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Regeneron Pharmaceuticals, Inc

Associate Director/Director Investigations (Quality Control)

Regeneron Pharmaceuticals, Inc, New York, New York, us, 10261


We are currently looking to fill an Associate Director/Director Investigations (Quality Control) position. This position is responsible for providing direction and oversight to the review, approval, and management of investigations and corrective and preventive actions.In this role, a typical day might include the following:Leads a team with direct oversight of review and approval for GMP DocumentsMay review, verify and approve system recordsCollaborates cross-functionally to provide succinct support to teams to strive for quality outcomesMay approve and review Policy/SOP revisionsProvides direction for cross-functional teams. Serves as an escalation point as well as determination when additional escalation is requiredIdentifies leading practices and recommends improvements to continuously improve compliance profileServes as a subject matter authority (SME) to present topics to management and during inspectionsSupervises relevant quality system metrics including deviations and corrective actions. Uses metrics to identify and pursue initiativesDrafts and implements long-term planning for the process and staffPerforms personnel management functions (i.e., annual employee evaluations, coaching, mentoring, performance feedback, etc.)Makes decisions and develops and implements policies.Ensures that policies and procedures are effectively administered and align with regulatory requirements and current good manufacturing practices (cGMPs)Participates on internal committees/teams, as requiredThis role might be for you if you:Have experience leading a large team of quality-minded individualsContinuously seek to improve processes for improved performanceHave detailed knowledge of cGMPsExcel in a quality-driven organizationHave an understanding of biologics manufacturing operationsTo be considered for this role you must hold a Bachelor’s degree in Life Sciences or a related field and the following amount of relevant cGMP manufacturing experience for each level:Associate Director – 10+ yearsDirector – 12+ yearsLevel to be determined based on qualifications relevant to the role. May substitute proven experience for education requirement.Does this sound like you? Apply now to take your first step towards living the Regeneron Way!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.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.Salary Range (annually):

$142,700.00 - $277,100.00

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