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2027 Co-op Cell Medicines Research & Development

Regeneron Pharmaceuticals

Cambridge, MAFull-time$17.9–50.9/hrSeen todaySeen in employer's feed today

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At a glance

Compensation
$17.9–50.9/hr
Location
Cambridge, MA
Role Type
Co-op
Schedule
Full-time
Work Authorization
Not specified

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Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

Regeneron seeks multiple 2027 Co‑ops for its Cell Medicines team, focusing on T‑cell therapy development. The full‑time, on‑site roles involve laboratory testing, method development, and support of GMP manufacturing, offering hands‑on experience in cutting‑edge cancer therapeutics.

Skills & qualifications

RequiredNice to have

Skills

In Vitro TestingFlow CytometryViral Vector ProductionHigh‑Throughput Protein ProductionAnalytical Method DevelopmentGMP ManufacturingDigital TransformationDocumentationCollaboration

Qualifications

Enrollment in Undergraduate or Graduate Degree ProgramCommitment to 40 Hours Per WeekDemonstrated Leadership PreferredCumulative GPA of 3.0 or Higher PreferredRelevant Majors: Biology, Biochemistry, Biomedical Engineering

Benefits

Medical Insurance
401(k) Match
Paid Time Off

Full job description

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking multiple 2027 Co-ops to join our Regeneron Cell Medicines (RCM) team, Regeneron's cell therapy unit developing next-generation T-cell therapies for cancer.

These positions offer the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & where:

Location: / Seattle, WA Cambridge, MA

Timeframe: Our Co-op positions are full-time and onsite from January-August (Spring-Summer), May/June-December (Summer-Fall), and August-December (Fall).

Pay : Intern and Co-op pay ranges are determined by level of education (year in school) and degree program. The hourly rate range for these locations is: $17.90-$50.90 per hour.

What you’ll do:

  • Support in vitro safety and efficacy testing of cell therapy candidates

  • Develop tumor antigen expression and flow cytometry methods

  • Contribute to viral-vector production and process development for cell engineering

  • Support high-throughput protein production activities

  • Contribute to analytical method development supporting Good Manufacturing Practice (GMP) manufacturing

  • Support digital-transformation initiatives for manufacturing operations

  • Document experimental procedures and results

  • Collaborate with scientists across the cell therapy team

Relevant majors: Biology, Biochemistry, Biomedical Engineering

Let’s find out if we’re a fit :

  • Must be enrolled in, or accepted to, an academic program pursuing an Undergraduate or Graduate degree (and be returning to school the semester following the position or graduating after the position)

  • Must be able to commit to 40 hours per week from January-August, May/June-December, or August-December

  • Demonstrated leadership in areas such as campus activities, clubs, sports, current or previous work, or within the community preferred

  • Cumulative GPA of 3.0 or higher preferred

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.

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