Medical Device Line Supervisor - Lead, Lean & Quality

Biomerics; Athens (TX); Hybrid; USD 60,000 - 90,000; Full time

Benefits offered by this job

Medical Insurance

Dental Insurance

Vision Insurance

Short-Term Disability

Long-Term Disability

Life Insurance

Paid Vacation Days

Paid Holidays

401k

Job summary

Biomerics is seeking a Line Supervisor to provide hands-on leadership to MF Operators, Floaters, and Lead Operators across shifts. The role ensures safety, quality, delivery, and production goals are met while overseeing day-to-day operations.

You will drive process improvements, support hiring and onboarding, and collaborate with Engineering and Quality to resolve production issues and implement corrective actions. Strong leadership and GMP familiarity are essential.

Qualifications

• 2+ years of supervisory experience in a manufacturing or medical device environment.
• 4–6 years of hands-on operational, technical, or quality experience preferred.
• Strong leadership, communication, and conflict resolution skills.
• Working knowledge of lean manufacturing tools and ISO 13485 QMS standards.

Responsibilities

• Lead and supervise daily production operations, ensuring adherence to work instructions and delivery schedules.
• Provide coaching, performance feedback, and development support for operators and leads; conduct reviews and merit recommendations.
• Ensure staffing and crew scheduling to meet production demands across centers.
• Monitor KPIs such as safety, yield, labor efficiency, scrap, and delivery performance; take corrective actions.

Skills

Leadership

Communication

Conflict resolution

Decision making

Time management

Education

High School Diploma or GED

Associate degree or technical certification

Tools

ERP

Data tracking systems

Microsoft Office

Job description

Biomerics is seeking a Line Supervisor to provide hands-on leadership to MF Operators, Floaters, and Lead Operators across shifts. The role ensures safety, quality, delivery, and production goals are met while overseeing day-to-day operations.

You will drive process improvements, support hiring and onboarding, and collaborate with Engineering and Quality to resolve production issues and implement corrective actions. Strong leadership and GMP familiarity are essential.