Software Quality Assurance Supervisor

Company Overview Jamieson Wellness Inc.
is Canada's leading health and wellness company, driven by a purpose to inspire better lives, every day.
Established in 1922, Jamieson is our 100 years old heritage brand, which is recognized as Canada's #1 consumer health brand.
In addition, we also market and manufacture a series of leading specialty supplements brands under the youtheory, Progressive, Smart Solutions, and Iron Vegan brands.
On top of our outstanding brand portfolio, Jamieson Wellness Inc.
has been recognized as one of the top ten most reputable companies in Canada and is well regarded for our industry leading commitment to quality - exemplified through award-winning innovations and meeting of rigorous manufacturing certification standards.
And, Jamieson is no longer just a Canadian success story, as our brands are established and growing rapidly in more than 50 countries around the world.
Our Jamieson Diversity and Inclusion Statement
At Jamieson Wellness, we cherish diversity, equity and inclusion and we know we must constantly listen, learn and take action to ensure these principles remain embedded in our culture.
We are accountable to build an environment free of bias in regard to citizenship, race, place of origin, ethnic origin, colour, ancestry, disability, age, creed, sex/pregnancy, family status, marital status, sexual orientation, gender orientation, gender identity, gender expression, and all other types of behaviours that are not conducive to an inclusive environment.
We hold ourselves and all stakeholders to a high standard of diversity equity and inclusion, because anything else is unacceptable.
• The QA Coordinator will support all Quality Systems to ensure quality manufacturing of products as defined by current Good Manufacturing Practices (cGMP).
Provide assistance to other departments concerning quality and GMP issues.Ensure appropriate compliance to all relevant regulatory requirements.
Meet Jamieson Wellness (JWEL) Quality standards.
This is an 16 month contract role.

Follow and maintain GMPs and GLPs for the facility.
Work in a team environment to ensure all Quality job functions are covered.
Support QC Samplers/Technicians on site for LIMS job tasks.
Support RD on site with LIMS tasks, including RD samples, testing, specifications and inventory management.
Assist other departments on handling and providing direction on quality related issues.
Track and manage Material retest/expiry program, including rejection process.
Lead specification update projects including supplier alignment.
Coordinate Environmental monitoring and trending results.
Review and trend Purified Water System testing results.
Responsible for rotational facility daily inspections.
Prepare and review documentation for facility customer, third party certification and government audits.
Maintain up-to-date and accurate QMS systems/databases including deviation investigations, complaints, change control and CAPA.
Investigate, trend and complete reports for deviations, complaints and OOS.
Complete RCA investigations and justifications for closure with scientific rationale and risk-based decision making.
Initiate continuous improvement training notices and operational communications.
Responsible for change control review and approvals and executing change control deliverables.
Back up to Quality Associate duties including SOP system, training files, document filing & archives, quality metrics and temperature/humidity monitoring.
Conduct new hire GMP orientation training.
Write or revise SOPs and controlled forms.
Review production logs, QC logs & facility records including calibration, equipment, facility, temperature/RH, preventative maintenance, pest control, and sanitation records.
Prepare or review VQ (vendor and contractor site qualification packages)
Review Validation protocols, data and reports.
Prepare technical documents and study protocols.
Prepare technical document requests.
Working in compliance with the company's Health & Safety Policies/SOPs including but not limited to the Safety Responsibilities Procedure.
Other duties and projects as required.

Minimum Bachelor's Degree in Science related field from an accredited post secondary institution.
Minimum 2 years practical Quality department experience in a pharmaceutical, nutritional, food or health products manufacturing environment.
Familiar with USP, AOAC, FCC and other compendia standard used in the food, nutritional and drug industry.
Experience in softgel and liquid manufacturing environment an asset.
Comprehensive knowledge of pharmaceutical, food and natural health product regulations.
Proficient with computers including Microsoft 365 application.
Experience with ERP, LIMS and QMS an asset.
Able to work shift work to provide job coverage as required.
Able to work overtime to meet production/customer deadlines and complete projects by due dates.
We take personal ownership for our work and actions and its impact on others and the business.

We challenge the status quo and bring forward innovative ideas in the continuous pursuit of quality.

We welcome new ideas and feedback, swiftly incorporating them to improve our performance.

How to Apply:
All those interested in applying for this job may do so by submitting an application to human resources by the closing date noted above.
All full-time employees who have been in their current position for six months are eligible to post for the said position.
In accordance with the Accessibility for Ontarians with Disabilities Act, 2005 and the Ontario Human Rights Code, Jamieson Laboratories Ltd.
Will provide accommodation throughout the recruitment, selection and/or assessment process to applicants with disabilities.