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Internship Downstream Process Development Scientist information

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

As of Sep 6, 2026, the average hourly pay for internship downstream process development scientist in Ridgefield, CT is $38.51, according to ZipRecruiter salary data. Most workers in this role earn between $28.27 and $45.96 per hour, depending on experience, location, and employer.

What does an internship downstream process development scientist do?

An Internship Downstream Process Development Scientist works in the biopharmaceutical industry, assisting with the development and optimization of processes that purify biological products such as proteins, antibodies, or vaccines after they are produced by cells. Their role often involves supporting laboratory experiments, analyzing samples, and documenting results to improve the efficiency and scalability of downstream processes like filtration and chromatography. Interns in this position gain hands-on experience with cutting-edge technologies and learn about regulatory requirements and industry standards. This role helps prepare students or recent graduates for a career in process development or biomanufacturing.

What types of projects and responsibilities can an internship downstream process development scientist expect to work on?

As an Internship Downstream Process Development Scientist, you can expect to be involved in hands-on laboratory work focusing on the purification and characterization of biopharmaceutical products. Typical responsibilities include preparing buffer solutions, operating chromatography and filtration systems, analyzing samples using various analytical techniques, and documenting experimental results. Interns often collaborate with experienced scientists and engineers, contributing to process optimization and troubleshooting. The role provides valuable exposure to industry-standard procedures and the opportunity to develop technical skills in a team-oriented environment.

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

To thrive as an Internship Downstream Process Development Scientist, you need foundational knowledge in biochemistry, molecular biology, or chemical engineering, often supported by ongoing or recent enrollment in a relevant degree program. Familiarity with laboratory techniques such as chromatography, filtration, and analytical instruments, as well as experience with lab management software, is typically expected. Attention to detail, problem-solving abilities, and effective teamwork are standout soft skills in this role. These skills and qualifications are crucial for conducting reliable experiments, analyzing data, and contributing to the optimization of bioprocesses in a collaborative research environment.

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Internship Downstream Process Development Scientist jobs near you
Infographic showing various Internship Downstream Process Development Scientist job openings in Ridgefield, CT as of July 2026, with employment types broken down into 1% As Needed, 79% Full Time, 16% Part Time, and 4% Contract. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $80,094 per year, or $38.5 per hour.

Process Development Engineer III, Analytical Science: Synthetic and Bioconjugation Scale-Up Tec[...]

Regeneron Pharmaceuticals, Inc (USA)

Tarrytown, NY • On-site

$100 - $130/hr

Other

Posted 19 days ago

Regeneron rating

8.5

Company rating: 8.5 out of 10

Based on 44 frontline employees who took The Breakroom Quiz

19th of 86 rated pharmaceutical

Job description

Process Development Engineer III – Synthetic and Bioconjugation Scale-up Technologies (SBST) Analytics Group

Regeneron’s Preclinical Manufacturing & Process Development (PMPD) organization in Tarrytown, NY is seeking a highly motivated Process Development Engineer III to serve as the analytical lead for developing, transferring, and troubleshooting analytical methods to advance bioconjugate pipeline programs.

A Typical Day in the Role
  • Independently design and execute analytical testing, method development and characterization to enable bioconjugate process development.
  • Serve as the subject matter expert to lead and design analytical deliverables: robust method development, method transfer to internal/external receiving labs, training, and troubleshooting to move the program forward.
  • Connect, interpret, and communicate complex results into clear actionable next steps to technical and non‑technical audiences to persuade and drive timely decisions.
  • Author high‑quality documentation (procedures, development and characterization reports, ELN entries) in a timely manner to support program timelines.
  • Drive, build, and improve business workflows: documentation standardization, data digitization, and sample management.
  • Maintain compliance with lab and environmental safety requirements and promote a safe lab environment.
  • Proactively scout, evaluate, and implement new or improved technologies for high-throughput analytics and real‑time decision making.
  • Lead equipment upkeep, troubleshooting, maintain an organized workspace, and proactively plan for lab resources.
  • Mentor and support peers and junior team members (direct and/or indirect via matrix).
Qualifications
  • This role requires a B.S. with 10+ years of relevant experience, or an M.S. with 7+ years, or a recent Ph.D. with 0‑3 years of relevant experience in chemistry, biochemistry, biology, chemical engineering, or a related field.
  • Hands‑on experience with analytical method development for antibody, bioconjugate, and/or synthetic molecules (e.g., small molecule, PEG, peptides, and/or siRNA) such as electrophoresis, HPLC, LC‑MS, UV spectroscopy, plus associated software (e.g., Empower).
  • Experience in transferring methods to internal/external labs and troubleshooting.
  • Demonstrated experience serving as an analytical lead for bioconjugate programs, collaborating effectively with internal teams and external CDMOs.
  • Strong written and verbal communication skills, including the ability to present data clearly to diverse audiences.
  • Experience drafting analytical methods, development and characterization reports to support regulatory filing.
  • Ability to work independently and collaboratively across cross‑functional teams to persuade and drive data‑based decision making.
  • Demonstrated initiative, learning agility, and a growth mindset in a fast‑paced environment.
Eligibility and Equal Opportunity Statement

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

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