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Entry Level Upstream Process Scientist Jobs in Philadelphia, PA

A Scientist is a mid-level individual with understanding of cell/molecular biology and previous experience in either upstream or downstream biopharmaceutical processing that utilizes bioreactors. A ...

Adecco Medical and Science is hiring for a Process Operator in Malvern, PA. Apply today if you meet ... Perform entry-level micronization and milling of both hazardous and non-hazardous pharmaceutical ...

Gelest Inc Gelest Inc. is recognized world-wide as a leader and innovator in materials science and ... The salary range for this position is $23.00 (entry level) - $30 per hour. Factors such as scope ...

Process Operator

Malvern, PA · On-site

$18.75 - $23.50/hr

Operator I Functions o Perform entry-level micronization and milling of both hazardous and non ... processes. o Report production on batch records following good documentation procedures (GDPs). o ...

Process Operator

Malvern, PA · On-site

$18.75 - $23.50/hr

... entry-level micronization and milling of both hazardous and non-hazardous pharmaceutical actives ... processes. o Report production on batch records following good documentation procedures (GDPs). o ...

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Entry Level Upstream Process Scientist information

See Philadelphia, PA salary details

$51K

$112.4K

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How much do entry level upstream process scientist jobs pay per year?

As of Aug 20, 2026, the average yearly pay for entry level upstream process scientist in Philadelphia, PA is $112,355.00, according to ZipRecruiter salary data. Most workers in this role earn between $95,400.00 and $138,200.00 per year, depending on experience, location, and employer.

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Infographic showing various Entry Level Upstream Process Scientist job openings in Philadelphia, PA as of August 2026, with employment types broken down into 83% Full Time, and 17% Contract. Highlights an 100% In-person job distribution, with an average salary of $112,355 per year, or $54 per hour.

(Associate) Scientist, Upstream Viral Process Development

Dispatch Bio

Philadelphia, PA

Full-time

Re-posted 29 days ago


Job description

The role:

Reporting to the Director, Upstream Process Development, the (Associate) Scientist will contribute to upstream viral process development to bring the company's pipeline of T cell and viral vector-based products to the clinic. Responsibilities will include, but are not limited to, performing the day-to-day activities of the viral process development lab, building the company's viral manufacturing capabilities, and executing experiments to support viral process development/characterization. This role will collaborate significantly with research and analytical development teams. 

Key responsibilities:

  • Contribute to the setup and organization of the company's vector process development capabilities. 
  • Perform day-to-day activities in the vector process development lab including maintaining equipment, ordering materials, managing inventory, and preparing buffers and process aids. 
  • Serve as a PD subject matter expert on both internal and external teams (CDMO, material & equipment suppliers, etc.). 
  • Develop bench scale suspension culture processes for viral vector generation within shake flasks and bioreactors. 
  • Design and execute experiments to support process characterization, and process transfer activities between the research team, TechOps, and external partners. 
  • Provide experimental execution, data review and analysis, and maintenance of accurate and detailed lab notebooks. 
  • Author and review technical documents, including but not limited to batch records, SOPs, development reports and process specific sections of regulatory documents. 
  • Represent the company externally at meetings (professional associations, with regulatory bodies, etc.) 

Required experience & skills:

  • Bachelor's Degree in chemical engineering, biochemical engineering/bioengineering, biotechnology or related discipline with at least 2 years of relevant experience- OR- Master's Degree in relevant discipline 
  • Hands-on experience with viral vector upstream processes, particularly experimentation in and operation of stirred-tank bioreactors 
  • Working knowledge of GMP guidelines for clinical manufacturing 
  • Strong scientific reasoning, problem-solving, and applied mathematics and statistics skills, including the ability to break down complex problems into manageable hypotheses 
  • Proficiency in using Microsoft Word, Excel, Power Point and data analysis/presentation software such as JMP and/or GraphPad 
  • Excellent interpersonal, verbal and written communication skills 
  • Strong organizational & problem-solving skills, with excellent attention-to-detail and the proven ability to collaborate in a dynamic team environment 

Preferred experience & skills:

  • Experience implementing processes in clinical and commercial manufacturing of cell and gene therapy products 
  • Demonstrated ability to apply knowledge of cell biology, chemical engineering, or bioengineering toward process development, scale-up /scale-down and troubleshooting 
  • Detailed understanding of bioreactor operation and control loops 
  • Experience drafting CMC sections for INDs 
  • Proven experience collaborating with internal and external partners 

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