GMP Sampling Associate – QC Raw Materials

Eurofins

Andover (MA)

On-site

USD 52,000 - 68,000

Full time

41 hours ago
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Benefits offered by this job

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

Job summary

Eurofins is seeking a detail-oriented GMP Sampling Associate to support QC raw material sampling in the warehouse and across multi-site laboratory environments. This role tests, tracks, documents, and coordinates samples to ensure accuracy, compliance, and timely availability for processing.

The position requires lifting 50–100 pounds, familiarity with cGMP and quality procedures, and proficiency with Microsoft Office and data analysis tools.

Qualifications

  • High School diploma or higher in science
  • 0–2 years of relevant experience
  • Ability to lift 50–100 pounds daily
  • Attention to detail and reproducible data in a controlled lab
  • Proficient with Microsoft Office and data analysis tools
  • Ability to work independently and in a team
  • US work authorization without sponsorship

Responsibilities

  • Perform Raw Material Sampling in GMP warehouse to support manufacturing operations
  • Daily sanitization of ISO classified sampling areas
  • Perform and review testing on raw materials (appearance, gas, Raman)
  • Contribute to continuous improvement in sampling areas
  • Plan and prioritize assignments to meet department goals
  • Record and maintain data per cGMP and QA procedures
  • Follow safety policies and perform additional QC tasks as needed

Skills

Attention to detail
Analytical thinking
Follow procedures
Teamwork

Education

High School diploma
Associates or Bachelors in chemistry/related science

Tools

Microsoft Office
Data analysis software

Job description

Eurofins is seeking a detail-oriented GMP Sampling Associate to support QC raw material sampling in the warehouse and across multi-site laboratory environments. This role tests, tracks, documents, and coordinates samples to ensure accuracy, compliance, and timely availability for processing.

The position requires lifting 50–100 pounds, familiarity with cGMP and quality procedures, and proficiency with Microsoft Office and data analysis tools.

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