Microbiology Lab Supervisor – 2nd Shift & Benefits

Eurofins; Centennial (CO); On-site; USD 65,000 - 85,000; Full time

Benefits offered by this job

Medical, dental, and vision benefits

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins USA Clinical Diagnostics is seeking a Laboratory Supervisor to lead a microbiology-focused department, ensuring GMP compliance and high-quality patient results. The role involves training staff, coordinating schedules, and driving process improvements to meet client expectations and company objectives.

The LS will review test results for accuracy, support QA investigations, and oversee data trending and reporting while maintaining regulatory adherence and staff competency under the

Qualifications

• 4 years of microbiology experience.
• Bachelor’s Degree in a relevant science field.
• Knowledge of CAP/CLIA and FDA regulations.
• Strong communication and leadership skills.
• Ability to interpret regulations and apply them.

Responsibilities

• Supervise the day-to-day operation of the department.
• Schedule staff to meet production schedules.
• Counsels staff regarding problems encountered in daily operations.
• Works with Quality Assurance to resolve client complaints by investigating problems, developing solutions and making recommendations to management.
• Identifies process improvements to better meet client expectations and company objectives.
• Oversees the monitoring of inventory/ordering by establishing par levels and restocking points for supplies and reagents.
• Performs timely generation of Phase I Out of Specification (OOS) Investigative Reports.
• Tracking and trending of department data.

Skills

Microbiology

Team leadership

Regulatory compliance

Communication skills

Problem solving

Education

Bachelor’s degree in a chemical, physical, biological science or clinical laboratory science

Job description

Eurofins USA Clinical Diagnostics is seeking a Laboratory Supervisor to lead a microbiology-focused department, ensuring GMP compliance and high-quality patient results. The role involves training staff, coordinating schedules, and driving process improvements to meet client expectations and company objectives.

The LS will review test results for accuracy, support QA investigations, and oversee data trending and reporting while maintaining regulatory adherence and staff competency under the