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3 jobs found in kentucky

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    • louisville, kentucky
    • temp to perm
    • $20 - $22 per hour
    job summary: Louisville KY based manufacturing company which develops and manufactures highly specialized products and has been providing innovative water-based specialty polymers since the 1960s is actively seeking (1) highly skilled Laboratory Technician starting immediately on a Temp to Hire basis. Working hours will be Monday thru Friday, 7:00am to 4:00pm or 8:00am to 5:00pm w/some extended hours - no weekends at this time. At this time the company is expanding its Laboratory Staff and will support new product development for their emulsion polymer platform. Great location in historic Louisville!! Dozens of great restaurants, shopping spots, historical attractions, sports teams and much more....!!!   location: Louisville, Kentucky job type: Temporary salary: $20 - 22 per hour work hours: 8 to 4 education: Associate   responsibilities: Perform laboratory experiments in support of technical projects and contribute to problem solving.Perform standard performance tests and develop new test methods where necessary.Use of Analytical instruments to characterize formulations and raw materialsMaintain a current inventory of chemical raw materials and laboratory consumables.Proficiently preform in a Laboratory setting by conducting polymer synthesis, characterization, and application testing in support of new product development.Be a problem solver.....leading to project success.Maintain a well-organized and efficient lab environment.Effective written and verbal communication.Maintain thorough records per Good Laboratory Practices (GLP).  qualifications: Prefer Technical Associates Degree with laboratory work experienceMinimum: High School Graduate > 3 years of relevant lab work experienceLiteracy in Microsoft Office software suite.Self motivated and excited to learn.Collaborative and team oriented.Ability to handle multiple tasks, work independently and complete assigned work with accuracy and efficiency.   skills: MS-WORD, MS-EXCEL, GLP (Good Laboratory Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: Louisville KY based manufacturing company which develops and manufactures highly specialized products and has been providing innovative water-based specialty polymers since the 1960s is actively seeking (1) highly skilled Laboratory Technician starting immediately on a Temp to Hire basis. Working hours will be Monday thru Friday, 7:00am to 4:00pm or 8:00am to 5:00pm w/some extended hours - no weekends at this time. At this time the company is expanding its Laboratory Staff and will support new product development for their emulsion polymer platform. Great location in historic Louisville!! Dozens of great restaurants, shopping spots, historical attractions, sports teams and much more....!!!   location: Louisville, Kentucky job type: Temporary salary: $20 - 22 per hour work hours: 8 to 4 education: Associate   responsibilities: Perform laboratory experiments in support of technical projects and contribute to problem solving.Perform standard performance tests and develop new test methods where necessary.Use of Analytical instruments to characterize formulations and raw materialsMaintain a current inventory of chemical raw materials and laboratory consumables.Proficiently preform in a Laboratory setting by conducting polymer synthesis, characterization, and application testing in support of new product development.Be a problem solver.....leading to project success.Maintain a well-organized and efficient lab environment.Effective written and verbal communication.Maintain thorough records per Good Laboratory Practices (GLP).  qualifications: Prefer Technical Associates Degree with laboratory work experienceMinimum: High School Graduate > 3 years of relevant lab work experienceLiteracy in Microsoft Office software suite.Self motivated and excited to learn.Collaborative and team oriented.Ability to handle multiple tasks, work independently and complete assigned work with accuracy and efficiency.   skills: MS-WORD, MS-EXCEL, GLP (Good Laboratory Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • lexington, kentucky
    • permanent
    • $90,000 - $100,000 per year
    job summary: The Senior Analytical Scientist will develop analytical methods for quality control and characterization of products, lead drug product development programs and provide analytical and technical support for process development and manufacturing. Responsibilities include developing appropriate quality measures for Summit Biosciences' products, developing, validating, transferring or verifying analytical methods, characterizing products and processes, training and creation of documentation.   location: Lexington, Kentucky job type: Permanent salary: $90,000 - 100,000 per year work hours: 9 to 5 education: Bachelors   responsibilities: Lead scientific aspects of nasal spray drug product development projectsProvide expertise in chemistry and analytics related to Summits' productsResponsible for the design and conduct of analytical development in accordance with company and regulatory standards to facilitate new product developmentResponsible for multi-department and multi-site communications required to facilitate new product developmentManage technical direction of projects by identifying key deliverables, next steps and communicating with teamsPrioritizes workload to ensure that key objectives are met on time and to budgetLead method development and product characterization for multiple projectsConducts technical projects with the appropriate use of company resources in mindMake recommendations for continuous improvement projects that improve effectivenessAuthor and review technical reports, regulatory submissions, SOPs, validation protocols and other cGMP documentsIdentify and implement new techniques and instrumentation to expand internal capabilitiesAssist junior staff to apply complex fundamental knowledge, laboratory procedures, or testing apparatus/ methods Knowledge, Skills and Abilities:Extensive technical experience in analysis and development of pharmaceuticalsComprehensive understanding of small molecule and large molecule chemistryDemonstrated knowledge of modern analytical techniques, including HPLC.Knowledge of nasal spray characterization a plus.Expertise in Pharmaceutical aspects of Leachables and ExtractablesExperience in development and validation of methods destined for QC in the pharmaceutical industryUnderstanding of current Good Manufacturing Practices (cGMPs)Proven team player with well-developed interpersonal and mentoring skills, excellent organizational skills, communication skills, including written documentation skills and presentation skills   qualifications: Degree in Chemistry, Pharmaceutics or related field; advanced degree is a plusExtensive experience in analytical and drug product development activities regulated by FDAOutstanding capabilities for adjusting priorities in response to changing conditions and schedules Experience with nasal spray drug product development and characterization is a plus   skills: Analytical Chemistry Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: The Senior Analytical Scientist will develop analytical methods for quality control and characterization of products, lead drug product development programs and provide analytical and technical support for process development and manufacturing. Responsibilities include developing appropriate quality measures for Summit Biosciences' products, developing, validating, transferring or verifying analytical methods, characterizing products and processes, training and creation of documentation.   location: Lexington, Kentucky job type: Permanent salary: $90,000 - 100,000 per year work hours: 9 to 5 education: Bachelors   responsibilities: Lead scientific aspects of nasal spray drug product development projectsProvide expertise in chemistry and analytics related to Summits' productsResponsible for the design and conduct of analytical development in accordance with company and regulatory standards to facilitate new product developmentResponsible for multi-department and multi-site communications required to facilitate new product developmentManage technical direction of projects by identifying key deliverables, next steps and communicating with teamsPrioritizes workload to ensure that key objectives are met on time and to budgetLead method development and product characterization for multiple projectsConducts technical projects with the appropriate use of company resources in mindMake recommendations for continuous improvement projects that improve effectivenessAuthor and review technical reports, regulatory submissions, SOPs, validation protocols and other cGMP documentsIdentify and implement new techniques and instrumentation to expand internal capabilitiesAssist junior staff to apply complex fundamental knowledge, laboratory procedures, or testing apparatus/ methods Knowledge, Skills and Abilities:Extensive technical experience in analysis and development of pharmaceuticalsComprehensive understanding of small molecule and large molecule chemistryDemonstrated knowledge of modern analytical techniques, including HPLC.Knowledge of nasal spray characterization a plus.Expertise in Pharmaceutical aspects of Leachables and ExtractablesExperience in development and validation of methods destined for QC in the pharmaceutical industryUnderstanding of current Good Manufacturing Practices (cGMPs)Proven team player with well-developed interpersonal and mentoring skills, excellent organizational skills, communication skills, including written documentation skills and presentation skills   qualifications: Degree in Chemistry, Pharmaceutics or related field; advanced degree is a plusExtensive experience in analytical and drug product development activities regulated by FDAOutstanding capabilities for adjusting priorities in response to changing conditions and schedules Experience with nasal spray drug product development and characterization is a plus   skills: Analytical Chemistry Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • lexington, kentucky
    • permanent
    • $90,000 - $100,000 per year
    job summary: This individual is responsible for independently planning and performing routine tasks in the development laboratory and directly contributing to project teams. Responsibilities include developing and transferring validation-ready analytical methods and manufacturing-ready formulations   location: Lexington, Kentucky job type: Permanent salary: $90,000 - 100,000 per year work hours: 9 to 5 education: Masters   responsibilities: Work in a safe manner in accordance with site procedures.Perform development stability testing and non-GMP production testing Maintain the laboratory in accordance with SOPs.Operate and maintain analytical instrumentation for development testing, including routine preventive maintenance and troubleshooting.Write, revise and review Standard Operating Procedures, Material Specifications, Forms, Protocols and Reports.Familiar with advanced analytical techniques for HPLC, UV/Vis, FTIR, GC, and Nasal Spray Testing and executes tasks without supervision or under the direction of a test method, standard operating procedure, or a protocol. Responsible for design and conduct of defined sets of experiments in support of a quality by design (QbD) process assisted by statistical design softwareUnderstanding of cGMPs and develop understanding EMEA regulationsExcellent oral and written communication skills.Recommend and implement innovative approaches to problem solving.Utilize investigative skills for aberrant result laboratory investigations.Mentor Development Scientist I and II levelsOther duties as assigned.  qualifications: Outstanding capabilities for multitasking and adjusting priorities in response to changing conditions and schedules.Team player with well-developed interpersonal, organizational, and communication skills.Demonstrates proper social etiquette and self-control to others when dealing with stressful situations.Advanced technical experience and knowledge in analysis and development of pharmaceuticalsExperience in development of validation-ready methods destined for QC in the pharmaceutical industry Minimum Qualifications: Relevant Technical Degree (years for guidance only) BS+6-12 yrs, MS+2-6 yrs, PhD+0-4 yrsExperience in FDA regulated environmentOutstanding capabilities for adjusting priorities in response to changing conditions and schedulesExperience with nasal spray drug product development and characterization is a plus   skills: Analytical Chemistry Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: This individual is responsible for independently planning and performing routine tasks in the development laboratory and directly contributing to project teams. Responsibilities include developing and transferring validation-ready analytical methods and manufacturing-ready formulations   location: Lexington, Kentucky job type: Permanent salary: $90,000 - 100,000 per year work hours: 9 to 5 education: Masters   responsibilities: Work in a safe manner in accordance with site procedures.Perform development stability testing and non-GMP production testing Maintain the laboratory in accordance with SOPs.Operate and maintain analytical instrumentation for development testing, including routine preventive maintenance and troubleshooting.Write, revise and review Standard Operating Procedures, Material Specifications, Forms, Protocols and Reports.Familiar with advanced analytical techniques for HPLC, UV/Vis, FTIR, GC, and Nasal Spray Testing and executes tasks without supervision or under the direction of a test method, standard operating procedure, or a protocol. Responsible for design and conduct of defined sets of experiments in support of a quality by design (QbD) process assisted by statistical design softwareUnderstanding of cGMPs and develop understanding EMEA regulationsExcellent oral and written communication skills.Recommend and implement innovative approaches to problem solving.Utilize investigative skills for aberrant result laboratory investigations.Mentor Development Scientist I and II levelsOther duties as assigned.  qualifications: Outstanding capabilities for multitasking and adjusting priorities in response to changing conditions and schedules.Team player with well-developed interpersonal, organizational, and communication skills.Demonstrates proper social etiquette and self-control to others when dealing with stressful situations.Advanced technical experience and knowledge in analysis and development of pharmaceuticalsExperience in development of validation-ready methods destined for QC in the pharmaceutical industry Minimum Qualifications: Relevant Technical Degree (years for guidance only) BS+6-12 yrs, MS+2-6 yrs, PhD+0-4 yrsExperience in FDA regulated environmentOutstanding capabilities for adjusting priorities in response to changing conditions and schedulesExperience with nasal spray drug product development and characterization is a plus   skills: Analytical Chemistry Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.

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