Downstream Process Scientist – Gene Therapy AAV (Houston)

Kelly Services; Houston (TX); On-site; USD 48,000 - 55,000; Full time

Job summary

A Houston-based biopharma company is seeking an Associate Scientist, Downstream Process Development, on a 6-month contract to support gene therapy manufacturing.

The role covers viral vector purification, development support, documentation, and cross-functional collaboration to advance AAV processes in a GMP environment. Candidates should have a BSc in a biological science and 2+ years in biotech, with hands-on purification experience and regulatory familiarity.

Qualifications

• BSc in Biological Science or related field.
• 2+ years in biotech/biopharma environment.
• Experience in virus/protein purification and aseptic technique.
• Familiarity with chromatography/filtration; AKTA preferred.
• Experience with viral vector bioprocessing (AAV preferred).
• Comfort in GLP/GMP regulated environments; FDA/EMA knowledge a plus.
• Strong documentation and teamwork skills.
• Proficiency with MS Office and precise record-keeping.
• Ability to lift up to 25 lbs regularly (50 lbs occasionally).

Responsibilities

• Execute viral vector purification and GMP batch runs.
• Support development operations and reagent prep.
• Draft SOPs and batch records; ensure compliant documentation.
• Collaborate with analytical/upstream teams on QC attributes.
• Maintain lab protocols, inventory, and safety procedures.
• Stay current with advances in viral vector process development.

Skills

Biotech lab experience

Team collaboration

Documentation skills

MS Office proficiency

Education

BSc in Biological Science

Tools

AKTA chromatography

Virus purification

Laboratory equipment

Job description

A Houston-based biopharma company is seeking an Associate Scientist, Downstream Process Development, on a 6-month contract to support gene therapy manufacturing.

The role covers viral vector purification, development support, documentation, and cross-functional collaboration to advance AAV processes in a GMP environment. Candidates should have a BSc in a biological science and 2+ years in biotech, with hands-on purification experience and regulatory familiarity.