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Research Associate Downstream Process Development Jobs in Philadelphia, PA

Genesis Global Group

Research Associate

Hamilton, NJ · On-site

... development of diagnostic and pre-clinical treatments. The Institute for Biomarker Research (IBR ... IBR is currently seeking a Research Associate . This position is in-person, in Hamilton, NJ.

Icon plc

Clinical Research Associate II

Blue Bell, PA · Remote

Ensuring protocol compliance, data integrity, and patient safety throughout the trial process ... Learning and development opportunities through structured training and career pathways Benefits may ...

ICON

Clinical Research Associate II

Blue Bell, PA · On-site

Ensuring protocol compliance, data integrity, and patient safety throughout the trial process ... Learning and development opportunities through structured training and career pathways Benefits may ...

ICON

Clinical Research Associate

Blue Bell, PA · On-site +1

Clinical Research Associate - Early Development XTA - Central ICON is a global healthcare ... Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.

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Research Associate Downstream Process Development information

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$19

$33

$49

How much do research associate downstream process development jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for research associate downstream process development in Philadelphia, PA is $33.99, according to ZipRecruiter salary data. Most workers in this role earn between $27.88 and $41.73 per hour, depending on experience, location, and employer.

What is a research associate downstream process development?

A Research Associate in Downstream Process Development works within biotechnology or pharmaceutical companies to optimize and scale up the purification and recovery of biological products, such as proteins or antibodies, after initial production. They focus on processes like filtration, chromatography, and centrifugation to ensure product quality and yield. These professionals design experiments, analyze data, and support the transfer of processes from laboratory scale to manufacturing. Their work is crucial for developing efficient, reproducible, and regulatory-compliant methods for producing biopharmaceuticals.

What are the key skills and qualifications needed to thrive as a research associate in downstream process development?

To thrive as a Research Associate in Downstream Process Development, you need a solid background in biochemistry, molecular biology, or chemical engineering, often demonstrated by a bachelor's or master's degree in a related field. Familiarity with chromatography systems (such as AKTA), filtration technologies, and Good Manufacturing Practice (GMP) standards, along with data analysis software, is typically required. Strong problem-solving skills, attention to detail, and effective teamwork and communication abilities help individuals excel in this role. These competencies are crucial for ensuring efficient, scalable purification processes and maintaining product quality in biopharmaceutical development.

What are the typical challenges faced by a research associate in downstream process development, and how can they be addressed?

A Research Associate in Downstream Process Development often encounters challenges such as optimizing purification processes for new biologics, troubleshooting equipment issues, and ensuring scalability from laboratory to production scale. Effective communication with cross-functional teams, such as upstream scientists and analytical specialists, is essential to resolve issues quickly. Staying current with new purification technologies and maintaining meticulous documentation can also help address these challenges and support successful process development.

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

AspectResearch Associate Downstream Process DevelopmentResearch Associate Upstream Process Development
Primary FocusPurification, filtration, chromatography of bioproductsCell culture, media optimization, bioreactor operation
Skills & CertificationsProtein purification, chromatography techniques, GMP complianceCell culture, aseptic techniques, bioreactor handling
Work EnvironmentLaboratory, manufacturing, quality controlLaboratory, bioprocessing facilities
Industry UsageBiopharmaceutical manufacturing, biotech researchBiopharmaceutical development, biotech research

While both roles support bioprocess development, Research Associate Downstream Process Development focuses on purification and filtration of bioproducts, whereas Research Associate Upstream Process Development emphasizes cell culture and bioreactor processes. Understanding these differences helps candidates align their skills with the appropriate role in biopharmaceutical production.

Research Associate Downstream Process Development jobs near you
Infographic showing various Research Associate Downstream Process Development job openings in Philadelphia, PA as of August 2026, with employment types broken down into 89% Full Time, and 11% Contract. Highlights an 95% In-person, and 5% Remote job distribution, with an average salary of $70,697 per year, or $34 per hour.

Research Associate

Hamilton, NJ • On-site

Genesis Global Group
See more jobs at Genesis Global Groupexternal

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 8 days ago

Job description

Job Summary: Genesis Global Group (GGG) is a consortium of entities and institutes, in the field of molecular biology, medicinal chemistry and biotechnology. Our mission is to improve the patient's quality of life by linking basic science and the development of diagnostic and pre-clinical treatments.
The Institute for Biomarker Research (IBR), a division of GGG, is dedicated to the innovation of multi-variant-based personal diagnostics to assess disease evaluation, progression, regression, and patient stratification in order to establish a targeted, pharmacogenomic-based treatment approach tailored to every patient's specific clinical situation.
IBR is currently seeking a Research Associate. This position is in-person, in Hamilton, NJ.
Responsibilities:
  • Design and validate microbiological and molecular diagnostic assays.
  • Design and perform experiments and analyze data using diverse procedures and laboratory equipment.
  • Properly record details of the procedures used and data collected; create reports to CLIA/CAP standards.
  • Conduct laboratory tests according to equipment specifications and standard operation procedures (SOPs).
  • Perform reagent preparation and proper handling of biological samples in a BSL 2 setting.
  • Collaborate with Reference Laboratories and the Clinical Laboratory division for projects.
  • Routinely participate in meetings and scientific journal article discussions.

Job Qualifications: General Knowledge, Skills, and Abilities (KSA's) required
  • Bachelor's degree in relevant field is required. Strong background in Molecular Biology and Genetics is a plus.
  • The ideal candidate would be well versed in aseptic, microbiological, molecular, and cellular biology techniques. Experience with CAP accredited laboratory practices and cGLP is a plus.
  • Experience in bacterial, fungal, viral, and parasitic pathogenesis, and culture is desirable.
  • Experience in test development, troubleshooting, optimization, and validation, particularly qPCR, would be desirable.

We Offer:
Competitive Salary
Medical, Dental & Vision Insurance
Short and Long-Term Disability
Life Insurance
Dependent Care Flex Spending Account
Legal Plan
401(k) Plan
Paid Vacation, Sick, and Holidays
Visit us at http://www.mdlab.com.
Medical Diagnostic Laboratories, LLC is an equal opportunity employer.

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