Quality Specialist I - Guelph, Canada - Kenvue

Kenvue

Verified Company

Guelph, Canada

6 days ago

Posted by:

Sophia Lee

beBee Recruiter

Description

Quality Specialist I (14-Months Contract) W

Description

Kenvue, part of the Johnson & Johnson Family of Companies (Kenvue), is currently recruiting for a Quality Specialist I for a 14-Months Contract from May 2023-July 2024.

This position reports into the Quality Systems Manager and is based in Guelph, Canada.

Who We Are

At Kenvue, part of the Johnson & Johnson Family of Companies (Kenvue), we believe there is extraordinary power in everyday care.

Built on over a century of heritage and propelled forward by science, our iconic brands—including NEUTROGENA, AVEENO, TYLENOL, LISTERINE, JOHNSON'S and BAND-AID —are category leaders trusted by millions of consumers who use our products to improve their daily lives.

Our employees share a digital-first mindset, an approach to innovation grounded in deep human insights, and a commitment to continually earning a place for our products in consumers' hearts and homes.

Join us in shaping our future-and yours

Watch us here:

What will you do?

The Quality Specialist I will support identified aspects of compliance related to products manufactured at the Johnson & Johnson MAKE Guelph Campus.

The Quality Specialist I will enable quality assurance activities that support product launch, product approval, post launch changes and quality laboratory processes.

The Quality Specialist I will assist in the management, development and implementation of processes/activities associated with the document and specification management process, Annual Product Quality Review, and Marketed Product Stability programs.

Key Responsibilities***- SOPs, Supplements, Test Methods, Worksheets, Forms

General Stability Protocols
Raw Material and Product Specifications
Support writing and routing Annual Product Quality Reviews, coordinating on time approval to adhere to Johnson & Johnson and regulatory metrics
Issuance of worksheets to the Quality Laboratories, and issuing master batch records to both processing and packaging functional areas
Collaborate with business partners to develop/improve processes in order to meet Regulatory requirements, and lead/facilitate the implementation phase
Create/review technical documents, including the APQR annual schedule and final report
Assist with Project Management activities, including owning change controls and/or deliverables related to site projects that are impactful to related quality systems
Supporting successful regulatory and Johnson & Johnson audit activities
Potential for crosstraining in laboratory administration activities

Qualifications

Required:

Bachelor of Science or related program
Knowledge of Good Manufacturing Practices and Good Documentation Practices

Desired:

Previous experience in a Laboratory or Quality Assurance setting
Prior experience with a food, water or pharmaceutical laboratory industry

What's in it for you

Competitive Benefit Package
Paid Company Holidays, Paid Vacation & More
Learning & Development Opportunities
Employee Resource Groups

Diversity and inclusion are central elements of the shared culture across the Johnson & Johnson Family of Companies.

Attracting, developing and retaining a workforce that reflects the diversity of our customers and communities is essential to our success.

We are committed to providing a respectful, inclusive and accessible work environment where all employees have the opportunity to achieve their potential.

LI-TA1

Primary Location NA-CA-Ontario-Guelph

Organization JNTL Consumer Health LLC

Travel No

Job Function Quality Systems