Regeneron
BIOTECHNOLOGY
Small Molecules, Biologics
LocationTARRYTOWN, NY
Employees13,000
Open Jobs408
Pipeline
Sodium-glucose cotransporter 2 inhibitorsN/A
Non-interventionalN/A
There is no interventionN/A
Non-InterventionalN/A
Process Development Associate, PAPD Operations
Regeneron
This listing was originally posted on Regeneron's careers page. Formulate is an equal opportunity job aggregator and is not involved in the hiring process. Where salary information is estimated, it is derived from BLS industry benchmarks and may differ from actual compensation.
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Upgrade to Pro — $25/moRegeneron, located in Tarrytown, NY, is seeking a Process Development Associate to support project management, technology transfer, and business operations for Regeneron Advanced Therapy Programs. This representative will work in the Advanced Therapy Project Management (AT-PM) group within Product, Analytical, and Process Development Operations (PAPD Ops) to help drive successful development and tech transfer of advanced therapies (e.g., AAV, bioconjugates, and synthetic chemistry programs) by enabling clear cross-functional ways of working, disciplined planning, and operational excellence with our internal partners and Contract Development & Manufacturing Organizations (CDMOs).
Lead cross-functional teams to complete process transfer and establish production processes at Contract Development & Manufacturing Organizations (CDMOs). Help ensure successful start-up and execution of manufacturing campaigns by driving team alignment, tracking deliverables, and escalating risks/issues as needed.
Own effective, accurate, and timely communication across functional areas within project/program teams. Serve as a primary point of contact for project status, decisions, and next steps, ensuring stakeholders have clear visibility to scope, timelines, and key risks.
Build and maintain integrated timelines for development and transfer activities, including assumptions, dependencies, and critical path.
Anticipate and address risks to manufacturing readiness related to process, documentation, training, and supply/logistics.
Lead recurring and ad-hoc technical forums to troubleshoot issues, drive decision-making, and capture lessons learned to improve future development and tech transfers across modalities.
Contribute to continuous improvement efforts to streamline and standardize AT-PM ways of working (templates, trackers, dashboards, and reference guides).
Partner with procurement and internal stakeholders to support CDMO engagement activities (e.g., RFPs, contracting coordination, and invoices) and help maintain a healthy vendor network to meet pipeline capacity/capability needs.
You take initiative, follow through on commitments, and enjoy working in a fast-moving environment with evolving priorities.
You enjoy coordinating across functions (technical and non-technical) and can balance independent work with team-based execution across multiple projects.
You have strong planning and organizational skills and are comfortable leading meetings, aligning on next steps, and driving closure on open actions.
You proactively identify risks/roadblocks, communicate tradeoffs, and know when and how to escalate to keep programs on track while maintaining strong partner relationships.
This role requires a BS in Chemical Engineering, Biochemical Engineering, Bioengineering, Biotechnology, Biochemistry, Biology, or Chemistry with an interest in Operations, Project Management, and Business, and 0–2 years of relevant experience in the biotechnology or pharmaceutical industry (internship/co-op experience may be considered). A strong customer-service mindset is essential. The ideal candidate can facilitate team collaboration, build and maintain clear project plans, and help design and improve repeatable business processes. Familiarity with cross-functional CMC concepts (e.g., process development, analytics, documentation readiness, and tech transfer to CDMOs) is preferred. Prior experience or knowledge of bioconjugation, gene therapy/AAV, or related advanced therapy process development is a plus.
If applicable, candidates may include GPA on their resume.
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 Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s 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 (annually)
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BIOTECHNOLOGY
Small Molecules, Biologics
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