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- Shakopee, MN
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Responsibilities for 3rd Shift Sanitation Supervisor:Manage cleaning and sanitation employees in a food manufacturing facility on the 3rd shift;Train new sanitation employees in proper cleaning SSOPs, chemical use and safety procedures;Ensure uniform pre-operational standards through inspection and training;Solve concerns in regards to GMP, SSOP, SQF, SDS, and Process Control programs;Inspect plant, stored equipment, and environment for cleanliness;Establish and maintain a Master Sanitation....


Excellent oppt'y for a Medical Technologist to work for a medical lab instrument manufacturer and utilize their lab knowledge as a Technical Support Specialist. Will be instrumental during the installation process as a trainer, and documenting the lab procedures. This position can be based almost anywhere in the greater Los Angeles CA area:Will also be involved with direct problem solving covering reagents, kits, procedures, adaptations, and software upgrades.Your lab knowledge will also be....


Our client is a world leader in laboratory equipment and services, and has an opportunity for a Technical Sales Representative (TSR) for its industry leading analytical instrumentation used in R&D laboratories. The TSR will be selling products for surface mechanical characterization include indentation testers, scratch testers, tribometers (high temperature and linear reciprocating), and calotest instruments (coating thickness characterization).This position will be covering MN, WI, MI,....


Our client is a world leader in the manufacturing and distribution of analytical instrumentation used in R&D Laboratories. They have an opening for a Product Specialist – Business Unit Measurement product line in their Houston offices. This is a new position due to company wide growth. Responsibilities: The Product Specialist applies scientific knowledge and principles to provide in-depth training and assistance to company salespeople and customers on the proper use of highly complex....


Traditional SHE leader's role dealing with a Chemical manufacturing facility. MUST HAVE PSM BACKGROUND AND EXPERIENCE. Will not even look at anyone without it. Lead the plant’s safety, health, environmental and security programs, as well as the operation of the Utilities function. Take the lead on all compliance with all safety and environmental regulations and policies. Lead effort in compliance with environmental regulations, permits and reporting requirements. Responsible for the operation....

- Cambridge, MA

My client seeks an outstanding scientist to contribute to drug discovery and development projects. The ideal candidate will work closely with medicinal chemists and other scientists – and apply methods to improve drug properties and efficacy. In addition, this person will apply and develop cutting-edge techniques and interpret data using modeling and data mining. Finally, the ideal candidate will possess leadership qualities to direct projects and collaborations. The level of the position is....


Our client, a nationally acclaimed interdisciplinary research center seeks an expert resource and thought leader to advise in all facets of data science and data management. You will build high-performance big data capabilities leveraging artificial intelligence and machine learning. You will actively contribute to data management and analysis activities across units within the research center in the creation of an eco-system of tools, applications and processes to support funded grant and....


Excellent oppt'y for a Medical Technologist to work for a medical lab manufacturer and utilize their lab knowledge as a Technical Support Specialist. Will be instrumental during the installation process as a trainer, and documenting the lab procedures. Area to be covered is approx 150 mile radius of San Jose (Sacramento - Stockton - San Jose), and maybe a bit south of San Jose. Can reside almost anywhere is this area. Will also be involved with direct problem solving covering reagents, kits,....


Clinical Research Coordinator needed for Alzheimer's studies. Entry Level and career transitions OK, employer is willing to train but candidate must have completed CITI Good Clinical Practice (GCP) and HIPS prior to starting. Associates degree or higher degree required, preferably in healthcare or life sciences. Download our white paper to understand how clinical research sites work. Responsibilities:Complete and ensure the quality of case report formsConducting study visits, including vital....


Global Pharmaceutical company in Madison, New Jersey is looking for a Pharmacovigilance Agreements & Alliance Management Specialist We are looking for candidates with a PharmD or RN/NP with individual case safety report processing experience and knowledge of global drug safety/PV regulations, i.e., Drug Safety Associate/Sr. Associate/Manager. I. POSITION SUMMARY: The PV Agreements & Alliance Management (PAAM) Specialist guides and facilitates effective working relationships with....


New need for Growing Global Pharmaceutical Company in New Jersey Contract R&D Project Planner III This R&D Project Planner is responsible for supporting Clinical Trial/Project Teams by strategically developing and maintaining clinical study timelines, providing evaluations of potential risks and conflicts, supporting the team on proactively resolving potential deviations, and presenting clear timeline reports. PP will work in a team orientated environment and is empowered to drive....


Global Pharmaceutical company is expanding in new offices in Madison, NJ This Clinical Trial Manager is an essential part of the Clinical Operations team. Looking for a strong Clinical Trials Professional with a operation experience for phase 2, 3 and 4 trials. Multiple therapeutic reas. -responsible for the delivery of studies , responsible for the execution and adherence of various aspects of the study operational plan (start up, conduct, close-out, and vendor oversight) with input from key....


Publicly Traded Top Tier Global Pharmaceutical Company is looking for a Clinical Study Manager or Senior level DOE to be located in their Cambridge, MA Headquarters competitive base salary and bonus, full relocation and stock and other long term incentives! This role requires a strong communicator: Duties and Responsibilities: 1.Manage clinical study/studies according to global regulatory requirements (including but not limited to US CFR, EU CTD, and ICH GCP) and Company SOPs, and supporting....


Large Global company is expanding their St. Louis team- They are in need of and Executive Director, Development In addition to a generous base salary: there is a bonus (30%) there is Equity Stock Grant Program and also Executives at this level have Stock purchase plan: (they can buy Stock options and company matches 75%) 3 weeks vacation PLUS – they ar eclosed during Christmas and New Years They will prvide FULL relocation This role reports into VP, Product Development Need Product Design....


New contract role (opportunity to convert to perm in future if desired) with Global Pharmaceutical company located in Cambridge, MA BACKGROUND: This Drug Product is an ALK Inhibitor for the treatment of patients with anaplastic lymphoma kinase-positive (ALK+) metastatic NSCLC. It was recently approved by the FDA under Accelerated Approval in April 2017, based on tumor response rate and duration of response, for previously treated anaplastic lymphoma kinase-positive (ALK+) metastatic....


Our client, a nationally acclaimed interdisciplinary research center seeks a talented Social Scientist to perform both basic and applied research in the areas of economic, workforce, business, and community development. You will collaborate closely in the development of proposals and research plans. You will provide technical and project management expertise, guidance, and support both internally and externally. Title: Associate Director Location: Mississippi. Multi-cultural, progressive....


My client seeks a Manager of Business Development to provide exceptional service to their biotechnology and pharmaceutical clients. This person will support the Director of Business Development, meet with decision makers of pharma and biotech firms, review their current R&D landscape, and offer solutions (both internal and external) to their clients. The focus of the position is to develop relationships with clients, build rapport with the R&D groups, and help the firm grow into the....


My client is expanding and looking to hire a Director for their Medical Affairs group. The ideal candidate will take on the following responsibilities:Direct collaborations with academic, pharmaceutical and biotechnology partners and ensure quality service to Directors & VPs, Principal Investigators and other clients.Develop and expand research and clinical collaborations with new partners.Work closely with Chief Medical Officer and ensure project deliverables are met.Understand the....


My client is expanding and looking to hire a Director for their Medical Affairs group. The ideal candidate will take on the following responsibilities:Direct collaborations with academic, pharmaceutical and biotechnology partners and ensure quality service to Directors & VPs, Principal Investigators and other clients.Develop and expand research and clinical collaborations with new partners.Work closely with Chief Medical Officer and ensure project deliverables are met.Understand the....


My client is focused in the oncology space, and they seek a Project Manager to take on the following tasks:Support project development activities and the overall coordination of proof-of-concept, proof-of-efficacy preclinical research projects, non-clinical toxicology and pre-IND activities for internal projects.Collaborate with a cross functional team including internal scientists and CROs to prepare study designs, manage budgets to perform the studies, and oversee the study from initiation....

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