Quality Control Specialist

Quality Control External Testing is currently looking to fill a QC Specialist position with a 1st shift, Monday-Friday, 8:00am - 4:30pm schedule. This position performs data review of analytical test results to support QC External Testing operations. In this role, a typical day might include the following: Conduct comprehensive data review for Release, In-Process, and Stability testing in Advanced Therapies, ensuring adherence to quality standards. Perform thorough evaluation of analytical test method Qualification, Verification, Transfer, and Validation documentation. Ensure all data complies with cGMP, GDP, FDA, EMA, and ICH Guidelines through meticulous review processes. Verify analytical data meets ALCOA+ principles (Attributable, Legible, Contemporaneous, Original, Accurate, plus Complete, Consistent, Enduring, and Available). Monitor testing compliance with established laboratory procedures, test methods, and approved protocols. Collaborate with laboratory personnel to address documentation errors and omissions while fostering a cGMP-oriented culture. Demonstrate exceptional attention to detail, focus, and multitasking capabilities when reviewing complex analytical laboratory data. Apply strong technical expertise in various analytical methodologies including liquid chromatography, pH measurement, iCIEF, ELISA, SEC, and CE-SDS. Engage with team members to implement continuous improvements to data review processes and methodologies. Provide strategic guidance to QC analysts for enhancing Good Documentation Practices within cGMP frameworks and applicable SOPs. Complete assigned tasks within established timeframes while managing organizational responsibilities including tracking open tasks and timelines. Support the development and review of QA events, deviations, and investigations as required. Maintain effective communication with QC Analysts, Group Leaders, and departmental managers to ensure seamless operations and quality compliance. This role might be for you if: You can effectively communicate issues and ideas with direct reports, peers, and with management You have a strong ability to achieve thoroughness and accuracy when performing tasks You have strong prioritization / organizational skills and are detailed-oriented. You have the capability to adjust to shifting priorities, manage multiple tasks and meet deadlines You have excellent written and oral communication skills You have experience in a GMP setting To be considered for this position you must have a BS/BA in a scientific field, or equivalent combination of education and experience. Specialist: Requires a BS/BA in a scientific field and 2 years of related experience or equivalent combination of education and experience. Level is determined based on qualifications relevant to the role. We have an inclusive and diverse culture that provides amazing benefits including health and wellness programs, fitness centers and stock for 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 maternity 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. 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, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship. Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit For other locations, additional information will be provided during the recruitment process. Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on-site. As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications. For jobs in Canada: this posting is for an existing position. Salary Range (annually) $67,400.00 - $110,000.00 #J-18808-Ljbffr