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Full Time Downstream Process Development Scientist Jobs in Virginia

As a Trex Process Development Engineer you'll be responsible for the design and development of new ... Full-Time/Regular EXPERIENCE We are looking for someone with a Bachelor's of Science in an ...

As a Trex Process Development Engineer you'll be responsible for the design and development of new ... Full-Time/Regular EXPERIENCE We are looking for someone with a Bachelor's of Science in an ...

Senior Scientist

Virginia Beach, VA

$82.40K - $112.50K/yr

The Senior Scientist will be responsible for hands‑on process development, prototyping, and characterization of tissue- and biomaterial-based devices with antimicrobial features. This includes ...

Senior Scientist

Virginia Beach, VA

$82.40K - $112.50K/yr

The Senior Scientist will be responsible for hands‑on process development, prototyping, and characterization of tissue- and biomaterial-based devices with antimicrobial features. This includes ...

Senior Scientist

Virginia Beach, VA · On-site

$86.80K - $118.60K/yr

The Senior Scientist will be responsible for hands-on process development, prototyping, and characterization of tissue- and biomaterial-based devices with antimicrobial features. This includes ...

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Full Time Downstream Process Development Scientist information

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 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 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 the most commonly searched types of Downstream Process Development Scientist jobs in Virginia? The most popular types of Downstream Process Development Scientist jobs in Virginia are:
What are popular job titles related to Full Time Downstream Process Development Scientist jobs in Virginia? For Full Time Downstream Process Development Scientist jobs in Virginia, the most frequently searched job titles are:
What job categories do people searching Full Time Downstream Process Development Scientist jobs in Virginia look for? The top searched job categories for Full Time Downstream Process Development Scientist jobs in Virginia are:
What cities in Virginia are hiring for Full Time Downstream Process Development Scientist jobs? Cities in Virginia with the most Full Time Downstream Process Development Scientist job openings:
Infographic showing various Full Time Downstream Process Development Scientist job openings in Virginia as of May 2026, with employment types broken down into 1% As Needed, 87% Full Time, 10% Part Time, and 2% Contract. Highlights an 70% Physical, 4% Hybrid, and 26% Remote job distribution.

Development Scientist

GSK Group of Companies

Richmond, VA • On-site

Full-time

Medical, Retirement

Posted 9 days ago


Job description

Welcome to Haleon. We're a purpose-driven, world-class consumer company putting everyday health in the hands of millions. In just three years since our launch, we've grown, evolved and are now entering an exciting new chapter - one filled with bold ambitions and enormous opportunity.
Our trusted portfolio of brands - including Sensodyne®, Panadol®, Advil®, Voltaren®, Theraflu®, Otrivin®, and Centrum® - lead in resilient and growing categories. What sets us apart is our unique blend of deep human understanding and trusted science.
Now it's time to fully realise the full potential of our business and our people. We do this through our Win as One strategy. It puts our purpose - to deliver better everyday health with humanity - at the heart of everything we do. It unites us, inspires us, and challenges us to be better every day, driven by our agile, performance-focused culture.
About the role
The Development Scientist supports new product development by developing formulation, combination products (IDDC) and device and/or providing analysis and evaluation of material and products at all stages of the development process, considering scientific and timing objectives. This individual would have various levels of involvement in the development of conventional and non-conventional solid, semi-solid, liquid, and other formulations and medical devices.
Role Responsibilities
This role will provide YOU the opportunity to lead key activities to progress YOUR career.
Execution Powerhouse
  • Manages or contributes to one or more projects in support of Brand Innovation strategy.
  • Execute a wide range of experiments/technical studies/scientific tasks.
  • Design & execute new methods and protocols.
  • Facilitate completion of outsourced support activity
  • Keep supervisor informed of progress and activities.
  • Ensures all work is conducted in accordance with written procedures as per EHS standards and expectations on site and within the laboratories.
  • Produces or contributes to departmental quality documentation (eg SOP's, batch doc, validation protocols & reports).
  • Safety & quality responsibilities for department and site (eg GMP, Audits, Health & Safety).

Growth Mindset
  • Maintains awareness of scientific literature to assist work progression& understanding, and present at internal R&D meetings.
  • Trains self and others in new technology and laboratory responsibilities.
  • Develops knowledge of regulations impacting areas of work (e.g. EP/USP/ICH/MDR).

Consumer and Customer-Obsessed
  • Participate in consumer engagement research to understand the category and needs.
  • Work with Consumer Understanding and Sensory scientists to development consumer-developed innovation.

Data-Driven
  • Maintains precise experimental records; issues report at project milestones; writes invention records to protect scientific discoveries.
  • Ensures all work is always conducted following good scientific practice and Good Manufacturing Practice (where required).

Agile
  • Sets and resets priorities to remain focused on objectives in rapidly changing circumstances.
  • Takes responsibility for specific equipment in accordance with site procedures.
  • Participates in general problem solving.
  • Develop networking skills though interactions with scientist outside of primary 'project' role.

Why you?
Basic Qualifications:
  • BS in Food, Chemical, Pharmaceutical, Biological or related science with 3 years of relevant experience working in a GMP lab setting.
  • Ability to apply scientific principles and techniques to assigned projects.
  • An ability to organize and report study data from internal and external sources.

Preferred Qualifications:
  • MS or PhD Chemical, Pharmaceutical, Biological or related science.
  • 2 years demonstrated experience of successful formulation and/or product development
  • Experience in Pharmaceutical or OTC industries.
  • Experience in development and formulation of oral solid dosage forms (eg. tablets, caplets, softgels, granules...) and liquids (eg. suspensions, syrups and solutions).
  • Practical application and technical proficiency of the R&D development processes and associated commercial environment.
  • Clear communicator in both oral and written form with both internal departments and external organizations.
  • Demonstrated ability to take initiative, think and work independently, problem-solve, work effectively in teams and contribute to multiple projects in parallel.
  • Ability to organize and report study data from internal and external sources.
  • Flair for creativity and innovation, with a desire to learn and have meaningful impact
  • Demonstrated computer proficiency.
  • Basic understanding of statistics and its application to experimental work.
  • Ability to connect consumer needs to product development

Location: This role is based in Richmond, VA with on-site requirements of 5 times per week.
Benefits
Haleon offers a robust Total Reward package that consists of competitive pay and a comprehensive benefits program. This includes a generous 401(k) plan, tuition reimbursement and time off programs including 6 months paid parental leave. On day one, you are eligible for benefits, including our healthcare programs where the company pays for the majority of your medical coverage for you and your family. We also offer the opportunity to receive a discretionary bonus based on the achievement of key business performance and other incentive/recognition programs as part of the offering.
Job Posting End Date
2026-06-06
Equal Opportunities
Haleon are committed to mobilising our purpose in a way that represents the diverse consumers and communities who rely on our brands every day. It guides us in creating an inclusive culture, where different backgrounds and views are valued and respected - all in support of understanding and best serving the needs of our consumers and unleashing the full potential of our people. It's important to us that Haleon is a place where all our employees feel they truly belong.
During the application process, we may ask you to share some personal information, which is entirely voluntary. This information ensures we meet certain regulatory and reporting obligations and supports the development, refinement, and execution of our inclusion and belonging programmes that are open to all Haleon employees.
The personal information you provide will be kept confidential, used only for legitimate business purposes, and will never be used in making any employment decisions, including hiring decisions.
Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, Haleon may be required to capture and report expenses Haleon incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure Haleon's compliance to all federal and state US Transparency requirements.
Accommodation Requests
If you require a reasonable accommodation or other assistance to apply for a job at Haleon at any stage of the application process, please contact us by sending an email to HR.AmericasSC-CS@haleon.com. Please include the following in your email:
Use subject line: 'Haleon Careers: Job Accommodation Request'
Your Name and contact information
Requisition ID and Job Title you are interested in
Location of Requisition (city/state or province/country)
Description of specific accommodation you are requesting
Please note: Resumes, CVs, or other requests outside of accommodation support submitted to this email box will not be accepted.
Note to candidates
The Haleon recruitment team will contact you using a Haleon email account (@haleon.com). If you are not sure whether the email you received is from Haleon, please get in touch.