Chemist Jobs in Hoboken, NJ

Primary Responsibilities • Support execution of scientific studies to support the development of active pharmaceutical ingredients (APIs), pharmaceutical formulations, and manufacturing processes using both traditional and advanced analytical tools. • Develop and implement analytical methods utilized during drug development as well as for the release and shelf-life assessment of clinical materials. • Document the execution, procedure, results, and conclusions of experiments in a detailed and organized manner. • Strong collaboration with fellow Analytical Research & Development colleagues as well as cross-functional partners. Quals-- Education Minimum Requirements: Minimum 3 years relevant industry experience for applicants with a Bachelor of Science degree, or 0 years of relevant industry experience for applicants with a Master of Science degree in Chemistry, Pharmaceutical Sciences, or related fields. Required Experience and Skills: Excellent written and oral communication skills, as well as strong collaboration skills, are required. Candidates will also be required to work in a team environment with cross-functional interactions. Preferred Experience and Skills: Hands-on experience in chromatography (e.g. LC, GC) method development, analysis and troubleshooting, spectroscopy analysis, and other analytical laboratory and data analysis techniques.

6 Month Contract (May extend or convert to permanenet) $30.34/hour - $35.34/hour W2 Primary Responsibilities: • Support execution of scientific studies to support the development of active pharmaceutical ingredients (APIs), pharmaceutical formulations, and manufacturing processes using both traditional and advanced analytical tools. • Develop and implement analytical methods utilized during drug development as well as for the release and shelf-life assessment of clinical materials. • Document the execution, procedure, results, and conclusions of experiments in a detailed and organized manner. • Strong collaboration with fellow Analytical Research & Development colleagues as well as cross-functional partners. Qualifications: Education Minimum Requirements: Minimum 3 years relevant industry experience for applicants with a Bachelor of Science degree, or 0 years of relevant industry experience for applicants with a Master of Science degree in Chemistry, Pharmaceutical Sciences, or related fields. Required Experience and Skills: Excellent written and oral communication skills, as well as strong collaboration skills, are required. Candidates will also be required to work in a team environment with cross-functional interactions. Preferred Experience and Skills: Hands-on experience in chromatography (e.g. LC, GC) method development, analysis and troubleshooting, spectroscopy analysis, and other analytical laboratory and data analysis techniques.

Outlier is the world's leading expert platform, connecting a network of over 100,000 contributors worldwide to improve AI models by providing expert human feedback. We partner with companies including OpenAI, Meta and Microsoft to enable advanced generative AI models to provide accurate responses and advanced reasoning capabilities. We are looking for advanced Chemistry experts to teach AI how to interpret and solve complex problems by: Evaluate AI-generated content for factual accuracy and relevance in Chemistry. Develop and answer Chemistry-related questions to refine AI understanding. Assess and rank AI responses based on scientific rigor. Required expertise and qualifications: Education: Master's degree or higher (PhD preferred) in Chemistry or a related field (can be currently enrolled) Research Experience: Strong preference for candidates with peer-reviewed publications, patents, conference presentations, research grants, or industry R&D contributions English Proficiency: Ability to read and write with minimal errors Bonus Skills: AI model training experience is not required but helpful Payment: Currently, pay rates for core project work by Chemistry experts range from $30 to $50 per hour USD but varies based on your geographic location (see note below) Opportunities for higher-paying research projects based on performance. Rates vary based on expertise, skills assessment, location, project need, and other factors. For example, higher rates may be offered to PhDs. For non-core work, such as during initial project onboarding or project overtime phases, lower rates may apply. Certain projects offer incentive payments. Please review the payment terms for each project.

Title: Analytical Associate Scientist Duration: 6 months with possible extension Education: Required Bachelors or Masters in Forensic Science degree - Madatory Experience using analytical instrumentation (FTIR, SEM/EDX, Microscopes) Summary The Associate scientist role within the Microscopy and Spectroscopy Lab (MSL) team in Manufacturing Sciences and Technology (MS&T) group will be responsible for investigations involving the physical and chemical characterization and identification of materials such as unknown components or foreign matter in manufacturing processes for cell therapy products. The role will also have responsibilities for investigating defective materials including but not limited to filters, single-use bioprocess containers, tubing, and polymeric fittings. Requirements: - Broad based experience in an area relevant to analytical and pharmaceutical chemistry with hands on exposure to state-of-the-art analytical technology, such as, microscopy, spectroscopy, FT-IR, confocal Raman, SEM/EDX, UV Vis, and NIR - Experience utilizing spectroscopic techniques including Raman, Mid-IR, Mass spectrometry, and others for protein identification and characterization is highly desirable. Knowledge of protein / cell chemistry related to structure and function is a plus. - GMP regulations, investigations (particulate and foreign matter). - "Bench" experience in forensics investigational work or analytical chemistry preferred. - Excellent scientific, analytical, and troubleshooting skills - Experience with the use of Scientific Software including Spectral data processing, hypercube spectral imaging, and MS Word, PowerPoint, and Excel. - Has high level of initiative, requires minimal direction/oversight. - Knowledge of cGMPs, compendial and FDA regulations.

Title - Forensic Scientist Months- 6+ Months (potential extension) Pay Range- $48-51/hr. on W2 Must Haves: Broad based experience in an area relevant to analytical and pharmaceutical chemistry with hands on exposure to state-of-the-art analytical technology, such as, microscopy, spectroscopy, FT-IR, confocal Raman, SEM/EDX, UV Vis, and NIR. Required Bachelors in Forensic Science degree, preferred Master's degree, or related field with at least 5 years of experience Summary The Associate scientist role within the Microscopy and Spectroscopy Lab (MSL) team in Manufacturing Sciences and Technology (MS&T) group will be responsible for investigations involving the physical and chemical characterization and identification of materials such as unknown components or foreign matter in manufacturing processes for cell therapy products. The role will also have responsibilities for investigating defective materials including but not limited to filters, single-use bioprocess containers, tubing, and polymeric fittings. Requirements: - Broad based experience in an area relevant to analytical and pharmaceutical chemistry with hands on exposure to state-of-the-art analytical technology, such as, microscopy, spectroscopy, FT-IR, confocal Raman, SEM/EDX, UV Vis, and NIR - Experience utilizing spectroscopic techniques including Raman, Mid-IR, Mass spectrometry, and others for protein identification and characterization is highly desirable. Knowledge of protein / cell chemistry related to structure and function is a plus. - GMP regulations, investigations (particulate and foreign matter). - "Bench" experience in forensics investigational work or analytical chemistry preferred. - Excellent scientific, analytical, and troubleshooting skills - Experience with the use of Scientific Software including Spectral data processing, hypercube spectral imaging, and MS Word, PowerPoint, and Excel. - Has high level of initiative, requires minimal direction/oversight. - Knowledge of cGMPs, compendial and FDA regulations. Education: Required Bachelors in Forensic Science degree, preferred Master's degree, or related field with at least 5 years of experience Experience using analytical instrumentation (FTIR, SEM/EDX, Microscopes) Duties: - Microanalytical investigations involving the physical and chemical characterization and identification of materials related cell therapy products. This includes characterization of unknown components or foreign matter, and/or the specialized analysis of reagents, starting materials, single-use consumables, process intermediates, and drug products. - Supporting day to day activities in the Microscopy and Spectroscopy lab including but not limited to, replenishment of lab supplies, analysis request distribution, interfacing with Facilities and EHS. - Application of a wide variety of analytical testing techniques such as, microscopy and spectroscopy techniques including, UV/Vis, FT-IR, Raman, NIR, SEM/EDX, particle sizing and counting, and wet chemistry. - Application of spectroscopic techniques to identify and characterize cell-therapy based drug products and intermediates. - Provide timely and efficient technical support. - Write comprehensive technical reports to document all analytical improvement or investigation projects. - Perform laboratory work to support defective material and foreign matter assessments - Perform analytical troubleshooting to solve manufacturing-related problems. Dexian is a leading provider of staffing, IT, and workforce solutions with over 12,000 employees and 70 locations worldwide. As one of the largest IT staffing companies and the 2nd largest minority-owned staffing company in the U.S., Dexian was formed in 2023 through the merger of DISYS and Signature Consultants. Combining the best elements of its core companies, Dexian's platform connects talent, technology, and organizations to produce game-changing results that help everyone achieve their ambitions and goals. Dexian's brands include Dexian DISYS, Dexian Signature Consultants, Dexian Government Solutions, Dexian Talent Development and Dexian IT Solutions. Visit ******************* to learn more. Dexian is an Equal Opportunity Employer that recruits and hires qualified candidates without regard to race, religion, sex, sexual orientation, gender identity, age, national origin, ancestry, citizenship, disability, or veteran status

Hi, My name is Gaurav, and I am a recruiter with Net2Source Inc. Our direct client is looking to hire a Scientist - II (Associate) - PA/NJ Only in their growing team. Please find below the job description. Title: Associate Scientist - II :: Ligand Binding Duration: 06 months (Extendable) Location: Rahway NJ 07065 No benefits Must Haves/Required skills: • Prior experience developing equilibrium and kinetic radioligand binding assays (e.g. 125I, 3H, 35S) in relevant formats is preferred, or willingness to do radioligand work. • Tissue culture including: (i) cell plating, (ii) cell stimulation and (iii) cell harvesting. • Experience in membrane preparation • Experience working with multiwell plates (96- and 384-well formats) • Note that this position is laboratory-based. **** is looking for a contractor for their early drug discovery team. This is a very dynamic, fast paced department. Our Mission statement: Mass Spectrometry & Biophysics Based in Rahway, NJ the Mass Spectrometry & Biophysics (MSB) team is an integral part of the Computational & Structural Chemistry Department within Discovery Chemistry. Working across all therapeutic areas & supporting teams at all network sites we focus our efforts in 3 principal areas to drive end-to-end pipeline impact: 1. Screening & Hit-to-Lead. Discovery & optimization of ligands across the modality spectrum (fragments, small molecules, bifunctional degraders, peptides, therapeutic proteins) to identify leads that modulate our targets of interest. 2. Elucidating Mode of Interaction. Detailed characterization of how our ligands interact with and modulate our targets of interest at the molecular level. 3. Understanding Mechanism of Action. Determining how perturbing our targets of interest affects disease pathology both in vitro and in vivo. Core responsibilities: • Run routine radioligand binding assay protocols, analyze data & generate weekly reports, carry out tissue culture and cell-based binding assays. • Fully document all experiments in our electronic laboratory notebook. Qualifications Education: B.Sc. with 6+ years or M.Sc. with 4+ year or PHD with 3+ years of laboratory experience practicing the required skills. Nice to haves/Preferred skills: • Experience with liquid handling automation systems (e.g. Echo, Bravo). • Familiarity with multi-mode plate readers such as the SpectraMax and EnVision Multilabel Reader. • Exporting and dose-response fitting of data from binding assays. • Running research operating plan assay and data upload (ROP assay, ActivityBase application) • Experience with traditional Western blot techniques, including requisite data analysis used to determine abundance of given protein targets. Knowledge of the Protein Simple high-throughput, automated western blotting system is preferred but not required. Computer/Software skills: • MS Office suite, Adobe PDF -must have • Prior experience with an electronic laboratory notebook system is desirable but not required. • Prior experience with data analysis packages including GraphPad Prism, Activity Base, etc. is desirable but not required.

Top-Tier Asset Management firm in Midtown, Manhattan is seeking a Investment Product Development Analyst for a permanent position! Responsibilities: Conducting competitive product analysis, market sizing, financial modeling, and database construction to support strategic decision-making. Construct and maintain financial models to analyze product performance, profitability, and risk metrics. Build and manage databases to organize and extract relevant investment data. Work with data from Morningstar and Evestment databases to support product comparisons and industry benchmarking. Develop and implement analytical frameworks for product evaluation and new investment product development. Conduct competitive product analysis, including gathering insights from third-party sources such as existing databases and competitor product profiles. Perform market sizing and pricing matrix analysis to assess the advisability of new and existing investment product opportunities. Qualifications: Bachelor's Degree Strong analytical skills with experience in financial modeling, investment analysis, data analysis, and market research. Familiarity with SQL, Python, or other data analysis tools is an added advantage. Proficiency in data analysis and visualization, with the ability to translate complex data into clear insights. Experience working with Morningstar and Evestment databases is highly preferred. Advanced Excel modeling skills with the ability to manipulate large datasets and create insightful financial models. Knowledge of different types of asset management products, including mutual funds, ETFs, hedge funds, and private equity. Prior experience in investment research, product strategy, or financial analysis is a plus.

The Associate scientist role within the Microscopy and Spectroscopy Lab (MSL) team in Manufacturing Sciences and Technology (MS&T) group will be responsible for investigations involving the physical and chemical characterization and identification of materials such as unknown components or foreign matter in manufacturing processes for cell therapy products. The role will also have responsibilities for investigating defective materials including but not limited to filters, single-use bioprocess containers, tubing, and polymeric fittings. Requirements: - Broad based experience in an area relevant to analytical and pharmaceutical chemistry with hands on exposure to state-of-the-art analytical technology, such as, microscopy, spectroscopy, FT-IR, confocal Raman, SEM/EDX, UV Vis, and NIR - Experience utilizing spectroscopic techniques including Raman, Mid-IR, Mass spectrometry, and others for protein identification and characterization is highly desirable. Knowledge of protein / cell chemistry related to structure and function is a plus. - GMP regulations, investigations (particulate and foreign matter). - "Bench" experience in forensics investigational work or analytical chemistry preferred. - Excellent scientific, analytical, and troubleshooting skills - Experience with the use of Scientific Software including Spectral data processing, hypercube spectral imaging, and MS Word, PowerPoint, and Excel. - Has high level of initiative, requires minimal direction/oversight. - Knowledge of cGMPs, compendial and FDA regulations. Education: Required Bachelors in Forensic Science degree, preferred Master's degree, or related field with at least 5 years of experience Experience using analytical instrumentation (FTIR, SEM/EDX, Microscopes) Duties: - Microanalytical investigations involving the physical and chemical characterization and identification of materials related cell therapy products. This includes characterization of unknown components or foreign matter, and/or the specialized analysis of reagents, starting materials, single-use consumables, process intermediates, and drug products. - Supporting day to day activities in the Microscopy and Spectroscopy lab including but not limited to, replenishment of lab supplies, analysis request distribution, interfacing with Facilities and EHS. - Application of a wide variety of analytical testing techniques such as, microscopy and spectroscopy techniques including, UV/Vis, FT-IR, Raman, NIR, SEM/EDX, particle sizing and counting, and wet chemistry. - Application of spectroscopic techniques to identify and characterize cell-therapy based drug products and intermediates. - Provide timely and efficient technical support. - Write comprehensive technical reports to document all analytical improvement or investigation projects. - Perform laboratory work to support defective material and foreign matter assessments - Perform analytical troubleshooting to solve manufacturing-related problems.

QC Chemist Job Title: Quality Control Laboratory Chemist - Radiopharmaceuticals Evergreen Theragnostics, Inc. is a radiopharmaceutical company headquartered in Springfield, NJ. We operate in a brand-new state-of-the-art facility, developing our own radiopharmaceutical products and providing contract development and manufacturing services for other radiopharmaceutical companies. We also operate our own cutting edge cancer research laboratories. Evergreen is a small team, where all team members support each other in a variety of activities. We are looking for team members who are motivated to take on new challenges and excited to help build the company. Job Description: We are seeking a highly skilled and experienced Quality Control Laboratory Chemist to join our team in the Radiopharmaceuticals division. This critical role involves the quality control processes documentation development, analytical methods improvement, and ensuring compliance with regulatory standards. The ideal candidate will have extensive experience in the pharmaceutical or radiopharmaceutical industry, a strong background in analytical chemistry, and well development technical writing capabilities. Key Responsibilities: Develop, optimize, and validate analytical methods for testing radiopharmaceutical products, including HPLC, GC, and TLC techniques. Troubleshoot and resolve issues related to laboratory equipment, ensuring proper functioning and accurate results and offering expertise and executing tasks related to department objectives and quality initiatives. Support the validation of analytical procedures, ensuring they meet internal specifications and regulatory requirements. Write, develop, and analyze methods and protocols for new and existing testing procedures. Serve as a key resource for the team, providing client support and managing communications related to reports, calls, and project updates. Contribute to the development of QC-specific protocols and reports, particularly for analytical method validation and related documentation. Collaborate with cross-functional teams and assist with the execution of client-driven requirements, ensuring that testing processes are aligned with regulatory standards. Lead and support efforts in continuous improvement projects that aim to optimize laboratory processes, increase efficiency, and enhance the overall quality system. Assist with departmental initiatives, including recruitment, training, and development of team members, as well as contributing to team scheduling and resource management. Ensure the accurate documentation of all testing results, protocols, and reports in compliance with GMP, GLP, and other regulatory guidelines. Qualifications: 5+ years of experience in the pharmaceutical, life sciences, or radiopharmaceutical industry Bachelor's degree in a scientific field (e.g., Chemistry, Biochemistry, Pharmaceutical Sciences), or equivalent relevant work experience. Extensive experience with laboratory techniques, including HPLC, GC, and TLC, with a strong ability to troubleshoot and resolve issues related to these methods. Proven ability to develop, modify, and validate analytical methods for a variety of testing procedures. Strong written and verbal communication skills, with experience developing and writing technical reports, protocols, and validation documents. Demonstrated ability to work independently as well as collaborate effectively with cross-functional teams. Experience in supporting client needs, including providing timely updates, addressing inquiries, and delivering high-quality reports. Knowledge of GMP, GLP, and other regulatory requirements for pharmaceutical testing and documentation. Working Environment: Laboratory setting with exposure to radiation and other chemical hazards. Fast-paced laboratory setting with responsibility for multiple concurrent projects and tasks. Opportunity to contribute to team improvement, including process optimization and team development. Collaborative environment with a focus on innovation and continuous growth in the radiopharmaceutical sector.

100% required Required Bachelors in Forensic Science degree, preferred Master's degree Lab w/ blood & animal Work Schedule: Mon- Fri(normal business hours) Duration: 6 months( possibility of extension beyond 6 months for the right candidate depending on performance). Must Haves: Broad based experience in an area relevant to analytical and pharmaceutical chemistry with hands on exposure to state-of-the-art analytical technology, such as, microscopy, spectroscopy, FT-IR, confocal Raman, SEM/EDX, UV Vis, and NIR Summary The Associate scientist role within the Microscopy and Spectroscopy Lab (MSL) team in Manufacturing Sciences and Technology (MS&T) group will be responsible for investigations involving the physical and chemical characterization and identification of materials such as unknown components or foreign matter in manufacturing processes for cell therapy products. The role will also have responsibilities for investigating defective materials including but not limited to filters, single-use bioprocess containers, tubing, and polymeric fittings. Requirements: Broad based experience in an area relevant to analytical and pharmaceutical chemistry with hands on exposure to state-of-the-art analytical technology, such as, microscopy, spectroscopy, FT-IR, confocal Raman, SEM/EDX, UV Vis, and NIR Experience utilizing spectroscopic techniques including Raman, Mid-IR, Mass spectrometry, and others for protein identification and characterization is highly desirable. Knowledge of protein / cell chemistry related to structure and function is a plus. GMP regulations, investigations (particulate and foreign matter). "Bench" experience in forensics investigational work or analytical chemistry preferred. Excellent scientific, analytical, and troubleshooting skills Experience with the use of Scientific Software including Spectral data processing, hypercube spectral imaging, and MS Word, PowerPoint, and Excel. Has high level of initiative, requires minimal direction/oversight. Knowledge of cGMPs, compendial and FDA regulations. Education: Required Bachelors in Forensic Science degree, preferred Master's degree, or related field with at least 5 years of experience Experience using analytical instrumentation (FTIR, SEM/EDX, Microscopes) Duties: Microanalytical investigations involving the physical and chemical characterization and identification of materials related cell therapy products. This includes characterization of unknown components or foreign matter, and/or the specialized analysis of reagents, starting materials, single-use consumables, process intermediates, and drug products. Supporting day to day activities in the Microscopy and Spectroscopy lab including but not limited to, replenishment of lab supplies, analysis request distribution, interfacing with Facilities and EHS. Application of a wide variety of analytical testing techniques such as, microscopy and spectroscopy techniques including, UV/Vis, FT-IR, Raman, NIR, SEM/EDX, particle sizing and counting, and wet chemistry. Application of spectroscopic techniques to identify and characterize cell-therapy based drug products and intermediates. Provide timely and efficient technical support. Write comprehensive technical reports to document all analytical improvement or investigation projects. Perform laboratory work to support defective material and foreign matter assessments Perform analytical troubleshooting to solve manufacturing-related problems.

To be considered for this position, you must be authorized to work for any US employer without sponsorship now or in the future. will be working the overnight shift, Mon-Fri from 10PM to 6:30AM. The Opportunity: A New Jersey-based flavor and fragrance company is seeking an experienced Chemist with a strong background in organic and process chemistry to develop new products and processes for flavor and fragrance ingredients for the food and cosmetics industry. Successful applicant will have excellent theoretical and practical knowledge as well as experience in organic synthesis including synthetic methodology, catalysis, upstream and downstream processing. The position also requires conceptual design and experimental validation of designed processes. Qualifications: Bachelor or Master Degree in organic chemistry or related field Experience in distillation, re-crystallization, sublimation, deposition and extractions, synthesis Two years of industrial experience or related Knowledge of various lab equipment Ability to design, execute and troubleshoot experiments and processes Capacity to work independently Possess strong written and oral communication skills Ability to work effectively in a team environment and individually Physical fitness is required

Job Title: Analytical/QC Research Scientist Position Type: Full-Time Reports To: Director, Analytical R&D/QC We are seeking a highly motivated Research Scientist to join our Analytical R&D and QC department within the CDMO (Contract Development and Manufacturing Organization) industry. The ideal candidate will have a strong background in analytical chemistry and experience in method development, validation, and quality control testing. Key Responsibilities: Conduct analytical method development and validation independently. Troubleshoot analytical methods as needed and gain more experience in the related area. Conduct release testing for GMP regulatory starting materials, intermediates, and final APIs. Conduct testing for stability studies and cleaning verification. Review test data to ensure completion and accuracy. Write raw material test procedures as needed under supervision. Write SOPs and protocols as needed under supervision. Write instrument operating, maintenance, and qualification/calibration procedures as needed. Participate in OOS and deviation investigations, as needed. Support Quality Assurance as needed during internal audits and audits by clients and regulatory agencies. Assist in the development and implementation of corrective actions related to QC/AD. Troubleshoot and maintain analytical instruments. Ensure that instrument calibration and qualification intervals are current. Perform structural elucidation of small molecule drug substances, intermediates, and starting materials. Independently troubleshoot and resolve issues with NMR instrumentation. Provide clear oral and written explanations of NMR data for structural elucidation Identify and elucidate the structures of related impurities and degradants from API synthesis, fate and purge, and stress degradation studies. Qualifications: BS, MS, or PhD in Analytical Chemistry, Chemistry, Pharmaceutical Sciences, or a related field. 3+ years of experience in analytical R&D and/or QC within the pharmaceutical or CDMO industry. Strong knowledge of analytical techniques, including HPLC, GC, UV-Vis spectroscopy, and dissolution testing. Familiarity with method validation protocols and regulatory requirements. Excellent problem-solving skills and attention to detail. Strong communication and interpersonal skills, with the ability to work effectively in a team environment. Proficient in data analysis software and laboratory information management systems (LIMS).

Ryan Gems Inc., founded in 1979, is a family-owned and operated fine jewelry manufacturer based in New York City. Specializing in crafting exquisite gemstone and diamond jewelry, we combine traditional craftsmanship with innovative techniques to create timeless pieces of exceptional quality. Our collection is meticulously designed and manufactured on-site, reflecting our commitment to precision and artistry. Role Description We're seeking a detail-oriented and dependable Quality Control Specialist to inspect finished jewelry pieces and components before they go out to retailers. You'll be responsible for ensuring that every item meets our company's quality standards in terms of craftsmanship, stone setting, polishing, symmetry, and overall appearance. Key Responsibilities: Inspect finished jewelry for defects in manufacturing, stone setting, polish, and overall craftsmanship Use calipers, loupes, and other tools to ensure measurements and tolerances are accurate Approve or reject products based on quality standards Record findings and communicate issues to production and design teams Ensure all jewelry meets customer and internal specs before packing Assist with tracking recurring quality issues and suggest improvements Inspect incoming castings, loose stones, and semi-finished goods Requirements: 2+ year experience in quality control or jewelry manufacturing preferred Strong understanding of jewelry construction, materials, and common issues Keen eye for detail and craftsmanship Ability to work under pressure and meet tight deadlines Basic documentation and communication skills Comfortable using a loupe, calipers, and scales Bonus Points: Experience with diamond and gemstone quality Background in jewelry repair, polishing, or setting Knowledge of 14K/18K gold, platinum, and silver jewelry What We Offer: A stable and supportive work environment Opportunity to grow within a long-standing NYC-based company Competitive pay based on experience Employee perks, clean working space, and a solid team culture

KLA is a global leader in diversified electronics for the semiconductor manufacturing ecosystem. Virtually every electronic device in the world is produced using our technologies. No laptop, smartphone, wearable device, voice-controlled gadget, flexible screen, VR device or smart car would have made it into your hands without us. KLA invents systems and solutions for the manufacturing of wafers and reticles, integrated circuits, packaging, printed circuit boards and flat panel displays. The innovative ideas and devices that are advancing humanity all begin with inspiration, research and development. KLA focuses more than average on innovation and we invest 15% of sales back into R&D. Our expert teams of physicists, engineers, data scientists and problem-solvers work together with the world's leading technology providers to accelerate the delivery of tomorrow's electronic devices. Life here is exciting and our teams thrive on tackling really hard problems. There is never a dull moment with us. Job Description/Preferred Qualifications Develop new chromatography methods for analysis of process solutions used in metal deposition and other areas of semiconductor manufacturing Validate analytical methods developed in R&D department and share findings within a team Plan and conduct experiments using GLP and write technical report of results Knowledge of Quality by Design/Design of Experiments Work with interdisciplinary groups to design commercial analyzers Provide documentation, testing and support for commercial and prototype equipment Perform assignments with minimal supervision Prepare scientific publications and present work at conferences International Travel up to 20% Minimum Qualifications Chemistry and/or Chemical Engineering background Experience with chromatography software packages Doctorate (Academic) Degree + 3 years Chromatography (HPLC/uPLC, GC, IC, MS) experience; Master's Level Degree + 6 years Chromatography (HPLC/uPLC, GC, IC, MS) experience Base Pay Range: $121,300.00 - $206,200.00 AnnuallyPrimary Location: USA-NJ-Totowa-KLAKLA's total rewards package for employees may also include participation in performance incentive programs and eligibility for additional benefits including but not limited to: medical, dental, vision, life, and other voluntary benefits, 401(K) including company matching, employee stock purchase program (ESPP), student debt assistance, tuition reimbursement program, development and career growth opportunities and programs, financial planning benefits, wellness benefits including an employee assistance program (EAP), paid time off and paid company holidays, and family care and bonding leave. Interns are eligible for some of the benefits listed. Our pay ranges are determined by role, level, and location. The range displayed reflects the pay for this position in the primary location identified in this posting. Actual pay depends on several factors, including state minimum pay wage rates, location, job-related skills, experience, and relevant education level or training. We are committed to complying with all applicable federal and state minimum wage requirements where applicable. If applicable, your recruiter can share more about the specific pay range for your preferred location during the hiring process. KLA is proud to be an Equal Opportunity Employer. We do not discriminate on the basis of race, religion, color, national origin, sex, gender identity, gender expression, sexual orientation, age, marital status, veteran status, disability status or any other status protected by applicable law. We will ensure that qualified individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us at ************************** or at *************** to request accommodation. Be aware of potentially fraudulent job postings or suspicious recruiting activity by persons that are currently posing as KLA employees. KLA never asks for any financial compensation to be considered for an interview, to become an employee, or for equipment. Further, KLA does not work with any recruiters or third parties who charge such fees either directly or on behalf of KLA. Please ensure that you have searched KLA's Careers website for legitimate job postings. KLA follows a recruiting process that involves multiple interviews in person or on video conferencing with our hiring managers. If you are concerned that a communication, an interview, an offer of employment, or that an employee is not legitimate, please send an email to ************************** to confirm the person you are communicating with is an employee. We take your privacy very seriously and confidentially handle your information.

Are you an experienced scientist who wants to work on the formulation of new and innovative products related to consumers' routines across the globe? Then L'Oréal Research & Innovation (R&I) might be exactly the place you have always been looking for! For more than one hundred years, L'Oréal believes that Beauty needs Science. In a world now transformed by digital technology and the emergence of new scientific Domains, we are confident in our ability to turn these opportunities into major innovations, closely linked to the new consumer expectations all over the world. Science & Technology are allowing us to invent safe, dependable, sustainable & responsible beauty products and experiences that will change people's lives. L'Oréal Research and Innovation has continuously invested upstream in its research with a high level of ambition. Our 3800+ L'Oréal R&I people are talented and highly skilled, located in major markets, working in a cooperative way, opened to the world. Inside L'Oréal's Research & Innovation Division, Development is responsible for working closely with our over 35 brands to adapt and innovate formulations into new and exciting products based on consumer and marketing insights. Development of great products requires building strong, international collaborations across different functions to ensure that products are seen from inception to officialization for our local and global launch deadlines. We are currently seeking a talented and innovative Senior Chemist I to join our Hair Care, Scalp, & Manageability Development Team located at our Clark, New Jersey facility for Research and Innovation. In this role you are responsible for coordinating development projects to ensure launch commitments are met in line with brand innovation strategies. You'll maintain awareness of scientific literature, patents, raw material technology, processing methodology, and marketing/consumer trends required to perform innovative product development assignments in an efficient manner. You'll regularly engage with key stakeholders to define evolving priorities and working methods. You'll also be overseeing a safe and orderly laboratory environment. You Will . . . * As an experienced researcher be responsible for initiating project concepts, developing objectives, and planning priorities to complete multiple, significant R&I projects under limited supervision * Independently manage multiple projects from inception to launch * Independently investigate and resolve research problems and issues as they arise * Mobilize and coordinate those involved in projects * Ensure implementation of necessary technical resources to meet targets and deadlines * Execute & develop new formulas for more complex hair projects * Monitor the quality and conformity of formulas * Provide scientific expertise and play an advisory role to ensure projects run smoothly; act as a project champion * Provide training and mentoring to technical project staff * Identify new efficacious raw materials suitable for product development * Interface with technical support groups including safety, regulatory, microbiology, analytical, Demi-grand and manufacturing * Have a clear and shareable vision of the objective, goal, and consumer insight for each project * Keep up to date with competitor landscape and project benchmarks * Have extensive inter-departmental/inter-divisional company interaction (e.g. Marketing, Manufacturing) and externally * Potentially manage some external vendor relationships when applicable to projects assigned You Have . . . * A minimum of a Bachelor's Degree in science or engineering is required * 3-5+ years of experience in hair care/ formulation required * Experience with sulfate free hair care formulation desirable * Knowledge of US hair market & global regulatory requirements desirable * Excellent communication, presentation and project management skills * Excellent interpersonal skills with the ability to share and teach in the area of expertise with experts and non-experts alike * Authorization to work in the US on a full-time, permanent, ongoing basis, without the need for sponsorship now or in the future. You Are . . . * Someone who plays well on teams and in collaborative environments * Someone who can work well under pressure and in a fast paced environment * Someone who can solve problems and make decisions * Someone who can quickly respond to changing priorities with initiative, creativity, and flexibility We are an Equal Opportunity Employer and take pride in a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, sexual orientation, national origin, age, marital or veteran status, medical condition or disability, or any other legally protected status.

We are seeking a QC Analytical Chemist to join our team. The successful candidate will be responsible for performing quality control analysis on essential oils, pre-shipment materials, and raw materials. This role involves generating Certificates of Analysis for customer requests, entering Quality Control Results in the QC module, and performing a variety of tests including Specific Gravity, Refractive Index, Optical Rotation, Aldehydes, Acid value, Flash Point, Solubility, and pH. Additionally, the QC Analytical Chemist will evaluate the sensory profile of tested items and manage samples in the QC database. Responsibilities * Perform QC analysis for essential oils, pre-shipment materials, and raw materials. * Generate Certificates of Analysis for customer requests. * Enter Quality Control Results in the QC module. * Conduct tests such as Specific Gravity, Refractive Index, Optical Rotation, Aldehydes, Acid value, Flash Point, Solubility, and pH. * Evaluate the sensory profile of tested items (odor, color, and physical appearance). * Enter samples into the QC database. * Set up samples on the GC Auto sampler Sequence file. Essential Skills * Proficiency in GCMS and Gas Chromatography. * Bachelor's degree in Chemistry, Chemical Engineering, Environmental Science, or a related field. * 5+ years of experience running GCMS/GC in the food/fragrance industry * Understanding of SQF Regulations and Procedures. * Experience with LIMS. * Development and GMP knowledge. Pay and Benefits The pay range for this position is $100000.00 - $120000.00/yr. Berjé provides medical, dental, and vision insurance options to ensure employees and their families have access to necessary healthcare services. Employees can participate in retirement savings plans, such as a 401(k), with company matching contributions to help secure their financial future. Berjé offers generous paid time off, including vacation days, sick leave, and holidays, allowing employees to balance work and personal life. The company provides life insurance and both short-term and long-term disability insurance to support employees in case of unforeseen circumstances. Employee Assistance Programs: These programs offer confidential counseling and support services to help employees manage personal and work-related challenges. Berjé encourages continuous learning and growth by offering opportunities for professional development, including training programs and tuition reimbursement. The company promotes overall well-being through wellness initiatives, such as fitness programs and health screenings. Workplace Type This is a fully onsite position in Carteret,NJ. Application Deadline This position is anticipated to close on Apr 28, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: * Hiring diverse talent * Maintaining an inclusive environment through persistent self-reflection * Building a culture of care, engagement, and recognition with clear outcomes * Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Department: Investment - Volatility Squarepoint Services US LLC seeks a Senior Quantitative Researcher for its New York, New York location. Duties: On behalf of an investment management firm, formulate mathematical and simulation models of investment strategies, relating constants and variables, restrictions, alternatives, conflicting objectives, and numerical parameters for the enhancement of trading through computerized algorithms, as well as implementation of models . Utilize comprehensive knowledge of mathematical models and technologies, statistical techniques including regression analysis, machine learning, and statistical inference, and financial and computer skills in order to enhance investment strategies based on equities or other asset classes. Produce and implement sophisticated analyses describing new statistical effects, assessing robustness of effects, and developing new quantitative strategies making use of such effects. Utilize KDB/Q and Python to analyze existing strategy behavior and propose and implement improvements. Utilize Excel/VBA mathematical models and KDB analysis tools to track market history of specific asset classes to evaluate future profit potentials and risk margins. Manage live trading automatons and perform continuous monitoring of risk related to live trading automatons. Leverage on asset-class-specific experience to find new patterns in market data and explore new methods to optimize execution costs. Assist team's quantitative researcher's efforts in building, validating, releasing, and maintaining highly complex automated trading models. Pilot research projects spanning multiple teams across multiple regions to develop new mathematical models and analytical tools for critical investment decision making. Required Qualifications: Must have a minimum of a Master's degree or foreign equivalent in any STEM (Science, Technology, Engineering, or Math) field of study and two (2) years of experience as a Quantitative Researcher, Investment Process Associate, or related position for an investment/asset management organization. Must have at least two (2) years of employment experience with each of the following required skills: Utilizing option's knowledge to perform asset specific research and engage in real trading; Analyzing time series data using auto-correlation, stationary test, autoregressive moving average model and conditional heteroskedasticity models; Transferring portfolio construction into mathematical optimization problem and obtain each name trade from the solution given signal values and restricted risk exposure. Backtesting different systematic trading ideas and evaluating performance metrics- sharpe ratio, return over gross, turnover and drawdown; Transferring idea into codes, implementing backtest framework, automating signal and report generation; and Analyzing and understanding large datasets using statistical techniques (regression and correlation). Salary / Rate Minimum/yr: $205,000 Salary / Rate Maximum/yr: $220,000 40 hrs/wk/ The minimum and maximum salary/rate information above include only base salary or base hourly rate. It does not include any other type of compensation or benefits that may be available. Squarepoint: Squarepoint is an EEO/AA employer.

Outlier is the world's leading expert platform, connecting a network of over 100,000 contributors worldwide to improve AI models by providing expert human feedback. We partner with companies including OpenAI, Meta and Microsoft to enable advanced generative AI models to provide accurate responses and advanced reasoning capabilities. We are looking for advanced Chemistry experts to teach AI how to interpret and solve complex problems by: Evaluate AI-generated content for factual accuracy and relevance in Chemistry. Develop and answer Chemistry-related questions to refine AI understanding. Assess and rank AI responses based on scientific rigor. Required expertise and qualifications: Education: Master's degree or higher (PhD preferred) in Chemistry or a related field (can be currently enrolled) Research Experience: Strong preference for candidates with peer-reviewed publications, patents, conference presentations, research grants, or industry R&D contributions English Proficiency: Ability to read and write with minimal errors Bonus Skills: AI model training experience is not required but helpful Payment: Currently, pay rates for core project work by Chemistry experts range from $30 to $50 per hour USD but varies based on your geographic location (see note below) Opportunities for higher-paying research projects based on performance. Rates vary based on expertise, skills assessment, location, project need, and other factors. For example, higher rates may be offered to PhDs. For non-core work, such as during initial project onboarding or project overtime phases, lower rates may apply. Certain projects offer incentive payments. Please review the payment terms for each project.

QC Analyst 3 Job Title: Quality Control Laboratory Analyst 3 - Radiopharmaceuticals About Us Evergreen Theragnostics, Inc. is a radiopharmaceutical company headquartered in Springfield, NJ. We operate in a brand-new state-of-the-art facility, providing contract development and manufacturing services for radiopharmaceutical companies, including therapeutics and centrally distributed diagnostics. We also operate our own cutting edge cancer research laboratories, developing proprietary, radiotherapeutic medicines. Evergreen is a small team, where all team members support each other in a variety of activities. We are looking for team members who are motivated to take on new challenges and excited to help build the company. Job Description: We are looking for an experienced and proactive Quality Control Laboratory Analyst 3 to join our team for our Monday-Friday day shift, Sunday-Wednesday 10 hour day shift, and Sunday -Wednesday 10 hour overnight shift. We offer a supportive team environment with room to grow in your career/ In this role, the candidate will participate in critical quality control processes for our radiopharmaceutical products, ensuring all operations comply with stringent industry standards and regulatory guidelines. The ideal candidate will have significant experience in pharmaceutical or radiopharmaceutical environments, a strong background in analytical techniques, and the ability to troubleshoot laboratory equipment. Key Responsibilities: Lead quality control testing and analysis of radiopharmaceutical products, ensuring adherence to both internal specifications and regulatory standards. Maintain a clean, safe, and organized lab environment, adhering to all safety and pharmaceutical regulations, including radiation safety protocols. Perform daily lab tasks, including solution preparation, drug product analysis, and documentation of all testing. Independently operate, maintain, and troubleshoot laboratory equipment such as GC (Gas Chromatography), TLC (Thin Layer Chromatography), and HPLC (High-Performance Liquid Chromatography). Perform routine and complex analysis, troubleshooting issues with laboratory instrumentation as needed to ensure accurate results. Ability to be the primary QC operator on all projects, taking ownership of testing and analytical activities across multiple initiatives. Mentor and train new team members on laboratory techniques, Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), and company-specific procedures. Ensure proper documentation practices, maintaining a high level of accuracy in lab notebooks. Collaborate with cross-functional teams to resolve quality issues and contribute to continuous improvement initiatives. Assist with management of QC materials, including ordering supplies, tracking inventory, and ensuring availability of materials necessary for testing. Qualifications: 5+ years of experience in the pharmaceutical, life sciences, or radiopharmaceutical industry Bachelor's degree in a scientific field (e.g., Chemistry, Biochemistry, Pharmaceutical Sciences), or equivalent relevant work experience. Extensive hands-on experience with laboratory techniques, including GC, TLC, and HPLC, as well as troubleshooting of each. Proven ability to be the primary QC analyst on complex projects, managing multiple responsibilities and ensuring quality deliverables. Strong experience in inventory management, including the ordering and monitoring of QC supplies and reagents. In-depth knowledge of GMP, GDP, and regulatory documentation standards. Strong troubleshooting and problem-solving skills related to laboratory equipment and procedures. Ability to mentor and train new team members on both technical skills and regulatory requirements, with a focus on GMP/GDP. Capable of maintaining detailed and accurate documentation in lab notebooks, with minimal QA corrections. Working Environment: Laboratory setting with exposure to radiation and other chemical hazards. Required to wear personal protective equipment (PPE) such as lab coats, gloves, and safety goggles. Fast-paced laboratory setting, requiring multitasking and prioritizing several projects. Occasional lifting and movement of materials; commitment to maintaining a safe and organized working environment.