GMP Sample Logistics Coordinator
: Job Details :

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 whilealso 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!Job DescriptionSupport efforts in acquisition, qualification, testing, and implementation of sample materials through the physical sampling, labeling, distribution (import and export), and monitoring of these samples globally.Serve as primary logistics coordinator for major vaccine and biologics franchises in BVA.Perform appropriate second scientist and second person review as required.Build and maintain Research LIMS specifications and specification lists for vaccine and biologics franchises.Serve as primary trainer and subject matter expert for BioInventory systems.As required, train on laboratory methods supporting key analytical method transfer activities.Ensure all work is compliant with all regulatory expectations.Conform to current Good Manufacturing Practices (cGMP) as they apply to the functions of the position.Perform aliquot of biological critical reagents and document in ELN.Perform Quarterly Equipment and logbook review.Perform Review of Equipment Temperature Data in OpenLab, DeltaV, or BAS PI.QualificationsBasic Minimum Qualifications :Bachelor's degree in biology, chemistry, or other related degree concentration with 2-3 years of related experience, or Master's degree with 0-1 year experience.Authorization to work in the United States indefinitely without restriction or sponsorship.The ideal candidate would possess :Strong scientific and organizational skills.Proficiency in MS Project and MS Visio.Excellent communication (oral and written) skills with both English and ESL speakers.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.Experience in statistical analysis using JMP, Minitab, or Excel.Technical writing experience.Experience with regulatory audits.Additional InformationPosition 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.What we offer: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 is an M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.#J-18808-Ljbffr