Packaging Technician

Overview

Type: 6 month contract, possibility of extension or FTE

Schedule: 12 hour shifts, 2-2-3 schedule, Saturday-Sunday week (not Monday-Sunday)

Location: Research Triangle Park site (RTP)

The Manufacturing Technician/Operator will work in the RTP Packaging area, where Lilly autoinjector devices are assembled and packaged. Technician/Operator will be responsible for the safe operation of highly automated equipment producing products of the highest quality for Lilly patients.

• Adhere to RTP Plant safety policies and procedures, contribute to a safe work environment.
• Setup and operate highly automated equipment in the Packaging area.
• Adhere to standard operating procedures and current Good Manufacturing Practices to ensure quality of product.
• Document process steps on appropriate batch documentation (Electronic Ticket, SAP, Cleaning Logs, etc.).
• Attain and maintain qualification for the operation of assigned process equipment and duties in the area.
• Identify opportunities for operational improvements.
• Proactively monitor documentation and product quality, properly documenting all activities and reporting issues to supervision.
• Contribute to the achievement of key departmental objectives including improving safety performance, reducing deviations, improving productivity, and training compliance.
• Will 12-hour shift (2-2-3 schedule)
• Currently in the startup phase of operations. Candidate must be flexible and be willing to perform non-routine work, with Safety & Integrity in mind at all times.

• High School Diploma/GED required.

• Previous experience working in a GMP environment preferably in the pharmaceutical industry.
• Strong ability to multitask.
• Ability to demonstrate attention to detail.
• Ability to develop independence in performing daily tasks.
• Collaborative work ethic with a strong bias for action
• Demonstrated ability to train and coach others.
• Ability to effectively communicate (written and verbal)
• Flexibility and problem-solving skills
• Basic computer skills (desktop software) are required.
• 3+ years relevant experience in pharmaceutical, or equivalent regulated industry
• Knowledge of current Good Manufacturing Practices (CGMPs)
• Previous experience with Manufacturing Execution Systems and electronic batch release.
• Knowledge of lean manufacturing principles

• Ability to wear safety equipment (safety glasses, safety shoes, protective gloves etc.)