Entry-Level Pharma Product Testing Scientist

null; Lancaster (Lancaster County); On-site; USD 42,000 - 58,000; Full time

Benefits offered by this job

Comprehensive medical coverage, dental

Vision options

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins USA BioPharma Services in Lancaster, PA is seeking an Entry Level Scientist to perform physical, chemical, and instrumental analysis of active pharmaceutical ingredients and finished products. The role requires a Bachelor's degree in chemistry or related field and US work authorization; hours are 7AM-3PM or 3PM-11PM, Monday to Friday, with full-time benefits.

You will operate instruments like HPLC, UV, Karl Fischer, and other methods, contributing to GMP-compliant documentation and

Qualifications

• Bachelor's degree in chemistry or related field.
• Authorization to work in the United States indefinitely without sponsorship.

Responsibilities

• Perform physical, chemical, and instrumental analysis of active pharmaceutical ingredients and finished products.
• Operate and maintain instruments such as HPLC, UV/Vis, Karl Fischer, and dissolution apparatus.
• Prepare samples and run analyses with minimal supervision.
• Set up and validate new analytical processes used by the department.
• Document work for GMP compliance and assist with method transfers.
• Perform monthly maintenance of laboratory equipment.

Skills

Analytical chemistry

Instrument operation

Laboratory safety

Education

Bachelor's degree in chemistry

Tools

HPLC

Karl Fischer

UV-Vis

ICP

IR

TLC

Job description

Eurofins USA BioPharma Services in Lancaster, PA is seeking an Entry Level Scientist to perform physical, chemical, and instrumental analysis of active pharmaceutical ingredients and finished products. The role requires a Bachelor's degree in chemistry or related field and US work authorization; hours are 7AM-3PM or 3PM-11PM, Monday to Friday, with full-time benefits.

You will operate instruments like HPLC, UV, Karl Fischer, and other methods, contributing to GMP-compliant documentation and