Job Description Job #219760
Chipton-Ross is seeking a Research Associate Scientific III for a contract opportunity in Deerfield, IL.
BASIC QUALIFICATIONS (REQUIRED SKILLS/EXPERIENCE)- Research lab experience may include research in GMP/QSR environment, cross-functional teamwork, and independent experimentation in method development and validation.
- Knowledge/experience with lyophilization
- Knowledge/experience with Class 2/ 510k/ PMA FDA approved medical devices
- Medical Device Product development experience
POSITION RESPONSIBILITIESEffectively contribute solid technical knowledge to a variety of projects within the relevant discipline with minimal assistance.
Display moderate technical understanding of related disciplines such as pH, temperature controlled reactions, and chemical reactions.
Conduct routine/non-routine research and design experiments with minimal assistance.
Essential Duties and Responsibilities:
The incumbent will perform other duties assigned.
- Without assistance, make sound technical recommendations regarding projects/matters that are more routine than not.
- Provide some analysis/redesign of key experimental procedures.
- Independently select techniques and procedures to solve problems within area of responsibility.
- Employ appropriate techniques/methods to successfully and independently execute routine assignments within negotiated deadlines.
Identify existing alternative methods and technologies for improving existing or new products/processes.
- Maintain knowledge of relevant QSR and safety requirements while building knowledge of other regulatory requirements related to R&D (product development, design and safety) to ensure compliance in all research, data collection and reporting activities. • Manufacturability/Scale Up of biomaterials- Transfer from lab scale experiements to manufacturing production.
- Contribute to technical feasibility analysis of complex research and design concepts.
- Monitor budgets and/or activity schedules of external testing (communication, shipment, analysis of results and documentation).
- In addition to having an in-depth knowledge and understanding of GxP and related regulations and guidance, is able to provide expert insights into such regulations so as to facilitate efficient product registration and/or is an active participant in the generation, review, adoption and interpretation of such regulations.
- Demonstrate ability to apply technical theories and principles to projects within area of expertise for non-routine tasks.
- Analyze and determine best solutions to non-routine experimental design or research problems with minimal assistance.
- Accurately assess results for validity and conformance to specifications.
PREFERRED QUALIFICATIONS (DESIRED SKILLS/EXPERIENCE)PHYSICAL REQUIREMENTSREQUIRED EDUCATION- Accredited Bachelor's Degree in a scientific discipline with at least 3-6 years lab experience or MS with at least 1-2 years of experience.
WORK HOURSADDITIONAL INFORMATION - Employment will be contingent on clearing a drug screen and background check. Both must clear prior to start date.
- Candidates responding to this posting must currently possess the eligibility to work in the United States. No third parties please.
For more information, please apply or contact:
Billy James 800.927.9318 x340
[email protected] 
