Quality Systems Technician

at  Johnson Johnson

WHO WE ARE

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® Brand Adhesive Bandages that you already know and love. Science is our passion; care is our talent. Our global team is made up of ~ 22,000 diverse and brilliant people, 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 the life of 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.

DESIRED:

• Previous experience in a Quality Assurance or Laboratory setting
• Prior experience within a GMP environment
  Qualifications
  What we are looking for

Required Qualifications

• Bachelor of Science or related program
• Strong consideration will be given to candidates with advanced knowledge of Microsoft Office suite of programs and technical writing experience.
• Knowledge of Good Manufacturing Practices and Good Documentation Practices

DESIRED QUALIFICATIONS:

• Previous experience in a Quality Assurance or Laboratory setting
• Prior experience within a GMP environment

WHAT YOU WILL DO

The Quality Systems Specialist will support aspects of compliance related to products manufactured at the Kenuve MAKE Guelph Campus. They will enable quality assurance activities relating to our Quality Systems that support product launch, product approval, post launch changes and quality laboratory processes. The Quality Systems Specialist will assist in the management and implementation of controlled documents, including SOPs, Work Instructions, Booklets, and manufacturing and packaging batch record instructions (MWI, PWI).

Key Responsibilities

• Responsible for controlled document management in the Tru Enovia application. This includes authoring/revising and routing the following document types:
• SOPs, Supplements, Test Methods, Worksheets, Forms/Booklets, MWI, PWI
• Issuance of controlled documents to the Quality Laboratories and Processing and Packaging functional areas
• Supporting successful regulatory and Kenvue audit activities

Required:

• Bachelor of Science or related program
• Strong consideration will be given to candidates with advanced knowledge of Microsoft Office suite of programs and technical writing experience.
• Knowledge of Good Manufacturing Practices and Good Documentation Practices