Quality Technician II in Guelph

At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent.

Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage.

This position reports into the Quality Laboratory Supervisor and is based in Guelph, Canada. This position resides on Weekend Shift (Friday-Saturday-Sunday-Monday; 7:00 am-5:00 pm).

As a member of the Analytical Quality Laboratory team, the Quality Technician II will:

• Test the chemical quality of raw materials, packaging components, bulk work in process and finished products.
• Perform the sampling of raw materials, procured bulk, and packaging components as required.
• Independently generate reports (LIRs, Near Miss/Accident Reports, Change Controls) as required.
• Identify non-value-added activities and own the implementation of innovative approaches to continuously improve current systems and processes.
• Identify risks within the laboratory and raise as appropriate.
• Support team activities to ensure completion in a timely and compliant manner according to written procedures.
• Ensure self and others are adhering to GMP and GDP requirements.
• Provide frequent feedback to peers and others to ensure high quality documentation.
• Provide training/share expertise with colleagues to ensure quality processes are followed.
• Ensure that testing and reporting of results meets the needs of the business and regulatory requirements.
• Lead in a team environment through open communication and demonstration of values consistent with the Kenvue values and Leadership Behaviours.
• Follow Kenvue policies, quality/technical standards, health, safety, and environmental regulations.

Required Qualifications:

• Minimum of bachelor's degree in science or a related field, or equivalent experience within the pharmaceutical industry.
• Minimum of 2 – 3 years experience in a Quality, or R&D environment in the pharmaceutical, food or water industries.
• Good knowledge of GMP regulations.
• Familiarity with USP guidance and guidelines is an asset.
• Strong digital literacy.

Desired Qualifications:

• Ability to work with limited supervision and function optimally in a team environment.
• Good interpersonal and collaboration skills.
• Excellent communication skills.
• Demonstrated ability to organize, multitask and prioritize workload.
• Good technical writing and problem-solving skills.
• Excellent attention to detail.
• Familiarity with computer software and strong personal computer skills.
• Enjoys working to multiple timelines in a dynamic and fast-paced team environment.
• Knowledge of Process Excellence/Lean is an asset.
• Knowledge of GC is an asset.

What’s In It For You:

• Competitive Benefit Package.
• Paid Company Holidays, and Paid Vacation!
• Learning & Development Opportunities.

Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.