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Research Associate Downstream Process Development Jobs in Conroe, TX

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Research Associate Downstream Process Development information

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How much do research associate downstream process development jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for research associate downstream process development in Conroe, TX is $28.84, according to ZipRecruiter salary data. Most workers in this role earn between $23.65 and $35.38 per hour, depending on experience, location, and employer.

What is a research associate downstream process development?

A Research Associate in Downstream Process Development works within biotechnology or pharmaceutical companies to optimize and scale up the purification and recovery of biological products, such as proteins or antibodies, after initial production. They focus on processes like filtration, chromatography, and centrifugation to ensure product quality and yield. These professionals design experiments, analyze data, and support the transfer of processes from laboratory scale to manufacturing. Their work is crucial for developing efficient, reproducible, and regulatory-compliant methods for producing biopharmaceuticals.

What are the key skills and qualifications needed to thrive as a research associate in downstream process development?

To thrive as a Research Associate in Downstream Process Development, you need a solid background in biochemistry, molecular biology, or chemical engineering, often demonstrated by a bachelor's or master's degree in a related field. Familiarity with chromatography systems (such as AKTA), filtration technologies, and Good Manufacturing Practice (GMP) standards, along with data analysis software, is typically required. Strong problem-solving skills, attention to detail, and effective teamwork and communication abilities help individuals excel in this role. These competencies are crucial for ensuring efficient, scalable purification processes and maintaining product quality in biopharmaceutical development.

What are the typical challenges faced by a research associate in downstream process development, and how can they be addressed?

A Research Associate in Downstream Process Development often encounters challenges such as optimizing purification processes for new biologics, troubleshooting equipment issues, and ensuring scalability from laboratory to production scale. Effective communication with cross-functional teams, such as upstream scientists and analytical specialists, is essential to resolve issues quickly. Staying current with new purification technologies and maintaining meticulous documentation can also help address these challenges and support successful process development.

What is the difference between Research Associate Downstream Process Development vs Research Associate Upstream Process Development?

AspectResearch Associate Downstream Process DevelopmentResearch Associate Upstream Process Development
Primary FocusPurification, filtration, chromatography of bioproductsCell culture, media optimization, bioreactor operation
Skills & CertificationsProtein purification, chromatography techniques, GMP complianceCell culture, aseptic techniques, bioreactor handling
Work EnvironmentLaboratory, manufacturing, quality controlLaboratory, bioprocessing facilities
Industry UsageBiopharmaceutical manufacturing, biotech researchBiopharmaceutical development, biotech research

While both roles support bioprocess development, Research Associate Downstream Process Development focuses on purification and filtration of bioproducts, whereas Research Associate Upstream Process Development emphasizes cell culture and bioreactor processes. Understanding these differences helps candidates align their skills with the appropriate role in biopharmaceutical production.

What cities near Conroe, TX are hiring for Research Associate Downstream Process Development jobs?

Cities near Conroe, TX with the most Research Associate Downstream Process Development job openings:

Infographic showing various Research Associate Downstream Process Development job openings in Conroe, TX as of August 2026, with employment types broken down into 88% Full Time, and 12% Contract. Highlights an 96% In-person, and 4% Remote job distribution, with an average salary of $59,981 per year, or $28.8 per hour.

Senior Scientist, Process Development with experience in lentivirus, extracellular vesicle (EV), exo

The Woodlands, TX • On-site

Cellipont Bioservices
Biotechnology Research and Development • 51 - 200 employees

$83K - $114K/yr

Full-time

Medical, Retirement, PTO

Re-posted 26 days ago


Key responsibilities

  • Design, optimize, and perform experiments to develop and improve processes for therapy programs, including cell culture, harvest, clarification, purification, and formulation.

  • Coordinate with analytical development and support process scale-up, scale-out, and transfer activities, including documentation and data analysis.

  • Lead discussions with clients, support process development projects, and assist in process gap analysis and equipment selection to ensure robust and reproducible processes.


Job description

"Bridging innovation to cure"Developing and Manufacturing your cell therapies from benchtop to bedsideJob SummaryCellipont Bioservices is growing, and we are looking for a Senior Scientist, Process Development with experience in Lentivirus, Extracellular vesicle (EV), Exosomes or EV/Exosome-based therapeutics who believes in the potential bridging clients discoveries to patient cures and who want to challenge the status quo and take Cellipont and it's clients to the next level. The Senior Scientist, Process Development will be part of the Process Development team and will participate in process development initiatives for our current and future therapy programs. This position plays a key role demonstrating the values, culture, and deliverables for the site. The Role Design, optimize and perform experiments to optimize the processes for various therapy programs.Design, optimize and perform mammalian cell culture processes using bench-scale to high-scale bioreactors. Design, optimize and perform harvest and clarification strategies using depth filtration, tangential flow filtration (TFF), or centrifugation.Design, optimize and perform purification workflows using chromatography (e.g., size-exclusion, ion-exchange, affinity) for isolation while removing host cell proteins (HCP) and DNA.Design, optimize and perform ultrafiltration/diafiltration (UF/DF) parameters for final concentration and buffer exchange into stable formulations. Perform cell isolation, modification, expansion, feeding and cryopreservation utilizing functionally closed systems.Assist in process gap analysis and provide process development recommendations/plan to close the gaps.Identify and implement appropriate equipment to develop highly robust and reproducible processes based on the cell type and unit operation. Develop scale-up and scale-out of processes based on the cell type and application.Coordinate with analytical development to test and characterize the product that is in development.Lead and support discussions with clients for process development projects. Prioritize the work to meet the timelines and deliverables.Provide support to the Business Development team by attending the technical calls with prospective clients.Assist in interaction with clients, key suppliers, and other external vendors.Successfully execute and document laboratory procedures and experiments with great attention to detail. Maintain detailed records in compliance with applicable cGMP, safety, and environmental requirements.Develop internal documentation, protocols, and reports to support transfer of processes to Manufacturing group.Perform data analysis and basic statistical analyses.Monitor and perform lab preventive maintenance activities as needed. Contribute at an individual level as well as part of an organized team in a fast-paced environment.Performs other duties as assigned.The Candidate Bachelors or Masters degree with 4-6 years minimum of industry experienceOR PhD with 1-2 years minimum of industry experience within pharmaceutical or biotech environmentPrior experience in Process Development for Cell and Gene Therapy is required.Prior experience with Lentiviral or EV upstream processing, including hands-on experience with mammalian tissue culture including both adherent and suspension cells, and bioreactors (e.g., stirred-tank and rocking-motion). Prior experience with Lentiviral or EV downstream processing, including purification unit operations such as preparative chromatography (affinity, ion-exchange), tangential flow filtration (TFF), and filtration. Experience with Formulation & Concentration, including ultrafiltration/diafiltration (UF/DF) parameters for final EV concentration and buffer exchange into stable formulations.Experience with common equipment used in lentivirus or EV therapy manufacturing such as Bioreactors, filtration, Tangential Flow Filtration (TFF) and Chromatography Systems is required.Experience working in a GMP environment preferred.Excellent verbal and written communication skills.Excellent organizational skills and attention to detail.Excellent time management skills, with proven ability to meet deadlines.Ability to design and execute experiments with minimal technical supervision.Strong analytical and problem-solving skills.Proficient with Microsoft Office Suite or related softwarePhysical Requirements: Prolonged periods of standing in clean room and at times, sitting at a desk and working on a computerMust be able to lift 15 pounds at timesManual dexterity to evaluate, install, and modify equipmentPosition BenefitsOpportunities for career growth within an expanding team.Defined career path and annual performance review & feedback process.Cross-functional exposure to other areas of within the organization.Robust benefit package designed for unique Health & Wellness needs, including coverage for your furry family members.401K strong employer match.Tuition Reimbursement.Employee Referral Bonuses.Flexible work schedules and PTO based on role/level, increasing 1 PTO day each year and paid holidays Gain experience in the cutting-edge cell therapy space. "At Cellipont Bioservices, we look for candidates with an innate desire to serve. Our "family" approach ensures you will get the mentorship you need to develop a satisfying career here!" Notice to Agency and Search Firm RepresentativesCellipont Bioservices is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Cellipont Bioservices employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Cellipont Bioservices. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.