Jeremy Fields

As a Lead Inspector am responsible for the in-process and Finish good activities at Legacy. The Quality Control Inspector must comply with all regulatory cGMP guidelines and Legacy Pharmaceutical Packaging standards and policies.

Promote and enforce cGMP and SOP compliance in an FDA regulated pharmaceutical manufacturing environment. Perform and document in-process and finish good inspections of product material. Perform and document line clearance of production room cleans. Perform daily review of in-process packaging batch records. Provide support to and coordinate with other departments to ensure product integrity.

The Lead oversees the activities of packaging rooms to ensure the safety,quality and throughput are maximized. As the Lead Operator i must comply with all regulatory/ cGMP guidelines and Legacy Pharmaceutical Packaging standards and polices.

Communicate with each stakeholder with respect and dignity. Demonstrate dependability and commitment to the organization and team by maintaining an acceptable attendance record. Work with team members to identify potential hazards or safety risk to employees and report them to shift supervisor. Coach and train assigned team members on the shift.

Machine operator operates packaging equipment to ensure that safety, quality output are optimized. The machine operator shall fully comply with all regulatory / cGMP guidelines and Legacy Pharmaceutical Packaging standards and polices.

Responsible for the start-up, operation, and shutdown of all packaging line equipment. Maintain and optimize existing packaging equipment to meet quality and customer exceptions. Perform changeover task on packaging equipment. Ensure packaging line equipment is kept clean and that housekeeping in the area is maintained at an acceptable standard. Works with a sense of urgency and pays attention to details to minimize errors and achieve the goals and objectives of the organization