R & D Jobs in Illinois

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117 Illinois R & D jobs found on Monster.

Jobs 1 to 20 of 117
ICON - Be a Part of our Journey. This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. Our Clinical Trial Assistants (CTA’s) play a key role within ICON. Working closely with our global clinical teams the Clinical Trial and Project Managers to...
Job ID: 4266 Position Description: - Consistently meet & exceed established program sales goals & market share targets within territory by delivering sales programs & utilizing effective sales techniques & promotional materials in order to influence targeted PCPs - Deliver a territory level business plan aligned with the national strategy and tactics - Achieve daily/monthly/quarterly sales call ac...
Fantastic Part Time Weekend Position 24 hours per week Skokie, Greater Chicago LanzaTech’s award winning technology is revolutionizing the way the world thinks about waste carbon by treating it as an opportunity instead of a liability. LanzaTech’s unique process provides a sustainable pathway to produce platform chemicals that serve as building blocks to products that have become indispensable in...
This section focuses on the main purpose of the job in one to four sentences. This position is responsible for complaint handling activities, specifically the processing of low-risk complaints (not associated with death or serious injury). Essential Duties and Responsibilities: This section contains a list of five to eight primary responsibilities of this role that account for 5% or more of the wo...
This section focuses on the main purpose of the job in one to four sentences. Under limited supervision within the Chemistry, Manufacturing, and Controls regulatory team, responsible for the implementation of complex regulatory strategies, obtaining and maintaining marketing authorizations for product(s) and communication of general regulatory requirements in support of licensing of Baxters produc...
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...
Develop products with superior design leveraging expertise in food chemistry, food ingredient functionality and experimental design supporting the Quaker and GNG businesses. Translate consumer needs and market trends into strategic and tactical product innovation and renovation projects Key Accountabilities Utilize scientific methods to develop knowledge that creates business opportunities that su...
Develop products with superior design leveraging expertise in food chemistry, food ingredient functionality and experimental design supporting the Quaker and GNG businesses. Translate consumer needs and market trends into strategic and tactical product innovation and renovation projects Key Accountabilities Utilize scientific methods to develop knowledge that creates business opportunities that su...
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...
Shall provide guidance to "New Indication" projects for previously approved therapeutic entity including: * Collaboratively identifying and proving new indication opportunities. * Developing of new clinical studies. * Gathering guidance and building advanced product support with healthcare organizations, payors, government entities and key opinion leaders. * Reviewing and translating data and stud...
PerkinElmer, Inc. is a global leader focused on improving the health and safety of people and the environment. The Software Engineer will participate as a member of the Radiometric Detection and Discovery Services R&D software development group in delivery of new product features and platforms across our radiometric detection instruments. Responsibilities: Technical leadership of software sustaini...
Your Clinical Consulting 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 Cli...
Job Title: Document Control Specialist Position Description Product/document configuration experience desired Intermediate level and document management (e.g. Word) software skills Project Management Skills, desired Must have excellent conceptual, analytical, written and verbal configuration skills Comprehension of design methodology, product configuration and complex manufacturing processes Abili...
Job Title: R&D Configuration Specialist Position Description R&D Configuration Specialist (Design & Control) will be responsible for managing the day-to-day operations for product/document configuration management within a section or functional area in the organization. Identify and assess regulatory and quality risks in activities and processes according to regulatory agency rules and guidelines...
PepsiCo Nutrition is central to the Company's future and instrumental in innovation efforts. This role is integral in helping to shape the organization in these efforts for the Global Nutrition Group and the Quaker food, snack and beverage businesses so they reflect company wide approaches. This position has responsibility for project and process management that requires a broad scope and understa...
G R Validation & Compliance Services, Inc., is a full service Validation, GMP Compliance, Engineering, Equipment Design and consulting firm dedicated to serve the FDA regulated Pharmaceutical, Biotechnology and Medical Device industries. We are currently looking for Validation Engineers with diverse background for multiple positions. Location: Milwaukee, WI (2 positions) Philadelphia, PA (3 positi...
Work closely with marketing and development teams to develop product strategy and ensure delivery of solid medical plans. Shall: * Gather guidance from healthcare organizations, government entities and key opinion leaders to advise medical planning. * Manage regulatory and safety issues. * Support development of a strategic publication plans. * Ensure that medical strategies reflect stakeholder ne...
Seeking board certified Gastroenterologist to advance professional relationships with healthcare organizations, government entities and key opinion leaders while communicating clinical data, health economics and outcomes research data on therapeutic products to physicians, researchers, managed markets medical and pharmacy directors, hospital decision makers, formulary committees, consultant pharma...
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