Pharma Manufacturing Tech II - GMP Operations

Takeda Pharmaceutical Company Limited; Los Angeles (CA); On-site; USD 55,931,000 - 88,166,000; Full time

Job summary

Takeda Pharmaceutical Company Limited is seeking a Manufacturing Tech II in Los Angeles, CA. The role involves hands-on execution of manual and automated production processes following cGMP and safety guidelines.

The position requires basic education with 1+ years of related experience or an AA or higher. You will work with automated equipment and participate in safety, quality and process improvement teams.

Qualifications

• High school diploma or GED plus 1+ years of related experience, or AA or higher with no prior experience required.
• Familiarity with pharmaceutical production equipment including centrifuges, filtration systems, and CIP/SIP.
• Proficient in English and understanding of cGMP regulations in a pharmaceutical manufacturing environment.

Responsibilities

• Follow all safety rules, SOPs, cGMP, work rules and other company policies and programs.
• Support all local manufacturing operations.
• Complete relevant paperwork following GDP/GMP guidelines.
• Hands-on execution of manual and automated manufacturing operations with equipment such as centrifuges, filtration systems, CIP/COP, and chromatography columns.
• Receive and distribute supplies into the production area.
• Remove hazardous waste per safety guidelines.
• Troubleshoot minor process problems and respond to process alarms.
• Communicate issues related to safety, quality, compliance and equipment to the manufacturing lead operator and supervisor.
• Help train team members on the manufacturing floor.
• Participate in revision and review of important documentation.

Skills

Automation basics

English proficiency

Quality/regulatory compliance

Education

High school diploma or GED

AA or higher

Tools

DeltaV automation

Electronic Batch Management

PLC

Job description

Takeda Pharmaceutical Company Limited is seeking a Manufacturing Tech II in Los Angeles, CA. The role involves hands-on execution of manual and automated production processes following cGMP and safety guidelines.

The position requires basic education with 1+ years of related experience or an AA or higher. You will work with automated equipment and participate in safety, quality and process improvement teams.