We are currently looking to fill a Quality Control (QC) Analyst position on our QC Analytical Science (AS) Clinical Bioassay Team. This position is a 1st shift, Sunday-Thursday 8 AM – 4:30pm schedule. Regeneron successfully manufactures a range of biopharmaceuticals for patients worldwide, including our approved therapeutic proteins and those involved in clinical studies. The QC Analysts at Regeneron perform the critical testing necessary to ensure the consistency and quality of both clinical and commercial products. The ideal candidate for this position would have experience with binding or bioassays used for potency testing in a GMP setting.

As a QC Analyst, a typical day might include the following:

• Perform QC testing on in-process, product, stability, and/or research samples.
• Perform associated support activities including maintaining laboratory supplies, preparing/aliquoting reagents and performing equipment maintenance.
• Completes test records and documents test results.
• Reviews test results to ensure compliance with standards; identifies/investigates any quality anomalies.
• Gather and/or summarize data for investigations.
• Review logbooks, notebooks or testing data.
• Compliance with all applicable SOPs as well as site and pertinent regulatory agency requirements.
• Participates in required training activities.
• Writes and revises control test procedures and SOPs.
• Interacts with outside customers or functional peer groups.
• May be responsible for maintaining specific projects.
• May assist in qualification and validation of methods.
• May be involved in establishing the transfer of methodology.
• May devise or develop new analytical methods and techniques.

This role might be for you if you:

• Have experience with potency assays or mammalian cell culture.
• Enjoy working in a fast-paced environment and balancing multiple tasks.
• Are able to work independently or as part of a team following both verbal and written instructions.
• Communicate effectively, respectfully, and with transparency.
• Continuously drive to improve processes for improved performance.
• Have a basic working knowledge of Microsoft Suite (Word, Excel, PowerPoint).
• Have effective time management skills.
• Possess strong interpersonal skills.
• Have excellent written and verbal communication skills.
• Can gather and evaluate data
• Maintain integrity and honesty at all times.

To be considered for the Quality Control Analyst on our QC AS Clinical Bioassay team, you must be willing and able to work Sunday-Thursday, 8 AM – 4:30 PM. You must have the following; BS/BA in Life Sciences or related field; or equivalent combination of education and 1 years of relevant experience. Experience with mammalian cell culture practices, bioassay and/or binding assay testing, and working in a GMP environment is preferred, but not required. Level is determined based on qualifications relevant to the role.

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)