Research and development technician jobs in Delaware

As an Entry Level Development Chemist, you will work in the laboratory as a member of automotive refinish technical team at Delaware, OH. You will support Refinish coatings R&D and contribute to the development of new products. You will work in the formulations laboratory under the supervision of an experienced chemist. Activities include paint formulation, spray application and physical and chemical property testing of standard and experimental color coatings. You will contribute to experimental design and planning with responsibility for conducting formulation experiments and communicating results to technical leadership and marketing organizations. PPG offers excellent Medical, Dental, & Vision Benefits; matching 401k + retirement savings; and Paid Vacation, Holiday pay. Key Responsibilities Safety first attitude for every task assigned. Follow experimental procedures and create reliable data promptly. Provide independent thoughts, contribute (or lead) design of experiments. Perform project tasks with the guidance from a senior chemist. Demonstrate use of scientific method for experimentation, observations. Provide recommendations that advances project goals. Build productive business relationships with suppliers, marketing/ sales, customers and within the broader PPG Technical community. Follow corporate policies and government regulations by compliance with established standards on business conduct, environmental issues, EEO. Qualifications Bachelor's degree in Chemistry or Chemical Engineering Experience with statistical tools for design of experiment 1+ years coating experience Experience with coating application techniques. PPG pay ranges and benefits can vary by location which allows us to compensate employees competitively in different geographic markets. PPG considers several factors in making compensation decisions including, skills and training, qualifications and education, licensure and certifications, and other organizational needs. Other incentives may apply. About us: Here at PPG we make it happen, and we seek candidates of the highest integrity and professionalism who share our values, with the commitment and drive to strive today to do better than yesterday - everyday. PPG: WE PROTECT AND BEAUTIFY THE WORLD™ Through leadership in innovation, sustainability and color, PPG helps customers in industrial, transportation, consumer products, and construction markets and aftermarkets to enhance more surfaces in more ways than does any other company. To learn more, visit *********** and follow @ PPG on Twitter. The PPG Way Every single day at PPG: We partner with customers to create mutual value. We are "One PPG" to the world. We trust our people every day, in every way. We make it happen. We run it like we own it. We do better today than yesterday - everyday. PPG provides equal opportunity to all candidates and employees. We offer an opportunity to grow and develop your career in an environment that provides a fulfilling workplace for employees, creates an environment for continuous learning, and embraces the ideas and diversity of others. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, color, creed, religion, national origin, age, disability status, marital status, veteran status, sexual orientation, gender identity or expression. If you need assistance to complete your application due to a disability, please email ******************. PPG values your feedback on our recruiting process. We encourage you to visit Glassdoor.com and provide feedback on the process, so that we can do better today than yesterday. Benefits will be discussed with you by your recruiter during the hiring process. PPG pay ranges and benefits can vary by location which allows us to compensate employees competitively in different geographic markets. PPG considers several factors in making compensation decisions including, but not limited to, skill sets, experience and training, qualifications and education, licensure and certifications, and other organizational needs. Other incentives may apply. Our employee benefits programs are designed to support the health and well-being of our employees. Any insurance coverages and benefits will be in accordance with the terms and conditions of the applicable plans and associated governing plan documents.

**Are you looking to power the next leap in the exciting world of advanced electronics?** Do you want to help solve problems that drive success in the rapidly evolving technology and connectivity landscape? Then bring your problem-solving, passion, and creativity to help us power the next leap in electronics. At **Qnity** , we're more than a global leader in materials and solutions for advanced electronics and high-tech industries - we're a tight-knit team that is motivated by new possibilities, and always up for a challenge. All our dedicated teams contribute to making cutting-edge technology possible. We value forward-thinking challengers, boundary-pushers, and diverse perspectives across all our departments, because we know we play a critical role in the world enabling faster progress for all. Learn how you can start or jumpstart your career with us. **Polish Lab Technician** The R&D CMP Technician will support clean room operations, materials development experimentation, operate lab equipment, record and analyze data, and support product development projects of senior scientists and engineers in our Applications Laboratory This position is scheduled for 5 day (M-F) 8-hour second shift assignment (3:00pm to 11:30pm). Candidate may be trained during day shift (7am-3:30pm) for first three months. **Your key responsibilities:** Perform daily experimental set up and tear down and lab housekeeping Properly handle and dispose of hazardous waste Comply with all safe chemical handling practices Record data in LIMS, first level troubleshooting and maintenance of electropneumatic equipment Perform chemical and/or physical analyses or scientific tests using routine techniques in compliance with all safety and control standards Record results of tests, organize data, perform basic computations, and prepare reports and analyses using standard procedures and guidelines Complete safety observations as required, participate in safety improvements **Qualifications:** + High School Diploma or Equivalent required. + Associate Degree in a technical field preferred + Mechanical aptitude. + Experience with high-tech machinery, and/or experience handling chemicals is a plus. **Physical Requirements:** + Candidate must be able to lift 50lbs with two hands. + Wear personal protective equipment for extended periods Join our Talent Community (*************************************************************** to stay connected with us! Qnity 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 (**************************************************** . Qnity offers a comprehensive pay and benefits package. To learn more visit the Compensation and Benefits page (*************************************************************************** .

Die Tracoe Medical GmbH mit Hauptsitz und Produktionsstätte in Nieder-Olm (Rheinland-Pfalz) gehört zu den führenden Entwicklern und Herstellern von Medizinprodukten und Hilfsmitteln für Patienten mit Luftröhrenschnitt. Der Schwerpunkt des Premiumproduktportfolios liegt auf Tracheostomiekanülen und Zubehör zur Patientenversorgung in der Klinik wie auch im HomeCare-Bereich. Tracoe Medical ist seit 2021 bzw. 2022 ein Unternehmen der Atos Medical / Coloplast Gruppe und beschäftigt insgesamt rund 300 Angestellte am Standort Nieder-Olm. Das Unternehmen blickt auf eine 60-jährige Geschichte zurück und wurde bereits dreimal in die Top 100 des Deutschen Mittelstands gewählt. DE - Stellenausschreibung Zur Verstärkung unseres Teams suchen wir zum nächstmöglichen Termin einen Quality Assurance Design Development Specialist (m/w/d) Stellenumfang: Vollzeit, 40 Wochenstunden Standort: TRACOE medical GmbH, Nieder-Olm / Deutschland Deine Hauptaufgaben und Verantwortlichkeiten: * Repräsentation der Qualitätssicherung in allen Entwicklungsprojektteams und stellt sicher, dass das in der Entwicklung befindliche Produkt den relevanten Entwicklungsprozessen (d.h. Designkontrolle, Risikomanagement, HF-Engineering) sowie den geltenden technischen Normen und Vorschriften entspricht * Überprüfung und Genehmigung der gesamten DHF-relevanten Dokumentation, die während des gesamten Design-, Entwicklungs- und Lebenszyklus erstellt wird * Leitung und Unterstüztung von Projektteams bei der Anwendung von Best Practices im Dokumentenmanagement (GDP) * Bereitstellung von Qualitätssicherung, Überwachung und Beratung bei allen technischen, Risikomanagement- und Human-Factors-Aktivitäten während der Entwicklungsprojekte, d. h. potenziell vom frühen Scoping/der Machbarkeit über die Entwicklung bis hin zum Designtransfer und der Industrialisierung * Unterstützung bei qualitätsbezogenen (Sicherungs-) Aspekten von Innovationsprojekten sowohl intern als auch mit externen Kunden und Entwicklungspartnern * Aufbau und Pflege von Schnittstellen zu Qualitätsmanagementeinheiten in der Produktion/im Betrieb, wie z. B. der Produktionstechnik für die Prozessvalidierung und der Qualitätskontrolle für die Validierung und Durchführung von Prüfverfahren * Unterstützung bei der Umsetzung von entwicklungsrelevanten Quality by design Konzepten (Regelstrategie) * Kooordinierung und Unterstützung bei der Umsetzung von internen Service Level Agreements * Leitung und Überwachung des Änderungs- und Abweichungsmanagement während der Entwicklung und darüber hinaus * Mitwirkung im change control Prozess bei dem Approval von Change Plans & bearbeitung Change Actions im bereich Quality Assurance * Eigenverantwortliche Leitung und/oder nimmt an Design Reviews im Zusammenhang mit der Entwicklung neuer Produkte und nachhaltiger technischer Aktivitäten teil. Deine Qualifikation: * Abgeschlossenes Hochschulstudium (Diplom, Master oder Bachelor) im Bereich Ingenieurwesen, Biomedizintechnik, Maschinenbau, Biochemie oder einer vergleichbaren Fachrichtung * Mindestens 5 Jahre Berufserfahrung im Qualitätsmanagement von Medizinprodukten oder in der Pharmaindustrie * Mindestens 5 Jahre Berufserfahrung in R&D-Projekten und im Design Control Prozess * Fundierte - praxiserprobte Kenntnisse der einschlägigen Normen und Regularien: * ISO 13485 (Qualitätsmanagement für Medizinprodukte) * ISO 14971 (Risikomanagement) * IEC 62366 (Usability Engineering - wünschenswert) * MDR/IVDR und CFR 820.30 * Praktische Erfahrung im Lebenszyklusmanagement von Medizinprodukten * Kommunikationsstärke, analytisches Denkvermögen und strukturierte Arbeitsweise * Fließende Deutsch- und Englischkenntnisse in Wort und Schrift * Sicherer Umgang mit MS Office Deine persönlichen Skills: * Fähigkeit zur Zusammenarbeit mit internationalen Partnern oder Teams, fließend in Wort und Schrift in Englisch und Deutsch * Proaktiv mit guten Kommunikations- und Selbstmanagementfähigkeiten, ergebnisorientiert * Durchsetzungsvermögen * selbsständige, effiziente und sorgfältige Arbeitsweise, Flexibilität zur Arbeit als Teamplayer und Moderator nach Bedarf * Starkes Engagement, Initiative und Pflichtbewusstsein * Erfahrung in der Arbeit in einem internationalen Umfeld * Reisebereitschaft, international EU (10 - 20% max.) Wir bieten dir: * Einen sicheren und verantwortungsvollen Arbeitsplatz in einem erfolgreichen Team * Eine Willkommenskultur und strukturierte Einarbeitung * Ein freundliches Arbeitsklima und Kollegen, die Ihnen auf Augenhöhe begegnen * Ideenmanagement, Freiraum zur Mitgestaltung von Prozessen und selbständiges Arbeiten * Aktive Förderung Ihrer fachlichen und persönlichen Weiterbildung durch interne und externe Fortbildungsangebote * Flexible Arbeitszeitmodelle und die Möglichkeit zum mobilen Arbeiten (bis zu 2 Tage pro Woche) * Firmenevents, kostenfreie Parkplätze uvm. Haben wir Ihr Interesse geweckt? Machen Sie den ersten Schritt und bewerben Sie sich auf der Karriereseite unserer Homepage mit einem Klick über "Apply now". ________ EN - Job Advertisement To strengthen our team, we are looking for the next possible date for a Quality Assurance Design Development Specialist (m/w/d) Job scope: fulltime, 40 hrs per week Loation: TRACOE medical GmbH, Nieder-Olm/ Deutschland Main tasks and key responsibilities: * Represents Quality Assurance in all development project teams, ensuring the compliance of the product under development to relevant development processes (i.e design control, risk management, HF engineering) as well as applicable technical standards and regulations * Reviews and approvals of all the DHF relevant documentation generated all along design and development and lifecycle * Guides and supports project teams in document management best practices (GDP) * Provides Quality assurance, oversight and consultancy in all technical, risk management and human factors activities during development projects, i.e. potentially from early scoping/feasibility through development until design transfer and industrialization * Supports in quality (assurance) related aspects with innovation projects internally as well as with external customers and development partners * Builds up and maintains interfaces with quality management units in production/operation such as production engineering for process validation and quality control for test method validation and execution Supports the implementation of Quality by design concepts relevant for development (control strategy) * Coordinates and supports the implementation of internal service level agreements if required * Lead/supervises the change & deviation management during development and beyond * Chairs and/or participate in Design Reviews related to new product development and sustaining engineering activities. * Support within Change control Activities for Change plan Approval and Quality support in Change Controls Your Qualifications: * University degree (Diploma, Master's, or Bachelor's) in Engineering, Biomedical Engineering, Mechanical Engineering, Biochemistry, or a comparable technical field * At least 5 years of professional experience in quality management of medical devices or within the pharmaceutical industry * At least 5 years of experience in R&D projects and the design control process * Solid, hands-on knowledge of relevant standards and regulations, including: * ISO 13485 (Quality management for medical devices) * ISO 14971 (Risk management) * IEC 62366 (Usability engineering - desirable) * MDR/IVDR and 21 CFR 820.30 * Practical experience in product lifecycle management of medical devices * Strong communication and analytical skills with a structured and solution-oriented working style * Fluency in German and English, both written and spoken * Proficiency in MS Office applications Personal Skills: * Strong collaboration skills with international partners and teams; fluent communication in English and German * Proactive, self-driven, and results-oriented with excellent communication and self-management skills * Confident and assertive personality with the ability to influence and motivate others * Independent, efficient, and detail-oriented work approach; flexibility to act as a team player and facilitator as needed * Strong commitment, initiative, and sense of responsibility * Experience working in an international environment * Willingness to travel within the EU (10-20%) We offer you: * A secure and responsible job in a successful team * A welcoming culture and structured induction programme * A friendly working atmosphere and colleagues who treat you as equals * Idea management, freedom to help shape processes and work independently * Active promotion of your professional and personal development through internal and external training programmes * Flexible working time models and the option of mobile working (up to 2 days per week) * Company events, free parking and much more... Have we piqued your interest? Take the first step and apply on the careers page of our homepage by clicking on 'Apply now'. Founded in 1986, Atos Medical is the global leader in laryngectomy care as well as a leading developer and manufacturer of tracheostomy products. We are passionate about making life easier for people living with a neck stoma, and we achieve this by providing personalized care and innovative solutions through our brands Provox, Provox Life and Tracoe. We know that great customer experience involves more than first-rate product development, which is why clinical research and education of both professionals and patients are integral parts of our business. Our roots are Swedish but today we are a global organization made up of about 1400 dedicated employees and our products are distributed to more than 90 countries. As we continue to grow, we remain committed to our purpose of improving the lives of people living with a neck stoma. Since 2021, Atos Medical is the Voice and Respiratory Care division of Coloplast A/S 58842 #LI-AT

As the first full-time scientist on the team, you will perform hands-on formulation, drive product improvements, help establish the new lab, and influence the company's technical direction. You'll Want to Explore this Opportunity Because: You will contribute immediately in the lab while also helping to build and shape a new product development function from the ground up in a company with an aggressive growth plan. (More chemists to be hired soon). You'll work directly with a passionate, visionary CEO who values collaboration, scientific insight, and real innovation. He's demonstrated an open mindset and is driven by continuous learning and improvement. Join an entrepreneurial team of people who are driven, curious, and deeply committed to building a brand that's changing the way things are done in their industry. What You'll Be Doing: This is a hand-on lab position with a build in progressing from formulation chemist to synthesis and project ownership. Lead the development of innovative chemical formulations and new product forms. This may also involve reverse engineering of 3rd party chemicals currently marketed and sold. Develop improvements to existing products to boost performance and address supply chain challenges. Participate with the R&D Consultant/Advisor in opening the new R&D lab. Translate market insights and company priorities into actionable product concepts. Oversee efficacy, user experience, safety, shelf life, and regulatory testing to ensure product excellence. Manage pilot studies and field trials to confirm real-world performance. Act as the scientific expert on water treatment chemistry, particularly in customer service and education. Collaborate with Operations and Marketing teams to take products from concept to commercialization. What You'll Bring to the Job: Ph.D. or M.S. in Chemistry or related field. 5+ years of hands-on experience in chemical product development, ideally in the specialty chemical or water treatment chemicals space Proven success in formulating products and bringing them to market. Strong analytical skills with expertise in experimental design and statistical analysis. Familiarity with regulatory frameworks (such as EPA, NSF etc.) and safety testing protocols. Experience with water treatment technologies is highly preferred. Must be authorized to work for any U.S. employer without sponsorship now or in the future. Our client is an Equal Opportunity Employer with fantastic benefits as described below: 20 days PTO Medical Insurance: 3 plan levels ($300-$6,350 deductibles; 80-100% coverage) Dental Insurance: PPO plan with $1,500 annual max; 100% preventive, 90% basic, 60% major; orthodontia up to $1,500 Vision Insurance: $10 copays; $150 frame or contact allowance every 12 months Life Insurance: 2× salary up to $500,000, company-paid Voluntary Life & AD&D: Employee up to $300K; spouse/child up to 50% of employee coverage Long-Term Disability: 60% of monthly earnings, up to $12,000, company-paid Continuing Education & Tuition Assistance Employee Assistance Program and Wellness Benefits If you're passionate about product development, eager to lead innovation in a fast-paced environment, and ready to make an impact, this opportunity is for you! Apply now!

A 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 Description Performs qualitative and quantitative chemical analysis of raw materials. Coordinates testing responsibilities to ensure QA test support according to the needs of Manufacturing to maintain continuous process flow. Functions as a team member in the QA Chemical Laboratories to provide timely test analysis information on the status of conformance to requirements. Investigates testing abnormalities and implements corrective action. Cross-trains in all testing responsibilities to ensure a fully cross-functional laboratory team environment. Assists with determination of root causes of non- conformance and recommends corrective actions. Maintains laboratory chemical supplies to ensure an adequate supply and prevent testing delays. Audits documentation, device history records, and test methods for compliance . Assists with special projects by supporting the development of new test methods of performing investigative test analyses as required. Assists in projects including the validation of test methods and transfer of new products/processes/test methods. Qualifications Minimum BS degree is required. Additional Information

Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications and expertise. Agilent enables customers to gain the answers and insights they seek - so they can do what they do best: improve the world around us. Information about Agilent is available at **************** We are looking for a talented Software/Firmware Engineer to join our R&D group at our Little Falls (Wilmington), Delaware site, located midway between Baltimore and Philadelphia. There, we have 800 people inventing, designing, building, and marketing products that dominate the market for Chemical Analysis. Our products are frequently behind the headlines in the news, from environmental regulations to new drug discoveries to Homeland Security. As a Software/Firmware Engineer in Agilent's R&D group, you'll play a vital role in designing and developing next-generation solutions for our Gas Chromatograph, Automated Sample Handling, and Automated Sample Preparation products. You'll be involved in all aspects of the development lifecycle-from requirements and design to implementation and testing-for embedded software applications, libraries, and development tools. This is a hands-on, collaborative role. You'll work closely with cross-functional teams including software and firmware engineers, mechanical and electrical engineers, and chemists to create complete systems. Location: Wilmington, DE Hours: Must be able to work between the hours 8:00 AM - 5:00 PM. Key Responsibilities: Design, develop, and test embedded software and supporting tools for R&D systems and instrumentation Translate product requirements into robust and scalable code. Collaborate with multidisciplinary teams to create complete hardware/software systems Integrate and validate third-party tools and libraries. Participate in code reviews, troubleshooting, and continuous improvement efforts Qualifications Bachelor's or Master's degree in Computer Science, Computer Engineering, or a related technical field Proficiency in one or more programming languages (C/C++) Experience with real-time control of hardware and embedded systems Development experience with microprocessors or microcontrollers for bare-metal applications Familiarity with device communication protocols such as TCP/IP, RS-232, and RS-485 Solid understanding of algorithms and data structures Ability to work effectively in a team-oriented, collaborative environment Added Bonus if you have: Experience with version control tools (e.g., Git, ClearCase) Integration of third-party libraries, software, or development tools Embedded Linux development experience Additional programming skills in Assembly, Python, C#, or Java Knowledge of Object-Oriented Analysis and Design (OOAD) principles Experience with the .NET framework and Visual Studio Familiarity with databases and SQL Understanding of Agile or Waterfall development methodologies GUI development experience Exposure to FPGA development Additional Details This job has a full time weekly schedule. Applications for this job will be accepted until at least October 22, 2025 or until the job is no longer posted.The full-time equivalent pay range for this position is $114,080.00 - $178,250.00/yr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: ************************************* Agilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_******************* or contact ***************. For more information about equal employment opportunity protections, please visit *************************************** Required: OccasionalShift: DayDuration: No End DateJob Function: R&D

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! QPS, LLC has an opening for an Associate Scientist I in our Bioanalytical department. In this role, you will play a pivotal part in QPS' continued expansion of our bioanalytical capabilities to support small molecule, antibody drug conjugate, protein, and gene therapy drug development. The LC-MS group's expertise lies in the quantitation of small molecules, oligonucleotides, peptides, proteins, and metabolite biomarkers by various mass spectrometric (LC-MS/MS, LC‑HRMS, hybrid/immunoaffinity mass spec), and hybridization-LC-fluorescence techniques. As an Associate Scientist I, you will be a fully-supervised trainee, responsible for sample preparation by various extraction methods; analysis of drug and metabolites in biological samples to support preclinical and clinical drug development programs under GLP regulations; and recording study results and observations. No visa sponsorship (e.g. H‑1B, L‑1, E) will be provided for this active position, now or in the future. Applicants must currently be authorized to work in the U.S. on a permanent or unrestricted basis. 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 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 (************ for more information and to see all current openings. The Job Perform routine lab operations, such as sample extraction, preparing reagents, operating automatic liquid handling equipment, pipetting, weighing, monitoring, and recording, in a neat/clean manner Assist Principal Investigator in performing quantitative analysis of drug and metabolites in biological samples utilizing validated liquid chromatography-tandem mass spectrometry (LC-MS/MS) methods under GLP regulations Document experiment details, calculations, results and observations in accordance with GLPs and SOPs Basic math skills to perform routine calculations Work Location This job will be 100% QPS-office/facility based Requirements The successful candidate will hold a degree in Analytical Chemistry, Biochemistry, Pharmacology, or related scientific discipline as follows: Bachelor's degree 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.

We are seeking motivated Production Chemists to join our GMP-compliant pharmaceutical manufacturing team working in both pilot plant and kilolabs. The Production Chemist will be responsible for performing production operations involving chemical processing, batch preparation, and in-process testing to support the manufacture of pharmaceutical products. In addition, the Production Chemist will provide day-to-day supervision and guidance to production operators, ensuring processes are carried out in full compliance with GMP and safety requirements. This position requires strict adherence to cGMP standards, safety regulations, and data integrity practices. The role involves working on a rotating shift schedule, including nights and/or weekends. Key Responsibilities Execute production processes involving weighing, charging, mixing, distillation, and chemical reactions in compliance with SOPs and batch production records. Operate and monitor process equipment (reactors, filtration systems, dryers, etc.) according to validated procedures. Collect, test, and interpret in-process samples to ensure product quality and batch consistency. Maintain accurate, real-time documentation in batch production records, logbooks, and electronic systems to ensure data integrity and regulatory compliance. Supervise and support operators during daily production operations, ensuring tasks are performed according to GMP and safety standards. Provide on-the-floor technical guidance and troubleshoot issues as needed. Adhere to all cGMP, safety, and environmental policies, including proper handling of raw materials, intermediates, and finished products. Support cleaning, equipment setup, and line changeover activities as required. Assist in deviation investigations, corrective and preventive actions (CAPA), and continuous improvement initiatives. Collaborate with Quality Assurance, Engineering, and Maintenance teams to ensure efficient production operations. Participate in training programs and maintain qualifications for GMP manufacturing operations.

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description Performs qualitative and quantitative chemical analysis of raw materials . Coordinates testing responsibilities to ensure QA test support according to the needs of Manufacturing to maintain continuous process flow. Functions as a team member in the QA Chemical Laboratories to provide timely test analysis information on the status of conformance to requirements. Investigates testing abnormalities and implements corrective action. Cross-trains in all testing responsibilities to ensure a fully cross-functional laboratory team environment. Assists with determination of root causes of non-conformances and recommends corrective actions. Maintains laboratory chemical supplies to ensure an adequate supply and prevent testing delays. Audits documentation, device history records, and test methods for compliance. Assists with special projects by supporting the development of new test methods of performing investigative test analyses as required. Assists in projects including the validation of test methods and transfer of new products/processes/test methods. The candidate should be able to work 2nd or 3rd shifts. Need to be flexible on working 2nd or 3rd. Qualifications The candidate should be able to work 2nd or 3rd shifts. Need to be flexible on working 2nd or 3rd. Additional Information Sneha Shrivastava Technical Recruiter (Clinical/Scientific) Artech Information Systems LLC 360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 Office: ************ | Fax: ************ Connect with us on - LinkedIn | Facebook | Twitter

Sirius Staffing is seeking multiple Associate Scientists (Formulations Chemistry) for a contract position at a leading agricultural research site in Newark, DE. This is an exciting opportunity to join the formulation team and contribute to advancing a robust product pipeline while supporting existing products. Rate: up to $36/hr + Benefits offered, PTO & Holiday Pay Schedule: Day shift, Mon-FriDuration: 6 months to 1 year+ Responsibilities: Work under the direction of a senior chemist with limited supervision. Prepare formulations for agricultural solutions using novel technologies. Perform physical tests on formulations to characterize products and simulate performance attributes. Conduct physical and chemical characterization of active ingredients. Support the evaluation of new technologies for the organization. Utilize wet and dry chemical techniques, including milling, extrusion, granulation, emulsification, suspensibility tests, and solution release tests. Operate physical-chemical instrumentation such as particle size analyzers and zeta potential analyzers. Use small-scale preparative equipment, including high-shear mixers and laboratory reactors. Interpret preliminary results and testing data. Manage small-scale or limited-scope projects as assigned. Key Responsibilities Preparation of laboratory-scale liquid and solid formulations. Planning and conducting experiments, troubleshooting issues, and suggesting improvements. Writing protocols and reports for assigned projects. Performing physical-chemical evaluations of formulations to ensure robust performance and shelf-life. Organizing and prioritizing activities within assignments. Analyzing and interpreting data and results. Communicating results and analyses promptly to chemists or management. Documenting experiments in a laboratory notebook. Ensuring compliance with all site, departmental, and group safety and GLP guidelines. Assisting in the training of new technical staff on laboratory procedures. Traveling to U.S. plant locations as needed (approximately 5% travel). Requirements Bachelor's degree in Chemistry, Biology, Physics, or a related field with 1-3 years of experience; or Associate degree in Chemistry or a related field with 5 years of laboratory research experience. Must be eligible to work for any U.S. employer without sponsorship now or in the future. Knowledge of computer systems and basic office applications (e.g., Excel, Word, PowerPoint, databases). Experience with laboratory equipment and apparatus. Experience conducting basic research in the field of chemistry. Proven ability to deliver high-quality results under tight timelines while managing competing priorities across multiple projects. Flexible and adaptable; able to adjust to changing demands and quickly learn new, unfamiliar materials and techniques, with a strong commitment to ongoing development. Strong commitment to safety, consistently following policies, procedures, and best practices in all work environments. Effective communicator with strong oral skills for presenting ideas, experiments, and results clearly. Strong written communication and interpersonal skills, including basic scientific writing, report preparation, and the ability to work well independently or as part of a team. Sirius Staffing is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to characteristics such as race, color, national origin, religion, gender, age, marital status, disability, veteran status, citizenship status, sexual orientation, gender identity, or any other status protected by law.

Reporting to the QC Analytical Lead, the QC Analytical Scientist will serve as a technical expert in analytical chemistry testing and laboratory operations in support of drug product manufacturing at WuXi STA's Middletown, DE site. This role includes advanced execution and troubleshooting of analytical methods, stability studies, method transfers, and equipment qualification, as well as maintaining compliance with GMP, corporate quality standards, and global regulatory requirements. The QC Analytical Scientist will play a critical role in both startup and steady-state operations, ensuring timely and accurate testing for product release, validation, and regulatory inspections. Responsibilities QC Analytical Testing and Support • Perform and review QC analytical testing for drug products, raw materials, packaging components, and stability samples in accordance with approved methods and SOPs. • Execute advanced analytical techniques including HPLC, UPLC, GC, dissolution, UV-Vis, TOC, Karl Fischer, and other relevant compendial and non-compendial methods. • Troubleshoot analytical instrumentation and methods, supporting investigations and continuous improvement. • Author, review, and revise test methods, SOPs, and technical documents. • Mentor and train QC Analysts and Associates in analytical techniques and best practices. • Other QC tasks assigned by analytical lead. Regulatory Compliance and Documentation • Ensure all activities are conducted in strict compliance with cGMP, safety, and quality standards. • Maintain accurate, complete, and inspection-ready laboratory documentation. • Participate in method transfer, qualification, and validation of analytical methods and equipment. • Support client and regulatory audits by presenting data, explaining technical approaches, and preparing responses. • Escalate deviations, out-of-specification (OOS) results, or atypical findings promptly to the QC Analytical Manager. Qualifications • Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or related scientific discipline with 5+ years of QC analytical laboratory experience in a GMP-regulated pharmaceutical or biotechnology environment; OR • Master's degree with 3+ years or PhD with 1+ years of relevant QC analytical laboratory experience. • Deep expertise in chromatographic and spectroscopic methods (HPLC/UPLC, GC, UV-Vis, TOC, KF, etc.) and data interpretation. • Demonstrated ability to lead laboratory investigations, troubleshoot instrumentation, and author technical reports. • Strong knowledge of GMP regulations, ICH guidelines, and data integrity principles (ALCOA+). Preferred Qualifications • Experience in method transfer, qualification, and validation of analytical methods. • Familiarity with LIMS, Empower, or other electronic laboratory management systems. • Prior experience in a CDMO or multi-client environment. • Strong communication and collaboration skills to support cross-functional teams, audits, and regulatory inspections. An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against based on disability This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. Employees holding this position will be required to perform any other job-related duties as requested by Management.

Job Description Signature Science, LLC is seeking highly motivated Forensic Scientists with specific expertise in human DNA analysis to contribute to our laboratory operations throughout the Mid-Atlantic region. These positions are contingent upon contract funding. The primary responsibility of this role is to perform DNA analysis on forensic casework samples, from initial sample processing to final report generation. This includes a range of tasks, such as DNA extraction, quantification, amplification, and genetic analysis. Additionally, the Forensic Scientist will contribute to research and validation efforts, ensuring the accuracy and reliability of our laboratory procedures. *This position can be located in Dover, DE* Essential Duties & Responsibilities: Laboratory Operations: Adhere to strict laboratory protocols and quality assurance standards. Utilize appropriate personal protective equipment (PPE) to maintain a safe working environment. Practice rigorous contamination control techniques to prevent sample cross-contamination. Handle and safeguard DNA samples and data in accordance with established procedures. Perform DNA analysis on diverse sample matrices, including touch DNA samples. Employ various DNA extraction methods, quantification techniques (e.g., Real-Time PCR), and amplification protocols. Utilize advanced genetic analyzer platforms to generate high-quality DNA profiles. Interpret complex DNA profiles, including single-source and mixture samples, using both manual and probabilistic genotyping methods. Prepare clear and concise forensic reports, summarizing findings and conclusions. Conduct technical reviews of casework to ensure accuracy and completeness. Collaborate with team members to efficiently process a high volume of casework. Adapt to changing priorities and deadlines to meet client needs. Maintain and troubleshoot laboratory equipment, such as Real-Time PCR instruments, thermocyclers, and genetic analyzers. Participate in validation studies of new DNA methodologies and established procedures. Required KSA's Strong understanding of forensic DNA analysis principles and techniques. Proficiency in using laboratory equipment and software (e.g., GeneMapper ID-X, STRmix). Excellent analytical and problem-solving skills. Attention to detail and ability to follow precise protocols. Strong written and verbal communication skills. Ability to work independently and as part of a team. Strong organizational and time management skills. Ability to obtain and maintain a security clearance. Education/Experience: Bachelor's degree in biological sciences, forensic science, or a related field. Minimum of 6 months of full-time laboratory experience, preferably in a forensic laboratory. Experience with DNA analysis techniques, including extraction, quantification, amplification, and genotyping. Adherence to FBI Quality Assurance Standards (QAS) for DNA analysis. Clearance: US Citizenship required; candidates will be subject to security screening. Working Conditions/Equipment/Travel: Laboratory environment requiring the use of PPE. Potential exposure to hazardous materials, including biological fluids. Ability to lift up to 20 pounds independently and 40 pounds with assistance. Limited ( Powered by ExactHire:160583

As we create a colorful, capable and cleaner world through chemistry, we invite you to join our team to harness the power of chemistry to shape markets, redefine industries and improve lives for billions of people around the world. CREATING ESSENTIAL CHEMISTRY THAT THE WORLD NEEDS At Chemours, our people are redefining how the world thinks of chemistry by approaching everything we do with a commitment to delivering Trusted Chemistry that creates better lives and helps communities thrive. That begins with how we use our science, data, and unmatched technical expertise to develop market-leading products with the highest levels of performance, sustainability, and safety in the industry. Powered by chemistry, our products are used in applications that make the products we rely on, processes, and new technologies possible. In key sectors such as clean energy, advanced electronics, high-performance computing and AI, climate friendly cooling, and high-quality paints and coatings for homes and industrial infrastructure---sustainable solutions and more modern living depend on Chemours chemistry. The Chemours™ Discovery Hub, a newly constructed 320,000 ft² world-class R&D/Application Development research facility located in Newark, DE, has an R&D Engineer position available in the Technology function. In Thermal & Specialized Solutions (TSS), we harness next-generation, low-Global Warming Potential (GWP) technology to provide market driven innovations to customers in the areas of Refrigerants, Propellants, Fire Protection, Foam Blowing Agents used in various systems for building and construction segments, and Mobile and Stationary heating and cooling systems. Our technical organization consists of experts in the areas of fluorine, catalysis, process development, analytical and formulation science, and application development to name a few. This key role will support R&D projects within the Refrigerants Test Center (RTC) with specific focus on operation of refrigeration equipment, system design, data collection and interpretation. This role is based in the Chemours™ Discovery Hub in Newark, DE. The responsibilities of the position include, but are not limited to, the following: Manage Refrigerant Test Center (RTC) projects, including and not limited to the testing of air conditioning, heat pump & refrigeration systems, data acquisition systems, instrumentation, operation and troubleshooting. Design and lead execution of experiments in laboratory environment. Perform thermodynamic cycle modelling and calculations. Analyze data, draw statistically based conclusions and determine next steps. Set project priorities and timeline in coordination with the relevant parties. Engage key external customers to develop and understand the tradeoffs on equipment design when adopting new solutions. Collaborate with cross-functional teams within the organization, customers and partners. Participate in conferences and share the findings under the format of technical papers. Knowledge or the desire to learn fluorochemical science and related application technologies. Travel 10% of time to customers and partners. The following is required for this role: Bachelors or Masters in an Engineering (Mechanical or Chemical Engineering is preferred). Relevant hands-on experience working on refrigeration or air conditioning equipment or components (e.g. compressors, heat exchangers, etc.) or system level (e.g. commercial, residential…). Good interpersonal and written/oral communication skills, excellent presentation skills, and the ability to work well with all levels in the organization. Ability to plan, prioritize and manage multiple, complex, time-sensitive projects. Ability to work in a team environment with high degree of initiative and self-motivation and flexibility to monitor and move projects forward quickly and safely. The following is preferred for this role: Relevant Internship/Co-op experience working on refrigeration or air conditioning equipment or components (e.g. compressors, heat exchangers, etc.) or system level (e.g. commercial, residential…). Benefits: Competitive Compensation Comprehensive Benefits Packages 401(k) Match Employee Stock Purchase Program Tuition Reimbursement Commuter Benefits Learning and Development Opportunities Strong Inclusion and Diversity Initiatives Company-paid Volunteer Day We're a different kind of chemistry company because we see our people as our biggest assets. Instead of focusing just on what our employees do each day, we look at how they do it-by taking a different approach to talent development, employee engagement, and culture. Our goal is to empower employees to be their best selves, at Chemours and in life. Learn more about Chemours and our culture by visiting Chemours.com/careers. Chemours is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, race, religion, color, gender, disability, national or ethnic origin, ancestry, marital status, family status, sexual orientation, gender identity or expression, or veteran status. Jurisdictions may have additional grounds for non-discrimination, and we comply with all applicable laws. Chemours is an E-Verify employer Candidates must be able to perform all duties listed with or without accommodation Immigration sponsorship (i.e., H1-B visa, F-1 visa (OPT), TN visa or any other non-immigrant status) is not currently available for this position Don't meet every single requirement? At Chemours we are dedicated to building a diverse, inclusive, and authentic workplace for our employees. So if you're excited about this role, but your past experience doesn't align perfectly with every qualification in the position description, we encourage you to apply anyways. You may just be the right candidate for this or other opportunities. In our pursuit to be the greatest place to work, we know that a critical element to enhancing our employee experience is to assure we're operating with a solid foundation of trust. At Chemours, this means being transparent about how we pay our employees for the work that they do. Pay Range (in local currency): $70,426.00 - $110,040.00 Chemours Level: 23 Annual Bonus Target: 6% The pay range and incentives listed above is a general guideline based on the primary location of this job only and not a guarantee of total compensation. Factors considered in extending a compensation offer include (but are not limited to) responsibilities of the job, experience, knowledge, skills, and abilities, as well as internal equity, and alignment with market data. The incentive pay is dependent on business results and individual performance and subject to the terms and conditions of the specific plans. At Chemours, you will find sustainability in our vision, our business and your future. If you want to work on the leading edge of your field and have a desire to make a difference, join Chemours and discover what it means when we say "We Are Living Chemistry."

Description Job Description: Set up and make operationally ready a wide variety of laboratory instruments and equipment. Write, review, and edit experimental protocols, standard operating procedures, and operating instructions for projects of experimental programs, service casework procedures and general laboratory management operations. Assist in quality assurance activities such as standards maintenance, equipment preventive maintenance, reagent testing & validation, proficiency testing, and accreditation and certification. Conduct inspections and provide oversight to the adherence to established quality assurance activities including maintenance of standards and controls, preventive maintenance and equipment calibration, reagent testing and validation, and proficiency testing programs for accreditation or certification. Perform general laboratory housekeeping activities such as maintaining appropriate working-stock levels of expendable supplies and maintaining a clean environment within laboratory work areas. Perform investigative studies on tissue identification by DNA typing technologies. Maintain documentation of methods development and research activities in accordance with standard practice. Supervise/perform service casework involving routine nuclear and mt DNA typing and profiling procedures. Prepare formal written reports of service casework or research reports that contain professional interpretations and conclusions from the test data, and that are suitable for legal presentation in a court of law. Review casework and formal written reports. Assist in program maintenance and development at the direction of their designated supervisor. Supervise staff performing investigative studies on tissue identification by DNA typing technologies, carry out DNA typing casework. Testify as an expert witness as required; provide technical assistance in the area of bioinformatics, information technology and laboratory automation; and support logistical or resource management activities. Participate in the organization and presentation of educational activities. Serve as a Supervisory DNA Analyst. Qualifications: Bachelor's degree or an advanced degree in biology, chemistry, forensic science, or a related disciple required. Must have successfully completed a minimum of 9 cumulative semester hours or equivalent (graduate or undergraduate level) course work covering the following subject areas: biochemistry, genetics, molecular biology; and course work and/or training in statistics and/or population genetics as it applies to forensic DNA analysis. Must have six (6) months of forensic human DNA laboratory experience. Desired knowledge and experience in filing techniques; administrative typing; preparing and editing technical or general documentation using various software packages such as Microsoft Word, Microsoft PowerPoint, Microsoft Excel and Windows; transcription of documents, data entry, and preparing and editing management support documentation. Positions are contingent and will begin upon contract award. Why Join Us? At CICONIX, we are committed to providing high-quality services to support military families. By joining our team, you'll make a direct impact on the lives of children and families in crisis while working in a supportive, mission-driven environment. We offer flexible remote options, competitive pay, and the opportunity to work on meaningful programs that serve those who protect our country. About the Armed Forces Medical Examiner System (AFMES): The Armed Forces Medical Examiner System (AFMES) is a vital Department of Defense entity responsible for providing medical-legal investigations, including autopsies and forensic services, for deaths involving military personnel, their families, and authorized civilians. AFMES plays a key role in identifying remains, investigating causes of death, and offering expert testimony, while also managing the Armed Forces DNA Registry. In addition to its forensic casework, AFMES supports research and development to enhance forensic techniques and contributes to the education and readiness of military forensic professionals. CICONIX, LLC is an Equal Opportunity Employer, including disability/veterans. We participate in E-Verify.

The entry-level Forensic DNA Technician (Forensic Scientist I - FSI) will perform DNA analysis on a wide range of complex samples in support of the Armed Forces DNA Identification Laboratory (AFDIL) in Dover, DE. The FSI will be responsible for performing analysis of forensic evidence in accordance with laboratory accreditation and standard operating procedures. This role is essential for effective laboratory operations and requires collaboration and productivity with laboratory staff and management. It is crucial to prioritize job responsibilities in a fast-paced environment while ensuring excellent customer service. Responsibilities will include: * Assisting in program maintenance and development at the direction of their designated supervisor. * Supporting investigative studies on biological materials using DNA typing technologies. * Supporting the logistical or resource management activities of the DNA Registry * Participating in the organization and presentation of educational activities. * Accessioning forensic evidence in the Laboratory Information Management System (LISA). * Maintaining accurate and complete chain of custody for evidence. * Entering data into LISA and the Armed Forces Medical Examiners Tracking System (AFMETS). * Preparing correspondence/documents ensuring proper format, mathematical correctness, grammar, punctuation, and spelling, in preparation for or editing of recurring reports regarding case status and case tracking. * Preparing reagents and maintain documentation of reagent prep and Quality Control testing in accordance with SOPs. * Performing laboratory housekeeping activities such as preparing common laboratory reagents. * Maintaining appropriate stock levels of expendable supplies and maintaining a clean environment within laboratory work areas. * Assisting in casework involving nuc DNA and mt DNA typing and profiling procedures. * Supporting validation projects focusing on systems with increased sensitivity and discrimination power and advanced development of automated systems. * Supporting research projects focusing on various research projects to include population databasing and working to increase sensitivity, discrimination power, and automated systems for casework applications. Minimum Education and Experience Requirements: * BA/BS degree in forensic science or in physical or life sciences. * Successfully completed course work (graduate or undergraduate level) covering the following subject areas: biochemistry, genetics, molecular biology; and course work and/or training in statistics and/or population genetics as it applies to forensic DNA analysis. * Must successfully complete a National Agency Check with Inquiries (NAC-I) background investigation. The position does not require a security clearance, but the individual may be required to obtain a government security clearance at a future date if handling classified information or materials. (Please note: US citizenship is required to obtain a government security clearance) * General knowledge of forensic DNA analytical methods, especially nuc DNA and mt DNA profiling. * Ability to maintain minimum standards of technical proficiency as demonstrated by acceptable performance by internal and external proficiency testing programs * Must be self-motivated, detail oriented, and able to work well in a team laboratory environment. * Possess strong written and verbal communication skills. * Familiar with MS Word, PowerPoint, Excel, and Adobe Acrobat. * A resume and a copy of unofficial transcripts must be submitted. Amentum is proud to be an Equal Opportunity Employer. Our hiring practices provide equal opportunity for employment without regard to race, sex, sexual orientation, pregnancy (including pregnancy, childbirth, breastfeeding, or medical conditions related to pregnancy, childbirth, or breastfeeding), age, ancestry, United States military or veteran status, color, religion, creed, marital or domestic partner status, medical condition, genetic information, national origin, citizenship status, low-income status, or mental or physical disability so long as the essential functions of the job can be performed with or without reasonable accommodation, or any other protected category under federal, state, or local law. Learn more about your rights under Federal laws and supplemental language at Labor Laws Posters.

As required by our governmental client, this position requires being a US Citizen, lawful resident alien, citizen of American Samoa or other territory owning permanent allegiance to the United States. Cherokee Nation Integrated Health (CNIH) seeks an experienced, highly qualified Forensic DNA Analyst 3 (FS3) with a strong work ethic to support a Federal program in Dover, DE. The FS3 will be responsible for performing analysis of forensic evidence in accordance with laboratory accreditation and standard operating procedures. The FS3 is critical to the successful laboratory operation and will be required to work collaboratively and productively with laboratory staff, management, and Government stakeholders. The ability to prioritize job responsibilities in a fast-paced environment while maintaining a focus on exceptional duty results and excellent customer service. Compensation & Benefits: Pay commensurate with experience. Full time benefits include Medical, Dental, Vision, 401K and other possible benefits as provided. Benefits are subject to change with or without notice. Forensic Scientist III Responsibilities Include: May serve as a Contractor Supervisory DNA Analyst. Shall be knowledgeable in a relevant field of the life sciences and have experience working in a research laboratory. Shall be required to work in one or more of the following functional areas and may be tasked to perform as a Contractor Supervisory DNA Analyst. Forensic Science Services, Past Accounting, Current Day Operations, Emerging Technologies, Family Reference Data Basing, Bioinformatics, Quality Management/Quality Control, and Laboratory Support Services. Assist in program maintenance and development at the direction of their designated supervisor. Supervise contractor DNA Analyst staff performing investigative studies on tissue identification by DNA typing technologies. Carry out DNA typing casework. May testify as an expert witness as required; provide technical assistance in the area of bioinformatics, information technology and laboratory automation; and support logistical or resource management activities. Participate in the organization and presentation of educational activities. Duties may include: Set up and make operationally ready a wide variety of laboratory instruments and equipment. Write, review, and edit experimental protocols, standard operating procedures and operating instructions for projects of experimental programs, service casework procedures and general laboratory management operations. Assist in quality assurance activities such as standards maintenance, equipment preventive maintenance, reagent testing & validation, proficiency testing, and accreditation and certification. Conduct inspections and provide oversight to the adherence to established quality assurance activities including maintenance of standards and controls, preventive maintenance and equipment calibration, reagent testing and validation, and proficiency testing programs for accreditation or certification. Perform general laboratory house-keeping activities such as: Maintain appropriate working-stock levels of expendable supplies. Maintain a clean environment within laboratory work areas. Perform investigative studies on tissue identification by DNA typing technologies. Maintain documentation of methods development and research activities in accordance with standard practice. Supervise and/or perform service casework involving routine nuclear and mt DNA typing and profiling procedures. Prepare formal written reports of service casework or research reports that contain professional interpretations and conclusions from the test data, and that are suitable for legal presentation in a court of law. Review casework and formal written reports Performs other job-related duties as assigned. Forensic Scientist III Experience, Education, Skills, Abilities requested: Bachelor's Degree, or an equivalent combination of education and experience, and 5 years of related experience is required related. Masters degree preferred. Experience supporting and leading teams of large-scale projects. Preferred experience with projects supporting forensic toxicology, medico-legal death investigations, and/or forensic DNA analytical services. Preferred experience in DoD forensic program support. Solution oriented with proven capability to realize. Excellent written and verbal communication skills. Ability to lead and advise mid-size teams. Working knowledge of MS product suite: Excel, Word, SharePoint; Project Management software and DoD reporting systems. Must pass pre-employment qualifications of Cherokee Federal Company Information: Cherokee Nation Integrated Health (CNIH) is a part of Cherokee Federal - the division of tribally owned federal contracting companies owned by Cherokee Nation Businesses. As a trusted partner for more than 60 federal clients, Cherokee Federal LLCs are focused on building a brighter future, solving complex challenges, and serving the government's mission with compassion and heart. To learn more about CNIH, visit cherokee-federal.com. #CherokeeFederal #LI Cherokee Federal is a military friendly employer. Veterans and active military transitioning to civilian status are encouraged to apply. Similar searchable job titles Senior Forensic Scientist Lead Forensic Analyst Forensic Scientist Supervisor Forensic Laboratory Manager Principal Forensic Examiner Keywords DNA analysis Crime scene investigation Expert testimony Forensic laboratory techniques Criminalistics Legal Disclaimer: All qualified applicants will receive consideration for employment without regard to protected veteran status, disability or any other status protected under applicable federal, state or local law. Many of our job openings require access to government buildings or military installations. Candidates must pass pre-employment qualifications of Cherokee Federal. Many of our job openings require access to government buildings or military installations. Candidates must pass pre-employment qualifications of Cherokee Federal. Please Note: This position is pending a contract award. If you are interested in a future with Cherokee Federal, APPLY TODAY! Although this is not an approved position, we are accepting applications for this future and anticipated need.

A 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 aretas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Job Description • Performs qualitative and quantitative chemical analysis of raw materials. • Coordinates testing responsibilities to ensure QA test support according to the needs of Manufacturing to maintain continuous process flow. • Functions as a team member in the QA Chemical Laboratories to provide timely test analysis information on the status of conformance to requirements. • Investigates testing abnormalities and implements corrective action. • ross-trains in all testing responsibilities to ensure a fully cross-functional laboratory team environment. • Assists with determination of root causes of non-conformances and recommends corrective actions. • Maintains laboratory chemical supplies to ensure an adequate supply and prevent testing delays. • Audits documentation, device history records, and test methods for compliance. • Assists with special projects by supporting the development of new test methods of performing investigative test analyses as required. • Assists in projects including the validation of test methods and transfer of new products/processes/test methods. • The candidate should be able to work in 3rd shift Qualifications • BS or Associate degree with any science related discipline preferred • BS degree in Chemistry would be highly desirable • 0-1 year of experience preferred Additional Information Warm Regards Ricky Bansal 732-429-1925

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 Translational Medicine (TLM) department of QPS is comprised of three laboratory operations units: Biomarker Analysis (BMA), Gene & Sequence Analysis (GSA), and Immunobioanalysis (IBA). An Associate Scientist in any of these units will be a fully-supervised trainee, responsible for gaining mastery of GCP and GDP, conducting assigned studies according to study protocols, and recording study results and observations. Our TLM department is continuing to expand, and has positions available in most of the above units. If you have a Bachelor's degree in Biology, Biochemistry, Immunology or other related disciplines, we would like to hear from you. No visa sponsorship (e.g. H‑1B, L‑1, E) will be provided for this active position, now or in the future. Applicants must currently be authorized to work in the U.S. on a permanent or unrestricted basis. 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 (************ for more information and to see all current openings. The Job Perform routine lab operations, such as preparing reagents, pipetting, weighing, monitoring, recording, and replenishing supplies Assist supervisor in performing analysis of drug or other targets in complex biologic matrices Set-up, use and maintain complex instrumentation Document experiment details, calculations, results and observations in accordance with GLPs and SOPs Perform routine mathematical & chemical calculations Work Location This job will be 100% QPS-office/facility based Requirements The successful candidate will hold an undergraduate degree in Biology, Molecular Biology, Biochemistry, Immunology, Pharmacology, Medical Technology, or a related field as follows: Bachelor's Degree Associate's Degree plus 2 or more years relevant experience Desire to learn and grow professionally 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.

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description Performs qualitative and quantitative chemical analysis of raw materials . Coordinates testing responsibilities to ensure QA test support according to the needs of Manufacturing to maintain continuous process flow. Functions as a team member in the QA Chemical Laboratories to provide timely test analysis information on the status of conformance to requirements. Investigates testing abnormalities and implements corrective action. Cross-trains in all testing responsibilities to ensure a fully cross-functional laboratory team environment. Assists with determination of root causes of non-conformances and recommends corrective actions. Maintains laboratory chemical supplies to ensure an adequate supply and prevent testing delays. Audits documentation, device history records, and test methods for compliance. Assists with special projects by supporting the development of new test methods of performing investigative test analyses as required. Assists in projects including the validation of test methods and transfer of new products/processes/test methods. The candidate should be able to work 2nd or 3rd shifts. Need to be flexible on working 2nd or 3rd. Qualifications The candidate should be able to work 2nd or 3rd shifts. Need to be flexible on working 2nd or 3rd. Additional Information Sneha Shrivastava Technical Recruiter (Clinical/Scientific) Artech Information Systems LLC 360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 Office: ************ | Fax: ************ Connect with us on - LinkedIn | Facebook | Twitter