What are the responsibilities and job description for the Packaging technician position at Lilly?
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana.
Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism.
We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world.
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.
Responsibilities :
- 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 begin as an 8hr shift with high likelihood to transition to work 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.
Basic Requirements :
High School Diploma / GED required.
Additional Skills / Preferences :
- Previous experience working in a GMP environment preferably in the pharmaceutical industry.
- Strong ability to multitask.
- 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
Additional Information :
- Ability to wear safety equipment (safety glasses, safety shoes, protective gloves etc.)
- Ability to work overtime as required.
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Last updated : 2024-09-10