1+ months


  • Jobs Rated


Shift Huddle




Zero Defects



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**QC** ****



Shift Huddle



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**** ****




**Role Details**


To be responsible for the chemical, physical test of raw materials, intermediate, finished products and special samples or environmental samples under the direction of QC Supervisor/Manager. To perform the validation of analytical or instrumental analysis method, product stability tests. To conduct the sampling of the raw material, packaging materials and water samples. Be responsible for the maintenance and calibration of related instruments and apparatus when necessary. To conduct the shift huddle in their own team.

**Responsibility scope**

To keep scientific advancements of lab according to the requirements of GMP GLP local regulatory and Pfizer. To ensure the safety by following the requirements of EHS strictly. To notice the management when the abnormal is occurred. To setup and maintain the harmonious team relationship, keep the open communication. To setup the quality culture and drive towards Zero Defects. To take part in the continuous improvement and ensure to achieve the high performance and quality compliance. To complete the tasks assigned by team leaders and Quality control management.

**Technical Service**

To conduct the maintenance and calibration of lab instruments under the direction of QC analysts and be responsible for the original data of calibration. To carry out the test method validation and verification, and complete the cleaning validation tests under the direction of QC analysts. Be responsible to the original data. To be responsible for printing and distributing LIMS reports.

**QC Operation:**

To be responsible for the preparation of test-required apparatus, glassware, reagents, reference standards. And to be responsible for the validity of all reagents and solutions. According to the QC testing and releasing plan to perform chemical, physical test of raw materials, intermediate, finished products, inner package material and special samples or environmental samples. To carry out sampling water samples, raw materials and packaging materials and perform related testing. To review the testing reports and original data timely and accurately. To ensure the data integrity. To implement and assist to the tests for method study and stability study. To initiate and take part in the investigation of LIRs and QARs. To conduct the shift huddle in the group as the facilitator. To be responsible for the retained sample storage. To be responsible for the sample disposition which have been completed testing To take part in the management of 6S in the lab and internal process improvement.

**Job requirements**


+ College Degree and above of pharmacy/pharmaceutical Analysis/chemistry major

**Special Knowledge**

+ Be familiar with the quality management system of Pfizer, GMP regulations and other pharmaceutical regulations


+ Ability to speak and write and understand English and use the computer.

+ Have the spirit of teamwork and strong sense of taking responsibilities

+ Have the capability of communicating, coordinating.

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

Quality Assurance and Control


Jobs Rated Reports for Chemist

Posted: 2021-03-11 Expires: 2021-05-12

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82nd2019 - Chemist
Overall Rating: 82/199
Median Salary: $76,890

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