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- Elmsford, NY

Staff Biostatistician (Or Senior Staff - Depending on Level of Experience) Elmsford NY or Newark, DE Competitive Salary, Bonus, 6% 401K, 4 Weeks PTO, Excellent Benefits We have a newly created opening for an experienced Senior (Staff or Senior Staff Level) Biostatistician with a longstanding client; a multi-billion global medical diagnostics/instrumentation company. They have strong revenue growth, a stable environment, very low turnover, and offer the opportunity to work on customized,....

- Newark, DE

Staff Biostatistician (Or Senior Staff - Depending on Level of Experience) Elmsford NY or Newark, DE Competitive Salary, Bonus, 6% 401K, 4 Weeks PTO, Excellent Benefits We have a newly created opening for an experienced Senior (Staff or Senior Staff Level) Biostatistician with a longstanding client; a multi-billion global medical diagnostics/instrumentation company. They have strong revenue growth, a stable environment, very low turnover, and offer the opportunity to work on customized,....

- Pocomoke City, MD

Our Client is seeking a talented and experienced Director of Supply Chain. The ideal candidate will have a strong background in Purchasing, Planning, Strategic Sourcing, and Logistics Management. This leader’s primary responsibility will be to develop, deploy, and lead supply and demand planning strategies for the Pocomooke, Trappe, and Wayne manufacturing locations. They will be responsible for all tactical and strategic sourcing, raw material planning and purchasing, supply chain production....


My client is a dedicated contract development and manufacturing organization (CDMO) focused on development and cGMP manufacturing of biopharmaceutical products derived from mammalian cell culture. They provide a comprehensive range of process development, high quality cGMP clinical and commercial manufacturing services for the biotechnology and biopharmaceutical industries. They have 25 years of experience producing monoclonal antibodies and recombinant proteins in batch, fed-batch and....


Staff Firmware / Embedded Software Engineer Elmsford, NY Competitive pay, Bonus, Excellent benefits This role is with a global leader in medical technology (imaging, diagnostics, healthcare IT), an organization dedicated to ongoing success by hiring top talent, investing in R&D, and commitment to engineering excellence for over 100+ years. This is a newly created Staff level role (seeking strong experience, team leadership, 7-15+ yrs exp), looking for someone to work in new project


Our client - a major Pharmaceutical Company - has a newly created opening for a Sr. Scientist /Principal Scientist. This position will provide Analytical R&D support to the Drug Substance / Drug Product areas. This position requires experience with HPLC / GC. The Sr. Scientist /Principal Scientist will oversee/perform Method Development / Method Validation in support of IND/NDA submissions. The Sr. Scientist/Principal Scientist will mentor/supervise Jr. level staff in the lab. They will....

- 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....

- Lancaster, SC

We are looking for an International Area Manager to be responsible for strategically planning and directing all business development initiatives, policies, and objectives for assigned foreign markets. Manage to execution all major strategic decisions to increase global market share and sales figures. Roles and Responsibilities:Helps to define the short and long-term international business strategies and goals to achieve growth and profitability in alignment with corporate objectivesDevelops....


Sr. Manager / Director, Medical Affairs Overview: Diverse and decentralized pharmaceutical company that is committed to focusing on our key stakeholders while delivering consistently high performance. Our values provide the overall direction for our company, and provide us with the tools necessary to rise to any challenge by leveraging our collective hard work and effort along with our unwavering competitive spirit. These values help us set goals based on our organization’s potential and what....


Medical Affairs – Fully integrated, global biopharmaceutical company developing innovative medicines for the treatment of central nervous system (CNS) diseases. The company has a diversified commercial product portfolio and a substantial clinical pipeline of product candidates for chronic diseases that include schizophrenia, depression, addiction and multiple sclerosis. In this highly visible leadership role in Medical Affairs, you will work closely with a cross-functional group that includes....


Position Overview Provide analytical expertise and leadership in the development of drug substances and pharmaceutical products from early development through commercialization. Plan analytical research and development activities, devise strategies for achieving project goals and independently manage CMC timelines. Make pivotal contributions to drug product development strategy at project team level. Independently manage multiple projects and ensure timely delivery of all deliverables to meet....

- Lancaster, SC

We are looking for a Research and Development Technician to assist formulation scientists by conducting lab scale formula trials, analyzing finished goods, reporting results to R & D team assisting production during the scale-up process and maintaining a clean and safe work environment. General Responsibilities:Effectively collaborate and communicate with R & D teamAccurately weigh appropriate raw materials for lab batchesPerform laboratory bench work to investigate formulations and....

- Lancaster, SC

We are looking for a Corporate Trainer who will develop, maintain, and administer training programs. General Responsibilities:Work with management to develop and/or implement company training programs and workshop to employees and manager such as training profiles, On the Job Training, Train the Trainer programs, supervisory, management, work skills, and communication.Monitors the effectiveness of training on employees using individual and/or group performance results. Collects feedback on....

- Lancaster, SC

We are looking for an Incoming Associate who will be responsible for inspecting and sampling materials. This person will reference Finished Product and Material Specifications for specific sampling instructions. General Responsibilities:Responsible for reading and understanding all the accompanied paperwork, which includes but is not limited to: Packing Slips, Bills of Lading, Certificates of Analysis (CoA), Certificate soft Compliance (Coca), Printed Material Proofs, & Material Safety....

- Marion, OH

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....


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 an In-House Service Engineer to be based in their Vernon Hills offices/service center. Requirements:Duties include the preventative maintenance, troubleshooting, repair, and calibration of instruments.Managing inventory and reporting for accuracy.The preferred candidate will possess a BS degree in Electric or Mechanical....


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....


Responsibilities: Manage project plan for assigned product launch which include working with the project team to create the project plan Set timelines, track milestones, and forecast budgetary and resourcing needs until plan completion Facilitate launch planning process for assigned product Build meeting agenda and conduct project meetings Review project plan periodically with the project team Ensure completion of assigned action items and deliverables in a timely manner Qualifications:....


Strategic opportunity as North American (NA) Team Leader supporting Analytical/ Synthesis (Methods Development); Product Metabolism, Product Safety (registration); and Regulatory Compliance (EPA). Participate on the Global Leadership Team while developing a challenged, problem-solving analytical team responsible for performing/ delivering scientific studies to ensure a sustainable product safety and registration success. The successful candidate will have a strong background in Scientific....


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

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