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Los Angeles Control Supervisor

Location:
Garden Grove, CA
Posted:
November 06, 2025

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Resume:

Beverage Corporation and LISI ar...

Linh M Ly

***** ******* ** ****** *****, CA 92841

Cell: 657-***-****

********.****@*****.***

Objective:

Passionate and result driven QC Sr Chemist/QC Supervisor with 20 years experience in

medical device, clinical diagnostic, and pharmaceutical industries. Seeking for Quality

Control Supervisor in a dynamic company with an opportunity for growth and career

advancement.

Education:

BA in Biochemistry and Molecular Biology at Boston University, graduated 1997.

Experience:

Quality Control Supervisor in Chemistry. Grifols, Los Angeles 2020 to 2024

* Manage and supervise quality activities in the Chemistry department.

* Plan, schedule, monitor, review and release testing results of raw material,

intermediate, in-process, final products, research, validation, and stability related

projects.

* Collaborate and interface with multiple departments to achieve product release

timelines and investigation of OOC, OOT, and OOS.

* Troubleshoot assays and instruments to drive efficiency and to identify problems.

* Provide and maintain cross training records, update SOPs to assure compliance

with regulation and to adhere to the highest quality standards and safety of the

products.

* Investigate and identify root causes and prepare reports for OOC, OOT and OOS.

* Prepare, conduct and approve timecards, attendance, and annual reviews to

employees.

* Maintain safety, housekeeping, instrument maintenance, SOPs, KPI, usage logs,

standards and control calibrations, inventory, and order supplies.

¢ Familiar with lim, SAP, Microsoft, and Excel.

Sr Chemist in QC Chemistry Grifols, Los Angeles 2006- 2020

* Schedule and perform testings by coagulation, chromogenic, electrophoresis,

immunology, enzymology, IC,GC, HPLC. UV, FTIR

* Review and approve results for product release, research, validation, stability, and

investigation projects.

* Participate and provide assistance with IQ, OQ and PQ validation plans and

reports.

* Participate in validation studies and transfer of approved LSPs for testing.

¢ Lead, train and mentor fellow Chemists.

¢ Assist in preparation of the lab for internal and FDA audits.



Contact this candidate