Lead Operator - Aseptic Filling (Night Shift)
BioSpace · Concord, NC · Today
Management$25.96–$38.08/hrFull-time
Company Overview
Lilly is a 140+ year strong global healthcare leader headquartered in Indianapolis, Indiana with manufacturing sites throughout the US, EU, and Asia. Our 35,000 employees 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.
Responsibilities
- Support start up activities required to bring the aseptic isolator barrier filling area into service.
- Become the experts within your assigned area and educate your team in the proper operation of the facility.
- Lead the training of new staff after the project phase is complete.
- Ensure continuous supply of medicines by expertly running the process, troubleshooting, and collaborating cross-functionally.
- Coordinate daily activities to meet capacity plans while developing your own and our team’s capabilities.
- Lead the site and be a technical leader for operations.
Qualifications/Requirements
- 5+ years of experience working with automated equipment in a GMP/cleanroom environment.
- Leadership experience and the ability to train / educate team members.
- Minimum education: High School Diploma or GED.
- Ability to effectively communicate (electronically, written and verbal).
- Flexibility - the ability to troubleshoot and triage challenges.
- Computer proficiency (desktop software, MS office).
Respect for People
- Support Site Leadership to build a diverse and capable site organization by delivering area operational procedures, quality processes and controls for the PAR areas.
- Assist Supervisor in development and performance evaluations of shift operators.
- Act as backup for Supervisor.
- Key liaison between operations and support functions.
Additional Preferences
- STEM degree or certification.
- Knowledge of aseptic filling, single use assemblies, isolator technology.
- Automated, semi-automated, and/or manual inspection experience.
- Knowledge of current Good Manufacturing Practices (cGMPs).
- Experience in operations or manufacturing environments.
- Pharmaceutical, medical device or food processing industries.
- Manufacturing Execution Systems and electronic batch release.
- Continuous improvement (Lean, Six Sigma methodologies).
- Highly automated equipment (inspection, packaging, filling, assembly, etc.).
- SAP, Electronic Batch Records.