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Cell Therapy Process Development Scientist Jobs in Massachusetts

Amgen

Process Development Senior Scientist

Cambridge, MA · On-site

$100K - $136K/yr

Process Development Senior Scientist What you will do Let's do this. Let's change the world. In ... Work in a coordinated group in which cell culture and purification scientists work together to ...

CEDENT

Senior Scientist, Process Development

Watertown, MA · On-site

$99K - $135K/yr

... therapies. We are seeking a Senior Scientist, Process Development, responsible for executing cell culture experiments, downstream processing, analyzing data, and contributing to process development ...

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Cell Therapy Process Development Scientist information

What is the difference between Cell Therapy Process Development Scientist vs Cell Manufacturing Associate?

AspectCell Therapy Process Development ScientistCell Manufacturing Associate
CredentialsTypically requires a Master's or PhD in biology, biochemistry, or related fieldsUsually holds a Bachelor's degree in life sciences or related areas
Work EnvironmentResearch labs, process development facilities, R&D settingsManufacturing floors, production facilities, GMP environments
Industry UsageDesigning and optimizing cell therapy processes, early-stage developmentExecuting manufacturing protocols, batch production, quality control

The Cell Therapy Process Development Scientist focuses on developing and refining cell therapy processes in research and development settings, often requiring advanced degrees. In contrast, the Cell Manufacturing Associate works primarily on executing manufacturing procedures in GMP environments, typically with a bachelor's degree. Both roles are essential in the cell therapy industry but differ in responsibilities, work environment, and required qualifications.

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Cities in Massachusetts with the most Cell Therapy Process Development Scientist job openings:

Cell Therapy Process Development Scientist jobs near you
Infographic showing various Cell Therapy Process Development Scientist job openings in Massachusetts as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 18% Part Time, and 3% Contract. Highlights an 90% Physical, 4% Hybrid, and 6% Remote job distribution.

Senior Process Development Scientist

Sun Pharmaceutical Industries

Billerica, MA • On-site

$97K - $132K/yr

Full-time

Posted 25 days ago

Job description

Job Summary

Lead new product formulation, process development, transfers into manufacturing, and continuous improvement of existing processes.

Area Of Responsibility

  • Manage tasks at independent level and contribute to cross-functional project management teams
  • Design experiments using Quality by Design principles, execute and author reports in support of:
  • Formulation, aseptic filling and lyophilization development of new products
  • Continuous improvement, troubleshooting and investigations of existing processes and products
  • Process transfers into manufacturing
  • Perform analytical testing in support of product development studies
  • Prepare cGMP documents such as SOPs, batch records and protocols
  • Design, execute and write technical reports to support FDA filings
  • May direct the work of junior Process Development staff
  • Other duties as assigned

Work Conditions:

  • Office
  • Lab
  • Warehouse
  • Exposure to noise, hazardous and non-hazardous chemicals, syringes and needles, toxic metals

Physical Requirements:

  • Stand, sit, walk, use hands and fingers to handle or feel, reach with arms and hands
  • Talk or hear
  • Close, and color vision; depth perception, ability to adjust focus
  • Use of repetitive motion
  • Operates Lyophilizer, HPLC, pH meter, analytical balance, compressed gas cylinders, fume hoods, heating mantles, stirring equipment, temperature controllers, and computer/office equipment
  • Requires wearing protective clothing in lab areas - lab coat, safety glasses, and gloves
  • Lift up to 50 lbs.

Travel Estimate

Up to 5%

Education and Job Qualification

  • Minimum  B.S. in related scientific field required

Experience

  • Minimum 7-10 years related experience preferred
  • Able to work with external contractors to find new technology, equipment or solutions to process issues
  • Experience with parenteral formulation, lyophilization and sterilization techniques preferred
  • Process validation experience
  • Cleaning validation experience
  • Analytical hands-on experience with techniques such as HPLC, Karl Fischer, DSC, and spectroscopic techniques
  • Experience with aseptic techniques in a clean room environment is highly beneficial
  • Experience working in a cGMP environment
  • Understanding of Quality by Design principles and statistics is preferable
  • Process development experience and manufacturing process investigation skills
  • Strong technical writing skills and resourceful problem solving skills
  • Ability to work independently and as a member of a cross functional team
  • Excellent verbal, written and interpersonal communications skills
  • Strong attention to detail and ability to manage multiple assignments concurrently
  • Able to lead cross functional teams to design experiments and address process issues

 

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