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Manufacturing Operator (Device Assembly, Day Shift)
Company | BioSpace |
Address | Durham, NC, United States |
Employment type | FULL_TIME |
Salary | |
Category | Internet News |
Expires | 2023-06-05 |
Posted at | 1 year ago |
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 35,000 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
Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and help our company develop talented individuals for future leadership roles. Our current groups include: Africa, Middle East, Central Asia Network, African American Network, Chinese Culture Network, Early Career Professionals, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinos at Lilly, PRIDE (LGBTQ + Allies), Veterans Leadership Network, Women’s Network, Working and Living with Disabilities. Learn more about all of our groups.
#WeAreLilly
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
- Identify opportunities for operational improvements.
- Attain and maintain qualification for the operation of assigned process equipment and duties in the area.
- Contribute to the achievement of key departmental objectives including improving safety performance, reducing deviations, improving productivity, and training compliance.
- Document process steps on appropriate batch documentation (Electronic Ticket, SAP, Cleaning Logs, etc.).
- Adhere to standard operating procedures and current Good Manufacturing Practices to ensure quality of product.
- Proactively monitor documentation and product quality, properly documenting all activities and reporting issues to supervision.
- Setup and operate highly automated equipment in the Device Assembly area.
- Adhere to RTP Plant safety policies and procedures, contribute to a safe work environment.
- Completion of Post Offer Exam or Completion of Work Simulation if applicable.
- 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., H-1B or TN status) for this employment position.
- High School Diploma/GED required
- Previous experience working in a GMP environment preferably in the pharmaceutical industry
- Strong ability to multitask
- Collaborative work ethic with a strong bias for action.
- Ability to demonstrate attention to detail
- Ability to develop independence in performing daily tasks.
Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and help our company develop talented individuals for future leadership roles. Our current groups include: Africa, Middle East, Central Asia Network, African American Network, Chinese Culture Network, Early Career Professionals, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinos at Lilly, PRIDE (LGBTQ + Allies), Veterans Leadership Network, Women’s Network, Working and Living with Disabilities. Learn more about all of our groups.
#WeAreLilly
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