Quality Systems Specialist II

Kenvue is currently recruiting for a:
Quality Systems Specialist II (15 month contract)

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 – and have brilliant opportunities waiting for you!

Join us in shaping our future–and yours. For more information, .

Compliance Lead

North America, Canada, Ontario, Guelph

フルオンサイト

The Quality Systems Specialist II – Technical Services supports identified aspects of compliance related to products manufactured. To enable quality assurance activities that support quality laboratory testing and release programs, product launches, product approval, post launch changes and quality laboratory equipment programs. The role assists in the management, development and implementation of processes/activities associated with quality laboratories computer systems, equipment, and applications.

Master data set up (Empower, etc.), systems administration including user access and audit trail reviews, equipment and software qualification and validation documents (protocols, reports, validation assessments, technical reports), troubleshooting, and laboratory equipment lifecycle management.

• Support compliance activities related to quality laboratory systems, computer system validation, ensuring adherence to quality and regulatory requirements, including Supporting successful regulatory and audit activities
• System administration including user access and audit trail reviews, equipment and software qualification and validation documents (protocols, reports, validation assessments, technical reports), troubleshooting, and laboratory equipment lifecycle management.
• Perform master data setup and maintenance within laboratory systems (e.g., Empower) to enable laboratory testing, product release, product launches, product approvals, and post-launch changes.
• Develop, execute, and maintain equipment and software qualification and validation documentation, including protocols, reports, validation assessments, and technical reports.
• Provide technical troubleshooting and support for laboratory computer systems, equipment, and applications.
• Manage laboratory equipment throughout its lifecycle, including qualification, maintenance, compliance, and retirement activities.
• Support quality laboratory equipment programs to ensure continued reliability, performance, and regulatory compliance.
• Facilitate External Contractor/Vendor visits and request for troubleshooting and qualification activities

• Bachelor’s degree or equivalent in a relevant field
• 3 to 5 years of experience supporting quality systems, laboratory operations, or related experience.
• Strong communication skills to effectively translate technical quality concepts
• Excellent analytical and problem-solving skills
• Proficient with computer applications and systems, including laboratory and quality management tools.
• Experience with Analytical and Microbiology Laboratory equipment, methods, and testing processes.