Manufacturing Tech III
Gilead Sciences
June 26, 2026
On-site
La Verne, CA
Operations
Knowledge & Skills:
- Working knowledge of Standard Operating Procedures (SOPs) and Master Batch Records (MBRs).
- Strong understanding of cGMP requirements and regulated manufacturing environments.
- Good verbal, written, and interpersonal communication skills.
- Proficiency in Microsoft Office applications and familiarity with administrative systems.
- Ability to follow direction while working independently with minimal supervision.
- Demonstrated capability to train and mentor others on manufacturing processes (e.g., filling, hydration, coating, granulation, compression).
- Ability to coordinate and organize complex manufacturing activities.
Key Responsibilities:
- Perform routine to moderately complex manufacturing operations in compliance with SOPs, MBRs, and cGMP standards.
- Execute operations across multiple unit processes (aseptic processing, dispensing, compaction, granulation, milling, coating).
- Assemble/disassemble/operate aseptic filling equipment and lyophilizer autoloading systems in cleanrooms.
- Prepare equipment/components for sterilization (autoclaves, ovens, vial washers, depyrogenation tunnels).
- Perform CIP/SIP of tanks and equipment; manual cleaning and assembly.
- Conduct sterile filtration and annealing; operate downstream equipment (vial cappers) and support unloading/packaging.
- Use Oracle and MES transactions; resolve inventory discrepancies.
- Maintain clean/compliant manufacturing areas; complete GMP documentation (logbooks, batch records, reports).
- Support MBR updates and batch documentation; dispense raw materials; manage batch prep.
- Operate solid dose equipment (drum coaters, compression machines); manual material handling.
- Create purchase orders for consumables; provide updates to Team Lead; troubleshoot equipment/process issues.
- May serve as a point of contact during compliance audits.
Basic Qualifications:
- High School diploma with 3+ years relevant manufacturing experience.
- FETAC Level 6 (GSL) or equivalent technical certification.
- Prior experience in a cGMP-regulated industry.
Shift:
- Night Shift: 4p–4:30a Sunday, Monday, Tuesday and every other Wednesday.
Application Instructions:
- Please apply via the Internal Career Opportunities portal in Workday.
Benefits (explicit):
- Company-sponsored medical, dental, vision, and life insurance plans.
- Working knowledge of Standard Operating Procedures (SOPs) and Master Batch Records (MBRs).
- Strong understanding of cGMP requirements and regulated manufacturing environments.
- Good verbal, written, and interpersonal communication skills.
- Proficiency in Microsoft Office applications and familiarity with administrative systems.
- Ability to follow direction while working independently with minimal supervision.
- Demonstrated capability to train and mentor others on manufacturing processes (e.g., filling, hydration, coating, granulation, compression).
- Ability to coordinate and organize complex manufacturing activities.
Key Responsibilities:
- Perform routine to moderately complex manufacturing operations in compliance with SOPs, MBRs, and cGMP standards.
- Execute operations across multiple unit processes (aseptic processing, dispensing, compaction, granulation, milling, coating).
- Assemble/disassemble/operate aseptic filling equipment and lyophilizer autoloading systems in cleanrooms.
- Prepare equipment/components for sterilization (autoclaves, ovens, vial washers, depyrogenation tunnels).
- Perform CIP/SIP of tanks and equipment; manual cleaning and assembly.
- Conduct sterile filtration and annealing; operate downstream equipment (vial cappers) and support unloading/packaging.
- Use Oracle and MES transactions; resolve inventory discrepancies.
- Maintain clean/compliant manufacturing areas; complete GMP documentation (logbooks, batch records, reports).
- Support MBR updates and batch documentation; dispense raw materials; manage batch prep.
- Operate solid dose equipment (drum coaters, compression machines); manual material handling.
- Create purchase orders for consumables; provide updates to Team Lead; troubleshoot equipment/process issues.
- May serve as a point of contact during compliance audits.
Basic Qualifications:
- High School diploma with 3+ years relevant manufacturing experience.
- FETAC Level 6 (GSL) or equivalent technical certification.
- Prior experience in a cGMP-regulated industry.
Shift:
- Night Shift: 4p–4:30a Sunday, Monday, Tuesday and every other Wednesday.
Application Instructions:
- Please apply via the Internal Career Opportunities portal in Workday.
Benefits (explicit):
- Company-sponsored medical, dental, vision, and life insurance plans.