Lead Process Technician

Thermo Fisher Scientific • Florence, SC

105d

About The Position

Be a Lead Process Technician at Thermo Fisher Scientific Inc., ensuring flawless operations and promoting collaboration in a dynamic setting.

Requirements

• High school diploma or equivalent experience.
• Minimum of 3-5 years' Process Technician experience working in the pharmaceutical industry.
• Successful completion of Phases I-IV of the Process Tech On-The-Job Training Program/process involving learning/applying Chemical Technology, Math, and Chemistry.
• Strong mechanical competence.

Nice To Haves

• Good understanding of basic equipment.
• Strong problem-solving skills and logical approach to problem-solving.
• Demonstrated interpersonal and communication skills for team collaboration.
• Capability to interpret technical procedures and governmental regulations.
• Proficiency in applying basic mathematical principles.

Responsibilities

• Ensure day-to-day manufacturing operations and activities are completed safely, compliantly, and in accordance with all applicable regulatory agency (e.g., FDA, OSHA) requirements and Company policies and procedures.
• Direct the workforce to meet production goals and process requirements.
• Schedule, control, and prioritize daily work assignments.
• Manage day-to-day workflow for a team of up to 8 Process Technicians.
• Resolve emergent issues, including troubleshooting process, equipment, and system malfunctions or failures on a 24-hour/7-day basis.
• Provide feedback to the Supervisor on work-related issues and employee performance appraisals.
• Ensure housekeeping and Asset Life Cycle Management responsibilities are maintained in assigned areas.
• Initiate and approve work orders when needed.
• Schedule maintenance activities around the production schedule to ensure cost-effectiveness.
• Write, develop, implement, and train employees on department SOPs.
• Suggest continuous improvement activities within LSM operations and assist with implementation.
• Enter Incident Reports, variance, and associated CAPAs.
• When needed, complete assigned CAPAs, start discrepancies, and aid in subsequent investigations.
• Coordinate, record, and uphold the Company's Quality Systems conformity to regulations and company policies as needed using the Company's Quality System tools and direct actions.

Benefits

• Standard work schedule (Mon-Fri)
• Ability to lift 40 lbs. without assistance
• Adherence to all Good Manufacturing Practices (GMP) Safety Standards
• Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
• Standing for full shift

What This Job Offers

• Job Type: Full-time
• Industry: Computer and Electronic Product Manufacturing
• Education Level: High school or GED