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Associate Process Development Scientist Jobs in Collingdale, PA

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Associate Process Development Scientist information

See Collingdale, PA salary details

$17

$34

$54

How much do associate process development scientist jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for associate process development scientist in Collingdale, PA is $34.01, according to ZipRecruiter salary data. Most workers in this role earn between $26.39 and $38.70 per hour, depending on experience, location, and employer.

What is the difference between Associate Process Development Scientist vs Process Development Scientist?

AspectAssociate Process Development ScientistProcess Development Scientist
Required CredentialsBachelor's or Master's in Life Sciences or Chemical EngineeringBachelor's or Master's, often with more experience or specialization
Work EnvironmentEntry-level, supporting process optimization in labs or manufacturingMore independent, leading process improvements and validations
Employer & Industry UsagePharmaceutical, biotech, or biotech manufacturing companiesSame industries, with increased responsibilities

The Associate Process Development Scientist typically supports process development tasks under supervision, focusing on experimental execution. In contrast, the Process Development Scientist takes on more independent roles, leading projects and process improvements. Both roles are common in biotech and pharmaceutical industries, with the main difference being experience level and scope of responsibilities.

Infographic showing various Associate Process Development Scientist job openings in Collingdale, PA as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, and 3% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $70,745 per year, or $34 per hour.

Process Scientist (Philadelphia, PA)

Cedent

Philadelphia, PA • On-site

Full-time

Re-posted 26 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