Senior Quality Control Analyst
Job description
Kenvue is currently recruiting for a: Senior Quality Control Analyst 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: Quality Control Manager Location: Asia Pacific, South Korea, Seoul, Geumcheon-gu Work Location: Fully Onsite What you will do Micro Testing Conduct Micro limit test, growth promotion test, environmental monitoring and method suitability Carried out OOS/OOT investigation To support receiving finished goods samples and test plan To conduct testing equipment maintenance and verification as stipulate in equipment SOP.
Reagent inventory control with MSDS and Media preparation To manage laboratory stock such as chemical reagent, consumables.. etc. To ensure all equipment are calibrated for routine analysis. To ensure the OOS procedure is strictly followed and compliance. To initiate non-conformance/OOS found and assist in non conformance/OOS investigation and support corrective actions to prevent future occurrence To ensure that equipment maintenance as per SOP.
Maintaining good condition of the laboratory, and that the laboratory reflects a high standard of housekeeping. To ensure that Good Laboratory Practice is strictly adhered to at all the time. To established and monitor the calibration schedule and to ensure lab equipment are adequately calibrated before expiration. Follow 5S in lab activities to keep it clean and arranged Data Integrity Follow ALCOA principal for lab activities Document control related to chemical test result Prepare log-book and maintenance it accordingly Maintain micro SOP or Work instructions periodically.
GMP and SHE (Safety Health and Environmental) compliance . Ensure GMP and SHE requirements are adhered at all the time To ensure workstation are clean and orderly Support the supervisor or Manager to make a right decision What we are looking for Required Qualifications: Micro lab experience including micro limit test minimum 3-5 years Knowledge/experience of GMP, Quality Systems, QA/QC compliance & especially for MFDS regulation Good communication skill with people (English skill is required) If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.