Entry-Level Microbiologist — Second Shift, GMP/GLP

Eurofins; Lancaster (Lancaster County); On-site; USD 42,000 - 62,000; Full time

Benefits offered by this job

Medical, dental, vision coverage

401(k) with company match

Paid vacation and holidays

Life and disability insurance

Job summary

Eurofins USA BioPharma Services is seeking a Second Shift Laboratory Analyst in Lancaster, PA. The role focuses on performing analyses of bio/pharmaceutical ingredients and products, reviewing standards, and producing quality data consistent with GMP/GLP requirements.

The candidate will work with an experienced analyst, review data for accuracy, and ensure timely, reliable results for clients. Full-time, on-site schedule with potential overtime and travel as needed.

Qualifications

• Bachelor's degree in microbiology, biology, or related field.
• Experience or ability to work under GMP/GLP conditions.
• Strong attention to detail and accurate data handling.

Responsibilities

• Applies GMP/GLP in all areas of responsibility.
• Maintains quality and productivity standards.
• Demonstrates strong client service and effective written and oral communication.
• Meets quality metrics and works well in a team.
• Performs laboratory operations with accuracy and precision.
• Prepares reagents, samples, and standards according to procedures.
• Documents testing, observations, deviations and results in compliance with regulatory requirements.
• Reads and follows analytical procedures and SOPs.
• Uses MS Windows applications (Excel, Word, Outlook).
• Processes data, generates reports, and evaluates data.
• Maintains a clean and organized workspace; accepts overtime as needed.

Skills

GMP/GLP knowledge

Analytical thinking

Communication skills

Attention to detail

Teamwork

Education

Bachelor's degree in microbiology or related

Tools

Excel

Word

Outlook

Job description

Eurofins USA BioPharma Services is seeking a Second Shift Laboratory Analyst in Lancaster, PA. The role focuses on performing analyses of bio/pharmaceutical ingredients and products, reviewing standards, and producing quality data consistent with GMP/GLP requirements.

The candidate will work with an experienced analyst, review data for accuracy, and ensure timely, reliable results for clients. Full-time, on-site schedule with potential overtime and travel as needed.