Regeneron successfully manufactures a range of biopharmaceuticals for patients worldwide, including our approved therapeutic proteins and those involved in clinical studies. Our Associate Biotech Production Specialists are on the front line, producing our life changing products and have a passion for assisting those in need by using biotechnology. They perform all tasks necessary for the manufacturing operations of both clinical and commercial manufacturing programs.

What to look forward to:

Competitive Compensation- Regeneron offers highly competitive base pay and employees working premium shifts receive incentive pay, such as shift differential and/or weekend pay. All employees receive equity awards and are eligible for annual performance bonuses. We offer comprehensive health coverage, tuition reimbursement, and qualified employees may receive assistance paying down student loans. Relocation assistance is also available for eligible new hires.

Work Life Balance- We provide an onsite gym and rock-climbing wall, daycare, physical wellbeing programs, tuition reimbursement, and generous paid time off and holidays.

Emotional Wellbeing Support – Regeneron prides itself in supporting employees. We provide onsite behavioral health counselors, emotional wellbeing webinars, and Employee Resource Groups (ERGs) to all employees. Employees enrolled in any of our health plans are eligible for additional mental health support.

Regeneron Culture- We pride ourselves on our outstanding culture! Regeneron has best-in-class onsite and offsite events throughout the year, onsite cafeterias, company affiliated sports teams and clubs, and a culture centered on diversity and inclusion.

As an Associate Biotech Production Specialist, a typical day may include the following (but may vary greatly due to Regeneron’s constantly evolving environment built on innovation):

Includes all aspects of biotech production activities related to cell culture

Reviews, edits, completes, and revises completed batch records, Logbooks, and SOPs in accordance with cGMP standards and aligned with written procedure

Performs manufacturing level maintenance on equipment

Participates in equipment start-up, commissioning, and validation activities

Works to optimize, trend, and report manufacturing process operational parameters during routine manufacturing campaigns

Creates process evaluation reports, process transfer documentation, and process characterization presentations

Assist with training of new employees

Performs in-process sampling, Quality Control Chemistry and Quality Control Microbiology

Keeps process area stocked with essential equipment and components

This job may be for you if:

You want to support our amazing team to produce the highest quality medicines for patients as efficiently as possible to change people’s lives

You are driven to challenge the status-quo and develop a culture where continuous improvement is not just a metric but rather an approach for everyone, every day, to do better

You are not easily frustrated with a meticulous process of change control, investigations, and corrective actions

You enjoy project oriented work with a career goal of becoming a subject matter expert

You thrive in a fast-paced setting where your priorities can quickly change based on the needs of the business and our patients

You are smart, adaptable and great at problem solving

You prosper in a culture of trust, teamwork and transparency

You are driven to constantly improve processes and procedures to find the most efficient and effective way to make it happen, everyday

Shift Requirements: Physical

Ability to perform physical requirements for entirety of shift (up to 10 hours):

Some physical requirements can include but not limited to: bending, climbing, crawling, kneeling, reaching, reaching overhead, sitting, squatting, walking, standing, driving, hand manipulation and ability to lift/push/pull up to 50lbs

Gowning and Environment

Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)

Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire

If you still are questioning what this role entails, please take the opportunity to view 'A Day in the Life' of one of our very own, Ashley Lebby, to learn more: https://www.linkedin.com/posts/regeneron-pharmaceuticals_learn-about-the-role-of-a-bps-and-apply-today-activity-6970862361234587648-vRzL?utm_source=share&utm_medium=member_desktop

To be considered for the Associate Biotech Production Specialist role, you must have one of the following; BS/BA in Industrial Engineering, Mechanical Engineering, or related field or AS/AAS Degree/Certificate in Biotechnology/Biological Science, or an equivalent combination of education and experience.

To be considered for the Biotech Production Specialist role, you must have one of the following; BS/BA in Industrial Engineering, Mechanical Engineering, or related field or AS/AAS Degree/Certificate in Biotechnology/Biological Science, or an equivalent combination of education and experience and a minimum of 2 years of relevant experience.

Level is determined based on qualifications relevant to the role.

#REGNEC

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 (hourly)