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Internship Downstream Process Development Scientist Jobs in Wayne, NJ

Lancesoft

Research & Development Scientist

Summit, NJ · On-site

Scientist 2, Research & Development Location: Summit NJ 07901 Duration: 07/28/2026 to 12/31/2026 ... Maintain comprehensive and accurate documentation of batch formulations, processes, and results in ...

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Internship Downstream Process Development Scientist information

See Wayne, NJ salary details

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

As of Jul 30, 2026, the average hourly pay for internship downstream process development scientist in Wayne, NJ is $38.35, according to ZipRecruiter salary data. Most workers in this role earn between $28.12 and $45.77 per hour, depending on experience, location, and employer.

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.

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.
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Internship Downstream Process Development Scientist jobs near you
Infographic showing various Internship Downstream Process Development Scientist job openings in Wayne, NJ as of July 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, and 2% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $79,758 per year, or $38.3 per hour.

Head of Biologics Development & CMC

Neion Bio

New York, NY

$170K - $230K/yr

Full-time

Medical, Dental, Vision, Retirement

Posted 22 days ago

Job description

About Neion Bio:

Neion Bio is harnessing nature's best molecular factory, the chicken egg, to make medicine affordable, accessible, and resilient. We turn farms into medicine factories using cutting edge genetic engineering and stem cell technology. These "living bioreactors" are fully autonomous 3D biomolecular printers that operate on existing industrial-scale infrastructure. Our platform can rapidly and scalably produce almost any protein, provide national resilience to drug shortages and de-risk complex supply chains, and ultimately take advantage of novel biological environments to solve unmet medical needs. Biomanufacturing, reinvented. Medicine, democratized. 

Role Summary:

We are looking for an exceptional Head of Biologics Development & CMC to lead the development of therapeutic proteins produced using Neion Bio's egg-based biomanufacturing platform. This person will own Neion Bio's protein development and CMC strategy, spanning downstream process development, analytical development, product characterization, and regulatory CMC.

This is a role for a technically rigorous and highly collaborative leader who can move fluidly between scientific and regulatory strategy and hands-on problem solving. The ideal candidate has deep experience in biologics (and in particular biosimilars) development, can critically evaluate protein quality and process data, and has led cross-functional CMC programs through regulatory interactions. This person will initially manage a small team of downstream process development and analytical scientists and will play a central role in building Neion Bio's broader protein development organization.

Key Responsibilities:

  • Lead Neion Bio's protein development function, including downstream process development, analytical development, product characterization, and CMC strategy
  • Define product-specific critical quality attributes and establish risk-based strategies for evaluating their potential impact on safety, efficacy, pharmacokinetics, immunogenicity, and biological function
  • Lead the design and interpretation of comparative analytical assessment and biosimilarity programs, including reference-product characterization, lot-selection strategy, analytical similarity, and structure-function studies
  • Provide technical oversight of purification-process development
  • Select and manage CROs, CDMOs, consultants, and other external technical partners, ensuring scientific quality, appropriate study design, and timely execution
  • Lead CMC development planning, including program timelines, technical risk assessments, budgets, resource plans, and decision-making frameworks.
  • Serve as the technical CMC lead in interactions with FDA and other regulatory agencies, including preparation for meetings, responses to agency questions, and implementation of regulatory feedback
  • Contribute to portfolio strategy, program selection, development timelines, budgets, hiring, and organizational planning

Requirements

  • Ph.D. in biochemistry, chemical engineering, bioengineering, pharmaceutical sciences, analytical chemistry, or a related field, with 10+ years of relevant industry experience; an M.S. with 13+ years of experience, or a B.S. with 15+ years of experience. 
  • Deep experience in biologics development, with a technical foundation in downstream process development, analytical development, protein characterization, or a closely related field
  • Deep technical knowledge of protein characteristics, especially glycosylation and other post translational modifications 
  • Substantial technical ownership of at least one biologic program through a major late-stage regulatory milestone, such as BLA or MAA submission, approval, process validation, or commercial readiness.
  • Experience managing scientists and leading cross-functional technical teams
  • Experience selecting and managing CROs, CDMOs, analytical laboratories, and other external development partners

Benefits

Compensation: base salary is expected to be $170K-$230K depending on experience, with additional bonus compensation, equity compensation, and benefits including health insurance, dental insurance, vision insurance, and 401(k).

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