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Biotech Process Development Jobs in Maryland (NOW HIRING)

Purification development experience for GMP process development in biotech/pharmaceutical or related industry (experience in clinical manufacturing is highly desirable). Must be a team player who can ...

... level financial processes or startup activities based on study needs. Accurate and timely ... We create intelligent connections to accelerate the development and commercialization of innovative ...

... level financial processes or startup activities based on study needs. Accurate and timely ... We create intelligent connections to accelerate the development and commercialization of innovative ...

... biotech, and self-care companies to accelerate the development, manufacturing, and delivery of life ... process development for clinical programs, with advanced development labs and cGMP cleanroom suites ...

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Biotech Process Development information

What is biotech process development?

Biotech process development refers to the design, optimization, and scale-up of manufacturing processes used to produce biological products, such as pharmaceuticals, enzymes, or vaccines. Professionals in this field work to turn laboratory procedures into efficient, large-scale industrial processes that meet regulatory and quality standards. This often involves selecting suitable equipment, optimizing conditions, ensuring reproducibility, and troubleshooting production issues. The ultimate goal is to produce high-quality products safely, consistently, and cost-effectively.

What is the difference between Biotech Process Development vs Biotech Manufacturing Associate?

AspectBiotech Process DevelopmentBiotech Manufacturing Associate
Primary FocusDesigning, optimizing, and scaling up bioprocesses for product developmentExecuting manufacturing processes to produce biopharmaceuticals at scale
Work EnvironmentLaboratories and pilot plant facilitiesProduction floors and manufacturing plants
Required SkillsProcess design, lab techniques, troubleshootingEquipment operation, quality control, adherence to SOPs
Typical CredentialsBSc/MSc in Biotechnology, Chemical Engineering, or related fieldsBSc in Biotechnology, Biology, or related fields

While both roles are essential in biotech, Biotech Process Development focuses on creating and optimizing processes during product development, whereas Biotech Manufacturing Associates handle the day-to-day production to ensure consistent product quality at scale.

What are the key skills and qualifications needed to thrive in Biotech Process Development, and why are they important?

To excel in Biotech Process Development, you need a strong background in bioprocess engineering, molecular biology, and chemistry, typically supported by a degree in biotechnology or related fields. Familiarity with tools such as bioreactors, chromatography systems, and data analysis software, along with certifications in Good Manufacturing Practice (GMP), is highly valuable. Strong problem-solving skills, attention to detail, and effective teamwork distinguish top performers in this role. These competencies are crucial for optimizing processes, ensuring product quality, and driving innovation in the biotech industry.

What are some common challenges faced by professionals in Biotech Process Development, and how are they typically addressed?

Professionals in Biotech Process Development often encounter challenges related to scaling up processes from the laboratory to commercial production, ensuring product consistency, and meeting strict regulatory standards. Addressing these challenges typically involves close collaboration with cross-functional teams such as quality assurance, regulatory affairs, and manufacturing. Continuous process optimization, thorough documentation, and robust validation protocols are essential strategies to overcome these hurdles and ensure successful product development and commercialization.
What are popular job titles related to Biotech Process Development jobs in Maryland? For Biotech Process Development jobs in Maryland, the most frequently searched job titles are:
What job categories do people searching Biotech Process Development jobs in Maryland look for? The top searched job categories for Biotech Process Development jobs in Maryland are:
What cities in Maryland are hiring for Biotech Process Development jobs? Cities in Maryland with the most Biotech Process Development job openings:
Infographic showing various Biotech Process Development job openings in Maryland as of June 2026, with employment types broken down into 100% Full Time. Highlights an 70% In-person, 10% Hybrid, and 20% Remote job distribution.
Scientist - NIH VRC

$53.33/hr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 12 days ago


Job description

Cape Fox Facilities Services is seeking an experienced Scientist support of the overall functions of the Vaccine Research Center (VRC) on the NIH Bethesda campus by supporting collaborative research in the intramural community of the NIH. The total hourly pay for this exempt position is $53.33 for up to 40 hours per week. This rate represents the company's good faith and reasonable estimate of possible compensation at the time of posting

In addition, for eligible positions we offer a variety of benefits including specified holidays, paid leave, health insurance, dental insurance, vision insurance, life and disability insurance, tuition reimbursement, as well as 401K with company match. This job will be posted until filled or withdrawn. Participate in projects that are complex and scientifically demanding within a specific area/field, specifically Bioanalytical separation.

Initiate, implement, plan, and execute scientific research and development. Determine scientific rigor in assessing own data and that of others, by providing detailed observations, analyzing data, and interpreting results. Ensure project goals are met within time and budget constraints.

Independently initiate, plan, design, evaluate, revise and execute projects within CGE, UPLC field, utilizing good scientific judgment. Utilize specific investigation and method development work in support of multiple projects at a time. Communicate and initiate investigations for project and process findings, draw conclusions, and act as project manager in the drafting of state-of-art work and publishing of papers.

Develop research findings and make recommendations to leadership for decision. Provide forward-looking perspectives that contribute to "go/no go" decisions by leadership. Research and recommend outside technologies for consideration.M.S degree in Chemistry, Biology, Biochemistry Life Sciences or a related discipline

Minimum of five (5) years of experience in recombinant protein purification development for GMP clinical-phase products. Demonstrated knowledge of maintaining accurate and detailed records. Demonstrated expertise in the following techniques or tools for protein purification and characterization: Column chromatography for protein purification by AEX, CEX, affinity, SEC, HIC.

Column packing and testing. AKTA chromatography system. Lab scale TFF systems.

Qualitative assays including SDS-PAGE and Western Blot. UV/vis spectrophotometer. Purification development experience for GMP process development in biotech/pharmaceutical or related industry (experience in clinical manufacturing is highly desirable).

Must be a team player who can effectively work with members from cross-functional departments. Strong oral and written communication skills. Familiarity with computer software including word processing and data evaluation.

Occupational Health/Physical Requirements and Worksite Hazards: Occupational health/physical requirements is required Cape Fox Corporation, its subsidiaries and affiliates provide equal employment opportunities to all persons and prohibit employment decisions on the basis of race, religion, color, creed, national origin, sex, age, disability, political affiliation, protected veteran status, or sexual orientation. Cape Fox Corporation, its subsidiaries and affiliates offer preference to Cape Fox Corporation shareholders, descendants and other Native Americans pursuant to Public Law 100-241.M.S degree in Chemistry, Biology, Biochemistry Life Sciences or a related discipline. Minimum of five (5) years of experience in recombinant protein purification development for GMP clinical-phase products

Demonstrated knowledge of maintaining accurate and detailed records. Demonstrated expertise in the following techniques or tools for protein purification and characterization: Column chromatography for protein purification by AEX, CEX, affinity, SEC, HIC. Column packing and testing.

AKTA chromatography system. Lab scale TFF systems. Qualitative assays including SDS-PAGE and Western Blot.

UV/vis spectrophotometer. Purification development experience for GMP process development in biotech/pharmaceutical or related industry (experience in clinical manufacturing is highly desirable). Must be a team player who can effectively work with members from cross-functional departments.

Strong oral and written communication skills. Familiarity with computer software including word processing and data evaluation. Occupational Health/Physical Requirements and Worksite Hazards: Occupational health/physical requirements is required Cape Fox Corporation, its subsidiaries and affiliates provide equal employment opportunities to all persons and prohibit employment decisions on the basis of race, religion, color, creed, national origin, sex, age, disability, political affiliation, protected veteran status, or sexual orientation.

Cape Fox Corporation, its subsidiaries and affiliates offer preference to Cape Fox Corporation shareholders, descendants and other Native Americans pursuant to Public Law 100-241.