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.
Perform physical sampling, labeling, distribution (import and export), and monitoring of samples globally
Perform aliquot of biological critical reagents and document in ELN
Perform Quarterly Equipment and logbook review
Perform Review of Equipment Temperature Data
Serve as primary logistics coordinator for major vaccine and biologics franchises in Analytical Research & Development
Perform appropriate second scientist and second person review as required
Build and maintain Research LIMS specifications and specification lists for vaccine and biologics franchises
As required, train on laboratory methods supporting key analytical method transfer activities
Ensure all work is compliant with all regulatory expectations
Follow current Good Manufacturing Practices (cGMP) as they apply to the functions of the position
Basic Minimum Qualifications :
Bachelor's degree in biology, chemistry, or other related degree concentration with 2-3 years of related experience
Authorization to work in the United States indefinitely without restriction or sponsorship
The ideal candidate would possess :
Strong scientific and organizational skills
Excellent communication (oral and written)
High level of attention to detail, in particular with the preparation of GMP documentation and the work associated with that documentation.
Ability to work independently and on a team
Highly self-motivated, expected to contribute to the work and take ownership of projects
Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
Experience in classical biochemical assays and molecular biological techniques
GMP experience
Technical writing experience
Experience with regulatory audits
Position is full-time, Monday-Friday, generally 8 a.m. - 5 p.m., but may vary to meet the assay needs; 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 options
Life and disability insurance
401(k) with company match
Paid vacation and holidays
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.
Originally posted by Eurofins. View original posting
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