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Manufacturing Technician - II; Upstream​/Downstream

Job in Oceanside, San Diego County, California, 92058, USA
Listing for: Lancesoft INC
Contract position
Listed on 2026-10-18
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Validation Engineer, Manufacturing & Industrial Operations
Salary/Wage Range or Industry Benchmark: 65000 - 90000 USD Yearly USD 65000.00 90000.00 YEAR
Job Description & How to Apply Below
Position: Manufacturing Technician - II (Upstream / Downstream) - 12+ months

Job Description

Job Description

Core JD – Common Requirements

  • Execute GMP manufacturing processes on the manufacturing floor while following batch records, SOPs, cGMP, and GDP requirements .
  • Support right-first-time manufacturing and maintain a strong safety/compliance culture.
  • Collaborate with MSAT, Facilities & Engineering, and Quality teams during GMP manufacturing runs.
  • Perform raw material weighing and electronic inventory transactions using MES/EBS systems.
  • Work with single-use systems , solution/buffer preparation, and filter integrity testing.
  • Follow proper aseptic technique and cleanroom/laboratory practices .
  • Assist with viral vector manufacturing, harvesting, and fill operations .
  • Escalate process, equipment, and manufacturing issues appropriately.
  • Assist with revisions of SOPs, Manufacturing Production Records (MPRs), and controlled documents .
  • Review in-process GMP documentation for accuracy, completeness, and compliance .
  • Work effectively in a cross-functional, team-based environment .
  • Must be able to work off-shifts and weekends .
  • Bachelor’s degree in Biology or related scientific discipline preferred; equivalent biotech/pharma manufacturing experience may be considered.

Group 1 - Viral Vector (Downstream Processing)

  • Experience with chromatography operations.
  • Experience with Ultrafiltration/Diafiltration (UF/DF) .
  • Experience supporting viral vector manufacturing using these downstream processing techniques.
  • Experience with manual and/or automated fill of harvested viral vector material.
  • Biopharmaceutical, cell therapy, or gene therapy manufacturing experience preferred.
  • Strong knowledge of cGMP manufacturing practices .
  • Ability to lift 40 lbs repeatedly and stand for extended periods.

Group 2 - Viral Vector (Upstream Processing)

  • Hands-on mammalian cell culture experience.
  • Experience maintaining cells in flasks, CellSTACK chambers, and single-use bioreactors .
  • Experience with cell culture and filling unit operations .
  • Experience with cell transfection and viral vector harvest .
  • Experience with solution formulation and filter integrity testing.
  • Prior cell/gene therapy or viral vector manufacturing experience strongly preferred.
  • Experience working with single-use bioreactor systems is highly relevant.
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