As a QC Analyst, you will perform a wide variety of analytical chemistry testing to support in-process and bulk drug substance manufacturing in a cGMP regulatory environment.
The successful candidate will be required to work shifts, including days and nights.
Typical responsibilities include, but are not limited to:
* Gathering data and documenting test results
* Reviewing test results to ensure compliance with standards and reporting any quality anomalies
* Ensuring compliance with all relevant regulatory requirements
* Participating in required training activities
* Maintaining laboratory supplies
* Conducting testing on raw materials, in-process, product, stability, and research samples
* Writing and revising control test procedures and SOPs
* Completing test records and reviewing data
* Calibrating or verifying calibration of instruments before use
* Interacting with outside customers or internal teams
* Owning responsibility for specific projects
* Developing new analytical methods and techniques
* Assisting in method validation
* Participating in transfer of methodology from R&D
This role might be for you if you:
* Enjoy working in shift patterns
* Can work independently or as part of a team
* Possess strong troubleshooting and problem-solving skills
* Have strong attention to detail and excellent communication skills
Qualifications include a BS/BA in Life Sciences or a related field.
Join us at Regeneron! We value diversity and offer comprehensive benefits, including health programs, fitness centers, bonuses, and paid time off, depending on location.
Regeneron is an equal opportunity employer. We provide reasonable accommodations for applicants with disabilities or chronic illnesses, unless it causes undue hardship.
Note: Salary ranges are provided according to local laws for U.S., Japan, and Canada roles. Please consult with your recruiter for details applicable to your location.
Background checks are part of our recruitment process to verify information such as identity, right to work, and qualifications.
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