As a QC Analyst you will perform a wide variety of analytical chemistry testing to support in-process and bulk drug substance manufacture in a cGMP regulatory environment.
The successful candidate will be required to work shifts which include days & nights.
This is a 12-month temporary contract.
A typical day might include, but is not limited to, the following:
* Gathering data and documenting test results
* Reviewing test results to ensure compliance with standards; reports any quality anomalies
* Complying with all pertinent regulatory agency requirements
* Participating in required training activities
* Maintaining laboratory supplies
* Conducting testing on raw materials, in-process, product, stability, and/or research samples
* Writing and revising control test procedures and SOPs
* Completing test records and reviewing data
* Calibrating or verifying calibration of instruments/devices prior to use
* Interacting with outside customers or functional peer groups
* Owning the responsibility for maintaining a specific project
* Devising or developing new analytical methods and techniques
* Assisting in validation of methods
* Participating in establishing the transfer of methodology from R&D
This role might be for you if:
* You enjoy working a shift pattern
* You have a proven ability to work independently or as part of a team
* You possess strong troubleshooting and problem-solving skills
* You have strong attention to detail & excellent written and oral skills
To be considered for this opportunity you should have a BS/BA in Life Sciences or related field.
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