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Medical Research Jobs in Missouri

Associate Scientist

Integrated Resources, Inc

Chesterfield, Missouri

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JOB DETAILS
JOB TYPE
Contractor
SKILLS
Analysis Skills, Antibodies, Biochemistry, Bioengineering, Biological Processes, Chemical Engineering, Chemical Processes, Chemistry, Clinical Research, Communication Skills, Computer Skills, Contract Manufacturing, Experiment Design, Information Technology & Information Systems, Laboratory, Laboratory Automation, Manufacturing, Manufacturing/Industrial Processes, Organizational Skills, Pilot Plant, Presentation/Verbal Skills, Process Development, Process Engineering, Process Validation, Regulations, Rehabilitation Nursing, Small Molecules, Team Player, Test Plan/Schedule, Vaccination, Writing Skills
LOCATION
Chesterfield, Missouri
POSTED
Today
Associate ScientistA Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.Job DescriptionThe successful applicant will support the development of innovative, robust, efficient, and scalable chemical and biochemical processes and technologies required for the advancement of a diverse and extensive portfolio of bio-conjugate- and polytide-derived biotherapeutic.The position will focus on process engineering, unit operation scale-up and scale-down and apply rigorous and engineering principals and approaches to all aspects of conjugate process development and equipment design.This position will support necessary purification activities to produce drug substances with appropriate quality attributes.The candidate will work across process development functions and projects covering a broad portfolio including vaccines, antibody-drug conjugates, therapeutic proteins, and oligonucleotides.QualificationsEDUCATION & EXPERIENCE:B.S. degree in Chemical/Biochemical Engineering, or equivalent or related field with 0-5 years of industry experience.Proven record of delivering results in a fast paced environment and effective communication to project teams.Desirable: 2-3 years of experience in process development of biotherapeutic.Experience in developing relevant purification processes for complex biologics.REQUIREMENTS:Demonstrated ability to drive for results and drive innovative research programs independently.Good understanding of chemical engineering/bio-chemical engineering, chemistry/biochemistry and macromolecule analytics.Familiarity with recent scientific literature is required.Applicants should be self-motivated, organized, and capable of working independently, and in a collaborative environment.The successful candidate will possess strong oral and written communication skills.Strong analytical and computer skills are required.Experience in laboratory automation and Lab-View software is desired.Hard working, capable of working independently and in collaborative environment, organized.Additional InformationCandidates will work with fellow scientists to designing and executing experiments including small-scale studies, and pilot plant and manufacturing studies in a variety of types and scales of equipment from bench top to pilot-scale, and, as required, technology transfer and validation in commercial plants.Based on the analyses of these studies, these positions will be expected to develop and test new hypotheses to improve fundamental understanding of the chemical and biochemical processes, including bio-conjugation or large and small molecule combinations.This position will support process validation, quality by design, regulatory approaches, and quality systemsThis position requires a highly motivated individual with the ability to work closely with other members of the laboratory and the department in a matrix environment.This position will also collaborate with the pilot plan and manufacturing staff on experimental studies, clinical manufacturing, and process validation, including work with external contract manufacturing organizationsJob LocationI'm interested

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Integrated Resources, Inc

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