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 Organisation 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 Organisations. It also has a rapidly developing presence in highly specialised 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 decentralised 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.

In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.

Job DescriptionPerform documentation review to ensure consistency (e.g. language, formatting, etc.) within the Redesign Team and across the Clinical Supply networkServe as communication channel between site personnelAssist with the coordination and collection of project metrics to support monthly operations review and project progressAssist with project management activities in support of various QMS topicsAssist and support other client department projects

Qualifications

Minimum Qualifications:

B.S. in Biology, Cell Biology, Bio/chemical Engineering, or related scienceMinimum of three years’ experience in the Pharmaceutical or equivalent industryAuthorization to work in the United States indefinitely without restriction or sponsorship

Desired Skills:

Strong computer, scientific, and organizational skillsExcellent communication (oral and written) and attention to detailAbility to work independently and as part of a team, self-motivation, adaptability, and a positive attitudeAbility to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policiesExperience directly related to Quality Assurance or Quality ControlExperience directly related to the development of Quality Standards and core requirements for Market Supply and / or Clinical SupplyExperience defining, generating and reporting Operational metrics Experience in Microsoft Office (Outlook, Word, Excel, PowerPoint, SharePoint, Teams, Project) strongly recommendedExperience with document editing in MS Word (e.g. formatting, forms, styles, templates, etc.) preferredExperience with electronic document management systems (e.g. VeevaVault) preferred

Additional Information

Position is full-time,Monday- Friday 8:00-5:00pm with overtime as needed. Candidates currently living within a commutable distance of West Point, PA are encouraged to apply.

Excellent full time benefits including comprehensive medical coverage, dental, and vision optionsLife and disability insurance401(k) with company matchPaid vacation and holidays

Eurofins USA PSS Insourcing Solutions is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.