Supervisor, Manufacturing 3rd Shift Packaging Dept.

Bausch + Lomb•US-SC-Greenville, SC

7d•Onsite

About The Position

Bausch + Lomb is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world. Our mission is to help you see better, to live better. We have a significant global research, development, manufacturing and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries. This position's objective is to supervise and hire employees who are responsible for observing, operating, and troubleshooting equipment in the Packaging/Accessories departments to ensure the manufacture of quality products to meet standard production quantities or better. This includes the primary, secondary, and tertiary packaging of sterile ophthalmic solutions. In some cases, this position may supervise multiple shifts within the same department.

Requirements

2-5 years of manufacturing experience in a regulated industry with automated packaging experience highly preferred.
Advance problem solving such as Six Sigma and Lean Training.
BS or BA degree, preferred
Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

Nice To Haves

Automated packaging experience highly preferred.

Responsibilities

Provide strong leadership with a focus on creating/maintaining a positive work environment.
Effective communication.
Effective performance management.
Establish department metrics and sustainability.
Review time and attendance for all department employees.
Manage staffing levels and budget spending.
Analyze product efficiencies, downtime and component waste.
Lead cross-functional teams to improve results.
Maintain safety within the department and employees.
Ensure all employees are current with their training.
Ensure that all SOPs and forms are current with process.
Maintain GMP (Good Manufacturing Practices) and GDP (Good Documentation Practices) in the department.
Write investigations and CAPA actions for non-conformances in the department.
Work with QA to quickly resolve any variance or document errors.