Manufacturing Senior Training Coordinator

Manufacturing Senior Training Coordinator

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About the role:

As the Manufacturing Senior Training Coordinator, you will oversee the assignment and delivery of manufacturing training curriculums for new employees, provide hands‑on instruction, and coordinate training events with supervisors. Assess the effectiveness of training, continuously improve materials in collaboration with quality and training groups, and perform personnel qualifications on critical operations such as aseptic technique and swab sampling. Maintain and report qualification status, address gaps, and support quality systems through CAPAs and Change Controls.

Present the training process during audits and inspections, ensure regulatory commitments, manage the MABioOps training lab, advise on training competencies, and participate in interviewing manufacturing associate candidates as needed. You will report into the Manufacturing Manager.

• Assign appropriate curriculum to new employees and provide a detailed overview of the manufacturing portion of the training program
• In collaboration with manufacturing supervisors, schedule training events to train manufacturing personnel
• Provide hands‑on training of manufacturing staff
• Assess training effectiveness and work with training and quality groups to continuously improve training materials and curriculum
• Perform qualification of manufacturing personnel on critical operations including aseptic technique and swab sampling
• Provide detailed qualification status via training reports and identify gaps or opportunities
• Support quality systems and implement action items stemming from CAPAs and Change Controls
• Present the training process during audits and inspections
• Ensure use of personal protective equipment and safety protocols during training
• Assist with gowning, entry to biotechnology/pharmaceutical areas, and handling of equipment up to 25‑50 lbs
• Operate within production suites, including standing for extended periods, climbing ladders, and working platforms

• High school diploma and 6+ years related industry experience, or Associate’s Degree in Life Sciences/Engineering with 5 years GMP manufacturing experience
• Biotech Certificate and prior leadership experience preferred
• Experience with SAP, LIMS, Track Wise, and lean principles is a plus
• 5+ years GMP training experience; coaching other training coordinators required
• Operational knowledge of upstream or downstream manufacturing, including CIP/SIP systems, autoclaves and related equipment
• Knowledge of cGMPs and applicable agency regulations (FDA, EMA) to ensure inspection readiness

U.S. Base Salary: $70,000 – $110,000 per year, with potential for short‑term and long‑term incentives. Eligible for medical, dental, vision, 401(k), disability, life insurance, tuition reimbursement, paid volunteer time, holidays, and well‑being benefits. Paid sick time up to 80 hours and vacation up to 120 hours.

Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, veteran status, or any other characteristic protected by law.

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