Sr Staff Fill/Finish MFG Engineer

Regeneron Pharmaceuticals, Inc (USA); United States; On-site; USD 130,000 - 210,000; Full time

Job summary

Regeneron Pharmaceuticals, Inc. in Rensselaer, NY seeks a Sr Staff Fill/Finish MFG Engineer to serve as an expert for formulation, aseptic filling, visual inspection, assembly, and packaging processes.

You will support equipment design, process development, tech transfer, and validation activities in a hands-on role within the operations team. Responsibilities include leading tech transfer studies, supporting cGMP start-up, and contributing to training and continuous improvement efforts.

Qualifications

• BS/BA in Engineering with 12 years of industry experience.
• Knowledge of cGMP manufacturing environment.
• Experience with formulation, aseptic filling, and packaging processes.

Responsibilities

• Lead tech transfer studies and continuous improvement initiatives.
• Support validation and training activities for equipment and processes.
• Collaborate with cross-functional teams and external vendors to source and implement materials.
• Review SOPs and regulatory documents as needed.
• Assist in capital expenditure recommendations and project realization.

Skills

Formulation

Aseptic filling

Visual inspection

Process development

Tech transfer

Equipment design

Education

BS/BA in Engineering

Job description

Build our future together: At Regeneron, we use science and innovation to develop life‑changing medicines for people with serious diseases. We are seeking a Sr Staff Fill/Finish MFG Engineer who will serve as an expert for formulation, aseptic filling, visual inspection (manual and automated), assembly, and/or packaging processes as assigned, directly supporting the operations team. They will support equipment design and selection as well as process development activities. They will be hands‑on, solving issues during technology transfer, cGMP start‑up, and routine manufacturing for Regeneron internal operations. This role will also support validation and training activities for the assigned equipment, processes, and operators.

When & where: Location: Rensselaer, New York, United States Work model: Monday‑Friday, 8:00am‑4:30pm Travel: 30% international & domestic Discover your roles: Interfaces with other departments such as Engineering, Validation, DP Process Development, Process Analytical Sciences, Combination Products, Regulatory, Quality Assurance and Quality Control. Leads tech transfer / tech transfer studies, investigations, innovative technology adoption and continuous improvement initiatives. Develops strategy for cycle development and other studies on manufacturing equipment as defined by end user needs. Stays abreast of latest technologies and industry benchmarks to make recommendations to senior management. Designs and executes cycle development and other studies on manufacturing equipment as defined by end user needs. Supports equipment / new technology design, install, and qualification. Leads material and component selection, design, and approval. Works with internal stakeholders and external vendors to design, source, and implement materials. Leads functional evaluation of new components and raw materials for feasibility of use on manufacturing equipment. Reviews Standard Operating Procedures, specifications, regulatory filing, or other controlled documents as needed. Supports SOP development and revision for assigned equipment and process operations. Recommends capital expenditures and aids in the realization of capital projects. May represent manufacturing during regulatory and client audits. Tracks and trends relevant technical and business process metrics to ensure operations are performing effectively and efficiently. May lead and/or manage others. Partners cross functionally to establish standards for formulation and filling. Identifies and solves customer problems with minimal supervision Negotiates with external parties on behalf of IOPS.

This role requires: Requires a BS/BA in Engineering with 12 years industry experience or equivalent combination of education and experience. Knowledge of cGMP manufacturing environment and familiarity with formulation, aseptic filling, visual inspection (manual and automated), assembly, labeling, and/or packaging of liquid and lyophilized injectable products.

We are committed to building a workplace with an inclusive culture. 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, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Please be advised that at Regeneron, we believe we do our best work when we are together.

Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process.

As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.

For jobs in Canada: this posting is for an existing position. Salary Range (annually) $126,300.00 - $206,100.00

Regeneron is a leading biotechnology company that invents life-transforming medicines for people with serious diseases. Founded and led for over 30 years by physician‑scientists, our unique ability to repeatedly and consistently translate science into medicine has led to nine FDA‑approved treatments and numerous product candidates in development, almost all of which were homegrown in our laboratories. Our medicines and pipeline are designed to help patients with eye diseases, allergic and inflammatory diseases, cancer, cardiovascular and metabolic diseases, neurology, infectious diseases and rare diseases. Regeneron is also proud of award winning culture of innovation, being recognized as a Great Place to Work in 2021, Fast Company’s Best Workplace for Innovators in 2020, and Forbes JUST companies in 2020, among others.