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- 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,....

- 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....

- Kansas City, KS
new job!

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....

- Pittsburgh, PA
new job!

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....

- Rockville, MD
new job!

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....


Location: San Diego, CA Employment Type: Permanent Context: Our client ss is seeking a Sr. Project Manager to manage research and drug discovery projects from the research/discovery phase through to early clinical development. Preference will be given to candidates who have experience with small molecule therapeutics. The ideal candidate will be an innovative, highly motivated project manager with a strong scientific background in preclinical drug discovery research and project management. The

- Cleveland, OH

Looking for an opportunity to combine your passion for marketing, artistry, and technology? A top Cleveland company is looking for UX Designers who want just that—to take a new name in a saturated market and grow it into something spectacular with a killer brand image and digital presence. So, if you’re looking to grow yourself on a fast-paced, creative, and diverse team, please read on: Required Skills: The User Experience Designer will lead the clients’ efforts to design and implement a....

- Cambridge, MA

Regulatory Affairs Advisor - Medical Device Cambridge, MA Overview: Our client is a leading provider of consumer, business-to-business, and industrial digital imaging solutions to the United States and to Latin America and the Caribbean markets. They are committed to the highest level of customer satisfaction and loyalty, providing 100 percent U.S.-based service and support for all of the products it distributes in the United States. They are currently seeking a Regulatory Affairs Advisor for....

- Cleveland, OH

Looking for an opportunity to combine your passion for marketing, artistry, and technology? A top Cleveland company is looking for UX Designers who want just that—to take a new name in a saturated market and grow it into something spectacular with a killer brand image and digital presence. So, if you’re looking to grow yourself on a fast-paced, creative, and diverse team, please read on: Required Skills: The User Experience Designer will lead the clients’ efforts to design and implement a....

- Cincinnati, OH

General Description:The QC Analyst IV will join chemistry group to provide technical coaching, perform analytical testing, instrument qualification as required to meet QC cycle times following cGMP. Responsibilities will also include reviewing, reporting test results and ensuring that all activities within the laboratory are performed in compliance with cGMP, internal written procedures and policies. The analyst IV will answer questions that arise regarding cGMP and internal requirements of a....


The job holder is accountable for driving improvement focused initiatives across Clinical Operations and for the development and implementation of effective processes and best practices for SP&CO and group functions. S/he aligns with the evolving business strategy throughout the organization and develops and maintains the strategic framework for efficient information management as well as the portfolio of projects/initiatives driving improved efficiency. The postholder is accountable for....


Global Specialty Pharmaceutical company in Bridgewater, New Jersey is looking to hire a Manager of Clinical Quality AssuranceThe Manager Clinical Quality Assurance is a key member of the company Research and Development organization. This role is responsible for Clinical QA activity related to the planning, conduct, and reporting of GCP audits in order to ensure that clinical studies are conducted in compliance with applicable regulations, guidelines and company standards. This role also has....

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Unless noted above, applicants MUST be authorized to work in the US without Visa Sponsorship. US citizens and Green Card holders ONLY. We do not provide relocation assistance for those living outside the continental US. Please only click apply if you meet the specific requirements of the job listing, you are able to work in the location listed, and are comfortable with the salary range indicated above. Thanks for your interest. We look forward to working with you.