Manufacturing Tech III

Gilead Sciences • La Verne, CA

10d

About The Position

At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference. Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact. We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together. Job Description Key Responsibilities Perform basic to routine manufacturing assignments in accordance with Standard Operating Procedures (SOPs), Master Batch Records (MBRs), and current Good Manufacturing Practices (cGMPs). Execute moderately complex manufacturing activities, including aseptic processing, dispensing, compaction, granulation, milling, and coating. Assemble, disassemble, and operate aseptic filling equipment and lyophilizer autoloading systems in classified cleanroom environments. Prepare equipment and components for sterilization; operate autoclaves, ovens, vial washers, and depyrogenation tunnels. Perform clean‑in‑place (CIP) and sterilization‑in‑place (SIP) activities for tanks and processing equipment. Perform annealing and sterile filtration of products. Operate vial cappers; unload product from lyophilizers; pack off vials from lyophilization and liquid fill lines. Perform more complex troubleshooting activities independently and support resolution of line performance issues. Report regularly to the Team Lead on manufacturing performance and escalate issues requiring resolution. Operate drum coaters and compression equipment; dispense ingredients for manufacturing batches. Perform manual material handling, including loading and unloading tablets and product. Execute detailed Oracle and MES transactions, including resolution of inventory discrepancies. Complete, review, and maintain accurate manufacturing documentation, including batch records, logbooks, and MBR updates. Create purchase orders for consumables and support material readiness. Clean manufacturing areas, including walls, ceilings, and floors, in compliance with GMP and safety requirements. Demonstrate capability to train others on manufacturing processes (e.g., filling, hydration, coating, granulation, compression). Organize and coordinate more complex manufacturing activities and assignments. May serve as a point of contact for compliance audits. Comply with all safety, GMP, and regulatory requirements at all times.

Requirements

• High School Diploma with at least 3 years of relevant manufacturing experience.
• Certificate to FETAC Level 6 (GSL) or equivalent.
• Prior experience working in a cGMP‑regulated industry.

Nice To Haves

• Working knowledge of written SOPs and Master Batch Records in a regulated manufacturing environment.
• Strong verbal, written, and interpersonal communication skills.
• Proficiency in Microsoft Office applications and familiarity with administrative policies.
• Ability to follow direction and work effectively with minimal supervision.
• Demonstrated experience training others on manufacturing processes.
• Ability to organize and execute more complex manufacturing activities.
• Experience operating aseptic, solid dose, or sterile manufacturing equipment.
• Familiarity with MES and ERP systems (e.g., Oracle).
• Strong attention to detail and commitment to documentation accuracy and data integrity.

Responsibilities

• Perform basic to routine manufacturing assignments in accordance with Standard Operating Procedures (SOPs), Master Batch Records (MBRs), and current Good Manufacturing Practices (cGMPs).
• Execute moderately complex manufacturing activities, including aseptic processing, dispensing, compaction, granulation, milling, and coating.
• Assemble, disassemble, and operate aseptic filling equipment and lyophilizer autoloading systems in classified cleanroom environments.
• Prepare equipment and components for sterilization; operate autoclaves, ovens, vial washers, and depyrogenation tunnels.
• Perform clean‑in‑place (CIP) and sterilization‑in‑place (SIP) activities for tanks and processing equipment.
• Perform annealing and sterile filtration of products.
• Operate vial cappers; unload product from lyophilizers; pack off vials from lyophilization and liquid fill lines.
• Perform more complex troubleshooting activities independently and support resolution of line performance issues.
• Report regularly to the Team Lead on manufacturing performance and escalate issues requiring resolution.
• Operate drum coaters and compression equipment; dispense ingredients for manufacturing batches.
• Perform manual material handling, including loading and unloading tablets and product.
• Execute detailed Oracle and MES transactions, including resolution of inventory discrepancies.
• Complete, review, and maintain accurate manufacturing documentation, including batch records, logbooks, and MBR updates.
• Create purchase orders for consumables and support material readiness.
• Clean manufacturing areas, including walls, ceilings, and floors, in compliance with GMP and safety requirements.
• Demonstrate capability to train others on manufacturing processes (e.g., filling, hydration, coating, granulation, compression).
• Organize and coordinate more complex manufacturing activities and assignments.
• May serve as a point of contact for compliance audits.
• Comply with all safety, GMP, and regulatory requirements at all times.

Benefits

• This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package.
• Benefits include company-sponsored medical, dental, vision, and life insurance plans.
• For additional benefits information, visit: https://www.gilead.com/careers/compensation-benefits-and-wellbeing
• Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: High school or GED