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Associate Scientist, Bioanalytical Sciences

Regeneron Pharmaceuticals

Tarrytown, NYJob$94–153K/yrSeen todaySeen in employer's feed today

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At a glance

Compensation
$94–153K/yr
Location
Tarrytown, NY
Work Authorization
Not specified

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Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

Regeneron seeks an Associate Scientist for its Bioanalytical Sciences Quality Control team in Tarrytown, NY, working on‑site. The role involves reviewing and verifying documentation, building GxP knowledge, and developing problem‑solving skills while collaborating with QC management and cross‑functional stakeholders.

Skills & qualifications

RequiredNice to have

Skills

Documentation ReviewQuality ControlGxP KnowledgeMulti‑TaskingProblem SolvingCommunicationProfessionalismScientific Curiosity

Qualifications

Bachelor's DegreeMaster's Degree0-3 Years Relevant Post‑Degree Experience

Benefits

401(k) Match
Medical Insurance
Dental Insurance
Vision Insurance
Paid Time Off

Full 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 an Associate Scientist to join our Bioanalytical Sciences Quality Control team in an on-site capacity. In this role, you will perform quality control review of documentation, building foundational GxP knowledge while beginning to independently interpret findings and solve problems within defined procedures while collaborating with QC management, peers, and cross-functional stakeholders.

This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & where:

  • Location: Tarrytown, NY

  • Work model/flexibility: On-site

Discover your role:

  • Build foundational knowledge of established QC processes by reviewing, verifying, and acknowledging documentation under the direct supervision of management

  • Assemble available resources to perform QC, learning to evaluate the quality of various forms of documentation

  • Manage multiple documentation types at once, sharpening your ability to multi-task effectively

  • Develop foundational problem-solving skills by learning appropriate approaches to resolve findings

  • Collaborate with and engage stakeholders across functions to improve documentation quality

  • Participate in QC sub-team and group meetings, sharing the results of your work with others

  • Provide cross-functional support as needed, broadening your exposure across the organization

This role requires:

  • Bachelor's or Master's degree and 0-3 years of relevant post-degree experience

  • Foundational knowledge of GxP principles and industry practices/standards is a plus

  • Conduct yourself with professionalism and integrity while maintaining a strong work ethic

  • You communicate clearly and concisely, and you listen actively to understand the needs of your team and stakeholders

  • You adapt readily to changing priorities in a fast-paced environment

  • You're invested in your own professional development and welcome giving and receiving feedback

  • You bring scientific curiosity to your work, asking thoughtful questions to deepen your understanding

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 (annually)

$93,900.00 - $153,300.00

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