We are currently looking to fill two Manager, QA (Drug Product Manufacturing) positions. These positions support facility start-up and operations of a new internal aseptic drug product facility. The position will be responsible for either the first or second shift on the floor Quality Operation Team. Available Working Schedule: + Monday-Friday, 2:00pm-10:30pm + Monday-Friday, 8:00am-4:30pm In this role, a typical day might include the following: + Builds and maintains a robust team of specialists by providing effective communication, motivation, mentorship, career development and performance feedback. + Lead cross functional teams and handles the results for the assigned projects. Drives projects through completion within timeline, quality and budgetary constraints. + Develops or supports program development for On the Floor Quality, Aseptic Qualification, Aseptic Process Simulation, and Filling batch records. + Develops functional processes, procedures and policies for areas. Works with senior management to report on project and program achievements and to present project needs. + Provides first response for Quality and Compliance issues on the manufacturing floor + Provides review and final QA approval of: Deviations, Change Documentation, CAPAs; SOPs; Electronic builds of Master Batch records + Interacts closely with Quality Systems, Manufacturing, Process Science, Manufacturing Science & Technology + Uses data trends to work with operating departments to facilitate process improvements. + Ensures product, facility, and equipment holds are placed when batch, equipment or system integrity is questioned + Ensures manufacturing quality staff are appropriately trained to support plant operations, ensuring risks are identified and resolved. + Ensures periodic formal and informal audits are completed in production + Directs the activities of resources, both internal and outside contractors/vendors, with similar technical or functional responsibilities. + Responsible for implementing operational and strategic policies and directives. + Ensures projects are on schedule and within budget. + Receives assignments in the form of general objectives with goals and processes defined. + Requires the ability to influence others to achieve results + Provide Leadership and direction to the manufacturing and support area departments to ensure a constant state of inspection readiness. + Accountable for ensuring policies, procedures, and standards are consistently followed and adhered to on a consistent basis; and changes policies, procedures and standards as appropriate to ensure the highest quality standards are maintained. This role may be for you if you: + Are able to set priorities within defined responsibilities and execute on results and goals per established timelines + Can adjust schedule based on facility start up, filling, and manufacturing needs. + Have strong decision-making skills + Possess the ability to multi-task and own multiple projects while ensuring each is progressing as planned + Excel at building relationships and working on cross functional teams + Are able to gown for an “A” classification clean room To be considered for this role you must hold a Bachelor’s degree in Life Sciences and the following minimum amounts of experience in a Quality Operations, Quality Assurance or manufacturing role, in a late stage or early stage start-up Drug Product company for each level: + Associate Manager -- 6+ years + Manager -- 7+ years Also requires 2+ years of work experience in a leadership role. May substitute proven experience for education requirement. Level is determined based on qualifications relevant to the role. \#REGNQA Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, 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. 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 (annually)** $104,300.00 - $170,100.00