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- South Region, MD

Choose a hospital-based career opportunity within our newly renovated laboratory, equipped with the latest technologies! During the consideration and selection process both your interests, skills and our immediate needs will assist in placement within our Core Lab. Hiring Med Lab Technicians and Medical Technologist. Must be able to run chemistry, hematology, coagulation, and urine analysis in accordance with written policies and procedures. Properly ascertain results, make necessary....


The Quality Control manager (QCM) reports to the Director of Quality Compliance. The QCM will stay current on publications released by USP, FDA and other pertinent regulating bodies to ensure the Quality Control Analytical & Microbiology Laboratories and the Incoming Inspection departments are complaint in the areas of applications, release specifications, and documentation practices. It will be necessary for the QCM to execute and understand all in-house test methods. This person will be....


Senior Clinical Research Manager Elmsford, NY or Glasgow, DE (Relocation Provided) Competitive Pay, Bonus, 4 weeks PTO, 6% 401K, Great benefits We have a new opening for a Senior Clinical Research Manager with a longstanding client; a multi-billion ($8B+) global medical diagnostics/instrumentation company. They have strong revenue growth, a stable environment, very low turnover, and offer the opportunity to work on customized, complex medical products that impact people's lives. A lot of....

- Parsippany, NJ

Our client - a growing Pharmaceutical company in Northern NJ - is looking for a Sr. Regulatory Affairs Associate. The Regulatory Affairs Associate will helps to put together and submit regulatory submissions to the FDA. These submissions will include: ANDAs, Amendments, Supplements, Annual Reports etc. (There may be additional work involving 505 (b)(2) submissions as well.) This position will also involve effective interaction with other departments with regards to the information required for


Job DescriptionSummary of the Position:Keeps Regulatory Affairs Director appraised weekly of all tasks and projects. Gather documentation and compile materials required for international product registrations. Coordinate with International Product Manager and the International Business Unit a viable timeline for registration approvals with the Regulatory Affairs Supervisor or Director of Regulatory Affairs & Technical ServicesRoles and Responsibilities:Maintains all (electronic/hard) files

- Charlotte, NC

Job DescriptionThe IT Service Desk is the central point of contact for all IT related incidents and service requests. The role of the Desktop Support Technician is to provide 1st level support for all company employees. The Desktop Support Technician is responsible for resolving support requests as well as meeting customer satisfaction and continuous service delivery demands. The position requires one to be able to work in a fast-paced environment which provides services via the phone, e-mail....

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