Associate manager , CQ at Kenvue
Shanghai, Shanghai, China -
Full Time


Start Date

Immediate

Expiry Date

26 Jun, 26

Salary

0.0

Posted On

28 Mar, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Supervision, Quality Assurance, Auditing, Training, Scheduling, Performance Appraisal, Problem Resolution, Quality Investigations, Process Deviations, Corrective Action, Nonconformance Investigation, Inspections, Reporting, Good Manufacturing Process, Documentation Approval, Process Monitoring

Industry

Personal Care Product Manufacturing

Description
Kenvue is currently recruiting for a: Associate manager , CQ What we do 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. Who We Are 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, click here. Role reports to: 质量与合规总监 Location: Asia Pacific, China, Shanghai, Shanghai Work Location: Hybrid What you will do Supervises the daily activities of the quality assurance auditors and other quality assurance activities. Carries out supervisory responsibilities in accordance with the organizations policies and applicable laws. Trains, plans, schedules and assigns work, appraises performance and resolves problems. Conducts and tracks quality investigations and process deviations and follows up to ensure corrective action has been taken. Investigates nonconformance's as they pertain to the manufacturing and testing of company products. Coordinates in-depth inspections of interdepartmental facilities and systems. Reports inspection findings to department and upper management in a timely fashion. Assists with conducting and developing site good manufacturing process training. Approves changes to documentation and processes. Monitors production deviations for trending purposes. Reviews, for approval or rejection, all procedures or specifications impacting on the identity, purity and quality of final products. Performs other related functions as required. If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation. At Kenvue, we foster a culture of belonging. In 2024, Kenvue was selected as one of Seramount’s 100 Best Companies for working parents and caregivers, recognizing our ongoing commitment to providing inclusive benefits for Kenvuers and families. Our community attracts curious and collaborative team members motivated by always striving to improve. Our team offers you plenty of opportunities to deepen your existing expertise and build on new skills by broadening your exposure outside of your own category. By working across the business, we harness the power of data and technology in new ways to better understand human insights and drive better health outcomes.
Responsibilities
This role involves supervising the daily activities of quality assurance auditors and other quality assurance functions, carrying out supervisory responsibilities in accordance with organizational policies. Key duties include conducting and tracking quality investigations, investigating nonconformances related to product manufacturing and testing, and reporting inspection findings to management.
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