QC Supervisor

• Responsible for formulating inspection procedures and procedures for raw materials product processes and finished products.

• Responsible for formulating the operation procedures of all relevant environmental testing and laboratory tests of the quality inspection department.

• Formulate the work plan of the quality inspection department implement and supervise the quality judgment and inspection of raw material inspection semi-finished product inspection (first inspection and patrol inspection) finished product inspection and packaging inspection.

• Responsible for implementing and supervising the endotoxin test dust particle test surface microbial test sedimentation bacteria test etc. of products and clean areas according to the specified frequency.

• Responsible for the work deployment of quality inspection department personnel comprehensive inspection skill training and quality training of other relevant personnel.

• Responsible for the quality monitoring of the production site timely report quality accidents to the superior analyze the causes and put forward preventive and improvement measures.

• Responsible for assisting QA to investigate customer quality complaints and return events analyze the causes and put forward solutions.

• Responsible for the configuration use calibration and maintenance of all quality inspection related instruments measuring tools experimental equipment and reagents.

• Responsible for the year-end summary of the quality inspection department and provide quality record data documents and test reports required for quality information statistics.

• Responsible for coordinating the communication between the quality inspection department and other relevant departments.

• Responsible for cooperating with technicians in trial production and quality control of new products.

• Responsible for the integrity effectiveness real-time and accuracy of inspection data to realize the traceability of product quality information.

• Other tasks assigned by leaders.

Disclaimer:
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities duties and skills required of employees assigned to this position. Avantor is proud to be an equal opportunity employer.

Why Avantor

Dare to go further in your career. Join our global team of 14000 associates whose passion for discovery and determination to overcome challenges relentlessly advances life-changing science.

The work we do changes peoples lives for the better. It brings new patient treatments and therapies to market giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his moms voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents learn new skills and grow your career at Avantor.

We are committed to helping you on this journey through our diverse equitable and inclusive culture which includes learning experiences to support your career growth and success. At Avantor dare to go further and see how the impact of your contributions set science in motion to create a better world. Apply today!

EEO Statement:

We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex gender identity sexual orientation race color religious creed national origin physical or mental disability protected Veteran status or any other characteristic protected by federal state/province or local law.

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