Regeneron is currently looking for an Associate Project Manager to join our QC (Quality Control) AS (Analytical Sciences) team. The Associate Project Manager - QC AS works to identify, define and progress the early phase project deliverables for Analytical Sciences for gene therapy programs. Working with internal SMEs, external contract manufacturing organizations, external contract labs and customer groups in a matrixed team environment, the Associate Project Manager ensures that analytical test methods and supporting quality deliverables are established to support product manufacturing.

As an Associate Project Manager, a typical day might include the following:

• Attends gene therapy CMC program meetings as a representative of Analytical Sciences to serve as the primary point of contact and identify timing of key program breakthroughs, changes to program strategies and issues/concerns for programs. Proactively disseminates this information to AS management and SMEs.

• May oversee programs and activities that are outsourced at external contract laboratories.

• May own the implementation of CAPAs for Analytical Sciences and/or assist with quality events.

• Communicates cross-functionally within Analytical Sciences to identify the method development needs and timing for each early phase program.

• Develops a cohesive strategy for each early phase program and is responsible for the execution of that strategy.

• Engages in technical discussions cross-functionality to ensure the appropriate analytical deliverables are identified.

• Uses technical knowledge to ensure customer groups are provided with the appropriate analytical services including ensuring appropriate assays are in place for manufacturing sampling plans.

• Ensures that team members are informed and accountable for their deliverables. Brings up any issues to management and proactively recommends solutions.

• Works cross-functionally with partner groups such as CMC Reg Sci, Quality Assurance, Manufacturing, Process Sciences and Tech Training to identify the need for supporting documentation for early phase gene therapy analytical programs including reports, technical documents and forms, and supports review of documents with impact to Analytical Sciences.

• Collaborates with CMC Reg Sci to support regulatory filings

• Identifies and implements effective tools for the group to improve the quality and efficiency of the matrix analytical development team.

• Regularly prepares and communicates program updates to senior management.

• Navigates a fast-paced and ambiguous environment to create a detailed program plan with defined deliverables and timelines.

This role night be for you if you have:

• Excellent organization, oral and written communication skills.

• Experience with MS Project or related project management tools.

To be considered for the Associate Project Manager – Quality Control you must have a BA/BS in Life Sciences or related field and 8+ years of experience.

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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)

$89,100.00 - $145,500.00