About this opportunity
BioTalent lists this Downstream Research Associates – Process Development opportunity in tustin, California. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Research Associate & Lead Research Associate - Process Development (Downstream)
Join a team developing the next generation of biologic therapies! We're looking for talented scientists with downstream purification experience to support the development and optimization of processes for monoclonal antibodies, recombinant proteins, and other biologics.
We're hiring for two levels:
1-2 years of biopharmaceutical industry experience
Perfect for early-career professionals looking to grow their expertise in downstream process development.
3-4 years of biopharmaceutical industry experience
We're looking for a technical leader who can drive downstream process development, lead purification studies, troubleshoot complex challenges, support process scale-up and technology transfer, and serve as a subject matter expert within cross-functional teams.
What you'll be working on:
Downstream process development and optimization
Protein purification using chromatography and filtration
Operating ÄKTA/FPLC systems
HPLC, SDS-PAGE, A280, and other analytical techniques
Experimental design, data analysis, and technical reporting
Supporting scale-up and technology transfer to manufacturing
Ideal background:
Downstream Process Development
Monoclonal Antibodies or Recombinant Proteins
Biopharmaceutical or CDMO experience
Hourly pay, bonus, equity, and comprehensive benefits.
Work on impactful products in a regulated, high-quality environment
Collaborate with cross-functional global teams
Grow your career in a dynamic and innovative organization
Work Authorization:
Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time
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Worksite address
tustin, CA, 92681, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.