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Internship Downstream Process Development Scientist Jobs in Hackettstown, NJ

PIM BRANDS LLC

R&D Process Engineer

NJ · On-site

$80K - $90K/yr

Advanced degree in food science desired * Product development in a food manufacturing plant or ... Statistical process control and quality systems experience required * Ability to anticipate as well ...

Ionbond

Process Engineer

Rockaway, NJ · On-site

... D curiosity with hands-on production-you'll feel right at home here. Our coatings are produced in ... The preferred candidate will have a Bachelor's Degree in Engineering, Materials Science/Metallurgy ...

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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 7, 2026, the average hourly pay for internship downstream process development scientist in Hackettstown, NJ is $39.95, according to ZipRecruiter salary data. Most workers in this role earn between $29.33 and $47.69 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 Hackettstown, NJ as of July 2026, with employment types broken down into 1% As Needed, 73% Full Time, 22% Part Time, and 4% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $83,097 per year, or $40 per hour.

Formulations Scientist/Sr. Scientist

NEVAKAR LLC

Bridgewater, NJ • On-site

$85K - $140K/yr

Full-time

Posted 5 days ago

Job description

Job Type
Full-time
Description
Company Description
Nevakar Pharmaceuticals, Inc. is a privately held specialty pharmaceutical company headquartered in Bridgewater, New Jersey. The Company develops enhanced sterile injectable products designed to address unmet clinical and commercial needs by improving existing FDA-approved molecules through innovative formulation, functional packaging, novel drug delivery approaches, and thoughtful regulatory and clinical strategies. Nevakar's work is focused on creating patient-centered products that improve quality of life and healthcare outcomes while providing value to the healthcare system. Its development programs include IP-protected dosage forms, such as ready-to-use infusion bags and prefilled syringes, and are primarily advanced through the FDA's 505(b)(2) regulatory pathway. As Nevakar enters its next chapter, the Company remains committed to scientific excellence, innovation, collaboration, and delivering accessible products that support better outcomes for patients and providers.
Position Summary
Nevakar Pharmaceuticals is seeking a Formulations Scientist onsite in Bridgewater, NJ to support the development of sterile injectable and ophthalmic drug products. The successful candidate will contribute to pre-formulation, formulation development, process development, and process optimization activities for small molecule drug candidates. This role requires strong scientific judgment, hands-on laboratory experience, and the ability to design experiments, analyze data, and communicate results in support of product development and regulatory submissions. Position title will be commensurate with experience. The formulation Scientist will be responsible for understanding small molecule chemistry, degradation pathways, characterization and stabilization techniques. The selected candidate will be supporting screening formulations for optimizing solubility and stability of drug candidates for ophthalmic and injectable drug products. Develop formulations for preclinical studies. Work with regulatory team in preparing PreIND meeting request and support IND and NDA submissions. Design and conduct pre-formulation, formulation development, process development and process optimization of parenteral and ophthalmic formulations and related alternate drug delivery systems such as solutions, lyophilized products, sterile injectable suspensions etc. Design and develop robust, scalable formulations, manufacture prototype dosage forms, and conduct drug product process development and process optimization activities in-house. Conduct literature search for the assigned projects. Demonstrate scientific creativity, initiative and contribution to the team and company goals. The individual will also be responsible for designing and executing different laboratory experiments, making observations, performing data analysis and reporting results.
Role and Responsibilities:
  • Design, conduct, and interpret pre-formulation, formulation development, process development, and process optimization studies for sterile injectable and ophthalmic drug products.
  • Develop and evaluate formulations for small molecule drug candidates, including solutions, lyophilized products, sterile injectable suspensions, and alternate drug delivery systems.
  • Support screening activities to optimize solubility, stability, manufacturability, and product performance.
  • Manufacture prototype dosage forms and support the development of robust, scalable manufacturing processes.
  • Conduct literature searches, evaluate scientific and technical information, and apply findings to assigned projects.
  • Prepare, review, and contribute to product development reports, technical documents, and regulatory submissions, including Pre-IND, IND, NDA, and ANDA filings.
  • Maintain accurate laboratory documentation in accordance with scientific, regulatory, and intellectual property requirements.
  • Collaborate with cross-functional development teams and external partners to support project goals, milestones, technology transfer, and commercialization activities.
  • Demonstrate scientific creativity, initiative, sound judgment, and a commitment to team and company objectives.

Requirements
  • Master's degree in Pharmaceutical Sciences, Chemical Engineering, or a related scientific discipline is required; Ph.D. is preferred.
  • Minimum of 2+ years of experience in early - or late-stage formulation development of small molecule drug products is required.
  • Experience with sterile dosage form development, including parenteral and/or ophthalmic formulations.
  • Experience with drug device combination product development.
  • Strong understanding of small molecule chemistry, degradation pathways, characterization methods, and stabilization techniques.
  • Demonstrated ability to independently design and conduct experiments, analyze data, troubleshoot technical challenges, and clearly communicate results.
  • Experience with hospital injectable products, 505(b)(2) product development, and container closure systems, including vials, syringes, and infusion bags, is preferred.
  • Knowledge of extractables and leachables considerations and familiarity with FDA and EMA pharmaceutical development expectations is preferred.
  • Experience managing or working with external CROs and CDMOs is preferred.
  • Strong organizational, written and verbal communication, technical writing skills for pIND & NDA filles required, and interpersonal skills.
  • Ability to work effectively in a collaborative, multidisciplinary team environment.

Salary Description
$85,000 to $ 140,000 based upon experience
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About Nevakar

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

11 - 50 Employees

Headquarters location

Bridgewater, NJ, US

Year founded

2015

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