cGMP Manufacturing Technician I — Production & Data Entry

Takeda Pharmaceutical Company Limited; Lexington (MA); On-site; USD 22,000 - 36,000; Full time

Job summary

Takeda Pharmaceutical Company Limited in Lexington, MA seeks a hands-on Production Operator to support cGMP manufacturing. You will follow SOPs and batch records, enter data into LIMS, and maintain logs and sample testing protocols.

This role emphasizes routine production tasks, safety, and quality compliance. The position also covers equipment management, including work orders, cleaning, and changeovers, with a strong training and development component.

Qualifications

• Experience with cGMP manufacturing operations using SOPs and batch records.
• Ability to enter data in LIMS and maintain logs.
• Willingness to complete required training on time.

Responsibilities

• Perform routine production operations.
• Complete Batch Record and Form Prep requests.
• Enter data in LIMS.
• Record data in log books.
• Prepare samples and perform testing.
• Propose document revisions.
• Complete required training on time.
• Carry out work safely and report safety issues.
• Initiate work orders for equipment.
• Perform cleaning of equipment as scheduled.
• Standardize equipment.
• Support changeover activities.
• Assist in assembly/disassembly of process equipment.
• Meet and maintain training requirements.
• Develop and maintain personal development plan.
• Provide annual performance self-assessment.

Job description

Takeda Pharmaceutical Company Limited in Lexington, MA seeks a hands-on Production Operator to support cGMP manufacturing. You will follow SOPs and batch records, enter data into LIMS, and maintain logs and sample testing protocols.

This role emphasizes routine production tasks, safety, and quality compliance. The position also covers equipment management, including work orders, cleaning, and changeovers, with a strong training and development component.