QCA Sampling Associate

Eurofins USA PSS Insourcing Solutions•Andover, MA

3d•Onsite

About The Position

Eurofins Scientific is an international life sciences company providing analytical testing services across multiple industries. Its laboratories help ensure the safety, authenticity, and accurate labeling of products, and its network includes 58,000 staff across 900 laboratories in more than 54 countries. The GMP Sampling Associate supports QC raw material sample operations in the warehouse and across multi-site laboratory environments. The role is responsible for testing, tracking, documenting, and coordinating samples to ensure accuracy, compliance, and timely availability for further processing. Work is performed in support of clinical and commercial manufacturing operations and in accordance with cGMP, quality procedures, and company safety policies.

Requirements

High school diploma, associate’s degree, and/or bachelor’s degree in chemistry or another science-related concentration.
0–2 years of relevant experience.
Ability to lift 50–100 pounds alone or with assistance daily.
Excellent attention to detail and ability to follow procedures to generate reproducible data in a controlled laboratory environment.
Excellent skills in Microsoft Office, data analysis software, and related applications.
Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies.
Critical thinking and troubleshooting/problem-solving skills.
Ability to work independently and as part of a team, with self-motivation, adaptability, and a positive attitude.
Authorization to work indefinitely in the United States without restriction or sponsorship.

Responsibilities

Perform raw material sampling in the GMP warehouse to support clinical and commercial manufacturing operations.
Perform daily sanitization of ISO-classified sampling areas.
Perform and review appearance, gas, and Raman spectroscopy testing on raw materials.
Participate in continuous improvement activities in sampling areas, identify improvement opportunities, and use site continuous improvement tools.
Plan and prioritize assignments to meet department and site goals.
Record and maintain related data and records in compliance with cGMP and quality procedures.
Perform work consistently with company safety policies and procedures.
Perform additional tasks as needed in the QC Analytical Department.