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Internship Downstream Process Development Scientist Jobs in Raleigh, NC

DivIHN

Process Engineer Pharmaceuticals I

NC · On-site

... scientists. This role does not carry people-management or long-term program ownership ... Process Development * Experience or familiarity with upstream and/or downstream bioprocess ...

Amgen, Inc.

Sr Engineer I - 2º Shift

Holly Springs, NC · On-site

$90.50K - $124.20K/yr

Our award-winning culture is collaborative, innovative, and science based. If you have a passion ... Manufacturing, Quality, Process Development, Maintenance, network partners) to ensure reliable ...

Amgen

Sr Engineer I - 2 Shift

Holly Springs, NC · On-site

$90.50K - $124.20K/yr

Our award-winning culture is collaborative, innovative, and science based. If you have a passion ... Manufacturing, Quality, Process Development, Maintenance, network partners) to ensure reliable ...

Amgen

Sr Engineer I - 2 Shift

Holly Springs, NC · On-site

$90.50K - $124.20K/yr

Our award-winning culture is collaborative, innovative, and science based. If you have a passion ... Manufacturing, Quality, Process Development, Maintenance, network partners) to ensure reliable ...

Amgen

Engineer I - 2 Shift

Holly Springs, NC · On-site

Manufacturing, Quality, Process Development, Maintenance, network partners) to ensure reliable ... and Downstream systems for plant operations. * Provide technical mastery and problem-solving ...

Amgen, Inc.

Engineer I - 2º Shift

Holly Springs, NC · On-site

Manufacturing, Quality, Process Development, Maintenance, network partners) to ensure reliable ... and Downstream systems for plant operations. * Provide technical mastery and problem-solving ...

Amgen

Engineer I - 2 Shift

Holly Springs, NC · On-site

Manufacturing, Quality, Process Development, Maintenance, network partners) to ensure reliable ... and Downstream systems for plant operations. * Provide technical mastery and problem-solving ...

AskBio

Process Engineer II

Durham, NC · On-site

... scientific discipline and 0 years of Biopharmaceutical Experience * Hands-on upstream or downstream ... development * Continuous improvement-oriented, seeking opportunities to optimize process operations ...

AskBio

Process Engineer II

Durham, NC · On-site

... scientific discipline and 0 years of Biopharmaceutical Experience * Hands-on upstream or downstream ... development * Continuous improvementoriented, seeking opportunities to optimize process operations ...

AskBio

Process Engineer II

Durham, NC · On-site

Pioneering science to create transformative molecular medicines. Our mission: Lead innovative ... Hands-on upstream or downstream biomanufacturing laboratory experience * Excellent written and ...

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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 May 28, 2026, the average hourly pay for internship downstream process development scientist in Raleigh, NC is $37.58, according to ZipRecruiter salary data. Most workers in this role earn between $27.60 and $44.86 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 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 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 are the most commonly searched types of Downstream Process Development Scientist jobs in Raleigh, NC? The most popular types of Downstream Process Development Scientist jobs in Raleigh, NC are:
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Internship Downstream Process Development Scientist jobs near you
KBI: US - Process Engineer III

KBI: US - Process Engineer III

KBI Biopharma, Inc.

Durham, NC • On-site

Full-time

Posted 26 days ago

Job description

Job Description
Process Engineering is responsible for all Manufacturing process equipment and ensures the equipment and site infrastructure is in an active state to support cGMP operations.
As a Process Engineer, you will act as member of a cross-functional team to support implementation of new systems and improvements to existing manufacturing processes and equipment. You will apply sound scientific and engineering principles to successfully define upstream and downstream process equipment requirements, specifications and standards for facility fit, and assess equipment design and operation in a commercial cGMP production facility. This may include upstream activities such as cell culture and harvest, and/or downstream processes such as chromatography, purification, and filtration. You will be at the forefront of existing best practices and evaluating technologies. Provide system ownership for Biopharmaceutical process equipment. Identify, support, and/or lead implementation of engineering-based improvements or upgrades to the equipment or facility systems. This may include development of business case for improvement and identification of design requirements and then translation of requirements into process equipment/system design, specification and supporting the construction, startup, and validation of process equipment.
Key Responsibilities
  • You will support equipment commissioning and qualification activities related to new or modified processes.
  • Collaborate with MS&T and Manufacturing teams to troubleshoot and resolve equipment and process-related issues in manufacturing systems.
  • Act the technical subject matter expert (SME) for upstream and/or downstream equipment and the site clean utilities ensuring proper installation, qualification, and maintenance of these systems.
  • Lead process engineering related projects to improve manufacturing operations or implementation of new processing equipment. As the project lead you will ensure on time delivery, compliance with project requirements, and project budget.
  • Lead the development, scale-up, and optimization of upstream (cell culture, fermentation) and/or downstream (purification, filtration) processes for biologics or advanced therapies
  • Design and execute experiments to improve process robustness, yield, and product quality
  • Collaborate with Engineering, Quality, Regulatory, and Manufacturing teams to ensure seamless tech transfer and GMP compliance
  • Author and review process documentation including SOPs, and Engineering Studies protocols
  • Serve as a technical lead in cross-functional project teams and represent process engineering in regulatory filings and audits
  • Evaluate and implement new technologies (e.g., single-use systems, PAT tools, continuous processing) to enhance scalability and efficiency
  • Support capital projects including facility design, equipment selection, and commissioning
  • Lead risk assessments, and root cause investigations for process deviations
  • Communicate with other KBI sites for problem solving and consistency of processes through the organization.
  • Contribute to developing a culture of continuous improvements on processes and tools in close collaboration with other.
  • You will perform facility fit activities for various production scenarios.
  • You should be able to apply engineering principles in-order to problem-solve and drive projects to successful completion within defined timelines.
  • The ability to manage multiple concurrent projects and resources.
  • Lead and support CAPA, Change Control, Deviation, Risk Analysis, Root Cause Analysis, and other Quality Systems.
  • Providing technical support for equipment modifications, deviations, change controls, and CAPAs.
  • Develop and maintain equipment SOPs (Standard Operating Procedures), training, and other process documentation.

Qualifications:
• Bachelor's in chemical engineering, Biochemical Engineering, or related field
• 10+ years of experience in bioprocess development or manufacturing within the biotech or biopharma industry
• Expertise in biologics, cell therapy, gene therapy, drug substance production processes
• Strong understanding of cGMP regulations, FDA/EMA guidelines, and validation principles
• Proficiency in process modeling and simulation tools
• Demonstrated leadership in cross-functional teams and project management
• Excellent communication, analytical, and problem-solving skills
• Experience with regulatory submissions (IND, BLA, MAA) is a plus
KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply.
I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary.
I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.

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