Quality Control Technician II

Join Takeda as a Quality Control Technician II, you will be responsible for ensuring compliance with procedures and regulatory requirements in the manufacturing facility. The incumbent is responsible for quality support and oversight of manufacturing operations, which includes presence on the floor and for performing Acceptable Quality Limit (AQL) sampling of finished product. Additional responsibilities include triage for potential issues on the floor, raw material investigations, Quality on the Shop Floor (QOTSF), online batch documentation review, sample management, kitting of batches, and raw materials release.

Quality Control Technician II is focused on ensuring the quality of processes and product outputs. This includes defining and specifying activities, processes, and standards to meet quality requirements, auditing and monitoring processes, and ensuring product integrity. This role contributes to Takeda's mission by maintaining high standards of quality and compliance.

• Performs Acceptable Quality Limit (AQL) sampling of finished product. Identifies and assesses quality risk in production operations daily.
• Executes Quality on the Shop Floor (QOTSF) and reviews checklists. Programs are part of manufacturing support and compliance enforcement.
• Initiation of JDE (inventory management system and preventive maintenance system) work orders if required to address issues in a timely manner.
• Performs sample management (Sterility, stability, etc.) to appropriate facilities and is responsible for the appropriate storage and disposal of retention samples. Performs triage with manufacturing, engineering, and maintenance to resolve potential issues on the floor and elevate if needed.
• Facilitates kitting operations for packaging – issue and return of preprinted materials physically and electronically.
• Handles movement of materials/products physically and electronically for quarantine and reject areas.
• Review Lead Manufacturing support activities, including batch record documentation review. Perform review and approval of batch documentation and consult with manufacturing to address any required corrections.
• Subject Matter Expert (SME) and provides training to other employees as required.
• Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, and cGMP regulations.
• Monitor product quality through the performance of required visual testing follow-ups.
• Actively contributes to a team setting within quality operations and potentially with other work teams to increase efficiency, solve problems, generate cost savings, improve quality, and provide new product support.

• Support regulatory audits as required.

• HS Diploma or GED with 2+ years, Associate’s degree or higher with 1+ years of relevant industry experience
• Team player with good problem-solving and good verbal and written communication skills.
• Knowledge of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP)
• Proficient in Microsoft Word, Excel, Outlook, and SharePoint.
• Able to learn and work with JDE, EBM, TW workflows, Systech, and other Learning Management and Document Management systems.
• Ability to work independently while contributing effectively in a multidisciplinary team environment.

At Takeda, our patients rely on us to deliver quality products. As a result, we must follow strict rules in our manufacturing facilities to ensure we are not endangering the quality of the product. In this role, you may:

• In general, the position requires a combination of sedentary work and walking around, observing the conditions of the facility.
• Must be able to lift, push, pull, and carry up to 50 lbs. without material…