Sample Handling Technician GMP Support

The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

If you’re looking for a rewarding career, a place to call home, apply with us today!

We’re seeking a detail-oriented individual to support sample management activities in a GMP environment. This role involves receiving, aliquoting, distributing, and documenting QC samples and reference standards across multiple labs. Ideal candidates are organized, collaborative, and thrive in a fast-paced, team-based setting.

Duties Include:

• Receiving, aliquoting, distributing, handling, and documenting GMP samples in support of multi-product and multi-site testing laboratories.
• Aliquoting, sampling, receiving,g and distributing QC samples and reference standards, all while providing appropriate GMP documentation.
• Adhere to established corporate and organizational procedures to ensure compliance with internal and regulatory standards.
• Interact effectively with peers and senior scientists as part of a multi-disciplinary team.
• Accurately record, document, and maintain all relevant sample information by GMP documentation practices.

• High School diploma with 2-5 years of experience, or AS degree with 1-3 years of experience
• Experience in a laboratory or manufacturing environment (bioprocess or chemical process industry preferred).
• Demonstrated capability to work as a team member in a matrix development team.
• Thrive in a fast-paced environment
• Knowledge of GMP concepts and documentation practices.
• Ability to follow established procedures under minimal supervision.
• Excellent interpersonal communication skills.
• Attention to detail, strong organizational skills, the ability to multitask, and effective interpersonal and communication skills are required.
• Ability to utilize electronic inventory management systems following established procedures.
• Highly effective in a team-based, fast-paced environment.
• Operational knowledge of computerized systems (ideally LabWare LIMS).
• Experience with quality systems such as LIMS
• Experience with database management.
• Capable of generating documents utilizing Microsoft Word and Excel.
• Position requires occasional light lifting and periods of standing, sitting, or walking.
• Authorization to work in the United States indefinitely without restriction or sponsorship

• 
  Position is full-time, 1st shift, Monday – Friday, 8:00am-5:00pm.

• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays
• #LI-EB1

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.