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Biotech Process Development Jobs in Philadelphia, PA

GenScript/ProBio

Automation Engineer, GMP

Pennington, NJ · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

About ProBio: ProBio, a subsidiary of GenScript, has a one stop biopharmaceutical R&D and ... Biotech Process Equipment/Systems. * Proficient in use of electronic systems, such as Microsoft ...

DPS Group

Process SME

Conshohocken, PA · On-site

Maintains current knowledge of relevant developments in their professional area of expertise ... biotechnology, and medical technology) and Advanced Technology (semiconductor, data center, and ...

USWM, LLC

Associate Scientist - MSAT

Philadelphia, PA · On-site

$70K - $110K/yr

Experience in a biotechnology company with emphasis on immunological systems, cell therapy, gene therapy, and large-scale process development and improvement. * Experience in a cGMP or GLP ...

IQVIA

CRA 1, IQVIA Biotech

Collegeville, PA · On-site

$71K - $145K/yr

... 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 ...

IQVIA

CRA 1, IQVIA Biotech

Philadelphia, PA · On-site

$71K - $145K/yr

... 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 ...

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Showing results 21-40

All JobsBiotech Process Development JobsBiotech Process Development Jobs in Philadelphia, PA

Biotech Process Development information

See Philadelphia, PA salary details

$19

$33

$49

How much do biotech process development jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for biotech 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 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 Philadelphia, PA?

For Biotech Process Development jobs in Philadelphia, PA, the most frequently searched job titles are:

What job categories do people searching Biotech Process Development jobs in Philadelphia, PA look for?

The top searched job categories for Biotech Process Development jobs in Philadelphia, PA are:

What cities near Philadelphia, PA are hiring for Biotech Process Development jobs?

Cities near Philadelphia, PA with the most Biotech Process Development job openings:

Biotech Process Development jobs near you
Infographic showing various Biotech Process Development job openings in Philadelphia, PA as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 18% Part Time, 1% Temporary, and 4% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $70,697 per year, or $34 per hour.

Process Scientist (Philadelphia, PA)

CEDENT

Philadelphia, PA

Full-time

Re-posted 28 days ago

Job description

Title: Process Scientist Report: CTO Location: Philadelphia, PA Position Type: Full Time, Exempt Travel: Occasional (0-10%) Position Summary This position is part of the Technology team responsible for Client technology development, process development, and assisting in transferring developed process to GMP manufacturing. 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 Scientist is responsible for hands-on execution of experiments and technology transfer, as well as authoring experimental protocols, SOPs, and batch documents.

A Scientist is expected to independently complete objectives given by supervisor, serve as a role model to junior scientists, collaborate cross-functionally, and provide support with any other technology, process development, and manufacturing needs. Key Responsibilities Independently contribute to technology/process development for specific bioprocessing steps, ensuring delivery in alignment with Client strategy Support Senior/Principal Scientist with experimental design, execution and data analysis, effectively communicating technical results to management Author protocols, SOPs, and batch documents to ensure the successful transfer of technology/process development to GMP manufacturing Perform as a Subject Matter Expert on a cross-functional team to implement novel process. Work closely with suppliers and other partners to drive forward technology development initiatives Serve as a good financial steward to the Technology team at Client and help to implement budgetary adherence and financial governance Coach and train junior scientists/employees on activities and documentation related to technology development, process development.

Other related duties as assigned. Education and Experience Minimum Bachelor's degree in Biological Engineering, Biotechnology, Biology, Biochemistry, or other related field. Master's preferred.

2-3 years of industry or academic experience in combination with Bachelor's or Master's degree. Knowledge, Skills and Abilities Experience with methodologies used for upstream or downstream viral vector production in either industry or academia Experience in experimental design, execution, and data analysis Excellent communication, collaboration, and technical writing skills Innovative and creative mindset, with problem solving capabilities Proficient in Microsoft Office products. Physical Requirements Ability to lift and carry up to 30lbs Ability to sit and stand for extended periods Excellent manual dexterity and ability to perform repetitive movements with fingers/hands Other Physical Requirements: PPE and gown training will be required as this individual will be required to enter into Laboratory and Cleanroom areas.

Work Environment: Work is performed primarily onsite in Philadelphia. 50% or more of the time, this role is in the laboratory.

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About Cedent

Sourced by ZipRecruiter

CEDENT strives to attract and retain the best people and provide an environment where they can all develop professionally and build a rewarding career. As a result, we create an inclusive environment that is rich in diversity, acknowledges each individual's uniqueness and promotes respect, personal achievement and stewardship. Our clients are global and so is CEDENT. We build and maintain a global workforce that includes people from different backgrounds, with a vast range of skills and experience all united by a common culture and commitment to help our clients achieve high performance. Cultivating a diverse workforce and inclusive work environment makes business sense. Our peoples varied skills are the talent engine that powers CEDENT, enabling it in turn to deliver the innovative solutions that help our clients outperform competitors.

Industry

It services

Company size

11 - 50 Employees

Headquarters location

Plano, TX, US

Year founded

2008

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