About this opportunity
Vita Global Sciences, a Kelly Company lists this Associate Scientist, Downstream Process Development opportunity in houston, Texas. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Are you ready to play a vital role in transforming the future of neurological disease treatment? An innovative, clinical-stage biopharma company is seeking a talented Associate Scientist, Downstream Process Development, to join their fast-growing team in Houston on a contract basis. This is a unique opportunity to advance your career in gene therapy, supporting a rapidly expanding pipeline and world-class manufacturing environment.
Position Title:
Associate Scientist, Downstream Process Development
Location:
Houston, TX
Rate
$37-40/hr.
Duration
6 months + potential extension
About the Opportunity
This hands-on technical role supports the design, execution, and optimization of breakthrough gene therapy products. Reporting to the Associate Director, Downstream Process Development, you will contribute across a spectrum of viral vector purification activities—empowering the company’s pipeline from research through clinical and commercial production.
Be part of a collaborative and mission-driven culture that is unwavering in its commitment to patients, innovation, and scientific excellence.
Key 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.
What We’re Looking For
BSc in Biological Science or related discipline
2+ years’ experience in a biotechnology or biopharma environment preferred
Practical experience in basic laboratory operations related to virus/protein purification, buffer preparation, and aseptic technique
Familiarity with chromatography and filtration purification methods; AKTA chromatography experience preferred
Hands-on experience with viral vector bioprocessing, especially AAV, is an advantage
Comfortable working in regulated environments (GLP/GMP); GMP experience is a plus
Understanding of bioprocess documentation (SOPs, batch records) and regulatory expectations (FDA/EMA/cGMP a plus)
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
Why Join Us?
Grow with a forward-thinking company at the cutting edge of gene therapy for neurological diseases
Collaborate with industry experts and contribute to life-changing therapies
Advance your skills in a highly supportive, innovation-focused culture
Be part of a Houston-based organization with an end-to-end manufacturing footprint, setting the stage for personal and professional growth
Take your next step in the gene therapy revolution. Apply your expertise in downstream process development to truly make a difference for patients and families facing rare diseases.
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Worksite address
houston, TX, 77246, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.