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- Marion, OH
new job!

Food Technologist Marion, Ohio area Salary up to 70K, depending on years of experience Due to an internal promotion, growing food manufacturer is seeking a Food Technologist to report to their Director of Product Development. Daily you will work within a team on development, quality and regulatory initiatives of their food product. Daily activities will includeCreating prototype productsManaging the final product costMaintaining current FDA labeling requirementsOverseeing sample request....

- Irvine, CA
new job!

This position is responsible for leading internal and outsourced Clinical Data Management activities in support of Clinical Research studies, managing the definition of Case Report Form (CRF) requirements, creation of the Data Management Plan, coordination of Centralized Data Review activities (a key component of Risk-Based Monitoring), and is accountable for data integrity, quality, and consistency at Database Lock. The employee must be able to lead data review activities and engage different

- Hartford, CT
new job!

Director of Statutory Reporting Hartford, CT USAThe Director of P&C Statutory Reporting (The Director) will report to the AVP of Statutory Reporting and will play a key leadership role within the Statutory Reporting Team and Corporate External Reporting and will lead a small and an experienced team. The Stat Team performs the following responsibilities for 16 P&C companies and 1 Life insurance company: closing the Stat Ledger, all NAIC reporting, Stat audited financial statements, the....

- Lancaster, SC
new job!

Roles and Responsibilities:The R&D Chemist (RDC) reports to Quality Control (QC) Management. The R&D Chemist (RDC) work closely with Product Development and Quality Control. The RDC will be the Liaison between Quality control, Product Development, and Contract laboratories by evaluating and Assessing testing methodologies and their application to different sample matrix. This responsibility also includes the evaluation of testing results from contract laboratories to be sure that the....


Join a leading global organization in their Product/ Metabolism discovery and safety studies team. Requires Scientific expertise in biological or chemical sciences of environmental, plant or mammalian studies. ---Participate as Lead Scientist with expertise in Data Chemistry, analysis testing utilizing Chromatography and other relative methodology. ---Support the use of data sets to optimize study design and overall understanding of the compounds behavior ---Manage studies placed with external

- Los Angeles area, CA
new job!

Our client is a world leader in the manufacturing and distribution of analytical instrumentation used in R&D Laboratories. Due to continuing growth they are adding a new Field Service Engineer to be based in the Los Angeles, CA area. The Field Service Engineer provides on-site service including preventative maintenance, calibration, installation, and training across all product lines.Responsibilities & QualificationsThis position will be based in or near the Los Angeles, CA area but....

- Pasadena, CA
new job!

The Clinical Trial Data Analyst is responsible for building programs to create datasets, listings, tables and figures from clinical databases, external data sources, and other sources. In addition, the position coordinates in-house data management activities (including vendor management) to ensure the accuracy and consistency of clinical databases for subsequent analysis and reporting. Responsibilities: Prepare data reports, tables and graphs for regulatory submissions, IRB submissions,....

- Irvine, CA
new job!

Education/ExperienceBS in life sciences or related field At least 2 years experience in clinical researchKnowledge of FDA regulations Prior Study Start-Up experience preferredAdvanced skills in Microsoft Word, Microsoft PowerPoint, Microsoft Excel, Microsoft Outlook Experience with Adobe Acrobat Professional and Microsoft Access a plusPresentation Delivery ResponsibilitiesExecute study start-up for assigned protocols within company timelines by identifying clinical team needs, Oversee Site....

- Moline, IL
new job!

Our client is a global leader in the manufacture of paints and coatings. They require an experienced industrial coatings chemist to join their team at a manufacturing facility in Moline, IL. ResponsibilitiesPerform experiments to develop, reformulate and improve industrial coatings products.Solve product or manufacturing process related technical problems. Demonstrate significant mastery in the use of chemical raw materials, instruments and substrates related to liquid industrial coatings.....


Our client is a multi-specialty chemical company committed to developing chemistry that addresses key societal challenges. They innovate and partner with customers in diverse global end markets. The company combines 50 years of technology heritage to bring a comprehensive product portfolio, expertise in material design, and extensive process engineering solutions to their customers. As the partner of choice for advanced materials development, they deliver optimal material solutions to address....


RETAINED RESEARCH Title: Director of Regulatory Affairs Direct Reports 2 Mgrs Indirect Reports: 8 -10 Responsible for coordinating quality regulatory submissions to the United States Department of Agriculture’s (USDA), specifically The Center of Veterinary Biologics (CVB), and following USDA licensure, coordinating dossier submissions to regulatory authorities in countries, including affiliates and distributors. Manage US Regulatory Affairs Department:Manage and oversee licensure of new....


My client is expanding and looking to hire a Director of Clinical Microbiology. The ideal candidate will direct a group and take on the following tasks:Oversee analytical testing ensure cutting-edge technologies for new test methods, research activities and product evaluations.Direct all technical standard operating procedures, including development, validation, and approval.Monitor and maintain standards of performance in quality control (QC) and quality assurance (QA); ensures key....


My client is seeking a Supervisor to launch a new group and oversee a team conducting in-vivo oncology work. The ideal candidate will take on the following tasks:Provides the oversight and leadership of technical proceduresProvides training, technical guidance and mentoring of team membersSchedules work within the department and manages overtimeReview and approve study protocolsLiaise with cross-functional groups, different departments, and project Leadership to facilitate and maximize....


This full time direct hire position will support the Enterprise Content Management (ECM) applications throughout the Company and is responsible for the design and development of document processing and workflow solutions for the Company. Responsibilities:Delivers first-class software solutions using a combination of out of the box Enterprise software and custom-coded solutions tailored to the company's requirements.Analyzes business needs and requirements to design and implement new....

- Mount Olive, NJ

Leading logistics company seeks a Manager of Data Operations to manage business critical data including data integrity, accuracy and timeliness and to lead a team in identifying data and systems issues, defining requirements, and recommending enhancements for system features and adapting processes to new anomalies. This position will work closely with operations and will establish and manage metrics and KPI’s vital to identifying issues and managing team progress. In addition, the position....


My established client seeks a Scientist for their Neurodegeneration group to take on the following tasks:Manage projects, develop work plans, and assist leadership team Perform stereotaxic surgeries and behavioral studies to support collaborationsManage data and perform statistical analysisPrepare and deliver presentations and reports, and contribute to manuscript preparationThe ideal candidate will possess the following qualities:PhD degree in Neuroscience or similarExperience with....

- Charlotte, NC

We are looking for a Lab Analyst to conduct analysis of water, waste, and soil samples using USEPA-approved methods. Job Requirements:BA/BS science degree and at least 3 years of laboratory experience and 2 years of experience utilizing ICP/MS instrument in an analytical chemistry lab.Must be a motivated self-starter capable of managing backlogs with short holding-time tests.Must be able to work productively in a high-volume, short-turnaround environment.Overtime will be required based upon....


We are looking for a Quality Assurance Specialist who will be responsible for the daily Quality Assurance support in the Manufacturing and Packaging process on site. They will be required to review all appropriate documents during the production process. In this role, the QA Specialist will be readily available to support the Quality Department and the production process; therefore, this position requires the QA Specialist to be flexible based on business need to support QA and business....

- Lancaster, SC

We are looking for a Photographer & Videographer who will be responsible for photography and video services to support company sales and marketing efforts. General Responsibilities:Take high quality photographs and edit the images as neededWork closely with Marketing team to determine video requirements and produce video footage accordinglyHelps set photo and video standards for brands and products in a brand with the ability to brainstorm with members of the Graphic Design / Marketing....


Los Angeles, CA Currently looking for an experienced Manager, Regulatory Affairs - CMC to fill an opening with a Fortune 100 Pharmaceutical Company located in Los Angeles, CA. Interested candidates should hold a Bachelor’s Degree (Regulatory Affairs, Life Sciences, or Engineering) and have 6+ years’ regulatory and/or compliance experience. Responsibilities of the Manager, Regulatory Affairs - CMC Responsible for generation of the region-specific regulatory documents Clinical Trial....

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