GMP Bioprocess Technician – Production Support

Bora Biologics; San Diego (CA); On-site; USD 56,000 - 75,000; Full time

Job summary

Bora Biologics in San Diego seeks a Manufacturing Technician, Production Support to perform routine manufacturing activities in GMP areas, solution preparation, dispensing raw materials, and bioprocessing support, including autoclave operation.

Under supervision, you will follow SOPs, WI, and MBRs, draft and revise documents, and maintain detailed logs. Flexible shift schedules and overtime may be required.

Qualifications

• cGMP manufacturing for biologics is expected.
• Fundamental knowledge of biologics regulations and cGMP for drug substance operation.
• Proficient with Microsoft Word and Excel.
• Ability to work with pressurized systems, steam, and corrosive chemicals with safety precautions.
• Detail-oriented and able to follow written procedures and logbooks.

Responsibilities

• Perform GMP manufacturing activities in assigned areas.
• Perform routine cleaning activities in GMP manufacturing areas
• Follow SOPs, cGMPs, safety guidelines during manufacturing to produce quality products.
• Set-up, operate, maintain and clean bioprocessing equipment.
• Demonstrate good aseptic technique.
• Perform dispensing raw material.
• Basic troubleshooting of bioprocess equipment.
• Manual cleaning and sterilization of parts and components.
• Maintain detailed process-related documentation of equipment logs and batch records.
• Draft and revise SOPs and batch records.
• Address production issues and report compliance concerns to supervisor.

Skills

cGMP knowledge

Biologics knowledge

Documentation

Safety compliance

Education

Bachelor's degree in life sciences

High School Diploma + 3+ years pharma/biotech experience

Tools

Bioprocess equipment

Job description

Bora Biologics in San Diego seeks a Manufacturing Technician, Production Support to perform routine manufacturing activities in GMP areas, solution preparation, dispensing raw materials, and bioprocessing support, including autoclave operation.

Under supervision, you will follow SOPs, WI, and MBRs, draft and revise documents, and maintain detailed logs. Flexible shift schedules and overtime may be required.