Analytical Chemist I – GMP Pharma (HPLC) | Lancaster, PA

Eurofins; Lancaster (Lancaster County); On-site; USD 65,000 - 85,000; Full time

Benefits offered by this job

Medical coverage

Dental coverage

Vision coverage

Life insurance

Disability insurance

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins USA BioPharma Services is seeking a chemistry-focused analyst to perform chromatographic testing and method transfer in a GMP environment. The role requires a Bachelor's degree in chemistry or related field and 1–2 years of pharmaceutical experience, with HPLC and validation experience.

The position is full-time, on-site in Lancaster, PA, with potential travel to client sites. Excellent benefits are offered, including medical and retirement plans.

Qualifications

• Excellent communication (oral and written) and attention to detail.
• Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude.
• Experience in cGMP environments is preferred.
• HPLC and validation experience is required.

Responsibilities

• Perform various types of testing using chromatographic systems including HPLC and related instruments.
• Execute specialized analyses and method transfer and feasibility testing.
• Document work as required for GMP compliance.
• Perform tests accurately and troubleshoot method and instrumentation problems.
• Use office and instrumentation-specific computer software.
• Produce written reports (e.g., SOP, OMC, client reports).
• Develop and execute validation plans.
• Carry out method transfers and feasibility studies.
• Train technical staff.
• Some travel to client sites for technical meetings could be required.

Skills

Excellent communication

Attention to detail

Independent work

Self-motivation

Education

Bachelor's degree in chemistry/analytical chemistry/biochemistry

Tools

HPLC

Job description

Eurofins USA BioPharma Services is seeking a chemistry-focused analyst to perform chromatographic testing and method transfer in a GMP environment. The role requires a Bachelor's degree in chemistry or related field and 1–2 years of pharmaceutical experience, with HPLC and validation experience.

The position is full-time, on-site in Lancaster, PA, with potential travel to client sites. Excellent benefits are offered, including medical and retirement plans.