Quality Control Technical Resources Specialist

We are currently looking to fill an Associate Specialist/Specialist Role in the QC Technical Resources Bioassay Team. This position is a Monday-Friday 8-4:30pm schedule. This position will be responsible for life cycle management of cell-based assays and binding assays utilized in Quality Control Biological testing. In this fast-paced environment with a strong pipeline, QC Technical Resources Specialists have the opportunity to develop scientifically and also gain insight into other areas of the business.

In this role a typical day might include the following:

• Work with Analytical Sciences to ensure method readiness to bring to QC commercial before process validation.
• Monitor day-to-day method performance in QC Commercial lab and provide subject matter expert support for any method-related issues.
• Participate in assay development, qualification, and validation
• Participate in troubleshooting/investigating technical and procedural issues
• Function as subject matter expert for analytical assay transfer internally and externally
• Review test procedures and assays
• Coordinate and review method performance reports and quality metrics.
• Coordinate post-transfer investigations between contract sites and collaborative partners.

This role might be for you if you:

• You enjoy working in a fast-paced environment and are flexible to changing requirements
• You are a team player who can work with a variety of different people on different tasks
• You have cell culture related experience or cell-based assay experience.
• You are able to multi-task, prioritize and execute projects independently and communicate cross-functionally to business units.
• You can take on new and sometimes ambiguous challenges and learn quickly.
• You possess effective time management skills, and the drive to meet deadlines.

To be considered for the Associate QC Technical Resources Specialist position you must being willing and able to work Monday-Friday 8-4:30pm and have a BS/BA in Biology, Biochemistry, Cell Biology or related field. Experience with binding assays, cell- based potency assays and ELISA testing preferred. Experience in a GMP setting is required. Level is determined based on qualifications relevant to the role.

Does this sound like you? Apply now to take your first steps toward living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits including health and wellness programs, fitness centers and equity awards, annual bonuses, and paid time off for eligible employees at all levels!

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. We will ensure that individuals with disabilities are provided reasonable accommodations to participate in the job application process. Please contact us to discuss any accommodations you think you may need.

The salary ranges provided are shown in accordance with U.S. law and apply to U.S. based positions, where the hired candidate will be located in the U.S. If you are outside the U.S, please speak with your recruiter about salaries and benefits in your location.

Salary Range (annually)

$55,700.00 - $103,700.00