Process Technician - Manufacturing Support​/Material Prep; Night Shift

Role Summary

Process Technician – Manufacturing Support/Material Prep (Night Shift). Role supports filling, dispensing, and formulation processes by performing material preparation and executing daily tasks as directed by the shift lead or supervisor.

Location:

Lilly Research Triangle Park (RTP). Night shift schedule: 1800–0630 (2-2-3).

• Execute daily operational tasks defined by the shift lead/supervisor.
• Focus on material preparation activities to support filling/dispensing/formulation processes.
• Adhere to plant safety policies and procedures to contribute to a safe work environment.
• Adhere to standard operating procedures and current Good Manufacturing Practices to ensure product quality.
• Document process steps on appropriate batch documentation (Electronic Ticket, SAP, Cleaning Logs, etc.).
• Attain and maintain qualification for operation of assigned process equipment and duties in the area.
• Identify opportunities for operational improvements.
• Proactively monitor documentation and product quality, documenting activities and reporting issues to supervision.
• Contribute to departmental objectives including improved safety, reduced deviations, increased productivity, and training compliance.
• Be willing to work 12-hour shifts (2-2-3 schedule) and perform non-routine work with Safety & Integrity in mind.
• Assist in checking execution documentation (PMX, SAP, Cleaning Logs, etc.).

• Required:
  
  Ability to gown and work in controlled classified areas (Grade C and Grade
  
  D).
• Required:
  
  legally authorized to work in the United States (no visa sponsorship expected).
• Required:
  
  Must pass a fitness for duty physical exam.
• Required:
  
  Availability to work 12-hour night shifts on a 2-2-3 schedule with overtime as needed.

• Preferred:
  Effective written and verbal communication.
• Preferred:
  Flexibility and problem-solving skills.
• Preferred:
  Basic digital literacy (desktop software).
• Preferred:
  Knowledge of current Good Manufacturing Practices (CGMPs).
• Preferred:
  Previous experience in operations/pharmaceutical industry.
• Preferred:
  Previous experience in a Grade C environment.
• Preferred:
  Knowledge of lean manufacturing principles.

• High School Diploma or equivalent.
• Bio Work Certification (preferred).