Manufacturing Supervisor — Cassette Production & Ops Lead

DiaSorin S.p.A.; Austin (TX); On-site; USD 70,000 - 117,000; Full time

Benefits offered by this job

Health benefits

Retirement plan

Annual incentive program

Job summary

DiaSorin is seeking a Manufacturing Supervisor to oversee consumables manufacturing staff, ensuring facilities, equipment, and documentation meet plans and cGMP/QSR requirements. You will coordinate manual, semi-automation and automation processes for cassette manufacture and testing.

The role requires 1+ year manufacturing experience in FDA-regulated environments, an engineering-related degree, and strong cross-functional collaboration with Engineering, R&D, QA and Production Control.

Qualifications

• Associate's Degree in engineering or related field required or Bachelor's degree preferred.
• 1+ years relevant manufacturing experience with an Associate Degree.
• Experience in an FDA-regulated industry and/or ISO-certified organization preferred.

Responsibilities

• Ensure resources are in place to deliver cassettes per plan.
• Schedule and manage Direct Labor to meet the plan.
• Monitor operational efficiencies, labor costs and BOM management.
• Train headcount on required procedures.
• Develop Training and Development Plans for all employees.
• Ensure compliance with cGMP and QSR requirements.
• Collaborate cross-functionally with Engineering, R&D, Production Control, QA and Manufacturing Engineering.

Skills

Direct labor scheduling

cGMP compliance

QSR compliance

SPC data analysis

Cross-functional collaboration

Education

Associate's Degree in engineering or related field

Bachelor's Degree in engineering or related field preferred

Tools

Bill of Materials management

Labor cost tracking tools

Job description

DiaSorin is seeking a Manufacturing Supervisor to oversee consumables manufacturing staff, ensuring facilities, equipment, and documentation meet plans and cGMP/QSR requirements. You will coordinate manual, semi-automation and automation processes for cassette manufacture and testing.

The role requires 1+ year manufacturing experience in FDA-regulated environments, an engineering-related degree, and strong cross-functional collaboration with Engineering, R&D, QA and Production Control.