Drug Production, Associate Manufacturing Specialist

Regeneron is currently looking for a Drug Production, Associate Manufacturing Specialist in the Global Manufacturing department. In this role, you will focus on manufacturing life changing medicines for patients around the world while working in a clean room environment.

A typical day for a Drug Production, Associate Manufacturing Specialist might include:

• Performing all aspects of drug production in a clean room including cell culture and purification of monoclonal antibodies

• Completing and reviewing batch records and logbooks in accordance with Current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP)

• Performing in-process sampling and analysis of buffer solutions, cell culture, and drug substance

• Operating automated equipment such as bioreactors, chromatography columns, and filtration skids

• Supporting equipment start-up, troubleshooting, and validation

• Partnering with R&D teams to implement new drug manufacturing processes and technologies

This role might be for you if you:

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

• Are highly organized, detail oriented and perform work accurately the first time

• Value trust and transparency in everyday work

• Work well in both small and large teams to accomplish tasks adhering to a schedule

• Can operate in a highly regulated environment strive to continuously improve processes and maintain compliance to manufacture safe and effective medicines for patients

• Are able to learn and use computerized systems for daily performance of tasks

• Are a good communicator and can give and receive feedback constructively

If this sounds like you check out this video to view 'A Day in the Life':  A Day in the Life

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

Shift & Physical Requirements

• Ability to perform physical requirements for entirety of shift (up to 10 hours) in a clean room environment

• To enable a healthy work life balance we offer multiple shifts that are 4 working days (10 hours) to support 24/7 production.

• 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

To be considered for this role you must meet the below minimum education and experience requirements:

Drug Production, Associate Manufacturing Specialist:

• HS diploma + 4 years of relevant work experience or

• AS, BS or BA in Life Sciences or related field

Regeneron offers an exciting and competitive benefits package! For details check out: https://careers.regeneron.com/en/working-at-regeneron/total-rewards/

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.