R & D Jobs in Wheeling, Illinois

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65 Wheeling, IL R & D jobs found on Monster.

Jobs 1 to 20 of 65
Highly visible position for individual with an executive presence, high energy and passion. Base salary starts at $350,000 plus bonus and equity potential in the seven figures range. Full company paid family benefits, tuition reimbursement, first class travel, expense account, club membership and executive perquisites. Seeking Medical Doctor with drug development experience in the area of Oncol...
Job Title: Sr. Clinical Supply Program Manager Position Description As a program and study lead for Global Clinical Trial Supply Chain (GCTSC) on the Global CMC Team (GCT) and the relevant Clinical teams, designs, develops and implements the global Clinical Supplies strategy for protocol development at the program level, to ensure appropriate processes are established and in order to achieve cli...
Why join our growing, dynamic team? Growth. Opportunity. Development. That’s what you can look forward to at Sensient. We provide a fast-paced, supportive and empowering environment in which employees can realize their full potential and take ownership in their career path. We are passionate about how we achieve great outcomes together for our customers and each other. Sensient fosters an cultu...
Job Summary: Responsible for Validation of thermal and non-thermal processing systems for the inactivation of vegetative pathogens for PepsiCo Foods and Beverages. Position Description: Implement PepsiCo Global Policy on the requirements for validation of all processes which have the potential to inactivate vegetative pathogens by thermal or non-thermal methods. Establish protocols, provide to...
To accelerate our progress against the Global PepsiCo Quality Program, Global Foods Quality Assurance is looking for a leader to oversee the execution of key change programs within the overall agenda. Specifically, the job holder will oversee the execution of the Global Foods Quality Forum agenda; development and adoption of harmonized Foods quality standards and audits; and the tracking and repor...
Responsibilities · Responsible for the development of validation protocols and reports to support the manufacturing and packaging processes of multiple solid dosage pharmaceutical products. Products manufactured include tablets, capsules, powdered blends and granulations. · Responsible for the generation of testing protocols covering all aspects of manufacturing and packaging processes for a giv...
Job Title: Forensic Investigator (Analytical Chemistry) Position Description The person in this position will perform day-to-day operations of the forensics laboratory including forensic analysis of suspected counterfeit pharmaceutical product. Under the supervision of the Forensic Program Manager, the position will be responsible for physical and chemical assessments of product packaging and p...
Job Title: Sr. Clinical Study Manager Position Description Provide leadership and expertise in the global clinical operational strategy, directing project teams to support the clinical studies defined in the Integrated Clinical Development plans for compounds within assigned Therapeutic Area ensuring all studies are executed in accordance with Code of Federal Regulations, Good Clinical Practices...
Job Title: Clinical Project Manager Position Description Project Manager leverages drug development, project management, operational, and technical expertise to: Independently manage a combination of R&D Project Management processes and Lead multiple small to medium size drug development programs. Responsibilities associated with drug development/R&D processes include developing, driving, manag...
Unusual position for strong leader who can scientifically guide drug development culture to efficiency not only guiding change but managing team and stakeholder morale and inspiring ownership and commitment to the process of change related to therapeutics being brought to market, changing healthcare management landscape, customers served, and business processes used. Key Position Activities: ***...
Seeking 5+ years of experience in Project Management for Medical Affairs, Clinical Drug Development and Product Launch activities; MBA or similar advanced business degree; PMP certification; general knowledge of regulatory and compliance standards and guidelines and risk management practices and techniques and super interpersonal skills to support Global Medical Affairs programs and apply critical...
1 Year Contract Position - H1's/Subcontractors will NOT be considered: · Associate Engineer/Scientist to tweak existing and create new products. · Ability to work independently under the direction of senior Scientists/Engineers leveraging strong problem solving skills. · Conduct bench top and pilot plant product development. · Plan and execute experiments, interpret and report results, and rec...
Job Title: Manager, Regulatory Affairs Position Description Supervisory responsibilities over a team of regulatory professionals for the on-time filing of high-quality regulatory submissions and for post-approval maintenance of regulatory dossiers. Mentors and provides regulatory guidance to team members. Interacts with all levels in the organization. Participates in discussions with manageme...
Trileaf Corporation is a nationwide environmental and architecture and engineering consulting firm that assists clients with environmental due diligence, regulatory compliance, and engineering & architectural design. Trileaf serves the wireless communications, real estate, financial, and petroleum industries from its headquarters in St. Louis, MO and branch offices in Baltimore, MD; Chicago, IL; D...
Thorough knowledge of analytical method development, validation and transfer in a cGMP setting. Utilize all applicable comprehensive chemistry knowledge including separations and wet chemistry, to aid in generic drug development and formulation support. Plans, performs, supervises laboratory work ranging from routine compendial work, stability testing t and data interpretation. Lead development of...
Senior Clinical Research Associate Home based throughout the Mid West Coast. Multiple positions available. If you have at least 5 full years of regional field monitoring, Provident Research is looking for you! This role is for individuals to be responsible for managing clinical activities at multiple study sites, as well as fostering strong, productive relationships with colleagues within the O...
AuraSense Therapeutics (AST) is a biopharmaceutical company developing first-in-class therapies based upon its proprietary Spherical Nucleic Acid (SNA) gene regulation and immune modulation strategies. AST is leading the translation of SNA constructs as innovative medicines. AuraSense Therapeutics' uniquely engineered SNA constructs possess attractive biocompatibility and versatility as therapeuti...
Job Summary: Develop both standard and innovative sweet good prototypes to demonstrate Sensient’s product line in support of existing and new business growth opportunities at targeted customers. Actively contribute ideas and physical assistance while further developing an expertise in the use of flavors and food ingredients. Can work independently and balance a multi-task workload. Effectively co...
Primary Responsibilities: Provide food safety support to the business unit in order to maintain safe design, processes and products within the current portfolio and with future innovation. Conduct documented Ingredient Risk Assessments and ensure all supporting analyses have been conducted, reviewed and acted upon. Assist with the development and execution of food safety strategies and plans in...
This individual will deliver expertise to the PepsiCo Americas Foods (PAF) Scientific Affairs function to enable innovation projects, new product development and new ingredient approval/development, as well as supporting crisis situations. This position will focus initially on support for the Quaker business and be recognized as a productive and collaborative team member supporting business goals ...

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