Evening Laboratory Team Lead - Microbiology & Chemistry

Aurora Lifesciences

Yorkshire, Northern (VA, KY)

Hybrid

USD 85,000 - 110,000

Full time

14 days+
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Benefits offered by this job

15% Shift Allowance
10% Bonus
36 Days Total Annual Leave
Annual Salary Review up to 5%
Private Healthcare

Job summary

Aurora Lifesciences is seeking an experienced Laboratory Team Leader to oversee an evening laboratory team supporting regulated medical device operations. You will balance people leadership with hands-on technical work.

You’ll supervise testing across microbiology, chemistry and quality, coach analysts, review data for trends and deviations, and ensure compliance with ISO 13485 and cGMP standards while driving continuous improvement.

Qualifications

  • Degree in a scientific discipline with relevant regulated lab experience.
  • Minimum 3 years of supervisory or team leadership experience.
  • Experience in microbiology and chemistry within regulated environments (medical devices/pharma).

Responsibilities

  • Lead daily lab activities across microbiology, chemistry and quality.
  • Coach analysts and build team capability.
  • Act as SME for lab operations and provide technical leadership.
  • Oversee testing, environmental monitoring and analytical work.
  • Review data for trends, non-conformances and improvements.
  • Support method development, qualification, validation and transfer.
  • Ensure calibration, maintenance and qualification of equipment.

Skills

People supervision
Microbiology knowledge
Chemistry knowledge
Quality systems
Data analysis & reporting
Cross-functional collaboration
Technical leadership

Education

Bachelor's degree in Chemistry/Biology/Biochemistry/Microbiology

Job description

Aurora Lifesciences is seeking an experienced Laboratory Team Leader to oversee an evening laboratory team supporting regulated medical device operations. You will balance people leadership with hands-on technical work.

You’ll supervise testing across microbiology, chemistry and quality, coach analysts, review data for trends and deviations, and ensure compliance with ISO 13485 and cGMP standards while driving continuous improvement.

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