Pharma Analytics Scientist – GMP/HPLC Expert

Eurofins BioPharma Product Testing North America

Lancaster (Lancaster County)

On-site

USD 60,000 - 80,000

Full time

27 hours ago
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Benefits offered by this job

Excellent medical, dental, and vision
401(k) with company match
Paid vacation and holidays
Life and disability insurance

Job summary

Eurofins USA BioPharma Services is seeking an analytical chemist to perform physical, chemical, and instrumental analyses of APIs and finished products. You will run HPLC and related systems, prepare samples, and help validate new processes in a GMP environment.

Responsibilities include sample preparation, method transfers, documentation, and routine maintenance of lab equipment. The role is full-time, on-site in Lancaster, PA, with standard hours and occasional travel.

Qualifications

  • Must have authorization to work in the US indefinitely without sponsorship.
  • Bachelor's degree in chemistry or related field or equivalent experience.
  • Minimum 1–2 years GMP industry experience.
  • 1–2 years HPLC industry experience.

Responsibilities

  • Perform physical, chemical, and instrumental analysis of active pharmaceutical ingredients and finished pharmaceutical products.
  • Run instrumentation independently including various chromatographic systems and related techniques.
  • Prepare samples for analysis and run instrumentation with minimal supervision.
  • Set up and validate new analytical or related processes used by the department.
  • Prepare standards and samples for analysis.
  • Execute method transfer protocols.
  • Document work for GMP compliance.
  • Perform monthly maintenance of laboratory equipment.

Skills

GMP experience
HPLC experience

Education

Bachelor's degree in chemistry or related field

Tools

HPLC

Job description

Eurofins USA BioPharma Services is seeking an analytical chemist to perform physical, chemical, and instrumental analyses of APIs and finished products. You will run HPLC and related systems, prepare samples, and help validate new processes in a GMP environment.

Responsibilities include sample preparation, method transfers, documentation, and routine maintenance of lab equipment. The role is full-time, on-site in Lancaster, PA, with standard hours and occasional travel.

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