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Internship Downstream Process Development Scientist Jobs in Crofton, MD

LifeSprout

R&D Engineer

Baltimore, MD · On-site

... and scientific disciplines. Position Overview: The Research and Development Engineer is responsible for planning and executing product and process development activities to support innovation ...

Govcio LLC

Data Scientist

Fort George G Meade, MD · On-site

$156K - $176K/yr

Early data science input during IOC ensures that data collected will be suitable for downstream AI development, reducing risk and accelerating capability maturation during follow-on implementation

Lab4U Inc

Lab4U's Internship Program

Washington, DC · On-site

Business Development Intern As the Business Development Intern, you will work directly with the ... Other Internships Areas If you'd like to help transform science education by joining our internship ...

Lab4U Inc

Lab4U's Internship Program

Washington, DC · On-site

Business Development Intern As the Business Development Intern, you will work directly with the ... Other Internships Areas If you'd like to help transform science education by joining our internship ...

Kaiser Permanente

Data Scientist III

Fulton, MD · On-site

$110 - $170/hr

Pursues self-development; creates plans and takes action to capitalize on strengths and develop ... downstream processes; writing and optimizing diverse SQL queries; and demonstrating a working ...

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Internship Downstream Process Development Scientist information

See Crofton, MD salary details

$20

$39

$62

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

As of Sep 4, 2026, the average hourly pay for internship downstream process development scientist in Crofton, MD is $39.10, according to ZipRecruiter salary data. Most workers in this role earn between $28.70 and $46.68 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 Crofton, MD as of June 2026, with employment types broken down into 16% As Needed, 34% Full Time, 23% Part Time, 12% Temporary, 2% Contract, and 13% Nights. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $81,330 per year, or $39.1 per hour.

R&D Engineer

LifeSprout

Baltimore, MD • On-site

Full-time

Re-posted 14 days ago

Job description

About LifeSprout:
LifeSprout was founded in September 2015 as a Johns Hopkins University spinout. We are a medical device company creating revolutionary products for aesthetic and reconstructive medicine. Our synthetic biomaterial platform mimics the look and behavior of native tissue and is being developed into a suite of products to restore form and function for millions of patients with soft tissue loss from aging, cancer, and metabolic disease. The company is led by a management team experienced across business, clinical, and scientific disciplines.
Position Overview:
The Research and Development Engineer is responsible for planning and executing product and process development activities to support innovation, product performance, and readiness for verification and validation. This role contributes across the development lifecycle, including process development, formulation screening, assay development, troubleshooting and root cause analysis, technical documentation, and preparation and execution of design verification and validation activities. The ideal candidate combines strong experimental skills with structured problem-solving, clear technical communication, and the ability to work effectively in a cross-functional, GMP-regulated environment.
Responsibilities:
  • Design and conduct experiments, analyze data, and interpret results to guide technical decisions and next steps.
  • Plan and execute formulation screening studies to evaluate candidate materials, compositions, and processing conditions.
  • Perform process development activities to improve product performance, manufacturability, robustness, and scalability.
  • Prepare for and execute design verification and validation activities, including protocol development, test coordination, data analysis, and report generation.
  • Develop, optimize, qualify, and document assays and test methods to support research, development, and product characterization.
  • Perform troubleshooting and root cause analysis for technical issues arising during development, testing, or manufacturing support activities.
  • Prepare clear and accurate technical documentation, including study protocols, reports, experimental records, and summaries of findings.
  • Collaborate with cross-functional teams such as Quality, Regulatory, Manufacturing, and Process Engineering to ensure development activities align with program goals and applicable requirements.
  • Maintain development records in accordance with internal procedures, quality system requirements, and good documentation practices.
  • Present technical findings, recommendations, and development updates to internal stakeholders.

Qualifications:
  • Master’s or PhD degree in Engineering, Biomedical Engineering, Chemical Engineering, Materials Science, Pharmaceutical Sciences, or a related technical field; advanced degree preferred.
  • 2+ years of experience in research and development, product development, formulation development, process development, assay development, or a related technical area.
  • Preferred experience working with biomaterials, hydrogels, electrospinning, high-shear mixing, separations, and sterilization processes
  • Hands-on experience designing experiments, analyzing data, and drawing conclusions to support product or process decisions.
  • Knowledge of verification and validation principles, test method development, and structured technical problem-solving.
  • Strong technical writing skills, with experience preparing protocols, reports, and development documentation.
  • Ability to troubleshoot effectively and apply root cause analysis tools to resolve complex technical issues.
  • Strong interpersonal and cross-functional collaboration skills.
  • Familiarity with regulated development environments, quality systems, and documentation practices is preferred.

Working conditions and what we offer:
  • Onsite presence required for laboratory activities with occasional travel (<10%).
  • Fast paced, collaborative environment balancing development and release activities.
  • Competitive compensation, benefits, and professional development opportunities.
  • Opportunity to shape analytical strategy for an innovative biomaterials platform with clear patient impact.

Eligibility to work in the U.S. is required.

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