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Internship Downstream Process Development Scientist Jobs in Mercer County, NJ

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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 Aug 15, 2026, the average hourly pay for internship downstream process development scientist in Mercer County, NJ is $40.89, according to ZipRecruiter salary data. Most workers in this role earn between $30.00 and $48.80 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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What job categories do people searching Internship Downstream Process Development Scientist jobs in Mercer County, NJ look for?

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Internship Downstream Process Development Scientist jobs near you
Infographic showing various Internship Downstream Process Development Scientist job openings in Mercer County, NJ as of July 2026, with employment types broken down into 1% As Needed, 81% Full Time, 14% Part Time, and 4% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $85,054 per year, or $40.9 per hour.

Process Scientist (Philadelphia, PA)

CEDENT

Philadelphia, PA

Full-time

Re-posted 28 days ago

Job description

Title: Process Scientist Report: CTO Location: Philadelphia, PA Position Type: Full Time, Exempt Travel: Occasional (0-10%) Position Summary This position is part of the Technology team responsible for Client technology development, process development, and assisting in transferring developed process to GMP manufacturing. A Scientist is a mid-level individual with understanding of cell/molecular biology and previous experience in either upstream or downstream biopharmaceutical processing that utilizes bioreactors. A Scientist is responsible for hands-on execution of experiments and technology transfer, as well as authoring experimental protocols, SOPs, and batch documents.

A Scientist is expected to independently complete objectives given by supervisor, serve as a role model to junior scientists, collaborate cross-functionally, and provide support with any other technology, process development, and manufacturing needs. Key Responsibilities Independently contribute to technology/process development for specific bioprocessing steps, ensuring delivery in alignment with Client strategy Support Senior/Principal Scientist with experimental design, execution and data analysis, effectively communicating technical results to management Author protocols, SOPs, and batch documents to ensure the successful transfer of technology/process development to GMP manufacturing Perform as a Subject Matter Expert on a cross-functional team to implement novel process. Work closely with suppliers and other partners to drive forward technology development initiatives Serve as a good financial steward to the Technology team at Client and help to implement budgetary adherence and financial governance Coach and train junior scientists/employees on activities and documentation related to technology development, process development.

Other related duties as assigned. Education and Experience Minimum Bachelor's degree in Biological Engineering, Biotechnology, Biology, Biochemistry, or other related field. Master's preferred.

2-3 years of industry or academic experience in combination with Bachelor's or Master's degree. Knowledge, Skills and Abilities Experience with methodologies used for upstream or downstream viral vector production in either industry or academia Experience in experimental design, execution, and data analysis Excellent communication, collaboration, and technical writing skills Innovative and creative mindset, with problem solving capabilities Proficient in Microsoft Office products. Physical Requirements Ability to lift and carry up to 30lbs Ability to sit and stand for extended periods Excellent manual dexterity and ability to perform repetitive movements with fingers/hands Other Physical Requirements: PPE and gown training will be required as this individual will be required to enter into Laboratory and Cleanroom areas.

Work Environment: Work is performed primarily onsite in Philadelphia. 50% or more of the time, this role is in the laboratory.

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About Cedent

Sourced by ZipRecruiter

CEDENT strives to attract and retain the best people and provide an environment where they can all develop professionally and build a rewarding career. As a result, we create an inclusive environment that is rich in diversity, acknowledges each individual's uniqueness and promotes respect, personal achievement and stewardship. Our clients are global and so is CEDENT. We build and maintain a global workforce that includes people from different backgrounds, with a vast range of skills and experience all united by a common culture and commitment to help our clients achieve high performance. Cultivating a diverse workforce and inclusive work environment makes business sense. Our peoples varied skills are the talent engine that powers CEDENT, enabling it in turn to deliver the innovative solutions that help our clients outperform competitors.

Industry

It services

Company size

11 - 50 Employees

Headquarters location

Plano, TX, US

Year founded

2008

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