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Internship Downstream Process Development Scientist Jobs in Sparta, NJ

... 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 ...

Material Scientist

Troy Hills, NJ ยท On-site

$104K - $144K/yr

Validate analytical and mechanical test methods for design verification and process development ... MS or PhD preferred * 3+ years of materials science and testing experience with preference to ...

Process Innovation Manager

Fairfield, NJ ยท On-site

$120K - $140K/yr

Participate as a member of the new program development/quoting team. * Participate as a member of ... Scientific molding expertise: Master Molder preferred * Must possess good analytical and problem ...

Process Innovation Manager

Fairfield, NJ ยท On-site

$120K - $140K/yr

Participate as a member of the new program development/quoting team. * Participate as a member of ... Scientific molding expertise: Master Molder preferred * Must possess good analytical and problem ...

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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 28, 2026, the average hourly pay for internship downstream process development scientist in Sparta, NJ is $40.67, according to ZipRecruiter salary data. Most workers in this role earn between $29.86 and $48.56 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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Infographic showing various Internship Downstream Process Development Scientist job openings in Sparta, NJ as of July 2026, with employment types broken down into 1% As Needed, 80% Full Time, 15% Part Time, and 4% Contract. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $84,592 per year, or $40.7 per hour.

Director, Large Scale Process Development

Socket.dev

Branchburg, NJ โ€ข On-site

$195 - $218/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 19 hours ago

Posted today


Job description

Description

About Century Therapeutics:

Century Therapeutics (NASDAQ: IPSC) is a biotechnology company advancing a pipeline of induced pluripotent stem cell (iPSC)-derived cell therapies with the potential to meaningfully address autoimmune diseases, including type 1 diabetes, and cancer. The companyโ€™s therapies are derived from its iPSC cell foundry and leverage its novel immune evasion engineering technology, Allo-Evasionโ„ข. Century believes its approach to developing off-the-shelf cell therapies will expand patient access and provide advantages over existing cell therapies which will ultimately advance the course of care.

Role:

The Director, Large Scale Process Development, is accountable for all scale up strategies, methodologies, and experiments that support the advancement of Centuryโ€™s product portfolio with the goal of developing and implementing cost-effective, productive, GMP-compliant, and large capacity processes for clinical and commercial manufacturing. This development includes bioreactor processes for cell expansion and differentiation, centrifugation and filtration processes for cell harvesting and isolation, and container filling for intermediate and final product presentation. This dynamic, scientifically motivated, operationally-savvy and highly collaborative individual will be a key leader and voice influencing critical areas of the technical development and operations organization and play an important role in collaboration with Research, Regulatory, Analytical and Manufacturing teams. This role is based in Branchburg, NJ, which is the location of our GMP manufacturing facility and our process development and analytical development teams.

The work expectation for this role is 5 days per-week on-site.

The expected annual salary range for this role is approximately $195,000-$218,000 depending on experience . Additional benefits offered include but are not limited to an annual performance-based bonus (prorated by start date), medical, dental, and vision insurance, matching 401K plan, and 20+ days per-year of PTO (prorated by start date). Additionally, employees not requiring sponsorship are preferred.

Requirements
  • Lead all efforts related to scale up of Centuryโ€™s cell processes, with the goal of implementation in clinical and commercial manufacturing.
  • Provide strategic, technical, and scientific leadership to a team of process development scientists and engineers, with responsibility for overall strategy and direction.
  • Oversee execution of scale up and scale-down experiments for cell expansion and differentiation, cell harvesting, and intermediate and final drug product container filling.
  • Function as a process development lead in mid to late-stage development programs to deliver on corporate objectives related to the advancement of the companyโ€™s pipeline programs.
  • Foster the growth of scale-up capabilities, including the implementation of state-of-the-art technologies, computational tools, and engineering principles in support of process scale-up, development, characterization, validation, tech transfer and GMP implementation.
  • Collaborate with other process development groups, MSAT and Manufacturing teams to tech transfer processes into clinical and commercial manufacturing.
  • Along with his/her team members, act as subject matter experts during the GMP manufacturing of our products, including side by side execution of GMP activities as necessary.
  • Lead authoring and internal review of regulatory submissions and engage in dialogue with health authorities supporting regulatory review of IND/CTA/IMPD/CTN applications for first-in-human clinical studies and associated internal source documents.
  • Communicate scientific data and information effectively through presentations, protocols, and reports, and where appropriate, through external presentation/publication in scientific, technical, and investor forums.
  • Responsible for resourcing, scheduling, and coordinating laboratory activities to meet organization objectives.
  • Estimate, report, and manage to a departmental budget.
  • Provide mentorship and guidance to his/her team members as well as additional team members and contribute to establishing and growing a strong, engaged culture within technical development, built on scientific competency and technical excellence, collaboration, and effective communication.
Qualifications:
  • BS, MS or Ph.D. in Biomedical Engineering, Chemical Engineering, Biotechnology, Biological Sciences, or related discipline.
  • PhD with at least 10 years relevant experience or BS or MS with at least 15 years relevant experience in biopharmaceutical or cell therapy process development, scale-up, tech transfer and GMP manufacturing.
Requirements:
  • Demonstrated experience in process scale-up, particularly cell therapy process scale-up, process development, process optimization, tech transfer, and GMP manufacturing
  • Technical excellence in scale-up engineering principles, theory and practical application
  • Sound understanding of, and the ability to interpret, GMPs for the production of clinical products
  • Ability to read, write and interpret technical and quality documents, such as batch production records, standard operating procedures (SOPs), change requisitions, non-conformances, and corrective action plans (CAPAs)
  • Demonstrated leadership skills, including the ability to manage scientific teams; work effectively within a matrix team; communicate, coach, and mentor employees
  • Strong scientific reasoning, problem-solving, and technical skills in process development, scale-up, cell culture, cell isolation, filling and GMP manufacturing.

Century Therapeutics is not accepting unsolicited resumes from search or staffing firms. All resumes submitted by search or staffing firms to any employee at Century Therapeutics via email, the internet, or directly without a valid written search agreement for this role, and without having been asked to participate in this by Talent Acquisition, will be deemed the sole property of Century Therapeutics, and no fee will be paid in the vent the candidate is hired. Firms not authorized to submit candidates will not be eligible for any fee or ownership claim.

Century Therapeutics Inc. is an Equal Employment Opportunity/Affirmative Action Employer - Minority/Female/Disability/Veteran. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, or veteran status or any other characteristic protected by federal, state, or local law.

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