Job Description

Join Jones Healthcare Group - Where Innovation Meets Purpose!
At Jones, we're committed to the environment, our team, communities, and consumers, and we're inspired to make a meaningful impact through advanced packaging and medication dispensing solutions.
Learn more about us here: .
Summary of position:
If you love ensuring products meet the highest standards and thrive in environments where precision matters, this role is for you.
If you get inspired by supporting teams to follow cGMP and quality processes that protect patients and consumers, you'll feel right at home here.
If you are driven by the challenge of solving problems, maintaining compliance, and keeping quality at the core of operations, you can make a real impact with us.
As a Quality Assurance Inspector, your responsibilities will include carrying out inspections using established procedures to ensure product quality, reviewing and verifying packaging operations, supporting production teams with compliance, and maintaining documentation in line with cGMP. You'll be an integral member of the Quality Assurance team, ensuring quality is at the forefront of every step of our packaging process.
More about your responsibilities:

• Production Start-Up: Participate in start-up meetings, confirm specifications for each job, and approve the production run.
• Line Clearance & Verification: Perform area clearances and cleaning checks, verifying that previous product and packaging materials are fully removed.
• Product & Materials Checks: Verify correct product, packaging, lot numbers, and control numbers against orders and release records.
• In-Process Inspections: Conduct sampling, inspection, and testing to ensure packaged product meets required specifications.
• Training & Support: Guide operators on sampling and testing requirements and promote adherence to quality plans.
• Documentation & Audits: Review and audit batch records, ensure results align with specifications, and support investigations into discrepancies with CAPAs and root cause analysis.
• Good Documentation Practices: Act as a champion on the shop floor, addressing issues and providing guidance to ensure traceability and compliance.
• Validation & Release: Carry out validation sampling and testing per protocol, document results, and support product release for both incoming and finished goods.
• Collaboration & Flexibility: Work closely with Production and QA teams to maintain a strong quality culture and take on additional duties as needed.

What you'll bring

• Values that mirror ours, from the Inside Out: Ingenuity, Nimble, Supportive, Inclusive, Driven, Empathetic
• High school diploma required; post-secondary diploma or bachelor's degree in a science-related field preferred.
• Additional training or certification in cGMP Quality Assurance is an asset.
• 1+ years of experience in quality assurance within a cGMP pharmaceutical environment preferred.
• Strong knowledge of cGMP and Good Documentation Practices (GDP).
• Excellent communication skills, with strong attention to detail and accuracy.
• Ability to manage time, prioritize tasks, and adapt to changing demands.
• Proficiency with Microsoft Office (Excel, Word, Outlook).
• Flexibility to work rotating shifts, including days, afternoons, midnights, and continental schedules.
• Experience within a pharmaceutical or food environment
• Understanding/familiarity of cGMP
• Experience within a regulated environment packaging/food/pharmaceutical (FDA, Health Canada)

We care about our colleagues, some benefits we offer are:

• A safe, respectful, diverse, and inclusive environment
• Competitive compensation and equitable people practices
• Comprehensive benefits and an RRSP program where we match up to 5% of your earnings
• Opportunities to grow and develop, alongside a supportive team
• Employee and family assistance program
• Referral bonuses
• Education reimbursement program
• Colleague appreciation events
• and more!

Join us in shaping the future of healthcare! Apply now to join our dynamic team and make a meaningful impact in a collaborative environment.
Please submit a resume and let us know why you are interested.
While we thank all candidates for their interest, only those selected for an interview will be contacted.
As part of our commitment to accessibility for all persons with disabilities, Jones Healthcare Group will, upon the request of the applicant, provide accommodation during the recruitment process to ensure equal access to applicants with disabilities. Please contact the Jones Human Resources department at 1.800.265.9093 about your needs, and we will consult with you to ensure suitable accommodation is provided.
For all feedback on equity and accommodation needs, please also contact the Human Resources department.

Skills Required