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Operations Technical Writer – 2407019680W
Description
Kenvue is currently recruiting for:
Operations Technical Writer
This position reports into Production Compliance Supervisor and is based at Guelph, ON, Canada
Who we are
At Kenvue (http://kenvue.com/careers) , 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. For more information, click here (https://www.youtube.com/watch?v=XhsbOsBiX_M) .
Role reports to: Production Compliance Superviso
Location: Guelph
Travel %: 0
What you will do
The Operations Technical Writer is responsible for leading and coordinating all Operations non-conformance investigations. Ensures investigations are thoroughly documented, root causes identified, and appropriate corrective measures implemented to prevent reoccurrence.
Key Responsibilities
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Investigate process deviations through discussion with all applicable parties, such as: Production Staff, Tech Ops, Plant Quality, and Maintenance.
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Draft reports to summarize the details surrounding the deviation for input into the EtQ Symphony system.
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Draft procedures and protocols for testing including QA Plans and Lab Requests in compliance with industry standards
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Make recommendations for corrective and/or preventative actions and obtain alignment from applicable parties.
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Update internal documents (SOPS, WIs, Job Aids) based on agreed upon actions and route for approval.
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Assist in monitoring corrective/preventative measures to confirm effectiveness
Participate in other projects/initiatives as assigned
Qualifications
What We Are Looking For
Required Qualifications
B.Sc., B.A.Sc., or B. Eng.
Prior experience in solid dose manufacturing in an OTC or Pharmaceutical facility is a benefit.
Desired Qualifications
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Experience with working effectively in a team-based environment.
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Good problem-solving skills, willing to dig deep to understand underlying issues.
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Excellent written and verbal communication skills.
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Self-directed to manage priorities and adhere to deadlines
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Clear and effective communication skills
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Strong experience using the Microsoft Office suite of applications (Word, Excel, Powerpoint)
What’s in it for you
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Competitive Total Rewards Package
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Paid Company Holidays, Paid Vacation, Volunteer Time & More!
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Learning & Development Opportunities
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Employee Resource Groups
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This list could vary based on location/region
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Note: Total Rewards at Kenvue include salary, bonus (if applicable) and benefits. Your Talent Access Partner will be able to share more about our total rewards offerings and the specific salary range for the relevant location(s) during the recruitment & hiring process.
Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on business needs, job requirements, and individual qualifications, without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, protected veteran status, or any other legally protected characteristic, and will not be discriminated against on the basis of disability.
Primary Location NA-CA-Ontario-Guelph
Travel No
Job Function Production
Organization : Johnson & Johnson Inc.
Req ID: 2407019680W
