GMP QC Analytical Scientist – Pharma Lab (Sanford, NC)

Eurofins

Sanford (NC)

On-site

USD 55,000 - 75,000

Full time

5 days ago
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Benefits offered by this job

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

Job summary

Eurofins USA is seeking a qualified analytical lab professional to perform routine and non-routine testing of pharmaceutical products and materials in a GMP-regulated laboratory in Sanford, NC. You will manage priorities, maintain instruments, and ensure accurate documentation while collaborating with Quality Operations and other teams.

The role requires a BS in Chemistry or Biochemistry with at least two years of lab experience, proficiency with analytical instruments (HPLC/UPLC, UV-VIS, pH,

Qualifications

  • BS in Chemistry or Biochemistry with a minimum of 2 years in a laboratory environment.
  • Experience with analytical standards, reagents and instruments used in GMP environments.
  • Hands-on analytical testing experience in a GMP (cGMP) setting.
  • Familiarity with UV-VIS, HPLC/UPLC, pH, osmolality, TOC and conductivity.

Responsibilities

  • Independently manage testing priorities and maintain analytical instrumentation.
  • Evaluate data for accuracy and compliance and document results thoroughly.
  • Collaborate with Quality Operations and other teams as needed.
  • Support investigations, CAPAs, inventory, and lab compliance while delivering quality results.
  • Create, review and approve GMP documentation (test records, methods, equipment records).

Skills

Analytical testing
GMP compliance
Data analysis
Pipetting
Multi-tasking
Self-motivated

Education

BS in Chemistry or Biochemistry

Tools

Empower 3
LIMS
HPLC/UPLC
UV-VIS
pH meters
TOC

Job description

Eurofins USA is seeking a qualified analytical lab professional to perform routine and non-routine testing of pharmaceutical products and materials in a GMP-regulated laboratory in Sanford, NC. You will manage priorities, maintain instruments, and ensure accurate documentation while collaborating with Quality Operations and other teams.

The role requires a BS in Chemistry or Biochemistry with at least two years of lab experience, proficiency with analytical instruments (HPLC/UPLC, UV-VIS, pH,

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