R & D Jobs in North Chicago, Illinois

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65 North Chicago, IL R & D jobs found on Monster.

Jobs 1 to 20 of 65
Biologist III: Looking for Biologist who have experience with ARCHITECT instrument. Bachelors Degree in Biology focus in a discipline 5+ years experience. Masters Degree in specified area of discipline and familiarity with techniques associated with that area. (Micro- Aseptic techniques, cell culture, cell plating and staining / Molecular- Assays, blotting, PCR, PAGE, electrophoresis). Ability to...
Work with lead scientist to perform preparative chromatographic separation and purification of starting material, intermediates and final products with desired quantity and quality to support process development and new drug discovery. Maintenance of chromatographic instrumentations to keep their condition operational. Manages separation and purification activities of preparative supercritical flu...
Job Description: M.S. in Analytical Chemistry or equivalent, and 0 to 3 years experience applied to pharmaceutical or related analyzes with use of computerized data handling systems. Formal knowledge of analytical separation and detection technology applied to pharmaceutical or related analyzes. Formal knowledge of basic organic chemistry, structure, functional groups and spectroscopic interpretat...
Your Medical Writing skills are needed just about anywhere. But is it where you want to go? Imagine working for one of the nation's most respected companies. Making a strategic contribution. Receiving the rewards and recognition you deserve. Whether you are pursuing a contract or permanent placement, Experis knows how and where to get you where you want to go. Are you interested? The ideal Medical...
Biochemistry, Gel electrophoresis, HPLC, Absorbance testing, pH conductivity, western blot basic chemistry background. Experis is an Equal Opportunity Employer (EOE/AA)...
Provide mechanical and electrical technician support for Engineering Department projects and other activities, such as, but not limited to, material (commodity, packaging, etc.) testing, manufacturing, process and laboratory equipment/instrumentation installation, startup and qualification, service and repair support for prototype instruments, and related facilities activities. Provide guidance to...
* 1 YEAR CONTRACT * eligible for benefits Business Systems Analyst Responsibilities: The Business Systems Analyst is able to work independently or as part of a team, will document business process and construct process models, for the identification of improvement opportunities or procedural and control deficiencies. In addition the Business Systems Analyst specifies, designs, documents, test’s an...
GENERAL: Participate in and manage both stability and sterility activities in the stability program for PharMEDium?s services. RESPONSIBILITIES: Assist in the design and acceptance of method validation protocols preparation and execution of stability testing protocols. Manage new product evaluations based on current stability data. Identify potential areas where current stability data and literatu...
Summary Responsible for the activities related to radiation processing and dosimetry across all Isomedix Services radiation operating facilities, including calibrations, generation of test methods, audits, scheduling, validations, and reporting as directed by the Radiation Physics Manager. Essential Job Functions 1. Contributes to successful product processing by performing dosimeter calibrations....
Manages global regulatory strategy and development of biological products for Hospira's business. Ensures that regulatory strategy and where necessary development resources are focused on harmonized goals in line with the strategic goals for the biologic. Manages regulatory issues related to the global development of biological products including timely compilation of global core dossiers. Ensures...
Summary : Review and evaluate safety issues related to medical device products and ensure compliance with worldwide regulations and/or guidelines. Provide medical approval and validation of safety reports ( as defined by SOP's ), including post-marketed, clinical, and periodic reports. Major Duties and Responsibilities: 1) Oversee the process and completion of medical assessment of medical device...
Summary Review and evaluate safety issues related to medical device products and ensure compliance with worldwide regulations and/or guidelines. Provide medical approval and validation of safety reports (as defined by SOP's), including post-marketed, clinical, and periodic reports. Major Duties and Responsibilities 1) Oversee the process and completion of medical assessment of medical device produ...
The Sr Manager, Corporate Strategy will be responsible for leading a number of strategic projects, problem-solve with leaders and within Hospira as requested by Strategy, and provide guidance to organization around problem structuring, action planning, and recommendation synthesis. The successful candidate will provide ongoing support to Head of Strategy and Corporate Development and other senior...
Job Number: 421658 Clinical Project Manager - Oncology Summary: Responsible for overall project management of one or more biosimilar clinical studies, including overall management of Clinical Research Organizations, vendors and cross functional teams. May also include personnel development, mentoring of Clinical Research Associates / Sr. Clinical Research Associates and other clinical staff. Major...
The Director, EPO Marketing: Provide commercial and cross-functional leadership for the launch of Hospira's first US biosimilar, EPO. Work closely with teams and business partners in the US to prepare for product launch and in Europe to gain understanding of marketing best practices and tactics. Help to shape the US strategy in an emerging regulatory and competitive landscape. Build foundational c...
Looking for clinical project management experience on multiple projects, budgeting, and monitoring (or site coordinator) experience. The candidate also needs to be willing to go out and monitor as well- sort of like a working supervisor that monitors in the field; not always but when needed based on needing their expertise in the field for site selection or interim monitoring visits. Someone who h...
1. Provide medical/clinical expertise related to products to internal (marketing, manufacturing, quality assurance, regulatory affairs, R&D, and legal) and external (healthcare professionals, patients, advocacy groups, etc.) customers from the U.S. and abroad, and assist in resolution of product inquiries. 2. Respond to telephone/written inquiries relating to product use in clinical settings. 3. M...
Sr Clinical Consultant - 140003U9 The Senior Clinical Consultant will utilize his/her therapeutic knowledge and expertise of various dialysis therapies (hemodialysis, peritoneal and acute) to contribute to the development of new renal products for the global market, including Europe, Korea and China. This position will work collaboratively with the Medical Director in the Renal Therapeutic Experti...
Job Title: Global Medical Affairs Project Manager Position Description Strong leadership, teamwork and interpersonal skills. Demonstrated ability to manage conflict situations and effectively interact with personnel at all levels of the organization. Strong ability to influence, initiate and accept change and address complex issues. Demonstrates exceptional follow-through with respect to tasks and...
SUMMARY: The Project Manager will support BioScience Global Medical Affairs (GMA) focusing on Medical Operations. He/she will report to the Director of Global Medical Strategic Project Planning & Metrics. This individual will be responsible for the implementation of appropriate procedures and tools to track progress, measure effectiveness and improve GMA performance. He/she will collaborate closel...
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