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Upstream Process Development Jobs in Hyattsville, MD

In this role, you will translate client and process development information into cGMP processes and act as a subject matter expert for biologic upstream and downstream processes. You will work hands ...

Principal Engineer

Beltsville, MD · On-site

$110 - $170/hr

As part of the Cell Engineering group, you will contribute to the development and optimization of a ... Partner with process/cell engineers to understand upstream process needs and downstream ...

Physical Therapist

Fulton, MD · On-site

$78K - $95K/yr

Continue learning and growing through Upstream's education and development programs Qualifications ... Specific details will be provided during the hiring process. Upstream Rehabilitation is an Equal ...

Physical Therapist

Fulton, MD · On-site

$1.6K - $2.1K/wk

Continue learning and growing through Upstream's education and development programs Qualifications ... Specific details will be provided during the hiring process. Upstream Rehabilitation is an Equal ...

Principal Engineer

Beltsville, MD · On-site

$174K - $191K/yr

... towards the development and optimization of first-of-its-kind prototyping line for ION's solid ... to understand upstream process needs and downstream implications of equipment design ...

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Upstream Process Development information

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How much do upstream process development jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for upstream process development in Hyattsville, MD is $26.58, according to ZipRecruiter salary data. Most workers in this role earn between $23.61 and $27.93 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in upstream process development?

Success in Upstream Process Development requires a strong background in biology, biochemistry, or chemical engineering, often with an advanced degree and experience in cell culture or fermentation techniques. Familiarity with bioreactors, process control systems, and analytical instrumentation, as well as knowledge of cGMP regulations, is essential. Critical thinking, problem-solving, and effective communication are important soft skills for optimizing processes and collaborating across multidisciplinary teams. These competencies ensure efficient development of scalable production processes, maintaining product quality and regulatory compliance.

What are some common challenges faced in upstream process development and how do teams typically address them?

One of the main challenges in upstream process development is optimizing cell culture conditions to consistently achieve high yields and product quality. Teams often encounter variability in biological systems and must troubleshoot issues such as contamination, scale-up inconsistencies, or nutrient limitations. Collaboration with analytical, downstream, and quality teams is essential to identify root causes and implement solutions. Regular data review meetings, cross-functional problem-solving, and continuous process improvement are standard practices to ensure robust upstream processes.

What is the difference between Upstream Process Development vs Downstream Process Development?

AspectUpstream Process DevelopmentDownstream Process Development
FocusDevelopment of cell culture, fermentation, and bioreactor processesPurification, filtration, and formulation of bioproducts
Skills & CredentialsBioprocess engineering, molecular biology, biochemistryBioprocessing, chromatography, analytical chemistry
Work EnvironmentLaboratories, bioreactors, pilot plantsPurification facilities, labs, quality control
Industry UsageBiotech, pharmaceutical manufacturingBiotech, pharmaceutical manufacturing

Upstream Process Development focuses on creating and optimizing cell culture and fermentation processes to produce bioproducts. In contrast, Downstream Process Development involves purifying and finishing these products. Both roles are essential in biopharmaceutical manufacturing and require similar scientific backgrounds, but they specialize in different stages of bioprocessing.

What are common upstream process development jobs?

Common upstream process development jobs include roles such as upstream process scientist, process engineer, and bioprocess development specialist. These positions focus on optimizing cell culture, fermentation, and bioreactor processes to improve product yield and quality, often requiring knowledge of bioreactor operation, cell biology, and process scale-up. Skills in laboratory techniques, process modeling, and regulatory compliance are also important in these roles.

What is an upstream process development job?

An upstream process development job involves designing, optimizing, and scaling the early stages of biopharmaceutical production, such as cell culture and fermentation processes. Professionals in this role typically work with bioreactors, laboratory equipment, and process analytical tools to improve yield and quality of biological products. Strong knowledge of microbiology, biochemistry, and process engineering is essential, along with adherence to regulatory standards.

What are popular job titles related to Upstream Process Development jobs in Hyattsville, MD?

For Upstream Process Development jobs in Hyattsville, MD, the most frequently searched job titles are:

What job categories do people searching Upstream Process Development jobs in Hyattsville, MD look for?

The top searched job categories for Upstream Process Development jobs in Hyattsville, MD are:

What cities near Hyattsville, MD are hiring for Upstream Process Development jobs?

Cities near Hyattsville, MD with the most Upstream Process Development job openings:

Infographic showing various Upstream Process Development job openings in Hyattsville, MD as of August 2026, with employment types broken down into 94% Full Time, and 6% Part Time. Highlights an 94% In-person, and 6% Remote job distribution, with an average salary of $55,278 per year, or $26.6 per hour.

Process Development Associate II (Upstream) *PC 986

Miltenyi Biotec

Gaithersburg, MD

$42.99 - $50.60/hr

Full-time

Medical, Dental, Vision, Retirement

Posted yesterday

New


Job description

Your Role:

As a member of the Miltenyi Biotec team, you will support the development, characterization, and tech transfer of processes to manufacture purified Lentiviral vectors used for pre-clinical and clinical gene therapy products. Additionally, you will apply your cell culture experience to support production, and characterization, of Lentiviral vectors using adherent and suspension-based production platforms. As a result of your attention to detail and keen ability to reliably produce Lentiviral vectors in a cross-functional team, you will support the continued success of Miltenyi Biotec as a whole.

Essential Duties and Responsibilities: 

  • Carry out all aspects of upstream vector production with the goal in mind that every effort is aimed at developing and qualifying processes required for clinical gene therapy products.
  • Order necessary supplies, maintain laboratory equipment and space, and prepare media and buffers.
  • Train team members as needed.
  • Track communication of data and ensure efficient progress towards achieving team objectives.

Requirements: 

  • B.S. Degree in the life sciences or engineering with minimum 2 years of relevant experience.
  • Previous biotech industry experience is preferred, specifically in the fields of gene therapy and virology.
  • Adherent and/or suspension mammalian cell culture, transfection and harvest of viral vectors and/or antibodies using aseptic techniques.
  • Strong experience utilizing stirred-tank bioreactors in the production of viral vectors and/or antibodies. Disposable and single use stirred-tank bioreactor experience preferred.
  • An understanding of DO/pH control loops, PID settings, and scale up and scale down parameters.
  • Practical knowledge in a range of bioprocess analytical techniques, such as but not limited to, cell-based assays, flow cytometry, qPCR, Western Blot analysis, and ELISA.
  • Superb documentation and organizational skills, capable of providing summaries and generating reports to support technical transfer to Manufacturing as well as process qualification.
  • Ability to work in a team and collaborative environment.
  • Highly proficient in the use of Microsoft Office products.
  • Weekend and holiday work may be required to maintain cell culture vessels or set up assays.
  • Experience with late-stage product development, application of QbD principles, as well as statistical design of experiments with JMP software is a plus.
  • Domestic Travel Requirements - 10% or less

Phyiscal Demands: 

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to walk; use hands or finger, handle, or feel; reach with hands and arms, talk, and hear. The employee is required to stand; climb or balance and stoop, kneel, crouch. The employee must occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, color vision, peripheral vision, depth perception and ability to adjust focus. Must have ability to handle more than one task at a time and must work at a rapid pace while maintaining attention to detail.

Work Environment:

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. This job is performed in a temperature-controlled facility without exposure to extreme hot or cold temperatures. Generally, this job is performed in a sanitized laboratory setting and routinely uses standard medical and research equipment such as centrifuges, biosafety cabinets, microscopes, incubators, pipettes and computers. While performing the duties of this job, the employee is frequently exposed to blood, viruses (e.g., HIV-1), bacteria, body fluids and/or other tissues which may be infectious and have the potential to cause disease. Employees entering and leaving the laboratory must wear appropriate clothing and protective equipment such as scrubs, coveralls, masks, face shield, glasses and gloves. The noise level in the work environment is usually moderate.

The hiring range for this position is expected to fall between $42.99/hr - $50.60/hr, reflecting the range candidates can reasonably expect to be considered for at time of offer, based on factors such as experience, internal equity, and qualifications. 

The salary of the finalist(s) selected for this role will be set based on a variety of considerations, including but not limited to internal equity, experience, education, specialization, skills, abilities, and training. The above range represents the Company’s good faith and reasonable estimate of possible compensation at the time of posting. 

In addition to your salary, the Company offers a comprehensive benefits package, including health, vision, and dental insurance, as well as a 401(k) plan. All benefits are subject to eligibility requirements. Certain positions may also be eligible for additional compensation such as bonuses or commissions. 

Miltenyi Biotec is an EO Employer – M/F/Veteran/Disability/Sexual Orientation/Gender Identity.

Miltenyi Biotec, Inc. participates in E-Verify.

The Company will provide reasonable accommodations to candidates and employees, unless doing so would impose an undue hardship on the Company, in accordance with applicable law.

Are you ready to start revolutionizing biomedical research? When you join Miltenyi Biotec, you join a family that is passionate about making a real impact – one breakthrough at a time. For over 30 years, we have played a pivotal role in the design, development, manufacture, and integration of products for sample preparation, cell separation, cell analysis, imaging, and cell culture needs. These developments have led to cutting-edge cell and gene therapies – transformative methods that mobilize the body’s own cells and genetic blueprint to tackle diseases such as cancer and autoimmune conditions. Today, our more than 18,000 solutions play a vital role in paving the way for the medicine of tomorrow.