<h3>Job Description</h3><div>Job Description<div>Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you! This is a laboratory role focused on the analysis of drug or other targets in complex biologic matrices using immunologic methods. Scientifically, you should possess, or be able to easily gain, command of the concepts of drug molecule and endogenous biomarker bioanalysis in support of pharmacokinetics, pharmacodynamics and other purposes. These might include anti-drug antibody and neutralizing antibody detection, as well as nucleic acid detection and sequence characterization. In addition, you will be expected to execute and then administer bioanalytical assays on various platforms, robots and detectors built for purpose, and sometimes per CLIA.Projects in translational medicine (TLM) include method transfer of assays originated from the sponsor's lab, validation of commercially available kits and methods, or a collaborative effort between the QPS team and our client for custom assays. In addition to LBA-based immunoassays for PK, biomarkers and immunogenicity assessment, QPS scientists also help develop cell-based assays for neutralizing antibody activity studies and biomarker evaluation in support of drug development programs.QPS’ Story:Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of Neuropharmacology, DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II – IV Clinical Research services. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life.Team members enjoy challenging and rewarding work, and are encouraged achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, team work and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals.If this sounds like your ideal work environment, then we would love to speak with you, so apply today! Please visit our website (www.qps.com) for more information and to see all current openings.The JobA senior role such as Research Scientist includes, but is not limited to, the following activities:<ul><li>Conceive and develop new, quantitative, bioanalytical methods; </li><li>Improve assay quality and technical operations; </li><li>Troubleshoot analytical issues and transfer existing assays from pharmaceutical organizations; </li><li>Prepare controlled procedures and reports of results with data interpretation;</li><li>Author scientific papers to be published in peer reviewed journals;</li><li>Present at scientific meetings as needed.</li></ul>Work Location<div><ul><li>This job will be 100% QPS-office/facility based</li></ul></div>RequirementsThe successful candidate will hold an advanced degree in Biochemistry, Immunology, Pharmacology, Medical Technology, Biology or a related field as follows:<ul><li>Ph.D.</li><li>Master’s Degree and 8 or more years of relevant industry experience </li><li>Experience in a Regulated industry laboratory required</li></ul>Why You Should Apply<ul><li>Great learning opportunities, especially for those new to the field. Our seasoned professionals are here to support and work with you to explore your learning potential and career goals.</li><li>Structured Career Ladders that provide excellent growth based on your personal aspirations.</li><li>Bonuses and merit increases are a part of the QPS total rewards approach and are linked to individual, team and company performance.</li><li>Solid Benefits package, including Company-matched 401(k), and Company-sponsored Group Life/AD&D and Short and Long-term Disability Insurance</li><li>Park-like setting in Newark, Delaware</li><li>Internal committees designed with the needs and enjoyment of QPS employees in mind.</li></ul>QPS, LLC is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans. </div></div>

At DuPont, we are working on things that matter; whether it's providing clean water to more than a billion people on the planet, producing materials that are essential in everyday technology devices from smartphones to electric vehicles, or protecting workers around the world.If you would like to be a part of a premier multi-industrial company that is delivering sustainable solutions that bring real purpose and value, of a company with collaborative spirit because it believes that we work best when we work together as a team and values the diversity of thought, then DuPont is the company for you!We are excited to share that on May 22, 2024, DuPont announced plans to separate(1) into three industry-leading, independent publicly traded companies. This strategic move will create focused businesses with distinct investment profiles. We believe the proposed separations will create opportunities for all three future companies to better serve their customers and unlock long-term value for stakeholders. This process is expected to take 18-24 months from the date of announcement to complete. We are committed to supporting our employees throughout this transition and ensuring a smooth and successful separation process. We look forward to welcoming new talent who are interested in contributing to the continued success and growth of our evolving organization.WHY JOIN US?Our purpose is to empower the world with essential innovations to thrive. We work on things that matter!Have the Opportunity to chart your own course, challenge yourself, and acquire new capabilities to build a rewarding and fulfilling career. We reward employees with competitive pay and incentives to recognize skills, competencies, and contributions to business results.Get to Experience a collaborative environment where teamwork is celebrated with flexibility that enhances balance and an inclusive atmosphere that is welcoming to all!Get to know our Purpose and make it yours by bringing innovations to market that improve the world, share a commitment to sustainability that makes our planet better and give back to communities in which we work and live.Pad Material Research ScientistJob Description:DuPont Chemical Mechanical Planarization (CMP) Technology group is seeking a Pad Material Research Scientist in Pad R&D team located in Newark, DE. The candidate will be responsible to develop innovative formulation and material technologies for DuPont's industrial leading CMP Pad portfolio and drive fundamental understanding of product performance in target applications. The candidate will work in a cross functional team in partnership with Marketing, Process Development, Scale-up, Application, and Analytical Science to resolve a variety of CMP pad material and engineering related problems.Key responsibilities are:* Develop innovative approaches to new material synthesis and processing to create novel polymeric materials with differentiated properties* Develop structure-property relationships with advanced knowledge of scientific principles, experimental design, and advanced characterization* Lead new product development and identification of new technology areas for DuPont CMPT's innovative pipeline* Collaborate with technical groups in R&D and manufacturing to facilitate the scale-up and commercialization of new products* Document work in a timely fashion in data books, internal reports, patent disclosures, and external publications as appropriate* Communicate results and progress to technical teams, management, and business leadership through written report and oral presentations* Demonstrate behaviors that exemplify DuPont's Core Values: Safety and Health, Respect for People, Highest Ethical Behaviors, and Protecting the PlanetThis position has travel requirements of up to 10% globally.Required Qualifications:* Ph.D. in Materials Science, Polymer Chemistry, Chemical Engineering, or other related disciplines* Strong background in polymer technology with proven record in synthesis and material development* Demonstrated ability to examine structure-property relationships of polymer formulations* Strong analytical and critical thinking with the ability to make data driven decisions and actionable recommendations* Excellent interpersonal and communication skills* Strong project management skills and ability to execute complex projects and navigate multiple priorities.* Familiarity with a variety of analytical techniques, such as NMR, GPC, FT-IR, SEM, DMA, TGA, DSC, etc.* Successful candidate should have strong collaborative R&D mindsetPreferred Qualifications:* Minimum of 3 years product R&D experience with a successful customer engagement and product development record. Formulating with polymeric system is preferred.* Experience in CMP or other semiconductor process technologies is preferred* Experience in polyurethane manufacturing and/or product development* Experience leading and driving complex technical projects to a successful completion* Experience in Stage Gate type of new product development process* Six sigma certification, experience in Design of Experiment principles and statistical data analysisJoin our Talent Community to stay connected with us!DuPont is an equal opportunity employer. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability or any other protected class. If you need a reasonable accommodation to search or apply for a position, please visit our Accessibility Page for Contact Information.(1)The separation transactions are subject to satisfaction of customary conditions, including final approval by DuPont's Board of Directors, receipt of tax opinion from counsel, the filing and effectiveness of Form 10 registration statements with the U.S. Securities and Exchange Commission, applicable regulatory approvals, and satisfactory completion of financing.? For further discussion of risks, uncertainties and assumptions that could impact the achievement, expected timing and intended benefits of the separation transactions, see DuPont's announcement.

Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you! The Bioanalytical department has an opening with our Method Development/Method Validation group as well as our Sample Analysis group.Our Bioanalytical Method Development / Method Validation staff has considerable experience with the conventional matrices (plasma, serum, whole-blood, urine, feces), as well as various animal and human tissues. As a professional in this group, you will work with our clients to identify assay requirements and intended use, and then to develop assays using the most appropriate technology platform.Serving as Principle Investigator (PI) on Bioanalytical studies for the Sample Analysis group, you will be responsible for study management, interpretation and reporting of study data, and in concert with team members and peers, will participate in method validation when needed.QPS' Story:Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of Neuropharmacology, DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II - IV Clinical Research services. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life.Team members enjoy challenging and rewarding work, and are encouraged achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, team work and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals.If this sounds like your ideal work environment, then we would love to speak with you, so apply today!Please visit our website (www.qps.com) for more information and to see all current openings.The Job* Independently manage multiple sample analysis projects OR method development/validation studies at the same time with minimum supervision.* Prepare, and/or review and understand study protocols.* Coordinate with client and internal resources to plan, design and conduct studies.* Evaluate significance of data and report findings.* Prepare Study summaries and/or reports.* Set-up, utilize, and maintain complex instrumentation.* Communicate project timelines, status, data, reports, and inquiries to client and/or study sites, effectively addressing any issues that may arise.* Maintain the proper level of regulatory compliance for each study, preparing QA related documents and addressing QA audit findings.* Maintain schedule of projects and timelines.* Supervise, train and/or mentor junior scientific staff* Develop, validate and run sensitive, reliable and efficient LC/MS/MS assays for TK/PK assessment OR Perform high-volume sample analysis and/or data analysis, data QC, and data interpretation.* Ensure that GLP regulations and SOPs are followed in all bioanalytical service activities.Work Location* This job will be 100% QPS-office/facility basedRequirementsThe successful candidate will hold an advanced degree in Analytical Chemistry, Biochemistry, Pharmacology, or related scientific discipline:* Ph.D. degree* Recent graduates must have with direct experience on LC-MS/MS analysis* If more than 2 years since graduation, candidates must have direct experience on method development of bioanalytical assays using LC-MS/MS, particularly having CRO experience* Understanding of experimental design and planning, and data collection and analysis software.Why You Should Apply* Great learning opportunities, especially for those new to the field. Our seasoned professionals are here to support and work with you to explore your learning potential and career goals.* Structured Career Ladders that provide excellent growth based on your personal aspirations.* Bonuses and merit increases are a part of the QPS total rewards approach and are linked to individual, team and company performance.* Solid Benefits package, including Company-matched 401(k), and Company-sponsored Group Life/AD&D and Short and Long-term Disability Insurance* Park-like setting in Newark, Delaware* Internal committees designed with the needs and enjoyment of QPS employees in mind.QPS, LLC is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.

<h3>Job Description</h3><div>Job Description<div><div><div><div>Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you! The Bioanalytical department has an opening with our Method Development/Method Validation group as well as our Sample Analysis group. Our Bioanalytical Method Development / Method Validation staff has considerable experience with the conventional matrices (plasma, serum, whole-blood, urine, feces), as well as various animal and human tissues. As a professional in this group, you will work with our clients to identify assay requirements and intended use, and then to develop assays using the most appropriate technology platform. Serving as Principle Investigator (PI) on Bioanalytical studies for the Sample Analysis group, you will be responsible for study management, interpretation and reporting of study data, and in concert with team members and peers, will participate in method validation when needed.QPS’ Story:Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of Neuropharmacology, DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II – IV Clinical Research services. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life.Team members enjoy challenging and rewarding work, and are encouraged achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, team work and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals.If this sounds like your ideal work environment, then we would love to speak with you, so apply today! Please visit our website (www.qps.com) for more information and to see all current openings.The Job<ul><li>Independently manage multiple sample analysis projects OR method development/validation studies at the same time with minimum supervision.</li><li>Prepare, and/or review and understand study protocols. </li><li>Coordinate with client and internal resources to plan, design and conduct studies.</li><li>Evaluate significance of data and report findings. </li><li>Prepare Study summaries and/or reports.</li><li>Set-up, utilize, and maintain complex instrumentation.</li><li>Communicate project timelines, status, data, reports, and inquiries to client and/or study sites, effectively addressing any issues that may arise.</li><li>Maintain the proper level of regulatory compliance for each study, preparing QA related documents and addressing QA audit findings.</li><li>Maintain schedule of projects and timelines.</li><li>Supervise, train and/or mentor junior scientific staff</li><li>Develop, validate and run sensitive, reliable and efficient LC/MS/MS assays for TK/PK assessment OR Perform high-volume sample analysis and/or data analysis, data QC, and data interpretation.</li><li>Ensure that GLP regulations and SOPs are followed in all bioanalytical service activities.</li></ul>Work Location<div><ul><li>This job will be 100% QPS-office/facility based</li></ul></div>RequirementsThe successful candidate will hold an advanced degree in Analytical Chemistry, Biochemistry, Pharmacology, or related scientific discipline:<ul><li>Ph.D. degree<ol><li>Recent graduates must have with direct experience on LC-MS/MS analysis</li><li>If more than 2 years since graduation, candidates must have direct experience on method development of bioanalytical assays using LC-MS/MS, particularly having CRO experience</li></ol></li><li>Understanding of experimental design and planning, and data collection and analysis software.</li></ul>Why You Should Apply<ul><li>Great learning opportunities, especially for those new to the field. Our seasoned professionals are here to support and work with you to explore your learning potential and career goals.</li><li>Structured Career Ladders that provide excellent growth based on your personal aspirations.</li><li>Bonuses and merit increases are a part of the QPS total rewards approach and are linked to individual, team and company performance.</li><li>Solid Benefits package, including Company-matched 401(k), and Company-sponsored Group Life/AD&D and Short and Long-term Disability Insurance</li><li>Park-like setting in Newark, Delaware</li><li>Internal committees designed with the needs and enjoyment of QPS employees in mind.</li></ul>QPS, LLC is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans. </div></div></div></div></div>

Local: Newark, Delaware, United States of AmericaCategory: Ciência & InovaçãoJob Id: 241834WJob Type: ExperienteNa DuPont, nós trabalhamos com as coisas que importam, seja ao fornecer água potável a mais de um bilhão de pessoas em todo o planeta, produzir materiais essenciais aos dispositivos tecnológicos que usamos diariamente, desde smartphones até veículos elétricos, ou proteger os trabalhadores do mundo todo. Se você quiser fazer parte de uma empresa multissetorial de primeira linha que está entregando soluções sustentáveis que geram propósito e valor reais, uma empresa com espírito colaborativo porque acredita que trabalhamos melhor quando trabalhamos juntos em equipe e valoriza a diversidade de pensamento, então a DuPont é a empresa certa para você!Pad Material Research Scientist Job Description:DuPont Chemical Mechanical Planarization (CMP) Technology group is seeking a Pad Material Research Scientist in Pad R&D team located in Newark, DE. The candidate will be responsible to develop innovative formulation and material technologies for DuPont’s industrial leading CMP Pad portfolio and drive fundamental understanding of product performance in target applications. The candidate will work in a cross functional team in partnership with Marketing, Process Development, Scale-up, Application, and Analytical Science to resolve a variety of CMP pad material and engineering related problems.<h3>Key responsibilities are:</h3><ol><li>Develop innovative approaches to new material synthesis and processing to create novel polymeric materials with differentiated properties.</li><li>Develop structure-property relationships with advanced knowledge of scientific principles, experimental design, and advanced characterization.</li><li>Lead new product development and identification of new technology areas for DuPont CMPT’s innovative pipeline.</li><li>Collaborate with technical groups in R&D and manufacturing to facilitate the scale-up and commercialization of new products.</li><li>Document work in a timely fashion in data books, internal reports, patent disclosures, and external publications as appropriate.</li><li>Communicate results and progress to technical teams, management, and business leadership through written reports and oral presentations.</li><li>Demonstrate behaviors that exemplify DuPont’s Core Values: Safety and Health, Respect for People, Highest Ethical Behaviors, and Protecting the Planet.</li></ol>This position has travel requirements of up to 10% globally.<h3>Required Qualifications:</h3><ol><li>Ph.D. in Materials Science, Polymer Chemistry, Chemical Engineering, or other related disciplines.</li><li>Strong background in polymer technology with proven record in synthesis and material development.</li><li>Demonstrated ability to examine structure-property relationships of polymer formulations.</li><li>Strong analytical and critical thinking with the ability to make data driven decisions and actionable recommendations.</li><li>Excellent interpersonal and communication skills.</li><li>Strong project management skills and ability to execute complex projects and navigate multiple priorities.</li><li>Familiarity with a variety of analytical techniques, such as NMR, GPC, FT-IR, SEM, DMA, TGA, DSC, etc.</li><li>Successful candidate should have strong collaborative R&D mindset.</li></ol><h3>Preferred Qualifications:</h3><ol><li>Minimum of 3 years product R&D experience with a successful customer engagement and product development record. Formulating with polymeric system is preferred.</li><li>Experience in CMP or other semiconductor process technologies is preferred.</li><li>Experience in polyurethane manufacturing and/or product development.</li><li>Experience leading and driving complex technical projects to a successful completion.</li><li>Experience in Stage Gate type of new product development process.</li><li>Six sigma certification, experience in Design of Experiment principles and statistical data analysis.</li></ol>DuPont é uma empregadora que promove a igualdade de oportunidades. Candidatos qualificados serão considerados sem que haja distinção de raça, cor, religião, credo, sexo, orientação sexual, identidade de gênero, estado civil, nacionalidade, idade, situação militar, deficiência ou qualquer outra classe protegida.
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<h3>Job Description</h3><div>Job Description<div><div>Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you! Our Bioanalytical Method Development / Method Validation staff has considerable experience with the conventional matrices (plasma, serum, whole-blood, urine, feces), as well as various animal and human tissues. As a professional in this group, you will work with our clients to identify assay requirements and intended use, and then to develop assays using the most appropriate technology platform. .QPS’ Story:Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of Neuropharmacology, DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II – IV Clinical Research services. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life.Team members enjoy challenging and rewarding work, and are encouraged achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, team work and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals.If this sounds like your ideal work environment, then we would love to speak with you, so apply today! Please visit our website (www.qps.com) for more information and to see all current openings.The Job<ul><li>Independently manage one or more method development/validation studies at the same time with minimum supervision.</li><li>Prepare, and/or review and understand study protocols. </li><li>Evaluate significance of data and report findings. </li><li>Prepare Study summaries and/or reports.</li><li>Set-up, utilize, and maintain complex instrumentation</li><li>Communicate project timelines, status, data, reports, and inquiries to client and/or study sites, effectively addressing any issues that may arise.</li><li>Maintain the proper level of regulatory compliance for each study, preparing QA related documents and addressing QA audit findings.</li><li>Maintain schedule of projects and timelines.</li><li>Supervise, train and/or mentor junior scientific staff</li><li>Develop, validate and run sensitive, reliable and efficient LC/MS/MS assays for TK/PK assessment.</li><li>Ensure that GLP regulations and SOPs are followed in all bioanalytical service activities.</li></ul>Work Location<div><ul><li>This job will be 100% QPS-office/facility based</li></ul></div>RequirementsThe successful candidate will hold an advanced degree in Analytical Chemistry, Biochemistry, Pharmacology, or related scientific discipline:<ul><li>Ph.D. degree<ol><li>Recent graduates must have with direct experience on LC-MS/MS analysis</li><li>If more than 2 years since graduation, candidates must have direct experience on method development of bioanalytical assays using LC-MS/MS, particularly having CRO experience</li></ol></li><li>Understanding of experimental design and planning, and data collection and analysis software.</li></ul>Why You Should Apply<ul><li>Great learning opportunities, especially for those new to the field. Our seasoned professionals are here to support and work with you to explore your learning potential and career goals.</li><li>Structured Career Ladders that provide excellent growth based on your personal aspirations.</li><li>Bonuses and merit increases are a part of the QPS total rewards approach and are linked to individual, team and company performance.</li><li>Solid Benefits package, including Company-matched 401(k), and Company-sponsored Group Life/AD&D and Short and Long-term Disability Insurance</li><li>Park-like setting in Newark, Delaware</li><li>Internal committees designed with the needs and enjoyment of QPS employees in mind.</li></ul>QPS, LLC is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans. </div></div></div>

Research Scientist Jobs in Newark, DE

Research Scientist
December 16, 2024

Pad Material Research Scientist
December 14, 2024

Research Scientist Bioanalytical Dept
December 14, 2024

Research Scientist Bioanalytical Dept
December 13, 2024

Pad Material Research Scientist
December 7, 2024

Mdmv Research Scientist Bioanalytical Dept
November 26, 2024

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Research Scientist Jobs in Newark, DE

Research ScientistDecember 16, 2024

Pad Material Research ScientistDecember 14, 2024

Research Scientist Bioanalytical DeptDecember 14, 2024

Research Scientist Bioanalytical DeptDecember 13, 2024

Pad Material Research ScientistDecember 7, 2024

Mdmv Research Scientist Bioanalytical DeptNovember 26, 2024