Chemist Jobs in Clifton, 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.

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

Job Title: Associate Scientist 100% onsite Duration: 06 Months Contract (Possibility of extension) Pay Rate: $45-$49/hr on w2 Must Haves: Required Bachelors in Forensic Science degree, preferred Master's degree (Must have) What make and model they used for SEM/FTIR 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 Job Description: 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. Additional Job Requirements: Lab w/ blood & animal

Our client, a leading CDMO, is seeking an Analytical Chemist to join their team! The Analytical Chemist is responsible for HPLC method transfer/validation, and quality control testing of raw materials and finished goods. Pay: Up to $45/hr Type: Contract Responsibilities Conduct and document chemical analyses for raw materials, in-process goods, and finished products. Design, validate, and resolve issues with analytical methods, including HPLC for cleaning verification. Collect and analyze equipment cleaning validation samples. Prepare Certificates of Analysis, analytical reports, and maintain lab documentation. Peer-review records and support OOS or OOT investigations as per SOPs. Ensure compliance with SOPs, cGMPs, and regulatory requirements. Assist with environmental monitoring and other tasks as assigned. Requirements Bachelor's in Chemistry-related discipline with 2+ years of analytical lab experience in pharma or biotech. 2 years hands-on method transfer/verification experience (HPLC). Method validation (HPLC) experience preferred. Experience with GC, UV-Vis, FTIR, KF, and Particle Size Analysis. Knowledge of cGMPs, pharmacopeia (USP, EP), and regulatory standards (21 CFR Part 210/211/820, ISO). This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

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.

About Us Imagine the innovation and expertise behind the world's leading cosmetic brands, brought to you by a distinguished Italian company with a legacy of excellence. Since 1972, Intercos Group has been at the forefront of color cosmetics, pencils, nail polish, skincare, and personal care products. We pride ourselves on being the only cosmetics manufacturer that combines top-tier quality and advanced technology with a global reach and a personalized touch. With 15 commercial offices and 15 production facilities across 12 countries, Intercos Group brings a local approach to a global stage. We continually set the standard for beauty, crafting exceptional product lines for brands worldwide. As one of the largest suppliers in the cosmetics industry, we are a leading force in the research, development, and production of beauty products, shaping the future of the industry with every season. Position Summary The R&D Lab Technician works on different color cosmetic projects from batching formulas, to preparing samples and performing testing in Congers, NY. Essential Functions Make daily lab batches as assigned by chemist or lab manager Assist the color chemist to perform shades counter-matching Prepare samples for submission to clients (lipsticks, pressed powders, lip-glosses) Prepare paperwork for formula submissions and document specifications for various batches Perform testing on formulation (viscosity, volatiles, break points, drop tests…) Maintain detailed, organized records in formulation and project management databases Collaborate with formulators and lab manager to ensure inventory of raw materials are replenished and maintained appropriately Assist the chemists in the development of new shades and formulations Participate actively to the organization of laboratory Keep track of all raw materials and organize them in the most efficient way Maintain and organize the color library Job Qualifications Bachelor's Degree in any related science, such as chemistry, Biology, Physics, etc. 1 year relevant work experience in a lab environment (ideally cosmetics) Color perception and color matching skills, Formulation skills in all color cosmetics technologies, raw material knowledge (especially pigments), FDA guidelines Ability to follow instructions Able to use a computer and enter data in the system Ability to record and document critical batch process documents Attention to accuracy and detail Familiar with measurement scales, mixing, blending, chemical mills and other formulation manufacturing equipment Follow established formulas to create laboratory batches color cosmetics. Observe, record, investigate, duplicate and validate successful procedures. Perform calculations during shade matching under chemist supervision. Prepare and maintain accurate technical data and required documentation. Job Benefits Health Insurance: Comprehensive medical, dental, and vision coverage Retirement Plans: 401(k) plan, often with company matching Life Insurance: Coverage for employees in the event of death or disability Paid Time Off (PTO): Vacation days, sick leave, and personal days Holidays: Paid company holidays and floating holidays Professional Development: Training programs and opportunities for career advancement Performance Bonuses: Annual merit increase and/or bonus based on individual performance Company Events: Team-building activities, social events, and company outings Employee Assistance Programs (EAPs): Confidential counseling and support services for personal and professional issues. EEO Intercos Group is committed to creating a diverse and inclusive workplace where everyone is valued and respected. We believe that a wide range of perspectives and experiences enhances our innovation and success. We are an Equal Opportunity Employer and do not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or any other legally protected status. All qualified applicants are encouraged to apply and will receive consideration for employment without regard to any of these characteristics. We are dedicated to providing a work environment that is free from discrimination and harassment and promotes equal opportunity for all.

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

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.

1. Capable of setting up benchtop, pilot plant experiments 2. Capable of managing product inventories, product entries, purchase orders 3. Support in pilot plant trials, product packing, shipping, labeling etc. 4. Capable of lifting up to 25 lbs 5. Capable of working in the lab under GLP/GMP practices 6. Accurate data entry, documentation, following the procedures is a must 7. Capable of interacting with other employees to independently identify and organize resources for conduct of experiments 8. Available for traveling to manufacturing sites to support trials when required. 9. Capable of engaging with suppliers in discussions associated with ingredient purchasing, and follow ups. Education: 1. Science degree/Experience in conducting experiments in science. REQUIRED SKILLS: 1. Diligent and perseverant 2. Excel/Word/MS Outlook - Microsoft product proficient 3. Good communication skills - oral and written 4. Good organizational skills 5. Attention to detail 6. Works well in a team setting, working with QA/R&D work team on other aspects of project 7. Self-motivated and with initiative

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).

Technician's responsibilities will include: support for Product Developers in the Citrus lab in the preparation, testing and evaluation of beverage batches. Accurately prepare beverage and beverage concentrates to support new product development, brand maintenance, etc. Support will also include: bench top batches, schedule and support pilot plant productions, sample submission for QC, Micro and any other required analysis, coordinate and collect data for product shelf life studies, keep thorough documentation of batches and experiments, maintain and document lab inventory, maintain a safe work environment and effectively work with team members, other PDs and support teams to complete projects. 1. Capable of setting up benchtop, pilot plant experiments 2. Capable of managing product inventories, product entries, purchase orders 3. Support in pilot plant trials, product packing, shipping, labeling etc. 4. Capable of lifting up to 25 lbs 5. Capable of working in the lab under GLP/GMP practices 6. Accurate data entry, documentation, following the procedures is a must 7. Capable of interacting with other employees to independently identify and organize resources for conduct of experiments 8. Available for traveling to manufacturing sites to support trials when required. 9. Capable of engaging with suppliers in discussions associated with ingredient purchasing, and follow ups. Education: 1. Science degree/Experience in conducting experiments in science. REQUIRED SKILLS: 1. Diligent and perseverant 2. Excel/Word/MS Outlook - Microsoft product proficient 3. Good communication skills - oral and written 4. Good organizational skills 5. Attention to detail 6. Works well in a team setting, working with QA/R&D work team on other aspects of project 7. Self-motivated and with initiative

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

*Hiring Organization*: Rose International * 481767 *Job Title: *Research and Development Technician *Work Model: *Onsite *Shift:* 8am-5pm, Mon - Fri *Employment Type*: Temporary *Estimated Duration (In months*): 13 *Min Hourly Rate($)*: 27.00 *Max Hourly Rate($)*: 29.00 *Must Have Skills/Attributes*: Communications, GMP, Inventory Control, QC *Job Description* *Required Education:* • Associates or Bachelor of Science Degree *Required Qualifications/Skills/Experience:* • Experience in conducting experiments in science • Diligent and perseverant • Microsoft product proficient (Excel, Outlook, Word) • Good communication skills • Good organizational skills • Attention to detail • Works well in a team setting, working with QA/R&D work team on other aspects of the project • Self-motivated and with initiative *Position Overview:* Support Product Developers in the Citrus lab in the preparation, testing and evaluation of beverage batches. Accurately prepare beverages and beverage concentrates to support new product development, brand maintenance, etc. Support will also include: bench top batches, schedule and support pilot plant productions, sample submission for QC, Micro and any other required analysis, coordinate and collect data for product shelf life studies, keep thorough documentation of batches and experiments, maintain and document lab inventory, maintain a safe work environment and effectively work with team members, other PDs and support teams to complete projects. *Job Details:* • Set up benchtop, pilot plant experiments • Manage product inventories, product entries, and purchase orders • Support in pilot plant trials, product packing, shipping, labeling, etc. • Lifting up to 25 lbs. • Work in the lab under GLP/GMP practices • Accurate data entry, documentation, and following the procedures is a must • Interact with other employees to independently identify and organize resources for conducting experiments • Travel to manufacturing sites to support trials when required • Engage with suppliers in discussions associated with ingredient purchasing, and follow-ups *\*\*Only those lawfully authorized to work in the designated country associated with the position will be considered.\*\** *\*\*Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client's business needs and requirements.\*\** *Benefits:* *For information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website.* *California Pay Equity:* *For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here.* *Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances.* *If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise, please contact our HR Department.* *Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify). (Posting required by OCGA 13/10-91.).* #UNI Job Types: Full-time, Temporary Pay: $27.00 - $29.00 per hour Benefits: * 401(k) matching * Dental insurance * Health insurance * Health savings account * Vision insurance Schedule: * 8 hour shift * Day shift * Monday to Friday Application Question(s): * Do you have a degree in a scientific field? * Do you have experience in a laboratory setting? * Do you have experience with pilot plants and setting up benchtops? * Are you authorized to work on Rose International's W2 without sponsorship? Education: * Associate (Required) Experience: * conducting experiments in science: 1 year (Required) Ability to Commute: * Valhalla, NY 10595 (Required) Work Location: In person

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.

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.