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Job Description

About the Role:

The Manufacturing Lead Operator executes processes in production while strictly following cGMP, environmental health and safety guidelines and any other related regulations which could apply. Under the overall direction of the supervisor, this person must aid in establishing daily shift priorities, and then communicate and delegate tasks to safely accomplish those priorities. They are expected to make Safety, Quality, and Production decisions. You can apply their subject matter expertise and their understanding of the capabilities and performance of their team members to quickly assess critical issues. You can escalate all relevant information and be prepared to recommend appropriate actions. They are expected to report all critical information to their respective teams and be able to communicate the appropriate shift-to-shift updates through all applicable communication tools and at shift handoffs. In addition to being accountable in production processes, you may help in other teams. They are expected to fully participate in both departmental projects and quality working teams. You will be a delegate to the supervisor and may conduct departmental activities in their absence. They understand the regulations and may make recommendations according to their interpretations. They have a high level of technical and administrative knowledge to perform complex troubleshooting tasks on manual and automated equipment, and they may assist during the transfer of new processes/methodologies into the manufacturing area. Manufacturing Lead Operators are expected to serve as a mentor and set the example for all team members since their team will interpret that behavior as acceptable. They must display the appropriate conduct, compliance, cleanliness, and culture while promoting Takeda's focus on Patient, Reputation, and Business

How you will contribute:

• Follow all safety rules, SOPs, cGMP, work rules and other company policies and initiatives.
• Complete relevant paperwork following GDP/GMP guidelines.
• Perform hands-on execution of manual and automated manufacturing operations. Equipment may include: Centrifuges, Filter Presses, Ultrafiltration, Tangential Flow Filtration and Nanofiltration systems, CIP/COP, Chromatography and material handling devices. Manual activities include weighing and addition of chemicals, paste suspension, equipment cleaning, room cleaning, equipment assembly/disassembly, transfer panel connections, titrations and other activities.
• Receive and distribute supplies into the production area as necessary.
• Perform removal of hazardous waste.
• Troubleshoot process problems and respond to process alarms.
• Act as the primary manufacturing personnel to resolve and communicate issues related to safety, quality, compliance and process to the supervisor. Main interface with other departments including maintenance, metrology, engineering and validation.
• Assist supervisor in organizing, scheduling, and directing other team members.
• May act as a delegate to the supervisor in their absence.
• Participate in the training and mentoring of team members on the manufacturing floor.
• Write, revise, and review manufacturing related documents as appropriate.
• Participate in Safety and Continuous Improvement Teams and may serve in a leadership role.
• Initiate and/or coordinate other process improvement projects.
• Drive performance of team members by promoting a positive work environment emphasizing Patient, Trust, Reputation, and Business.

What you bring to Takeda:

• High school diploma or GED. 6+ years of experien