Biopharma Downstream Manufacturing Associate - Onsite

Avid Bioservices

Tustin (CA)

On-site

USD 30,000 - 36,000

Full time

14 days+
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Job summary

Avid Bioservices in California is seeking a Manufacturing Associate, Downstream, to support multi-product production in a CGMP environment. You will be involved in production, documentation, materials procurement, and equipment scheduling to ensure timely release of high-quality biologics.

Role requires cleanroom gowning ability and experience with chromatography and GMP documentation. This full-time onsite position offers a collaborative team, growth opportunities, and a strong patient-impact

Qualifications

  • 2+ years of related manufacturing experience in biopharma.
  • Experience with large-scale liquid chromatography columns or similar equipment.
  • GMP and aseptic technique proficiency.
  • Ability to gown for cleanroom environments (class 10,000 to 100) and work aseptically.
  • Strong documentation and batch-record skills.

Responsibilities

  • Set up equipment and materials for production runs.
  • Plan resources for various processes and activities.
  • Operate and maintain chromatography skids.
  • Handle packing, unpacking, and cleaning of production-scale chromatography columns.
  • Perform antibody and enzyme purification using multiple chromatography methods.
  • Calibrate pH and conductivity meters.
  • Manage filtration processes including sterile and viral filtration.
  • Maintain aseptic techniques during operations and fills.
  • Keep cleanroom facilities and equipment in good condition.
  • Document GMP-compliant records and batch production records.

Skills

Attention to detail
Team player
Communication
Multitasking
GMP awareness

Education

BSc Biology
AS Chemistry

Tools

Chromatography
Sartocheck
Autoclave

Job description

Avid Bioservices in California is seeking a Manufacturing Associate, Downstream, to support multi-product production in a CGMP environment. You will be involved in production, documentation, materials procurement, and equipment scheduling to ensure timely release of high-quality biologics.

Role requires cleanroom gowning ability and experience with chromatography and GMP documentation. This full-time onsite position offers a collaborative team, growth opportunities, and a strong patient-impact

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