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.
Responsibilities
* Gathering data and documenting test results
* Reviewing test results to ensure compliance with standards; reporting 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
Requirements
* A proven ability to work independently or as part of a team
* Strong trouble-shooting and problem-solving skills
* Strong attention to detail & excellent written and oral skills
* A BS/BA in Life Sciences or related field
Work Environment
This role may involve working a shift pattern. We have an inclusive and diverse culture that provides comprehensive benefits, including health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels.
Regeneron Values
We are an equal opportunity employer and welcome applications from all qualified candidates. We provide reasonable accommodation to known disabilities or chronic illnesses unless it would impose undue hardship on our business operations. Certain background checks will be conducted as part of the recruitment process.