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Internship Downstream Process Development Jobs in Stamford, CT

Head of Biologics

New York, NY · On-site

$170K - $230K/yr

Lead Neion Bio's protein development function, including downstream process development, analytical development, product characterization, and regulatory strategy and interactions * Define product ...

This individual will own upstream and downstream process development, analytical development, and ADC conjugation/manufacturing - from early clinical supply through late-stage development - ensuring ...

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Internship Downstream Process Development information

See Stamford, CT salary details

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$18

$25

How much do internship downstream process development jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for internship downstream process development in Stamford, CT is $18.17, according to ZipRecruiter salary data. Most workers in this role earn between $15.38 and $20.53 per hour, depending on experience, location, and employer.

What is an internship in downstream process development?

An Internship in Downstream Process Development is a temporary position, typically for students or recent graduates, focused on learning and supporting the processes involved in purifying and formulating biopharmaceutical products after the initial production stage. Interns in this field gain hands-on experience with techniques such as filtration, chromatography, and quality control, and often work within a research and development or manufacturing environment. This internship helps build skills in laboratory methods, data analysis, and process optimization, making it valuable for those interested in careers in biotechnology or pharmaceuticals.

What types of hands-on projects can I expect to work on during an internship in downstream process development?

As an intern in Downstream Process Development, you will typically assist with projects focused on purification and recovery of biological products, such as proteins or antibodies, from complex mixtures. This often includes tasks like preparing chromatography columns, performing filtration techniques, and conducting sample analysis using methods such as SDS-PAGE or HPLC. You’ll also collaborate closely with experienced scientists and engineers, participate in team meetings to review data, and help troubleshoot process challenges. These experiences provide valuable insight into both laboratory workflows and the broader bioprocess development pipeline.

What are the key skills and qualifications needed to thrive as an internship in downstream process development, and why are they important?

To thrive in an Internship Downstream Process Development role, a solid background in biotechnology, chemical engineering, or a related field, along with foundational lab skills, is essential. Familiarity with bioprocessing techniques, analytical instruments, and data analysis software is typically required, and experience with GMP environments can be advantageous. Strong problem-solving abilities, attention to detail, and effective communication are important soft skills for collaborating with team members and documenting results. These competencies ensure interns can contribute to optimizing purification processes and maintaining high standards in biopharmaceutical development.

What is the difference between Internship Downstream Process Development vs Downstream Process Technician?

AspectInternship Downstream Process DevelopmentDownstream Process Technician
CredentialsTypically pursuing or holding a degree in biotech, chemistry, or related fieldsUsually requires technical diploma or associate degree in biotech or related areas
Work EnvironmentLaboratory and development settings, focusing on process optimization and experimental workManufacturing floor, operating equipment, and performing process runs
ResponsibilitiesAssisting in process development, data analysis, and protocol documentationExecuting downstream processing steps, equipment setup, and process monitoring

In summary, Internship Downstream Process Development focuses on learning and supporting process optimization in a lab setting, while Downstream Process Technicians handle the hands-on execution of downstream manufacturing processes in production environments.

Process Development Engineer I, Purification Development

Regeneron Pharmaceuticals, Inc (USA)

Tarrytown, NY • On-site

$70 - $90/hr

Other

Medical, Retirement, PTO

Posted yesterday

New


Regeneron rating

8.4

Company rating: 8.4 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

22nd of 86 rated pharmaceutical


Job description

Overview

Regeneron's Preclinical Manufacturing & Process Development Group (PMPD) in Tarrytown, NY seeks a Process Development Engineer to support purification development and assist in technology transfers to internal manufacturing sites.

Key Responsibilities
  • Perform process development for pre‑clinical and clinical purification processes
  • Document experiments, results, and findings in an electronic laboratory notebook
  • Read and understand scientific literature and technical documentation, then verify literature findings with experimental plans
  • Maintain instruments and troubleshoot instrumental and experimental problems
  • Develop technology and automation to increase throughput and efficiency of pre‑clinical manufacturing and support improvement initiatives
  • Present work at group and department meetings
  • Build relationships within the subgroup, train and mentor peers, co‑op students, and interns
  • Assist colleagues in experiment execution and seek support when necessary
Who We’re Looking For
  • Enjoy working in a fast‑paced, team environment
  • Show initiative and drive to complete ambitious tasks and learn new technologies
  • Contribute to lab equipment maintenance, safety, and SOP compliance
  • Anticipate and prevent potential problems with laboratory supplies and equipment
  • Keep up with SOP training and compliance responsibilities
Qualifications
  • Bachelor’s and/or Master’s degree in Chemical Engineering, Biochemical Engineering, or Biochemistry
  • 0–3 years’ experience in the biotech or pharmaceutical industry
  • Strong fundamental understanding of protein purification and technology transfer principles (preferred)
  • Experience with downstream development and equipment such as Akta systems, centrifuges, filtration, chromatography, HPLC/UPLC, ultrafiltration, laminar flow hood, fume hood, Empower, Unicorn, JMP, LIMS, PI Historian (preferred)
  • Experience with robotic liquid handlers, Raman spectroscopy, or software programming (preferred)
Benefits

Regeneron offers a competitive and comprehensive total rewards package that may include annual bonuses or incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, insurance benefits, paid time off, and family support benefits. Additional benefit details are provided during the recruitment process.

Equal Opportunity Employer

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, Regeneron will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

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