Associate Scientist, Process Development jobs in United States
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Kelly Science, Engineering, Technology & Telecom · 5 hours ago

Associate Scientist, Process Development

Kelly Science & Clinical is seeking an Associate Scientist for a contract opportunity with a gene therapy biotechnology company focused on neurological disorders. This hands-on role involves supporting the design, execution, and optimization of gene therapy products, particularly in viral vector purification activities.

Staffing & Recruiting

Responsibilities

Execute routine and complex viral vector purification, from buffer preparation and sampling to small-scale purification runs and GMP batch execution
Support process development operations including development and toxicology production runs, reagent prep, inventory control, and lab upkeep
Draft and review critical documentation, including SOPs, batch production records, process forms, and laboratory records, adhering to best practices in biotechnology and compliance
Collaborate cross-functionally with analytical and upstream teams to define and deliver critical quality attributes and process performance for AAV purification
Maintain accurate laboratory protocols and data capture, participating in inventory and equipment management, waste disposal, and lab safety procedures
Stay engaged with the latest advances in viral vector process development and proactively contribute to the success of the process development team

Qualification

Viral vector purificationChromatography methodsGMP experienceAseptic techniqueBioprocess documentationMS Office proficiencyTeam playerCommunication skillsProblem-solving skills

Required

BSc in Biological Science or related discipline
Practical experience in basic laboratory operations related to virus/protein purification, buffer preparation, and aseptic technique
Familiarity with chromatography and filtration purification methods
Hands-on experience with viral vector bioprocessing, especially AAV, is an advantage
Comfortable working in regulated environments (GLP/GMP)
Proven team player with strong organizational, communication, and problem-solving skills
Tech-savvy with proficiency in MS Office, accurate documentation practices, and attention to detail
Ability to work flexibly, lift up to 25 lbs frequently (50 lbs occasionally), and thrive in a laboratory setting

Preferred

1-2 years' experience in a biotechnology or biopharma environment preferred
AKTA chromatography experience preferred
GMP experience is a plus
Understanding of bioprocess documentation (SOPs, batch records) and regulatory expectations (FDA/EMA/cGMP a plus)

Benefits

Medical
Dental
Vision
Telemedicine
Term life
Whole life
Accident insurance
Critical illness
A legal plan
Short-term disability
Retirement savings plan
Service bonus
Holiday pay plans (earn up to eight paid holidays per benefit year)
Transit spending account
Paid sick leave under the applicable state or local plan

Company

Kelly Science, Engineering, Technology & Telecom

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Kelly Science, Engineering, Technology & Telecom specializes in science, engineering, technology, and telecom.

Funding

Current Stage
Late Stage

Leadership Team

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Linda Stuit
Senior Vice President, Engineering Specialty
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