QC Analytical Scientist - GMP Lab, Growth & Benefits

Eurofins; Sanford (NC); On-site; USD 52,000 - 75,000; 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 is seeking a qualified candidate for a GMP‑regulated analytical testing role in Sanford, NC. The position focuses on routine and non‑routine testing of pharmaceutical products and raw materials, with collaboration across QA Operations and production teams.

The role requires a BS in Chemistry or Biochemistry, hands‑on GMP experience, and proficiency with HPLC/UPLC, UV‑VIS, and analytical equipment. Join a comprehensive benefits program and contribute to safe, compliant laboratory

Qualifications

• BS in Chemistry or Biochemistry with at least 2 years in a laboratory
• Experience with analytical standards, reagents and lab instruments
• Hands-on analytical testing experience in a GMP/cGMP environment
• Ability to operate UV-VIS, HPLC/UPLC, pH, osmolality, TOC and conductivity
• Strong organizational skills and ability to multi-task
• Authorized to work in the United States indefinitely without sponsorship

Responsibilities

• Manage testing priorities and operate/maintain analytical instrumentation
• Collaborate with Quality Operations and cross-functional teams
• Support investigations, corrective actions, inventory management and compliance
• Create, review and approve GMP documentation (test records, validation protocols/reports, methods, equipment records)

Skills

Strong organizational skills

Self-motivated

Multi-tasking

Analytical data analysis

Accurate pipetting

Work authorization in US (no sponsor)

Education

Bachelor's degree in Chemistry or Biochemistry

Tools

Empower 3

LIMS

Job description

Eurofins is seeking a qualified candidate for a GMP‑regulated analytical testing role in Sanford, NC. The position focuses on routine and non‑routine testing of pharmaceutical products and raw materials, with collaboration across QA Operations and production teams.

The role requires a BS in Chemistry or Biochemistry, hands‑on GMP experience, and proficiency with HPLC/UPLC, UV‑VIS, and analytical equipment. Join a comprehensive benefits program and contribute to safe, compliant laboratory