Entry-Level Analytical Scientist – Pharma QC

Eurofins; Lancaster (AZ); On-site; USD 42,000 - 56,000; 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 in Lancaster, PA, is seeking an entry-level analyst to perform analytical testing on active pharmaceutical ingredients and finished products. You will run chromatography systems, prepare samples, and help validate processes with minimal supervision.

The role emphasizes accuracy, teamwork, and adherence to GMP. Full-time, Monday–Friday, 8:00 a.m.–5:00 p.m., with benefits and opportunities for growth within a global life sciences company.

Qualifications

• Bachelor's degree in chemistry or related field.
• Authorization to work in the United States without sponsorship.
• Ability to work independently and as part of a team.
• Strong attention to detail and excellent communication.

Responsibilities

• Perform physical, chemical, and instrumental analysis of active pharmaceutical ingredients and finished pharmaceutical products.
• Run the instrumentation independently including various chromatographic systems.
• 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 as required for GMP compliance.
• Perform monthly maintenance of laboratory equipment.

Skills

Strong computer skills

Excellent communication

Attention to detail

Teamwork

Self-motivation

Adaptability

Learning agility

Education

Bachelor's degree in chemistry

Tools

Chromatography systems

Job description

Eurofins USA BioPharma Services in Lancaster, PA, is seeking an entry-level analyst to perform analytical testing on active pharmaceutical ingredients and finished products. You will run chromatography systems, prepare samples, and help validate processes with minimal supervision.

The role emphasizes accuracy, teamwork, and adherence to GMP. Full-time, Monday–Friday, 8:00 a.m.–5:00 p.m., with benefits and opportunities for growth within a global life sciences company.