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
External Manufacturing Specialist
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/moWe are currently looking to fill a Specialist position within the Advanced Therapies External Manufacturing team that specializes in synthetic or fermentation-based processes. Regeneron successfully manufactures a range of biopharmaceuticals for patients worldwide, including our approved therapeutic proteins and those involved in clinical studies. This role oversees all aspects of contract manufacturing organizations and partners including day-to-day operations, ensuring timely completion of associated operations/documentation, and assisting in the monitoring of cGMP compliance.
As a Specialist of External Manufacturing (Advanced Therapies), a typical day might include the following:
Serving as the operational contact for contract manufacturing and/or partner sites concerning day-to-day activities.
Coordination of external manufacturing activities at contract and/or business partner sites, including but not limited to scheduling of all batches, supply of materials, providing direction on shipment of material, tracking and monitoring of cycle times, providing support for manufacturing activities and enlisting support from others who will provide any required associated reports and technical expertise.
Functioning as a liaison between Regeneron Quality Control, Quality Assurance, Supply Chain, Operations/Logistics Departments and contract manufacturers or business partners.
Leads a sub-team in continuous process improvements, system/equipment implementation and/or strategy development.
Supporting investigations which concern external manufacturing activities and associated shipping operations, as required.
Supporting and informing strategic initiatives and contract negotiations that drive long-term relationship stability and success.
Ensuring product integrity and company reputation by assisting in the monitoring of cGMP compliance at contract manufacturers and business partners.
Support tech transfer and/or development work of programs at a CMO to ensure scalability toward GMP manufacturing.
Performing reviews of pre-production master batch records and executed batch records.
This role might be for you if:
You have experience in any of the following areas: synthetic based processes, small molecule synthesis, antibody drug conjugates, fermentation.
You have knowledge of bulk manufacturing techniques (recommended) – fermentation, chemical synthesis, downstream purification, conjugation and/or formulation.
You have basic knowledge of regulatory compliance inclusive of cGMP, FDA regulations, familiarity with ICH guidelines, and EU regulations.
You lead continuous improvements, system implementations and/or strategy development to reduce cycle times and improve efficiencies for area.
You have strong interpersonal, written, and oral communication skills.
You exhibit a degree of ingenuity, creativity, and resourcefulness in evolving and ambiguous environments.
You can gain understanding from the instructions provided and work towards goals with minimal supervision
Can travel to contract manufacturers or business partners, as required (up to 25%).
Are comfortable with leading a sub-team in continuous process improvements, system/equipment implementation and/or strategy development.
Shows resiliency and flexibility in the face of challenging and dynamic environment
To be considered for a Specialist of External Manufacturing, a BS/BA in business or scientific discipline and 3+ years of related experience in either cGMP manufacturing operations or equivalent combination of education and experience.
To be considered for a Senior Specialist of External Manufacturing, a BS/BA in business or scientific discipline and 5+ years of related experience in either cGMP manufacturing operations or equivalent combination of education and experience.
Level is determined based on relevant education and experience.
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.
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BIOTECHNOLOGY
Small Molecules, Biologics
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