Job Description

Company Description

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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

Join a dynamic team dedicated to advancing pharmaceutical innovation. In this role, you will perform comprehensive physical, chemical, and instrumental analyses of active pharmaceutical ingredients (APIs) and finished dosage forms-including tablets, capsules, injectables, liquids, creams, and gels. Your work will directly support clients in the development and regulatory approval of a wide variety of medications.

This is a great opportunity to contribute to cutting-edge pharmaceutical development in a fast-paced, collaborative environment.

Key Responsibilities:

• Prepare solutions, standards, and samples for analytical testing
• Operate a range of laboratory instruments, including HPLC, GC, IC, Karl Fischer titrators (Coulometric and Volumetric), UV/Vis and IR/FTIR spectrophotometers, disintegration testers, and dissolution equipment
• Process and interpret analytical data, comparing results against client-provided specifications
• Execute and document all laboratory work in accordance with Good Manufacturing Practices (GMP)

Qualifications

The Ideal Candidate would possess:

• Strong computer, scientific, and organizational skills
• Excellent communication (oral and written) and attention to detail
• Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
• Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies

Minimum Qualifications:

• Bachelor's degree in chemistry or other related degree concentration, or equivalent directly-related experience
• Authorization to work in the United States indefinitely without restriction or sponsorship

Additional Information

This position is a full-time role, Monday-Friday, 8 a.m.-5:00 p.m., with overtime as needed. Candidates who live within a commutable distance from Lancaster, PA are encouraged to apply.

Excellent full-time benefits including:

• Comprehensive medical coverage, dental, and vision options.
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays

Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

Job Tags

Full time, Contract work, Monday to Friday,

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