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Quality Control Analyst

Posted as of: Friday, March 28, 2014

Status: Archived

Company: JM Tolmann Laboratories Inc.

Number of available position(s):  2


Duties and Responsibilities:

Receives all incoming Bulk / In-Process product samples from QA inspector.

Performs physical parameters and to analyze the product sample based from the official / verified monograph.

Conducts testing on all bulk / in-process samples based on established parameters prior to disposition

Observe proper keeping of product retention sample (bulk / in-process) after analysis to serve as reference for future problems.

Accurate cGMP documentation of data.

Aware of the GMP Guidelines approved by FDA.

Maintain and develop Standard Operating Procedure (SOP)

Perform other duties and responsibilities that may be asked or assigned by the superior.

Candidate must possess at least a Bachelor's / College Degree in Chemistry, Biochemistry, Chemical Engineering or Pharmacy.
Good in written and verbal commuication.
Highly analytical, has good attention to details, and can work with minimal supervision.
Willing to be assigned in Diliman, QC and undergo shifting schedules.
Male / Female
Fresh Graduates / Entry level applicants are encouraged to apply.


Problem Solving/Reasoning, Good Communication (listening, verbal, written), Leadership/Management, Critical Thinking, Computer/Technical Literacy

Work Location:

Interested to apply? Send your application letter and CV to:

Contact Person

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