Bio/Pharma Lab Technician - 2nd or 3rd Shift (Full-Time)

Eurofins-USA-Medical-Device

Lancaster (Lancaster County)

On-site

USD 55,000 - 75,000

Full time

13 hours ago
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Benefits offered by this job

Excellent full-time benefits (medical,
Dental and vision options
Life and disability insurance
401(k) with company match
Paid vacation and holidays

Job summary

Eurofins USA Medical Devices in Lancaster, PA, is seeking a Lab Analyst with a Bachelor’s degree in microbiology, biology, biochemistry, or related field to join our bio/pharmaceutical analyses team. The role emphasizes GMP/GLP compliance and data accuracy, working on 2nd or 3rd shift with potential overtime.

Responsibilities include preparing samples, running equipment, and generating clear reports while ensuring quality and client satisfaction.

Qualifications

  • Bachelor's degree in microbiology, biology, biochemistry, or related field.
  • Authorized to work in the US indefinitely without sponsorship.
  • Med device experience is a plus.

Responsibilities

  • Applies GMP/GLP in all areas of responsibility.
  • Maintains high quality standards in all tasks.
  • Demonstrates strong client service, teamwork and collaboration.
  • Performs laboratory operations with accuracy and precision.
  • Prepare reagents, samples and standards per procedures.
  • Document testing, observations and results in compliance with regulations.
  • Read and follow analytical procedures and SOPs.
  • Use Excel, Word and Outlook for reporting.
  • Communicate effectively, both orally and in writing.
  • Commit to occasional overtime when workload requires.

Skills

Client service
Teamwork
Multitasking
Communication skills
Safety compliance

Education

Bachelor's degree in microbiology, biology, biochemistry, or related degree concentration

Tools

Excel
Word
Outlook
MS Windows

Job description

Eurofins USA Medical Devices in Lancaster, PA, is seeking a Lab Analyst with a Bachelor’s degree in microbiology, biology, biochemistry, or related field to join our bio/pharmaceutical analyses team. The role emphasizes GMP/GLP compliance and data accuracy, working on 2nd or 3rd shift with potential overtime.

Responsibilities include preparing samples, running equipment, and generating clear reports while ensuring quality and client satisfaction.

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