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. Please continue to review the job duties if you are interested in working 3rd shift (10pm-8:30am) with the potential for weekends.

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

• Able to work 3rd shift (10pm-8:30am) with the potential for weekends

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 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.

 

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.  If you have any questions, please speak with your recruiter. 

Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.

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 (hourly)

$21.78 - $39.13