Eurofins: QCA Sampling Associate — Andover, MA, United States

About Eurofins

Eurofins provides analytical testing and laboratory services across life sciences and other industries. Its work includes assessing food, water, pharmaceutical and cosmetic products for qualities such as safety, authenticity, composition and accurate labelling. The employer also describes activities in genomics, clinical-study support, biopharmaceutical development and manufacturing, and diagnostic testing. Scientific methods and dependable information are central to this business, supported by the technology and operational functions used to deliver laboratory services.

The position and its setting

Eurofins lists QCA Sampling Associate in Andover, MA, United States, under reference REF82490B. The details below separate the work described by the employer from essential conditions, preferred experience and practical preparation advice.

• Department: Testing & Laboratory
• Employment type: Full-time
• Employer listing date: 23 October 2026
• Legal Entity: CUS206 - Eurofins Professional Scientific Services NBLSC, LLC
• Sub-Business Line: Biopharma Product Testing
• Contract Type: Permanent
• Business Lines: Biopharma Services

Responsibilities and work described

• We are seeking a detail-oriented and organized GMP Sampling Associate to support QC raw material sample operations in the warehouse and across multi-site laboratory environments
• This role is responsible for the testing, tracking, documentation, and coordination of samples to ensure accuracy, compliance, and timely availability for further processing
• Execution: Raw Material Sampling in the GMP warehouse to support clinical and commercial manufacturing operations
• Execution: Daily Sanitization of ISO classified Sampling Areas
• Execution: and Review Appearance, Gas, and Raman Spectroscopy testing on Raw Materials
• Participate in continuous improvement culture within sampling areas
• Identify opportunities for improvements and utilize site continuous improvement tools
• Plan and prioritize assignments to meet department and site goals
• Record and maintain all related data and records in compliance with cGMP and quality procedures
• Execution: work in a manner consistent with company safety policies and procedures
• Execution: additional tasks as needed in the QC Analytical Department

Essential requirements and candidate background

• High School diploma, associate’s degree and/or a bachelor’s degree in chemistry or other science related degree concentration
• 0-2 years of relevant experience
• Lift 50-100 pounds alone or with assistance daily
• Attention to detail and ability to follow procedures to generate reproducible data in a controlled laboratory environment
• Skills in Microsoft Office, data analysis software, and other related applications
• Learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
• Think critically and demonstrate troubleshooting/problem solving skills
• Work independently and as part of a team, self-motivation, adaptability, and a positive attitude
• Authorization to work in the United States indefinitely without restriction or sponsorship

Location, schedule and contract conditions

For this overseas or regional listing, confirm work authorisation and any location restrictions with the employer. The location does not establish visa sponsorship or permission to work remotely from India.

• Work arrangement: On-site
• Advertised location: Andover, MA, United States

Employer details to confirm

• The employer’s seniority category and its stated experience requirements do not agree. Follow the role-specific requirements above rather than assuming this is a fresher opening.

Pay and application dates

A verified salary figure is not established in this article. An online estimate for another QCA Sampling Associate vacancy is not an offer for reference REF82490B; use the employer’s own pay disclosure and recruitment communication.

A closing date is not confirmed in this article. Check the current employer page before submitting: an undated posting can change or be withdrawn.

How to apply to Eurofins

Applications follow the official employer page linked below.

Open the official Eurofins posting below and match the title and reference REF82490B.

Compare your qualifications and experience with the essential conditions for the Andover, MA, United States position, then read the preferred criteria separately.

Prepare an accurate CV and the supporting items requested in that employer’s application. Provide only information and documents you are authorised to share.

Use the employer’s application option, complete the required fields and review the submission. Retain the acknowledgement when one is provided. Job Alerts World does not receive the application.

Practical preparation: GMP

GMP references concern work performed within a controlled manufacturing or quality environment. In an application, explain your actual involvement with procedures, records, deviations or other controls relevant to the post.

Relevant skills

• MS Office
• GMP
• ISO
• manufacturing
• laboratory testing
• compliance
• warehouse operations
• data analysis
• chemistry
• problem resolution