QC Analyst- Material Qualifications

Company: Regeneron Pharmaceuticals, Inc.
Location: East Greenbush
Posted on: January 8, 2026

Job Description:

Regeneron is currently looking for a Quality Control (QC) Analyst on our Materials team with a 1st shift, Monday-Friday, 8am-4:30pm schedule. Regeneron successfully manufactures a range of biopharmaceuticals for patients worldwide, including our approved therapeutic proteins and those involved in clinical studies. Our QC Analysts are responsible for the operations of the QC Reference Standard and QC Materials functional area activities. They openly communicate with Regeneron QC Laboratory Managers, Regeneron Regulatory Sciences, Regeneron Procurement, Regeneron Warehouse and Logistics (WHL), Regeneron Protein Group in Tarrytown, and partners. As a QC Analyst you will culture customer service for all internal and external clients. As a Quality Control Analyst Materials, a typical day might include the following: Responsible for QC Reference Standard and Materials processes. Sets and maintains internal requirements for product reference standards. Ensures timely procurement and implementation of product reference standards and qualified materials. Oversee and maintain appropriate inventory levels of product reference standards and qualified materials. Work with members of QC Labs, Tarrytown, and Business Partners for reagent and product reference standard forecasts. Provide excellent customer service. Evaluates and documents deviations in the appropriate Quality System. Oversight of the preventive and corrective maintenance monitoring program. Prepare and provide regular data updates to the management and group. Lead and coordinate the improvement effort of streamlining processes. This role might be for you if : Data analysis using excel spreadsheets or other software applications. You can work independently and drive projects to completion. You have a passion for technical writing and excel at quickly understanding and interpreting complex or new information. You can adhere to established procedures. You can collaborate effectively with people who may not be on your immediate team and willing to ask others for information. Are familiar with GMP(good manufacturing practices) and GDP (good documentation practices). You can work independently and drive projects to completion. You can work in a hood in a lab and utilize a pipette. To be considered for the Quality Control Analyst on the Materials team you must be willing and able to work Monday-Friday, 8am-4:30pm. You must have a BS/BA in Biology, Chemistry, Biochemistry or related Life Sciences field; or an equivalent combination of education and experience. For the various levels you must have the following: Associate QC Analyst: BS/BA in Biology, Chemistry, Biochemistry or related Life Sciences field QC Analyst: 12-18 months of related experience Or an equivalent combination of education and experience Level is determined based on qualifications relevant to the role. Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries specific benefits, please speak to your recruiter. Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regenerons roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regenerons on-site policy and expectations for your role and your location. 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. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business. For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location. Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc. Salary Range (hourly) $24.38 - $38.13

Keywords: Regeneron Pharmaceuticals, Inc., Hartford , QC Analyst- Material Qualifications, Science, Research & Development , East Greenbush, Connecticut