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.
Viatris Inc., Ireland,
Recruiters.ie, Ireland,