Chemist Jobs in Madison, NJ

"Education Requirements" B.S. in Chemistry required M.S. or Ph.D. in Organic or Medicinal Chemistry strongly preferred Job Title: Regulatory Chemist - CMC Documentation Duration: 6-month Contract (W2) Possibility to extend Job Description: This position requires a minimum of 50% onsite presence. The role focuses on compiling detailed information from scientists, authoring the Chemistry, Manufacturing, and Controls (CMC) sections of regulatory documents, and conducting data integrity checks to support the timely submission of both investigational and marketing applications for small and large molecules. A solid understanding of organic chemistry principles and the ability to critically evaluate analytical data are essential for success in this position. Experience with drug substance and/or drug product CMC development is highly preferred. Key Responsibilities: Author and compile CMC sections of regulatory submissions, ensuring accurate and comprehensive documentation. Perform data integrity checks to support regulatory applications for investigational and marketing approvals. Collaborate with scientists and cross-functional teams to gather and assess relevant data. Utilize computer-assisted tools for document preparation to ensure quality and compliance with regulatory standards. Qualifications: Strong Regulatory Documentation and Authoring experience (not limited to formatting). A mandatory B.S. in Chemistry is required, with M.S. or Ph.D. in Organic or Medicinal Chemistry strongly preferred. In-depth understanding of Organic Chemistry and Medicinal Chemistry. Excellent written and verbal communication skills with attention to detail. Ability to multitask and work collaboratively within a team-oriented environment. A background in pharmaceuticals is essential, particularly in drug substance or drug product CMC development.

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.

At Benjamin Moore, our success is attributable to the employees who dedicate their time and talents to the brand and exemplify our core values of openness, integrity, community, excellence, and safety. Benjamin Moore employees enjoy a competitive and well-rounded benefits package, career development options, business resource groups, and opportunities to come together and connect with colleagues. We facilitate growth, development, and purpose for all through an inclusive and engaging workplace. Join us and be part of a brand that inspires creativity, innovation, and passion while supporting locally owned stores in 65 countries. Click here to see how you can paint your future! Job Summary Benjamin Moore & Co., a Berkshire Hathaway company, is a leading manufacturer of innovative, high-quality coatings for the architectural and industrial maintenance markets. We are currently seeking a Product Development Chemist I to join our Research and Development team. In this role you will collaborate with the product formulation team working to improve existing products and develop and commercialize new products. This position requires solid technical skills and a desire to innovate as well as problem solve. The Product Development Chemist I role offers many opportunities for growth and development into higher technical or managerial roles. The Product Development Chemist I job is an exciting chance to join a team that promotes and recognizes innovation. We are seeking motivated individuals who will produce world-class products and add to the skillset of an already successful product formulation team. Please review the responsibilities and requirements for the position. We look forward to reviewing your resume. Soft Skills Leadership: Supervises 1-3 direct reports with the ability to develop personal growth opportunities, while managing multiple projects for organizational growth. The ability to inspire and motivate others towards a shared vision or goal. Emotional intelligence (Self-awareness): The ability to recognize and manage one's own emotions, as well as recognizing the emotions of others. Adaptability The ability to be flexible and adaptable in response to changing situations and demands. Conflict resolution: The ability to manage and resolve conflicts constructively and respectfully. Coaching Skills: The skill for growing and developing others. Knowing how to ask the right questions, active listening, and empowering others, as well as building rapport with colleagues. Trust Building: Building a team environment where the employees feel safe. Leaders need to be authentic, honest, transparent, and compassionate. Problem Solving: The ability to identify and analyze problems and produce effective solutions. Creativity (critical thinking): The ability to be forward-thinking and strategic and present innovative solutions. Time management: The ability to prioritize tasks and manage one's time effectively. Teamwork: The ability to work collaboratively with others towards a common goal, recognizing different perspectives and strengths. Empathy: Genuinely caring for others and being able to understand another person's situation and perspective. Cultural competence (The ability to work across cultures): The ability to understand and appreciate diverse backgrounds, perspectives, and ways of thinking. Key Responsibilities Develop new products, in partnership with Quality, Marketing and Manufacturing teams Initiate, design and execute multidimensional experiments Actively seek and leverage internal and external best in class knowledge Plan and support plant scale-ups Coordinate with quality and manufacturing to improve performance and ease of manufacturing Capable of managing a team and working as a member on larger complex teams Manage multiple projects simultaneously Record test results accurately Analyzes data, thoroughly documents results and recommends next steps Perform product physical and application testing Manage and train junior chemists and technicians Monitor competitive and industry trends Adhere to all laboratory safety and cleanliness guidelines Supports resolution of quality issues Required Skills BS in Chemistry or related discipline and 5+ years of experience Knowledge of coatings, formulation tools, techniques, performance metrics and manufacturing processes Strong people and cross-functional team management skills Excellent communication, presentation & organizational skills Possess good analytical problem-solving skills to make timely & accurate decisions Compensation Philosophy At Benjamin Moore, our brand represents excellence, and we strive to provide a comprehensive total rewards package to match. In addition to a competitive base salary, every exempt and non-exempt role in our organization is eligible for a performance-based annual raise and bonus in recognition of their efforts that contribute to the success of our organization. We conduct regular pay audits using external market data and internal comparisons to ensure our employees are compensated fairly and equitably. During our annual compensation review, we implement merit, equity, and promotion increases after a full calibration across all roles. In addition to our monetary Engagement, Inclusion + Social Impact At Benjamin Moore, we don't just accept difference - we celebrate it, support it, and thrive because it benefits our employees, customers, and community. We remain steadfast in our commitment to cultivating an environment where all are provided the tools and opportunities to thrive in the workplace. Our efforts allow each of us to authentically live our corporate values of Openness, Integrity, Community, Excellence, and Safety. Our Social Impact initiatives, including strategic partnerships, in-kind donations, and volunteerism, further amplify our ability to positively impact the lives of our stakeholders. We believe that fostering a culture of inclusion and belonging is the right thing to do and essential for our continued success. Student Loan Repayment Assistance Program Benjamin Moore provides Student Loan Repayment Assistance Program to support eligible active employees who graduated from an accredited post-secondary educational institution. The Repayment Program is intended to contribute to reducing employee's student loans. The Company follows all rules and regulations concerning the taxability of student loan repayments provided under applicable law. EOE Benjamin Moore is an equal-opportunity employer that is committed to a culture of inclusion and belonging. We do not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status, or any other basis covered by appropriate law. Our commitment to these principles means all employment decisions are made based on qualifications, merit, and business needs.

Job Title: Process Chemist Department: Process R&D Job Type: Full Time Director of Process Chemistry We are seeking a highly motivated and skilled Process Chemist to join our Process R&D Department at Porton J-STAR. In this role, you will be responsible for the development, optimization, and scaling of chemical processes for pharmaceutical production. You will collaborate with cross-functional teams to ensure that our processes are efficient, cost-effective, and compliant with regulatory standards. This job description applies to activities and responsibilities associated with the process chemistry development group and support of GMP Operations. Responsibilities Follow existing synthetic routes, making processing improvements where necessary, while conducting multi-step organic synthesis Plan and organize routine operations to maximize production output. Design novel synthetic routes and carry out multi-step organic synthesis. Operate simple open access HPLC/UV, LC/MS, MS, NMR, GC/MS, and other analytical instruments required to monitor reaction processes. Consult with management, the Analytical Department, the Director of GMP Operations and others on issues concerning experiments prior to and during GMP production. Accurately make and check calculations, prepare raw materials, reagents and solutions in accordance with company SOP's. Faithfully record procedures and results in Batch Records or Solution Preparation Forms, notebooks, or other appropriate forms in an organized manner as dictated by departmental SOP and GMP regulations. Write reports on research as required. Promote compliance with cGMP regulations. Attend GMP training sessions. Support management and maintenance of the SOP and Document Control system. Work with clients to develop material release tests and specifications for materials supplied by J‑STAR. Help ensure that client project needs, requirements, and timelines are communicated to, and coordinated between, GMP Operations and Quality Control. Conduct process chemistry R&D for clients as an individual contributor, which includes, but is not limited to, research on synthetic routes to active pharmaceutical ingredients and chemical intermediates by route discovery, process optimization, safety evaluation, enabling technologies, high throughput screening and chemo/biocatalytic reaction discovery and optimization. This will include R&D under c-GLP and potentially under c-GMP conditions. Develop safe, timely and efficient chemical processes by using established, new and/or novel chemical methodologies and processes. Coordinate analytical chemistry methodology to process and/or catalysis discovery, development optimization and problem solving. Maintain an uncompromising focus on quality, documentation, confidentiality and scientific execution. Participate in idea generation for selective quotes/proposals to clients as well as successfully execute against accepted quotes. Initiate cross-department communication and develop coordinated R&D, processing schedules and deliverables Lead and contribute to scientific and technical discussions with co-workers and clients to plan, execute, resolve issues and problem solve. Communicate candidly, clearly and timely with clients, management and peers. Participate in weekly client updates as needed, prepare weekly reports, contribute to and lead campaign reports and participate in process chemistry technology transfer. Coordinate and author professional campaign reports, research summaries, and tech packages. Follow all company, site and laboratory Environmental, Health and Safety (EHS)-related protocols, processes, guidelines and SOPs. Actively participate in EHS discussions with peers and management for continuous improvement of EHS practices. Maintain a clean and well-organized hood, bench, glove-box and common work area that is free of clutter, excess chemicals/samples. Advocate for these principals and positively influence others in this regard. Qualifications Required MS, PhD degree in Organic Chemistry. Proven track record meeting aggressive targets as related to safe, timely and successful synthetic organic chemistry projects. Knowledge and experience base of working in a c-GMP environment is preferable, but not required Excellent written, verbal and presentation skills. Experience in small molecule drug development is preferable, but not required. Track record of scientific success as measured by publications and presentations. Ability to prioritize and manage numerous activities simultaneously. Ability to interact in an effective and appropriate manner with diverse population sets. Experience in working on and positively contributing to scientific teams. Ability to perform the physical requirements of the position.

Our client, a well-established company in the cosmetic and personal care industry, is looking for an Associate Chemist to join their team. This role operates fully onsite in their Clark, New Jersey location. Responsibilities: Assist with the formulation of cosmetic products, including batching, stability studies, and product evaluations. Conduct physicochemical characterizations, including pH, viscosity, rheology, and microscopy. Perform regulatory compliance assessments for raw materials and final formulations in alignment with industry standards. Operate lab equipment (e.g., rheometers, viscometers, microscopes) to assess product performance. Conduct quality control measurements and microscopic analysis. Required Qualifications: Bachelor's degree in Chemistry, Chemical Engineering, or a related scientific field. 0-3 years of professional experience in a laboratory environment (internships or academic projects in related fields are also considered). Previous experience in the cosmetic, pharmaceutical, or related industries is a plus. Strong proficiency in Microsoft Excel and other relevant computer programs. Experience with lab equipment (rheometers, viscometers, microscopes) is a plus. Ideal candidate will be quick learner, detail oriented with good communication skills and able to thrive in fast-paced team environment Strong attention to detail, organized, and methodical. If you meet the required qualifications and are interested in this role, please apply today. The Solomon Page Distinction Solomon Page offers a comprehensive benefit program for hourly employees. We pride ourselves on offering medical, dental, 401(k), direct deposit and commuter benefits to our employees, including freelancers - which sets us apart in the industries we serve. About Solomon Page Founded in 1990, Solomon Page is a specialty niche provider of staffing and executive search solutions across a wide array of functions and industries. The success of Solomon Page reflects an organic growth strategy supported by a highly entrepreneurial culture. Acting as a strategic partner to our clients and candidates, we focus on providing customized solutions and building long-term relationships based on trust, respect, and the consistent delivery of excellent results. For more information and additional opportunities, visit: solomonpage.com and connect with us on Facebook, and LinkedIn. Opportunity Awaits.

Job Details: Chemist Global Pharmaceutical Company Contract, Long Term Will start in Skillman, NJ and move to Summit, NJ in the summer Pay up to $33-34/hr The Scientist, Analytical Advanced Models and Methods is responsible for planning and conducting moderately complex experiments, analyzing results, and providing solutions to problems of moderate complexity. You will also keep accurate records, review case report forms, and present data at in-house meetings: Key Responsibilities Develop advanced analytical models and methods to solve complex scientific problems Utilize innovative techniques to analyze data and generate insights Collaborate with cross-functional teams to design and implement cutting-edge solutions Stay current with industry trends and advancements in analytical methodologies Conduct in-depth research in assigned areas using cutting-edge methodologies Analyze and interpret complex data to provide actionable insights Continuously explore and integrate new technologies to enhance analytical capabilities Present findings and recommendations to stakeholders in a clear and compelling manner Present findings and recommendations to stakeholders in a clear and concise manner Qualifications What we are looking for Required Qualifications Bachelor's Degree in Chemistry, Materials Science or equivalent in a related field 2-4 years of experience in developing analytical models and methods using instrumentation techniques such as SEM, DSC, TGA, HPLC, UPLC, FTIR, LC/MS and GC/MS Proven track record of developing and implementing analytical solutions Strong proficiency in statistical analysis and data visualization tools Ability to think critically and problem-solve creatively Excellent communication skills and ability to work effectively in a team environment Desired Qualifications Experience with chemometrics and statistical tools such as PCA, PCR, and PLS Experience with programming languages such as Python, SAS, MATLAB Strong understanding of statistical methods and machine learning algorithms Experience with formulation chemistry across a wide variety of product types (e.g. emulsions, suspensions, solid oral dosage forms)

Specialty paint, coatings, and additives company is looking for a Coatings Chemist with application development experience. The position is located in Fairfield, NJ Responsibilities: Solve customer problems by applying our additives to the customer coatings problems. The employee is primarily responsible for working in a lab to test and evaluate those solutions Explore R&D teams new additives for potential applications Daily working on the bench Spraying and testing of formulations Extensive tracking of data Work from formulation to plant scale up. Interact with internal and external customers. Requirements The employee must have at least a Bachelor's degree in Chemistry. Masters or PHD is a plus. 5 years Coatings work experience is required Confident working in a lab Strong Application Development skills Strong organization skills are important to effectively manage the wide range of responsibilities. The employee must be able to clearly and effectively communicate in person and in writing. PLEASE NOTE THIS POSITION IS LOCATED IN FAIRFIELD, NJ. Relocation Assistance is provided.

RESPONSIBILITIES: Must be able to perform assigned sampling, physical, chemical tests and assay on raw materials, active pharmaceutical ingredients, in-process, finished and stability products, using various wet chemicals, physical and instrumental techniques (HPLC, GC, UV-Vis, IR, Particle Size Analyzer, KF Auto titrator, Bulk Density, and other routine QC instruments) as per as per USP monograph / In-house / any other Compendial monographs. Must record data and results as specified in documentation procedures. Documents work clearly and perform tests accurately. Must comply with regulatory/in-house requirements (may include but not limited to safety, housekeeping, laboratory chemical waste, cGMP, cGLP, documentation) when performing the assigned activity. Must prepare and review the analytical documents. Associate Chemist II will be responsible to prepare and/or Review Test Procedures, SOPs, and Protocols as assigned Responsible for maintaining independent verification testing programs with 3rd party contractor. Perform routine laboratory analysis, such as finished product testing, dissolution testing, stability testing, raw material testing, cleaning verification testing and manufacturing in-process testing. Must provide the necessary document to Support for the ANDA filing Associate Chemist II must perform troubleshooting and investigations under the direction of a supervisor/senior QC chemist. QUALIFICATIONS: Must have BS with chemistry 3+ years of experience as associate chemist in pharmaceutical industry. QC experience in Generic pharmaceutical industry. Must have good documentation practices. Knowledge in USP/ICH/FDA. BENEFITS: Medical Insurance Dental Insurance Vision Insurance Contract to Hire

Perform chemical and physical testing for complex inhalation product formulations under general supervision. Conduct testing in a cGMP laboratory and document those experiments per cGMP requirements. Calculate, organize, and communicate results using standard data templates and reports. Provide general laboratory assistance including planning, designing and executing experiments. Edit SOPs, protocols, methods, and reports. Position Description: • Perform analytical testing for inhalation products according to established testing method, per cGMP requirements. • Analyze samples, process data and document in laboratory notebook. • Organize and maintain the functionality of the lab. • Edit SOPs, protocols, methods, and reports. • Plan, design, and execute experiments with guidance from supervisor/senior staff. Necessary Skills: • Possess good organizational skills, a commitment to quality work, and good oral and written communication skills. • Work effectively as part of a team. • Experienced with HPLC, GC, KF, FTIR, or other analytical instrumentation necessary.

Our client, a skincare brand, is looking to hire a Senior Chemist to join the team at their corporate office onsite in Edison. Candidates must be able to work a 5 day, in office schedule. Job Duties Include: Lead reformulation initiatives to enhance product performance, stability, and to ensure alignment with regulatory and market demands Develop skin, hair, and body care formulations that prioritize technical excellence, consumer appeal, and market relevance Serve as the technical lead on cross-functional projects, facilitating communication between R&D, Regulatory, QC, and Manufacturing teams Troubleshoot and resolve technical challenges related to stability, viscosity, pH, compatibility, and texture to meet quality and performance standards Collaborate to transform concepts into feasible, trend-driven products Scale formulations from bench prototypes to pilot and full-scale manufacturing Oversee stability testing and analyze results to ensure formula integrity across varying conditions Mentor junior chemists, fostering skill development and enhancing lab efficiency Job Qualifications Include: 10+ years of experience in formulation development for skin care, hair care, or body care products Bachelor's degree (or higher) in Chemistry, Chemical Engineering, or a related scientific field Demonstrated success in cross-functional collaboration with Marketing, Product Development, and Regulatory teams to bring innovative concepts to market Expertise in formulating emulsions, serums, creams, gels, cleansers, and treatments Proven track record of resolving complex technical challenges Strong knowledge of raw materials and their functionalities, focusing on performance-driven applications Understanding of global regulatory standards and compliance requirements for beauty and personal care products Excellent problem-solving, technical leadership, and project management capabilities Salary: $115k - $120k annually *While PCG appreciates all applicants, only those qualified will be contacted. Thank you for your application. We look forward to hearing from you! If you believe you are a great candidate for this position, and the salary listed does not meet your expectations, we would still love to speak to you! PCG, in good faith, believes that this posted range of compensation is the accurate range for this role at this location at the time of this posting. PCG and our clients may ultimately pay more or less than the posted range depending on candidate qualifications. This range may be modified in the future. Pyramid Consulting Group, LLC is an Equal Opportunity Employer that takes 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. Please refer to our website: ***************** for access to our Right to Work and E-Verify Participation Posters.

Job Title: Laboratory Scientist - Pharmaceutical Manufacturing Support Key Responsibilities :Routine Testing and Analysis : Conduct routine analysis of finished products and raw materials, including weight, chemistry tests for raw materials, and stability sample testing under different ICH conditions .Testing and Assays : Perform a range of tests, including assay, identity (ID), content uniformity, blending uniformity, impurity testing, water content determination, content resolution, disintegration, and hardness testing .Instrument Proficiency : Operate and troubleshoot laboratory instruments such as HPLC, UPLC, GC, Karl Fischer, FTIR, visualization testers, and pH meters. Experience with chromatography software (e.g., Empower 3) is highly preferred .Methodology Compliance : Follow approved testing procedures and methods according to internal SOPs and USP monographs. Report data accurately and promptly .Data Review and Trending : Conduct peer data reviews and analyze data trends to ensure consistent results. Participate in laboratory investigations using TrackWise software .Collaboration and Support : Assist other scientists and laboratory personnel to ensure timely completion of projects. Support routine lab activities such as balance calibration, pH calculations, and other day-to-day tasks .Stability and Medical Testing : Perform stability testing of pharmaceutical products and excipients under ICH conditions, and assist with medical testing as necessary .Software Utilization : Utilize Empower 3 chromatography software for HPLC and UPLC analysis . Position Requirement s:4-8 years of hands-on experience in a laboratory setting, with a focus on oral solid dosage forms (tablets, capsules, sub-gels) and raw material s.Strong working knowledge of pharmaceutical testing, including stability testing and compliance with USP standard s.Experience with laboratory instrumentation such as HPLC, UPLC, GC, Karl Fischer, FTIR, and pH meter s.Prior experience with Empower 3 software or similar chromatography software is a significant advantag e. Skills and Knowled ge:Strong understanding of pharmaceutical testing methods, including assay, identity testing, content uniformity, and impurity analys is.Knowledge of data review processes, trending, and documentation of test resul ts.Ability to adhere to SOPs, USP monographs, and GMP regulatio ns. We are looking for a candidate who is proactive, detail-oriented, and possesses a strong understanding of modern pharmaceutical testing methods. If you have a passion for contributing to the development of high-quality pharmaceutical products and have the required experience, we would love to hear from you.

Jacobs Levy is seeking a Senior Quantitative Equity Researcher for our Florham Park, NJ office with a strong background in technical computing and statistics to join our research team. The team is responsible for researching all aspects of the investment process from data processing and alpha modeling through to portfolio optimization. Our researchers work collaboratively to contribute to our firm's leading edge, innovative investment process. We seek people who are passionate about equity investment and motivated to outperform the market . Responsibilities include: Conducting exploratory data analysis Empirical research into U.S. and global equity market inefficiencies Reviewing financial literature Developing new and improving existing investment models by identifying novel investment ideas and innovative data sources Creating innovative investment strategies Ideal candidates will look to combine creative insights with research to make sound investment decisions. Requirements include: PhD in Finance, Econometrics, or related quantitative discipline Familiarity with fundamental, expectational and market data Solid knowledge of asset pricing literature Strong programming skills (C++, C#, Fortran, Java, Julia, Python etc.), preferably experienced with large datasets and also familiar with parallel programming Version control experience (such as Git) An understanding of Bayesian Statistics, Machine Learning, Non-Linear Estimation Methods, Optimization, Transaction Cost Modeling, or Data Visualization is a plus At least 3 years of empirical equity research experience Independent thinker with good economic intuition and demonstrated record of original research Ability to work collaboratively across departments and to explain challenging technical concepts

Our Client, a Fortune 100 energy company who specializes in pioneering new research and pursuing new technologies to create more efficient forms of energy, is seeking a R&D Technician to join their growing team. Responsibilities: Carry out characterization and analytical studies on a variety of sample types in support of researchers (GC, SEM, TEM, etc.) Perform data analysis of experimental results Set up, calibrate, and troubleshoot instrumentation Operate lab and pilot scale equipment along with analytical instrumentation Qualifications: Bachelor degree in chemistry or related field OR HS diploma with relevant chemical industry experience Strong understanding of safety regulation Prior experience in the laboratory OR in production environment for chemical/oil & gas industry 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!

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

This position is for an experienced scientist with significant skills and interests in bench-level technical work. The individual will be part of a successful team focused on delivering innovation. Conduct laboratory bench research in the area of chromatography and sample preparation. Primary activities include execution of technical work under general supervision of senior technical staff. This will include carrying out chromatography sample preparation and testing as well as basic method development in GC. The ability to develop technical approaches and plans, solve appropriate technical problems and work independently is also expected. This position will require development of a detailed understanding of chromatographic theory. Key Responsibilities: Plan, setup and execute experiments Analyze data, accurately document experiments, propose next steps Follow safe laboratory practices and keep areas clean Participate in Department meetings and other R&D facility activities Requirements BS in Chemistry with 1-5 years of industry experience, or fresh MS in chemistry. Preferred: Familiarization with Agilent OpenLAB and ChemStation GC software.

Driven by a commitment to research, quality, and service, PDI provides innovative products, educational resources, training, and support to prevent infection transmission and promote health and wellness. Encompassing three areas, our Healthcare, Sani Professional and Contract manufacturing divisions, we develop, manufacture, and distribute leading edge products for North America and the world. We have several locations across the US and are looking for new Associates to join our team! POSITION PURPOSE This role is part of the R&D Microbiology team and involves leading the application and interpretation of standards and regulations related to PDI's microbiological and sterility assurance control programs. Key responsibilities include analyzing data, developing tactical plans, implementing procedures, and leading remediation projects. Additionally, you'll conduct scientific research to support PDI's growth strategies, ensuring that our products meet stringent microbiological and sterility standards. The position is a key component of scientific advancement in skin antiseptics and medical device sterilization. Primarily, the role supports new market launches with input across all facets of project progression including scientific insights, prototype assessment and registration testing to meet regulatory requirements. This position requires strong cross-functional collaboration and communication. In addition, developing equity building studies that enhance PDI's current portfolio to provide a competitive edge in a challenging marketplace. ESSENTIAL FUNCTIONS AND BASIC DUTIES RESEARCH & DEVELOPMENT: Act as a sterilization and microbiology subject matter expert (SME), by supporting new product development, changes to existing commercial products. Guide product development teams with scheduling, budget estimates, deliverables, as needed to ensure project and product launch success, and compliance with applicable regulations, industry standards. Develop innovative microbiology solutions to support product development and meet regulatory requirements. Provide technical solutions to product development and engineering teams using various fields of science and sterilization theory and practice. Lead cycle development, validation, requalification activities, as well as product-specific sterilization qualifications and adoptions. LABORATORY SUPPORT: Analyze samples, ensure compliance, and prepare, sterilize, and evaluate products with precision. Optimize laboratory space to ensure an efficient flow of work. Develop and refine methods, utilizing various techniques and instrumentation for accurate results Create new SOPs where gaps exist. Maintain SOP version revisions for continuous improvement initiatives. Maintain detailed records and partner with teams to ensure compliance and efficiency. CROSS-FUNCTIONAL SUPPORT: Lead formulators to determine the correct method and dosage for sterile products Work with packaging and operations to ensure appropriate sterility assurance level Identify technical and project risks. Drive quick problem-solving, manage risks, and align teams on project goals. Prepare technical reports and technical presentations for internal meetings. Provide input to regulatory strategies as it relates to sterilization validation and verification PERFORMANCE MEASUREMENTS Ability to work in partnership with the product development and regulatory functions. Communicate scientific findings clearly and make meaningful contributions to projects. Support work stream timelines and be able to balance priorities according to stakeholder needs. Able to communicate and cooperate with other team members and cross function teams effectively. Demonstrate ability to add value to the organization through scientific excellence. Take ownership for assigned projects and self-lead initiatives. QUALIFICATIONS EDUCATION/CERTIFICATION University Degree in a Biological Science required Masters/Ph.D. an advantage REQUIRED KNOWLEDGE Previous experience in a regulated R&D environment supporting Sterile Products. Strong Microbiology understanding. Working knowledge of FDA regulations EXPERIENCE REQUIRED 5+ years' experience in sterilization or microbiology for regulated products Responsible for ensuring compliance with standards governing Ethylene Oxide, Dry Heat, X-Ray and Gamma sterilization Experience in working in GxP laboratory facilities. SKILLS/ABILITIES Excellent communication skills (verbal / written). Ability to explain science to management. Prudent risk taker. Identifies opportunities and takes risks to achieve objectives. Simplify complex ideas, collaborate effectively, deliver results, and innovate in sterility assurance. Able to work on multiple projects of varying complexity. Computer literate (Outlook / Word / Excel). SALARY RANGE $65,000 - $90,000 annually BENEFITS PDI is pleased to offer comprehensive and affordable benefits for our associates, which includes: Medical, behavioral & prescription drug coverage Health Savings Account (HSA) Dental Vision 401(k) savings plan with company match and profit sharing Basic and supplemental Life and AD&D insurance Flexible Spending Accounts (FSAs) Short & long-term disability Employee Assistance Program (EAP) Health Advocacy Program PDI also offers many voluntary benefits such as: Legal services, critical illness, hospital indemnity, accident coverage, ID theft and fraud protection, pet insurance and employee discounts. At PDI, we are also committed to helping our associates maintain a healthy and sustainable work/life balance and are proud to provide associates with paid time off programs including: sick & safe leave, vacation, company & floating holidays, paid parental leave, and depending on the position we also offer summer hours and flex place/flex time options.

Job Title: Quality Control Specialist Responsibilities: Perform routine testing of raw materials, in-process, and finished products per SOPs. Ensure lab compliance with GMP, GLP, and other regulatory standards. Maintain and calibrate laboratory instruments and equipment. Document and review analytical data accurately and timely. Support investigations for out-of-spec (OOS) and deviations as needed.

QC Microbiology Analyst II - Allendale, NJ Our vision is creating future cell therapy miracles together. We are a leading global contract development and manufacturing organization dedicated to the advancement of cell and gene therapy products. We believe in the transformative potential of cell and gene therapies and we are shaping the future of medicine. We open doors in the regenerative medicine industry for those looking to transform medicine while continuously improving an innovative, growing company. This position will report to the Supervisor of QC Microbiology. The Quality Control Microbiology Analyst II serves as a support role to clinical and/or commercial production. The QC Microbiology Analyst will perform environmental monitoring activities including, but not limited to, non-viable particulate testing, active air viable, passive air viable, surface viable, and personnel monitoring. Essential Functions and Responsibilities: Environmental monitoring in controlled environments: Non-viable particulate monitoring Active viable air monitoring Personnel monitoring Surface sampling Passive air monitoring Equipment monitoring: Ensure equipment is in proper working conditions Ensure all equipment is properly maintained/calibrated Assist with routine laboratory testing Plate reads and incubations Shipping of test samples and equipment to contract laboratories for testing Produce documentation according to written Standard Operating Procedures in accordance with current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP) Writing/conducting investigations pertaining to environmental monitoring and testing Develop and train QC Microbiology Analyst I personnel on relevant business processes Qualifications:BA/BS in a science or relevant field required Minimum 2-4 years of experience with environmental monitoring or within the biopharmaceutical industry Proficient with computer software such as Microsoft Office, MODA, LIMS Familiar with ISO and EU standards Strong written and oral communication skills Must be detail oriented, can multi-task, work in a team environment, and have the flexibility to adapt to company growth as well as its evolving responsibilities Employment as a QC Microbiology Analyst II is contingent on the ability to obtain a qualified gowning status within 90 days of start date.

We are Bentley Labs, a cutting-edge formulation and manufacturing partner to the World's Best Beauty Brands! Our product formulation and production capabilities are wide-ranging and distinctive - with innovative, exciting products across skin care, bath and body, hair, and lip categories. Over the past 16 years, the Bentley team has grown to include some of the industry's brightest stars. Our diverse and talented group are ever and truly a unit -working together toward an all-consuming vision to be the best. In the past 2 years, our formulation team has won over 20 industry awards for best products in wide range of categories. We launch over 200 new products a year, and growing rapidly and seeking new R&D Chemists to join our team! As a valued member of our R&D team, this position will have hands-on responsibility to work with our formulation chemists to produce customer-winning formulas for skin care, sun care and bath & body care products including but not limited to creams, gels, lotions, serums, anhydrous and surfactant systems. This is a place where we create products that matter, relationships that last, and where ambition is supported and rewarded! We know you work hard and we want you to be successful. What will we do for you? Let us help you with tuition reimbursement. Don't know something? Let us send you to classes. Come on in and we will show you what else we have to offer you! Who you are…you celebrate your success and others too. You focus on the right solution with each customer. Your passion for providing outstanding service contributes to our high level of customer satisfaction. Building relationships is your strong suit. You like to have fun at work too! Loud laughing encouraged. Main Responsibilities: The R&D Chemist is a key member of the company's Research and Development Team. The primary responsibilities required for this role are: Review new Product Development Requests (PDR's) and collaborate with SE's for additional clarification; assign tentative project completion dates. Prepare lab batches of formulas needed for submitting samples for customer analysis within lab schedule, and reformulating / resubmitting them based on customer's feedback. Maintain detailed and organized lab notebook with detailed observations while making lab batch. Develop detailed lab scale process for success including order of addition, critical raw materials and processing parameters, bench standard and benchmark, and lab scale preliminary specification and test results Work closely and collaboratively with lab technicians, to teach, coordinate and collaborate on projects leading to well-planned and executed bench work and successful sample submissions Perform and monitor stability with lab technician, utilizing approved stability protocol, and re-formulate if initial formula is unstable. Meet with raw material vendors to learn about new technologies and new raw materials that can be utilized to create/improve Bentley's innovative technology offerings. Collaborate as a key team member across the R&D department, contributing innovative ideas, expertise, knowledge, experiences with strong team spirit, and pride in organization's contribution to the company Perform/Monitor calibration and validation of all lab instruments with Lab Technicians. Maintain clean, safe and well-organized lab working area. Required Outcomes: Stable and compliant personal care, cosmetics and OTC products Timely shipment of lab samples to customers/marketing/testing facilities Documentation of detailed observations and specifications Learning of new technology via researching new raw materials and processes Establishing preliminary product specifications and detailed lab process Education and Experience Requirements: BS in Chemistry 3 + years of R&D experience in Personal Care Excellent lab processing techniques and data management Must have strong analytical, communication and organizational skills Must have a bias for action and initiative to collaborate and contribute value to the overall R&D effort