Job Description

OBJECTIVES / PURPOSE OF JOB

Perform assembly, subassembly, and packaging functions in accordance to product specifications and standards. Meet productivity and quality standards on a consistent basis.

LOCATION: Clearwater, FL

SHIFT: 6:45 PM - 6:45 AM EST

KEY ACTIVITIES / RESPONSIBILITIES

• Performs various lens fabrication and inspections duties to include lens molding, machining, lens polishing, finished production inspections and primary packaging.

• Function as a member of a high-performance team and rotate routinely to all positions related to Manufacturing. Maintain acceptable productivity levels. Team member's success will be measured by the overall team's effectiveness.

• Ensure product meets all acceptable criteria per SOP's. Follow all regulatory guidelines and regulations regarding traceability, and safety procedures.

• Alert supervision of any equipment out of calibration.

• Support Team's Improvement activities with ideas and feedback as well as assist in troubleshooting of defect causes and problems and routinely review process issues with leadership and aid in Root cause analysis.

• Report unusual conditions and problems to Team Leader.

• Follow the practice of good housekeeping.

• In addition to the listed duties, the associate is expected to perform other similar related duties as assigned.

• Other Duties and responsibilities include: performing job responsibilities to the best of an individual's abilities and at the required skill levels; knowing and observing B&L work /safety rules, policies and SOPs; protecting B&L assets and treating fellow employees with dignity and respect in accordance with the principles of Affirmative Action, Equal Employment Opportunity and a working environment free from harassment

QUALIFICATIONS / TRAINING

Desired Education:

• High school diploma or general education degree (GED) preferred. Proficient in math and reading.

Desired Experience:

• Previous manufacturing in assembly, subassembly, packaging of small parts.

• One or more years manufacturing related work experience; or equivalent combination of education and experience.

• Knowledge of regulatory requirements for medical device or pharmaceutical industry.

• Clean room experience and knowledge specific to proper clean room behavior

• Previous overnight shift work

You should be proficient in:

• Experience in a Manufacturing Environment

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