Easter Seals Jobs

Company Description Consider joining Eurofins Lancaster Laboratories where people are the most important element in our chemistry. Celebrating 50 years of service, Lancaster Laboratories is a leading contract lab providing testing and research services in the environmental, pharmaceutical, and biopharmaceutical sciences to clients worldwide. Interested in contributing globally to improving and saving lives? Work for one of the largest global testing laboratories at the forefront of one of our state-of-the-art laboratories, each day testing for life and making the world a safer and healthier place. We are seeking immediate talent to support our clients to help make our world a safer place. We are seeking any and all experience levels including recent graduates with a life science degree in chemistry, biology or related sciences. Additional training will be provided.Perform cutting edge science in world class laboratories to develop your skills and advance your career. Job Description Responsible for administration aspects of the Regulatory Affairs support. The team member will work with Regulatory Affairs colleagues and will support the following key areas: Product Dictionary data entry, compiling regulatory documents and facilitating document legalization and manufacturing documents (such as ISO Certificates and certificates of analysis), study risk assessment coordinator, and document maintenance within the document control system (VV/ETS or other). Will work with the Global Diagnostics Regulatory Affairs Team and/or independently, based on the tasks, supporting both the Veterinary and Human Health Diagnostics Product inquiries (30%). Document Management support will include archiving of regulatory documents, review of documents in compliance with VMRD document handling requirements, interaction with internal customers to provide support (collaboration tools or document management related issues). Responsibilities: * Collaborate with the Global Diagnostic Strategists to ensure Product Dictionary information for Global Diagnostic products is up to date in product dictionary website * Gather manufacturing documents and other documents needed to support registration as requested by the regulatory team. * Maintains information systems (electronic and paper) for regulatory information * Assist in the development of instructional guidance's and processes, as applicable - Provide status updates on tasks as appropriate. * Manages study risk assessments process including risk assessment intake, assignment, compilation, signatures, and final archival * Visually identify and record pre-defined metadata values from electronic document headers and abstracts. Metadata values may be recorded into Microsoft Excel spreadsheets and/or into an electronic document management. * Upload electronic documents and respective metadata into electronic document management systems. * Perform simple to complex electronic library searches. * Perform page merges/extractions using existing PDF documents to create new documents in preparation for further processing and filing. * Support the departments document management operations. * Adhere to the appropriate use of the publishing and document management systems, through use of working practices and QC regimens, such that regulatory compliance is preserved. * Participate on global/local teams to complete assignments and tasks within a specific task force/project. * Maintain a working knowledge of electronic publishing systems and tools and how these are applied. * Proven ability to perform complex electronic library searches using advanced query techniques. * May assist with the compilation and processing of electronic regulatory submission documents. * Regulatory document submission assembly and publishing experience within a pharmaceutical or other highly-regulated environment is desirable. Qualifications A degree in Science, Pharmacy, Library Science or related business. Knowledge or experience of Di