QCA Sampling Associate

Eurofins•Andover, MA

6h•$22 - $26

About The Position

Eurofins Scientific is an international life sciences company providing analytical testing services across multiple industries. The QCA Sampling Associate supports QC raw material sample operations in the warehouse and across multi-site laboratory environments. The role is responsible for testing, tracking, documentation, and coordination of samples to ensure accuracy, compliance, and timely availability for further processing. The position includes raw material sampling in a GMP warehouse, sanitizing ISO-classified sampling areas, and performing and reviewing appearance, gas, and Raman spectroscopy testing on raw materials. The associate also contributes to continuous improvement, plans work to meet department and site goals, maintains records in accordance with cGMP and quality procedures, follows safety policies, and performs additional tasks in the QC Analytical Department as needed. This is a full-time position, Monday through Friday, 8:00 a.m. to 5:00 p.m., with overtime as needed. Candidates living within commuting distance of Andover, Massachusetts, are encouraged to apply. Compensation is $22–$26 per hour.

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.
Ability to think critically and demonstrate troubleshooting and problem-solving skills.
Ability to work independently and as part of a team, with self-motivation, adaptability, and a positive attitude.
Authorization to work in the United States indefinitely 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 within 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.