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Quality Control Analyst (계약직)

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Posting Date:

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Job ID:: 2507038717W

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Kenvue is currently recruiting for a:

Quality Control Analyst (계약직)

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

Laboratory Responsibilities

To carry out physical and chemical testing as per stipulated timeline & SOP (HPLC, GC, IR, UV, AAS, pH, Viscosity….etc)
To support receiving finished goods samples and test plan
To conduct testing equipment maintenance and verification as stipulate in equipment SOP.
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

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

Control and update the reference standard & column for HPLC/GC

To update the receiving reference standard reagent with expiry date
To control MSDS and CoA of reagent
To update column master list

Requirements

Analytical lab experience including HPLC/GC/IR..etc minimum 2-3 years
Knowledge/experience of GMP, Quality Systems, QA/QC compliance & regulation
Good communication skill with people (English skill would be preferred but not mandate)

If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.

Analytical lab experience including HPLC/GC/IR..etc minimum 2-3 years

Knowledge/experience of GMP, Quality Systems, QA/QC compliance & regulation

Good communication skill with people (English skill would be preferred but not mandate)