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Manufacturing Process Technician - Device Assembly (Night Shift)

Eli Lilly and Company

Durham (NC)

On-site

USD 60,000 - 80,000

Full time

30+ days ago

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Job summary

Join a forward-thinking company that is dedicated to improving lives through innovative healthcare solutions. As a Manufacturing Operator, you will play a crucial role in assembling devices that deliver life-changing medicines to patients worldwide. This position offers the chance to work in a state-of-the-art facility that emphasizes safety and quality while utilizing advanced manufacturing technologies. If you are passionate about making a difference and thrive in a collaborative environment, this is the perfect opportunity for you to contribute to meaningful advancements in healthcare.

Qualifications

  • High School Diploma/GED required for all candidates.
  • Experience in a GMP environment is preferred.

Responsibilities

  • Operate highly automated equipment in the Device Assembly area.
  • Document process steps and maintain product quality.

Skills

Attention to Detail
Multitasking
Collaboration
Operational Improvement

Education

High School Diploma/GED

Tools

SAP
Electronic Ticket

Job description

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.

Organization Overview:

For 140 years, Lilly has manufactured medicines that improve people’s lives around the world. We produce our medicines using some of the most sophisticated manufacturing technologies and rigorous quality standards. Lilly Manufacturing strives for excellence in its process, standards, procedures, and behaviors to develop medicines with safety first and quality always. Lilly is designing and building a new Parenteral, Device Assembly, and Packaging Facility in Raleigh-Durham, North Carolina. This is an exciting opportunity to help build a state-of-the-art, paper-less, highly automated facility, and Quality System from the ground up with a mission to produce safe and highest quality medicine. The Manufacturing Operator will be a part of Device Assembly team, where Lilly autoinjector devices are assembled. Operators will be responsible for the safe operation of highly automated equipment producing products of the highest quality serving Lilly patients worldwide.

Responsibilities:

  1. Adhere to RTP Plant safety policies and procedures, contribute to a safe work environment.
  2. Setup and operate highly automated equipment in the Device Assembly area.
  3. Adhere to standard operating procedures and current Good Manufacturing Practices to ensure quality of product.
  4. Document process steps on appropriate batch documentation (Electronic Ticket, SAP, Cleaning Logs, etc.).
  5. Attain and maintain qualification for the operation of assigned process equipment and duties in the area.
  6. Identify opportunities for operational improvements.
  7. Proactively monitor documentation and product quality, properly documenting all activities and reporting issues to supervision.
  8. Contribute to the achievement of key departmental objectives including improving safety performance, reducing deviations, improving productivity, and training compliance.

Basic Requirements:

  1. High School Diploma/GED required.
  2. Completion of Post Offer Exam or Completion of Work Simulation if applicable.
  3. Qualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H1B or TN status) for this employment position.

Additional Preferences:

  1. Collaborative work ethic with a strong bias for action.
  2. Previous experience working in a GMP environment preferably in the pharmaceutical industry.
  3. Strong ability to multitask.
  4. Ability to demonstrate attention to detail.
  5. Ability to develop independence in performing daily tasks.
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