Quality Systems Management:

Establish, monitor, and maintain Quality Management Systems to ensure compliance with Good Manufacturing Practices (GMP) and regulatory requirements (e.g., HC, FDA, etc). Develop, review, and update Standard Operating Procedures (SOPs), batch records, and documentation relevant to operations. Implement corrective and preventive actions (CAPA) for any quality issues identified during audits or inspections.

2. Process Oversight and Validation:

Oversee the production processes to ensure they meet quality standards and regulatory guidelines. Manage process validation, cleaning validation, and equipment validation to confirm consistent product quality.

3. Batch Record Review and Release:

Review batch manufacturing records and documentation to ensure accuracy and completeness. Authorize the release of finished product batches after thorough review of quality test results, batch records, and deviation reports. Ensure that any deviations from the process are documented, investigated, and resolved before product release.

4. Quality Control and Testing:

Collaborate with the Quality Control (QC) team to ensure that raw materials, in-process materials, and finished products are tested and meet specified quality standards. Address out-of-specification (OOS) results and ensure proper investigation and resolution.

5. Audits and Inspections:

Prepare the facility and team for internal audits and external inspections by regulatory authorities. Conduct internal audits to identify compliance gaps and drive continuous improvement initiatives. Coordinate responses to audit findings and ensure timely implementation of corrective actions.

6. Training and Compliance:

Develop and deliver training programs for employees on quality assurance, GMP, and safety procedures. Ensure that all personnel involved in operations are adequately trained and comply with SOPs. Promote a culture of quality and compliance within the facility.

7. Risk Management:

Conduct risk assessments related to the production processes, equipment, and facility environment. Implement strategies to mitigate risks, such as contamination, cross-contamination, or equipment failure.

8. Change Control Management:

Manage change control processes to ensure that any changes to equipment, processes, or formulations do not impact product quality. Review and approve changes in formulation, packaging, or equipment to ensure they meet quality standards.

9. Continuous Improvement:

Analyze quality metrics and performance data to identify areas for process improvement. Implement Lean Manufacturing, Six Sigma, or other quality improvement methodologies to enhance efficiency and reduce waste.
10.

Managing Departments

Ability to manage their team and departments. Delegate and monitor work load and ongoing tasks in order to make sure work is distributed correctly, followed up in a timely manner, and dealt with accordingly. Ability to conduct performance reviews, to hire/terminate personnel to make sure the team is running smoothly, efficiently and to its full potential.

SKILLS AND QUALIFICATIONS

Educational Background: Bachelor's in Engineering or in sciences, chemistry, biology, or science related field. Experience: Extensive experience in a manufacturing environment + managed departments successfully. Knowledge: Strong understanding of GMP, FDA regulations, quality control, and validation processes. Skills: Attention to detail, analytical thinking, problem-solving, project management, leadership, and communication skills. Fluent in both French and English, mandatory

Impact on the Organization:

The QA/QC Manager ensures that products are manufactured in compliance with strict regulatory standards., maintaining the company's reputation, and avoiding costly rejects or recalls or regulatory penalties.

WHY DELTA PHARMA?

Join a deeply experienced, privately held company recognized for its turn-key manufacturing and R&D excellence. Enjoy meaningful impact, regulatory leadership, and collaboration in a GMP-driven environment that values innovation, quality, and strong client relationships.

TO APPLY:

Submit your resume and cover letter via our Careers page.

https://www.deltapharmainc.com/en/apply-online/

We're excited to learn how your leadership in Quality Assurance can support Delta?Pharma's ongoing mission of excellence and compliance.

Job Types: Full-time, Permanent

Pay: $80,000.00-$110,000.00 per year

Benefits:

Dental care Extended health care On-site parking Paid time off RRSP match
Education:

Bachelor's Degree (preferred)
Experience:

quality assurance: 1 year (preferred)
Work Location: In person