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Process Engineer - New College Graduate

Summary of Role\:GlobalFoundries Fab 9, the world leader in RF semiconductor manufacturing in Essex Junction, VT, is seeking an entry level Semiconductor Process Engineer. The individual selected for this position will be part of the Manufacturing Engineering organization with primary responsibilities focused on development, support and continuous improvement of 200mm semiconductor manufacturing processes.Essential Responsibilities include\:Establish and manage the equipment quality control planDrive continuous improvement efforts in support of throughput improvement, cost reduction, and yield learningDefine and maintain equipment installation process qualification roadmaps - Drive process qualifications, implement process control plans and configuration with the area equipment engineers, including qualification, start up and volume ramp of process equipmentDesign, execute, and analyze experiments to screen and optimize manufacturing processes to meet technology (performance, yield, and reliability) and manufacturing (process stability, cost of ownership) targetsMust be technically inclined and able to lead hands on, tactical troubleshooting efforts to resolve long term performance issues; must be able to deconstruct and understand complex systemsCollaborate with GlobalFoundries integration, equipment and quality engineering to support the development of improved next generation technologies.Support technology transfer to other fabricatorsAbility to marry both the equipment and process sides of issues, focusing on delivering the right results on productOther Responsibilities\: Perform all activities in a safe and responsible manner and support all Environmental, Health, Safety & Security requirements and programs.Qualification:Required Qualifications\:Technology related Bachelor’s Degree in Chemical Engineering, Electrical Engineering, Materials Science, Solid State Physics or other relevant disciplineFluent in English10% travel may be requiredPreferred Qualifications\:COOP/Intern in semiconductor or manufacturing industryKnowledge of semiconductor/silicon processingUnderstanding and knowledge of Statistical Process Control (SPC) and Design of Experiments (DOE)Prior experience working in a semiconductor cleanroom environmentTechnology related Master’s and/or PHD degree\: Chemical Engineering, Electrical Engineering, Materials Science, Solid State Physics or other relevant disciplineAbility to work effectively and efficiently with diverse teams, customers, internal and external partners

Careerbuilder • Essex Junction, U.S.

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Research Associate

A Pharmaceutical Company is seeking a Research Associate in Frederick, MD. Role Description This role will provide process engineering and analytical support for commercial manufacturing of cell therapy. Working cross functionally with quality, operations, material management, facility and engineering functions, the role is expected to provide technical input for product/process response and investigations, technology implementation, technology transfers, process validation and regulatory filings. • Execute scientific laboratory studies to support process/product understanding and continuous improvement projects • Execute analytical testing of cell therapy products – flow cytometry, ELISA and PCR assays. • Ability to follow laboratory procedures with attention to detail, and successfully execute experiments at the bench • Provide technical input to the execution of process validation and comparability campaigns. • Participate in evaluation of new technology and process automation for introduction into GMP manufacturing • Participate and support process FMEAs to understand process and product risks as a pre-requisite for process validation. • Participate and report to a cross-functional team to advance production activities. • Participate in Operational Excellence activities within Tier Structure. • Participate continuous improvement projects supporting commercial manufacturing site • Ensure systematic DMAIC based approach utilization for process/product related investigations to identify root cause and provide impact assessment to maintain routine manufacturing operations and determine process improvements for manufacturing. • Support technology transfers of launch and commercial cell therapy products • Effectively & efficiently communicate manufacturing process performance internally. • Support the implementation of automation and IT infrastructure projects • Assist in writing technical documentation (protocols & reports for equipment/instrument qualifications, comparability, and cell therapy manufacturing process validation) Skills & Requirements • Bachelors Degree in Biochemical Engineering, Tumor Immunology, Biotechnology or Life Sciences. • Basic understanding in Bioprocessing, Cell Culture and Biochemistry. • Knowledge of ELISA and/or PCR testing • Knowledge in flow cytometry and data analysis (FACSDiva, FlowJo, GraphPad Prism, Excel) is a plus • Ability to think critically, demonstrate troubleshooting and problem-solving skills • Excellent interpersonal, verbal and written communication skills are essential in this collaborative work environment • Previous experience with other technologies is a plus • Experience with the use of Microsoft word, Excel, Power Point, Smartsheet, Prism, JMP, and other data analysis applications • Highly collaborative with excellent interpersonal, verbal and written communication skills • Ability to think critically with demonstrated problem-solving and troubleshooting skills • Comfortable working in a fast-paced company environment with minimal direction and able to adjust workload/assignments based upon changing priorities • Self-motivated, detail-oriented, and willing to accept temporary responsibilities outside of initial job description

HAYS PLC • Frederick, U.S.

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Statistician II/III

An American Company is seeking a Statistician II/III in Gaithersburg, MD. Role Description We are seeking a Statistician II/III to join our Data Science and Statistics team. This position directly supports all our nonclinical groups, and provides guidance in the utilization of appropriate statistical methodology to scientists and management. • Provide sound strategic, scientific, and statistical input to support our nonclinical research and development projects, through design of experiments and by using appropriate statistical methodology and sample size. • Prepare statistical analysis plans; analyze experimental and historical data. • Create design of experiments and perform various types of statistical analyses to develop predictive models and optimize conditions for processes, methods, and drug product/drug substance storage. • Perform stability analysis to identify degradation rates and expiration dates. • Prepare the statistical section of technical reports and presentations. • Engage in discussions and research to ensure the central place of applied statistics in research, development, quality, and validation projects. • Manage one's projects effectively, and meet deadlines with high quality of standards • Explain statistical designs and concepts to non-statisticians • Meet company milestones Skills & Requirements • A degree in Statistics/Biostatistics, Bioengineering, Chemical Engineering, or a related field, with at least 5 year of relevant experience is preferred. • Sound knowledge of theoretical and applied statistics is required, with an emphasis on experimental design in biotechnology, power calculations, survival analysis, etc. • The candidate should have hands-on experience with using and scripting statistical software packages including JMP, SAS, and R. • Familiarity with ICH guidelines • Experience in the drug development field is preferred. • Must be an effective team player, able to thrive in a fast-paced team environment, and also work independently on projects. • Excellent interpersonal, oral, and written communication skills. • Leadership ability to influence team members and communicate statistical concepts across functions.

HAYS PLC • Gaithersburg, U.S.

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Analytical Development Labs Head – Life Sciences – F/M

Our client, one of the largest Contract Development & Manufacturing Organizations (CDMO) in Europe is currently looking for their future Analytical Development Labs Head. Your responsibilities:Based in the Innovation and Development group, you will bring a deep understanding of development and validation of modern analytical methods, with a passion for leading dynamic and high performing teams in an evolving environment (internally, externally).  External collaboration with clients and technology partners is an important part of the role.Lead and support a team of technicians and scientists.Maintain an up-to-date understanding of trends, requirements, and regulations in analytical methods.Ensure that a comprehensive analytical platform is in place for all aspects of Safety, Identity, Strength, Purity and Quality.Provide quality, on time, analytics for external client projects in various phases of development (pre-clinical, clinical), and ensure the transferability of methods into QC labs to support clinical and commercial release testing. Your profile:PhD in Life Sciences preferred, with a focus on proteins or biochemistry.Ideally 8+ years of experience in an applied setting, with experience of working in multi-disciplinary teams.Previous experience in management of teams.Strong understanding of biological production processes.Solid understanding of analytical method development and validation (accuracy, precision, robustness, etc), including regulatory expectations (e.g., ICH, EP, etc).Great experience in Project Management.Strong oral and written English skills Business fluent English (B2-C1 level); similar level in French (B1-C2).

Approach People Recruitment • Paris, France

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Lab Supervisor

LabCorp is seeking a Clinical Laboratory Supervisor to join our team in Charlotte, NC. In this position, you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives" as we combat the COVID-19 pandemic.Job Duties/ResponsibilitiesSupervise the day to day operations of the laboratoryEnsure laboratory tests are accurately performed and results are reported in a timely mannerDirectly supervise, train, and mentor laboratory personnel of the departmentMonitor daily workflow in the lab and schedule adequate assay coverageResponsible for ensuring all shifts in the department are properly staffedResearch and resolve any production errors while escalating when necessaryEngage in continuous process and service level improvementsEnsure all equipment is being properly maintained through Quality ControlPrepare and maintain Quality Assurance records and documentsEvaluate new process improvements and make appropriate recommendationsMeet regularly with direct reports to provide coaching and feedback for their developmentPerform bench work as needed and maintain proficiency/competency in technical operationsEnsure all work is in accordance with state and Federal regulationsResponsible for administering and managing policies and proceduresProcess and maintain payroll and personnel filesPerform administrative duties as neededBachelor's degree in Medical Technology or a Science related majorMinimum 2 years of experience as a Medical Technologist in a clinical laboratoryPrior experience in Chemistry, Hematology and Urinalysis is highly preferredPrevious supervisor experience is preferredASCP and/or AMT Certifications are a plusStrong working knowledge of CLIA, CAP and relevant state regulationsUnderstanding of laboratory operations as well as policies and proceduresProficient with Laboratory Information Systems and Microsoft OfficeStrong communication skills; both written and verbalHigh level of attention to detail with strong organizational skillsComfortability making decisions in a changing environmentAbility to handle the physical requirements of the position

Careerbuilder • Charlotte, U.S.

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Research Associate /Senior Research Associate – Translational Biology

A Pharmaceutical Company is seeking an Research Associate /Senior Research Associate – Translational Biology in Lexington, MA. Role Description • Play a role in guiding creative and rigorous biological research programs aimed at fully understanding the disease mechanism of our pipeline. • Conduct efficacy, pharmacokinetic, pharmacodynamics, structure-activity-relationship and mechanisms of action studies of drug candidates • Use appropriate in vivo models to understand the mechanisms by which our drug candidates may contribute to adverse events in patients • Present working progress to team members in group meeting • Work closely with members of our research team to develop in vivo strategies to quickly and effectively address key questions related to the safety and efficacy of our drugs. • Review literature and provide insights to research directions, while predominantly making hands-on contributions to the research Skills & Requirements • Bachelor’s or Master’s Degree in Biology, Pharmacology, or related field, with a minimum of 1-3 years of experience. • Proficient in animal handling, dosing and surgery. Proficient in techniques including but not limited to oral gavage, intravenous injection, subcutaneous injection, blood collection and basic surgery • In depth knowledge of, and hands-on experience with, in vitro and in vivo models used for mechanistic investigation with small molecule or RNAi therapeutics • Experience performing molecular and cellular biology techniques, including but not limited to RNA preparation, RT-qPCR, ELISA, immunohistochemistry, urine biomarker analysis, plasma biomarker analysis • Broad and deep understanding of signaling pathways and biological processes implicated in rare genetic liver diseases as well as the mechanism of action of RNAi therapies is desirable • Previous experience in drug discovery is preferred • Outstanding written and oral communication skills • A high level of motivation and demonstrated record of accomplishment throughout your career • The ability to work effectively as part of a team, in a fast-paced environment

HAYS PLC • Lexington, U.S.

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Research Scientist

JOB SUMMARY: Conduct biological research associated with one or more complex projects within the NASA Ames Research Center’s Bioengineering Branch. Primary focus will be on designing, building, and analyzing a microbiology experiment for the International Space Station (ISS). The goal of the experiment is to complete multi-omics analysis of Arthrospira platensis during 6-months of continuous photoautotrophic growth. BASIC REQUIREMENTS: ● Master's degree from an accredited university in a biological discipline with 3+ years’ professional experience or a Doctoral degree with 0-3 years’ of experience. ● Laboratory experience in genomics, molecular biology, microbiology/plant biology, biochemistry/analytical chemistry, omics sample preparation, and omics data analysis. ● Familiarity with best practices for working with hazardous materials and willingness to adhere to NASA-defined processes. ● Experience with Microsoft Office and command line computer operating systems such as Linux, Unix, or R. ● Ability to communicate effectively with scientists, engineers, and external scientific service providers from a wide range of technical backgrounds. ● Excellent written and verbal communication skills as well as analytical problem-solving abilities. ● Track record of communicating scientific results through conference presentations and peer-reviewed journal articles. ● Capacity to work independently and efficiently with minimal instruction. ● Demonstrated ability to work in a team environment. ESSENTIAL FUNCTIONS: ● Complete experimental research to determine spaceflight experiment design requirements, develop/build the flight payload, and prepare samples for omics analysis. ● Support science components of flight operations that may require travel and/or extended hours. ● Conceive and design laboratory experiments and actively participate in project planning. ● Generate, record, analyze, and compile experimental data. ● Complete statistical analysis of whole genome sequences, transcriptome sequences, proteomics, and metabolomics data. ● Submit data to appropriate public databases. ● Prepare figures for presentation/publication and collaborate with other scientists in publishing research findings. ● Draft scientific materials for public outreach and/or publication. ● Present research at scientific conferences. ● Maintain a safe and organized laboratory area. ● Perform laboratory duties including management of materials and supplies, equipment, and operations. ● Identify materials and equipment needed for experiments, obtain product information, identify vendors, and assist in the preparation of material and supply acquisition. ● Oversee general state of the laboratory, including scheduled waste removal, decontamination of surfaces, and instrument calibration/upkeep. ● Carry out assigned duties in a manner consistent with defined safety policies and report any safety incidents, potential hazards, or close calls. Assist with identifying and eliminating any unsafe conditions.

Careerbuilder • Mountain View, U.S.

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Ingénieur projets – Medical devices

Vos Missions :• Rédiger et exécuter des protocoles d’essais en respectant les standards internes. • Définir et participer aux étapes d’industrialisation et / ou amelioration de procedés de fabrication • Définir la stratégie et exécuter les validations initiales des nouveaux procédés et équipements complexes • Participer au transfert technologique des procédés de fabrication définis et communiqués par les équipes Développement et projets, • Créer ou mettre à jour la documentation projet ou du système du SMQ dans le cadre de son activité en conformités avec les standards internes. • Soutenir les activités de production en prodiguant une expertise pour la résolution de difficultés process Proposer, harmoniser et implémenter les méthodes de travail en vue de cette amélioration • Participer et/ou animer le processus d’analyse de risque, • Participer si nécessaire au processus de déviation, investigation et CAPA • Participation aux validations ou revues périodiques, • Réaliser un reporting régulier de son activité, • Veiller au respect du système Qualité en vigueur, des bonnes pratiques de fabrication, des règles d’hygiène et de sécurité, des règles de fonctionnement de l’entreprise. • Préparer la documentation technique nécessaire pour soutenir un examen des autorités compétentes concernées, en accord avec les normes applicables en vigueurQualifications & Experience• Diplôme d’ingénieur ou équivalent, • Expérience d’au moins 2 ans en R&D ou en Engineering, idéalement acquise dans le domaine de la chimie des polymères, des dispositifs médicaux. en qualification / validation • Connaissances de la norme ISO13485, des BPF et autres normes applicables au dispositif médicaux • Maîtrise des outils informatiques de bureautique standards • Français et anglais courant • Expérience projet en tant qu’acteur ou gestionnaire ayant permis de démontrer une aisance relationnelle, des capacités à dialoguer avec des interlocuteurs variés internes et externes à l’entreprise

Approach People Recruitment • Lausanne, Switzerland

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Lipid Nanoparticle Scientist

A Pharmaceutical Company is seeking a Lipid Nanoparticle Scientist in San Diego, CA. Role Description The successful candidate will design, manufacture and characterize lipid nanoparticles for the delivery of nucleic acids as well as other novel nanoparticle-based drug delivery formulations containing small molecules, RNA, DNA and proteins. The work is multi-functional and includes formulation design, analytical methods development, physical characterization, experimental design, sample analysis and interpretation of results. The candidate with be expected to bring prior experience in the field and interact closely with other researchers in the design of lipid nanoparticle delivery formulations. This is a hands-on, laboratory-based role in a highly collaborative early development environment. Job Description: • Must have experience with lipid nanoparticle delivery of RNA or DNA for transfection to mammalian cells or in-vivo models. • Must have experience in nanoparticle formulation and nanoparticle drug delivery. • Must have experience in development of methods to analyze and characterize nanoparticle formulations, components and functionality. • Background in the biology of gene transfection and expression is a plus. • Experience and technical proficiency with HPLC and other methods for analysis and quantification of small molecules, DNA and proteins is preferred. • Previous experience and technical proficiency in the physical characterization of nanoparticles, including particle sizing is a plus. • Familiarity with lab-scale nanoparticle preparation techniques, including microfluidics technology, is preferred. • Experience with alternate pharmaceutical manufacturing technologies homogenization, lyophilization, micronization, etc. is a plus. • Strong interpersonal, communication, collaboration and problem solving skills. • Ability to document work and proven record of scientific technical writing. Skills & Requirements • Qualifications: Ph.D. in Chemistry, Biochemistry, Pharmaceutical Sciences, Chemical Engineering, Biomedical Engineering or closely-related discipline with an emphasis in delivery of nucleic acids. M.S. or B.S. in similar fields acceptable with a minimum of 6+ years of relevant industrial experience.

HAYS PLC • San Diego, U.S.

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Chemical Process Engineer - Staff

Location: Bayport, TXThe Chemical Process Engineer – Staff will be responsible for engineering needs demonstrating skills in plant troubleshooting, process design, process control and monitoring, project management and implementation, capital budget developments and management, new technology development and implementation. The Chemical Process Engineer – Staff will be responsible for interfacing with other parts of the organization which include safety, environmental, process safety management, and product quality. Primary ResponsibilitiesConduct process troubleshooting. Identify and implement process improvements;Maintain and improve process control systems;Identify and manage capital and other various projects through completion;Process Safety Management (PSM) - Complete various PSM responsibilities including Management Of Change (MOC) and Standard Operating Procedures (SOPs);Implement safety and environmental improvements; andMonitor and improve product quality. Required Education and ExperienceBS in Chemical Engineering or other Engineering discipline is required;Minimum of five (5) years experience as a process engineer in a chemical manufacturing environment is required;Experience leading cross-functional teams and projects also required;Strong computer skills including Microsoft Office Suite, SAP required;Ability to configure and maintain process control systems such as Delta V and PLCs ( Desired) Experience leading small to medium size capital projects required; and Experience with the following unit operations and equipment (reaction, distillation, heat exchange, pumps, scrubbers, cooling towers) also is required.

Goodyear Tire & Rubber Company • Pasadena, U.S.

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