Biopharma Downstream Manufacturing Associate III

Avid Bioservices, Inc.; Tustin (CA); On-site; USD 31,000 - 39,000; Full time

Job summary

Avid Bioservices, Inc. in Tustin, CA, seeks a Manufacturing Associate III - Downstream to drive virus purification and filtration in our GMP biopharma facility. You will execute complex downstream operations, support batch records, and mentor junior staff in aseptic techniques.

The role requires a BS in biotechnology or biology, 2+ years of GMP biologics manufacturing, and strong problem-solving in an audit-ready, fast-paced environment. Monday–Friday; potential overtime.

Qualifications

• BS in Biotechnology, Biology, or chemistry (Biochemistry preferred).
• 2+ years GMP biologics manufacturing, downstream experience.
• Aseptic practices and clean room operations; knowledge of GMP, FDA and EMA requirements for biologics.

Responsibilities

• Prioritize and execute the daily manufacturing schedule for downstream operations including virus purification techniques such as harvest, clarification, purification (TFF and chromatography) and filtration.
• Troubleshoot equipment and processes in partnership with Manufacturing Science and Technology.
• Conduct osmolality, pH and conductivity tests and perform filter integrity testing.
• Communicate problems clearly to management and train junior associates.
• Ensure timely setup of equipment and materials for each production run.
• Maintain cleanrooms, inventory, and audit readiness; plan material kitting for operations.
• Adhere to GMP documentation; update batch records, SOPs, protocols and reports.

Skills

GMP manufacturing experience

Biologics downstream processing

Analytical problem-solving

Education

BS in Biotechnology/ Biology/ Chemistry

Job description

Avid Bioservices, Inc. in Tustin, CA, seeks a Manufacturing Associate III - Downstream to drive virus purification and filtration in our GMP biopharma facility. You will execute complex downstream operations, support batch records, and mentor junior staff in aseptic techniques.

The role requires a BS in biotechnology or biology, 2+ years of GMP biologics manufacturing, and strong problem-solving in an audit-ready, fast-paced environment. Monday–Friday; potential overtime.