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Full Time Downstream Process Development Scientist Jobs in Raleigh, NC

PD Sr Engineer

Holly Springs, NC · On-site

$90K - $124K/yr

Our award-winning culture is collaborative, innovative, and science based. If you have a passion ... In this vital role you will be a part of the Process Development Drug Substance Technology group ...

PD Sr Engineer

Holly Springs, NC

$90K - $124K/yr

Our award-winning culture is collaborative, innovative, and science based. If you have a passion ... In this vital role you will be a part of the Process Development Drug Substance Technology group ...

Our award-winning culture is collaborative, innovative, and science based. If you have a passion ... In this vital role you will be a part of the Process Development Drug Substance Technology group ...

Our award-winning culture is collaborative, innovative, and science based. If you have a passion ... In this vital role you will be a part of the Process Development Drug Substance Technology group ...

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Full Time Downstream Process Development Scientist information

See Raleigh, NC salary details

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

As of Jul 31, 2026, the average hourly pay for full time 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 does a Full Time Downstream Process Development Scientist do?

A Full Time Downstream Process Development Scientist is responsible for designing, optimizing, and scaling up processes that purify biological products such as proteins, antibodies, or vaccines after they are produced in cells or microbes. This role involves developing and improving techniques like filtration, chromatography, and centrifugation to ensure high purity and yield of the final product. The scientist also conducts experiments, analyzes data, and collaborates with cross-functional teams to transfer processes from the lab to manufacturing. Their work is critical for producing safe and effective biopharmaceuticals on a large scale.

What is the difference between Full Time Downstream Process Development Scientist vs Downstream Process Engineer?

AspectFull Time Downstream Process Development Scientist
Primary FocusDesigning, optimizing, and developing downstream purification processes for biopharmaceuticals
Required CredentialsBachelor's or Master's in Biotechnology, Biochemistry, or related field; experience in process development
Work EnvironmentLaboratories, R&D settings, collaborative teams in biotech or pharma companies
Typical ResponsibilitiesProcess scale-up, method validation, troubleshooting, documentation

While both roles involve downstream bioprocessing, the Full Time Downstream Process Development Scientist focuses on process development and optimization, whereas the Downstream Process Engineer typically handles process implementation and manufacturing support. The scientist role emphasizes research and development, while the engineer role is more operational. Candidates often hold similar degrees and certifications, but their daily tasks and focus areas differ.

What are some typical challenges faced by a Downstream Process Development Scientist, and how can they be addressed?

Downstream Process Development Scientists often encounter challenges such as optimizing protein purification processes to achieve high yield and purity, troubleshooting unexpected impurities, and scaling up processes from laboratory to manufacturing scale. These tasks require strong problem-solving skills, meticulous attention to detail, and effective collaboration with upstream teams, analytical scientists, and manufacturing staff. Addressing these challenges involves staying current with new purification technologies, maintaining robust documentation, and participating in cross-functional meetings to ensure seamless process integration and regulatory compliance.

What are the key skills and qualifications needed to thrive as a Full Time Downstream Process Development Scientist, and why are they important?

To thrive as a Full Time Downstream Process Development Scientist, you need a strong background in biochemical engineering, protein purification, and analytical techniques, typically supported by a degree in biochemistry, biotechnology, or a related field. Proficiency with chromatography systems (e.g., HPLC, FPLC), filtration technologies, and knowledge of regulatory and quality systems like GMP is essential. Strong problem-solving abilities, teamwork, and effective communication skills help you collaborate with cross-functional teams and troubleshoot process challenges. These skills are crucial for developing robust purification processes that ensure product quality, regulatory compliance, and efficient production in biopharmaceutical environments.
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:
What are popular job titles related to Full Time Downstream Process Development Scientist jobs in Raleigh, NC? For Full Time Downstream Process Development Scientist jobs in Raleigh, NC, the most frequently searched job titles are:
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What cities near Raleigh, NC are hiring for Full Time Downstream Process Development Scientist jobs? Cities near Raleigh, NC with the most Full Time Downstream Process Development Scientist job openings:
Infographic showing various Full Time Downstream Process Development Scientist job openings in Raleigh, NC as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $78,175 per year, or $37.6 per hour.

Senior Scientist - Downstream Process Development

Novartis Pharmaceuticals Corporation

Durham, NC • On-site

$88K - $120K/yr

Full-time

Posted 14 days ago


Job description

Band

Level 4


Job Description Summary

Role type: Full time onsite, #LI-Onsite
Location: Durham, North Carolina, United States
Relocation Support: Yes
Join the team shaping the future of Cell and Gene Therapy and help bring transformational medicines to patients worldwide. As a Senior Scientist - Downstream Process Development, you will play a critical role in advancing viral vector technologies across adeno-associated virus (AAV) and lentiviral vector (LVV) platforms. Combining scientific expertise, innovation, and hands-on laboratory leadership, you will drive process development strategies that support breakthrough therapies from pre-clinical development through clinical manufacturing. This is a unique opportunity to influence cutting-edge science, collaborate with world-class experts, and accelerate the delivery of life-changing treatments to patients with urgent unmet needs.


Job Description

Key Responsibilities

You will serve as the downstream technical lead for one or more gene therapy programs. This role is responsible for defining the overall downstream development plan for assigned gene therapy programs; designing, executing, and interpreting downstream process development studies; performing hands-on process operations at both small scale and large scale; and collaborating with cross-functional teams to advance AAV and LVV programs from pre-clinical development through clinical manufacturing.

Other responsibilities will include:

  • Perform hands-on downstream process operations at both small scale and large scale, delivering high-quality experimental outputs within program timelines.

  • Apply a strong statistical and data-driven mindset to analyze process study results, draw scientifically sound conclusions, and inform development strategy.

  • Drive downstream innovation by evaluating emerging technologies, current scientific advances, and state-of-the-field approaches relevant to viral vector process development.

  • Promote adoption of technical standards, platform approaches, and best practices across multiple programs and modalities.

  • Author technical reports, summarize process development outcomes, and contribute downstream content to regulatory filings, including IND submissions.

  • Present study results, technical recommendations, and development strategies to internal and external stakeholders in cross-functional forums.

  • Be a technical coach and mentor, fostering an innovative, collaborative, and scientifically rigorous culture.

  • Present technical recommendations and mentor colleagues to foster scientific excellence and collaboration.

Essential Requirements

  • Bachelor's degree in biological sciences, pharmaceutical sciences, chemical engineering, or a related technical field with 8+ years of relevant experience; Master's degree with 6+ years of relevant experience; or PhD with 4+ years of relevant experience.

  • Strong technical background in downstream process development for biologics and/or viral vector-based therapies, with hands-on experience designing, executing, and interpreting process development studies.

  • In-depth expertise across multiple downstream unit operations such as chromatography, depth filtration, precipitation or flocculation, tangential flow filtration, ultracentrifugation, impurity clearance, and adventitious virus clearance.

  • Proficiency in statistical analysis principles, Design of Experiments (DoE), and data-driven decision-making.

  • Proven ability to define technical plans, solve complex process development challenges, and deliver scientific objectives within program timelines.

  • Demonstrated ability to influence cross-functional stakeholders, communicate technical recommendations clearly, and contribute to program strategy in a matrixed environment.

  • Innovative mindset with experience advancing continuous improvement, technical standards, best practices, or platform approaches across programs.


EEO Statement:

The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential.


Accessibility and reasonable accommodations

The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an e-mail to tas.nacomms@novartis.com call +1 (877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
https://www.novartis.com/careers/careers-research/notice-all-applicants-us-job-openings


Salary Range

$119,700.00 - $222,300.00


Skills Desired

Data Science, Materials Science, Process Simulation, Technical Writing, Waterfall Model