Manufacturing Technician

Takeda • Los Angeles, CA

7h • $19 - $30 • Onsite

About The Position

About the role: Responsible for the hands-on execution of production operations in full compliance with cGMP, Environmental Health and Safety (EHS) requirements, and all applicable regulations. Under the direction of the Manufacturing Lead Operator, Supervisor and Manufacturing Lead, this role supports daily manufacturing and departmental initiatives, participates in quality-focused project work, and may lead a small team around specific equipment or act as a delegate for the Lead Operator as needed. The position applies strong technical knowledge to operate and troubleshooting manual and automated systems, supports technology transfer activities, and contributes to creating, revising, and improving procedures, including developing new or complex procedures when required. The role also provides meaningful exposure to validation and qualification work, partnering closely with engineers and external vendors to help ensure facility and equipment readiness while building technical capability and contributing to the continued advancement of Takeda’s manufacturing operations. Throughout all activities, the incumbent upholds Takeda’s focus on Patient, Trust, Reputation, and Business.

Requirements

• High school diploma or GED
• 2+ years of experience or AA or higher and 1+ years of related work experience.
• Advanced process knowledge of related manufacturing techniques and specialties.
• Thorough automation experience using DeltaV, Electronic Batch Management, PLC, etc.
• Familiarity with pharmaceutical production equipment including but not limited to centrifuges, filtration systems and CIP/SIP (Clean in Place/Steam in Place).
• Experience operating material handling equipment such as pallet jacks and forklifts.
• Must have strong communication skills (both verbal and written) and understanding of cGMP regulations in a pharmaceutical manufacturing environment.
• Must be able to read and follow detailed written procedures.
• Must be able to apply quantitative analysis to analyze process performance.
• Must be proficient in a variety of mathematical disciplines and be able to work with both the metric and USA standards of measurement.
• Good interpersonal skills and be able to work effectively and efficiently in a team environment.
• Knowledge of basic chemical and biological safety procedures.
• Good computer skills.

Responsibilities

• Execute day-to-day manufacturing operations in full compliance with safety policies, cGMP/GDP, SOPs, validation protocols, work rules, and applicable company policies/initiatives.
• Perform hands-on manual and automated manufacturing activities, including operating/monitoring process equipment (e.g., centrifuges, filter presses, ultrafiltration/nanofiltration systems, CIP, chromatography and material-handling equipment) and completing associated tasks (e.g., weighing/adding chemicals, transfers/connections, titrations, equipment assembly/disassembly, equipment/room cleaning).
• Complete all required documentation/paperwork accurately and contemporaneously per GDP/GMP, ensuring activities are properly recorded and compliant.
• Partner with Quality and Quality Validation to ensure work is performed correctly, deviations are addressed, and documentation meets requirements.
• Troubleshoot process deviations and equipment/process issues; respond promptly and effectively to alarms; escalate and communicate safety, quality, compliance, and equipment concerns to lead operator/supervisor as needed.
• Coordinate with Maintenance/Engineering/Metrology to resolve equipment, utilities, and systems issues and to support preventive and corrective maintenance execution.
• Coordinate with Schedulers and RTMS to ensure project/manufacturing steps are executed as planned, including making RTMS updates/adjustments when required.
• Receive, stage, request/order, and distribute materials, parts, supplies, and tools to support production activities.
• Remove, segregate, and properly handle manufacturing and hazardous waste in accordance with established procedures.
• Perform sanitization, bio-cleaning, and facility/area cleaning activities; coordinate with ISS as needed; ensure cleaning activities are completed and documented.
• Collaborate with leadership, engineers, PETs, and cross-functional project team members to ensure successful execution of manufacturing/validation/project activities.
• Participate in project meetings, daily huddles, and other required communications to maintain alignment and execution readiness.
• Support operational excellence/continuous improvement by developing/refining micro-steps, using CI tools, and initiating/coordinating process improvement projects.
• Support team capability by assisting the lead operator (including leading small teams around equipment), acting as delegate when needed, and training/mentoring manufacturing-floor team members.
• Contribute to the creation, revision, and review of manufacturing-related documents (e.g., SOPs, batch records, protocols) as required.
• Maintain flexibility to work extended hours (up to 12 hours per day) and/or alternative shifts to support operations, validation, and project needs.
• Perform other duties as assigned.

Benefits

• U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short-term and long-term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits, among others.
• U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: High school or GED
• Number of Employees: 5,001-10,000 employees