Biologics GMP Manufacturing Associate – Swing Shift

Miltenyi Biotec; Bilibiran; On-site; PHP 4,202,000 - 4,937,000; Full time

Benefits offered by this job

Health insurance

Vision insurance

Dental insurance

401(k) plan

Job summary

Miltenyi Biotec is seeking a Senior Manufacturing Associate I for a swing shift (1:00 pm – 9:30 pm) in a high‑volume biologics manufacturing environment in San Jose, CA. The role follows cGMP procedures and requires adherence to gowning and cleanroom SOPs while supporting production schedules and equipment readiness.

The candidate will execute batch records, GMP documentation, and assist in investigations and corrective actions, contributing to SOPs and GMP documentation updates in a fast-paced

Qualifications

• Completion of High School; 2+ years of related experience.
• Previous GMP and aseptic technique experience is desired.

Responsibilities

• Adhere to clean room SOPs for gowning, traffic flows, and operation modes.
• Support manufacturing schedules, ensure equipment availability, maintain materials supply, and perform setup and monitoring.
• Execute batch record instructions, SOPs, GMP documentation, and review records for completeness and accuracy.
• Assist Manufacturing team Leads in investigations and corrective actions.
• Contribute to development and review of SOPs, MSs, SMPs, BPRs and related GMP docs.
• Maintain cleaning and proper operation of production equipment per cGMPs and safety policies.

Skills

Production equipment

Process troubleshooting

Communication

Excel

Education

High School Diploma

Job description

Miltenyi Biotec is seeking a Senior Manufacturing Associate I for a swing shift (1:00 pm – 9:30 pm) in a high‑volume biologics manufacturing environment in San Jose, CA. The role follows cGMP procedures and requires adherence to gowning and cleanroom SOPs while supporting production schedules and equipment readiness.

The candidate will execute batch records, GMP documentation, and assist in investigations and corrective actions, contributing to SOPs and GMP documentation updates in a fast-paced