Demo

Temp QC Analyst (Day 1)

POSTED ON 4/20/2025 AVAILABLE BEFORE 6/15/2025

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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