Chemist Jobs in Fords, NJ

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 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)

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.

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

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.

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.

Opportunity for an experienced Upstream Manufacturing Scientist (multiple levels) to continue their career in downstream/upstream manufacturing. This role will be with our client who has a global footprint in both R&D and manufacturing within the biopharma industry. Location- Middlesex County, NJ Terms: Direct Hire Salary: $80-100k/yr. What you will be doing: Work closely with manufacturing associates and engineers to execute upstream batch processes. Perform cell culture and bioreactor operations (single-use fed-batch bioreactors) across various scales. Carry out harvest clarification processes using centrifuges and depth filters at multiple scales. Ensure timely execution of engineering and clinical batches. Develop equipment specifications and optimize manufacturing techniques. Leverage programs to collect and analyze operational data, making real-time adjustments to products, instruments, and equipment. Interpret and follow instructions in written, oral, diagrammatic, or scheduled formats. Adhere to GMP standards in the manufacturing area and lead compliance with environmental health and safety regulations. Review completed manufacturing and packaging batch records and supporting documentation. Coordinate investigations and implement corrective actions for any issues identified during batch execution. Perform additional duties as assigned. Comply with all company policies and standards. What you bring to the company: Bachelor's or Master's degree in Chemical, Biological, or Biochemical Sciences, with at least 3 years of relevant experience in the biopharmaceutical industry. Proven expertise in independently designing, executing, analyzing, and documenting all phases of process development. Strong foundational knowledge and subject matter expertise in executing both engineering and clinical batches. Hands-on experience in GMP and aseptic manufacturing environments. Familiarity with single-use manufacturing consumables, such as bags, tube sets, columns, and process manifolds. Proven ability to work both independently and collaboratively within a team; excellent interpersonal skills. Strong verbal and written communication skills, with advanced computer and organizational abilities. High attention to detail and proficiency in basic software, including Word, Excel, and spreadsheets. In-depth understanding of GMP batch manufacturing and packaging documentation, including audit and review procedures. Knowledge of cleaning verification and validation processes. ** 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**

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.

6-month Contract Onsite in Piscataway, NJ Responsibilities: Analyze samples of finished products using chromatographic, spectroscopic, wet chemistry, and other analytical techniques Process analytical data and prepare reports to communicate results and findings to key stakeholders. Qualifications: Bachelor's degree in Chemistry 3+ years of Analytical Chemistry experience Experience in the cosmetics/consumer goods industry

Analyze samples of finished products using chromatographic, spectroscopic, wet chemistry, and other analytical techniques; process analytical data and prepare reports to communicate results and findings to key stakeholders. Qualifications: Position requires a Bachelor's degree in Chemistry 3+ years analytical chemistry Experience in cosmetics/consumer goods industry and good communication skills.

Adecco is recruiting for an Analytical Chemist at a leading global cosmetic manufacturer in Piscataway, NJ. Apply today! Qualifications: Education: Bachelor's degree in chemistry. Experience: Minimum of 3 years in analytical chemistry, preferably within the cosmetics or consumer goods industry. Skills: Strong communication skills are essential. Pay Rate- The anticipated wage for this position is between $34 and $36.76 per hour. Hourly wage depends upon experience, education, geographic location, and other factors. Job Description: Analyze Samples: Utilize chromatographic, spectroscopic, wet chemistry, and other analytical techniques to analyze samples of finished products. Data Processing: Process analytical data and prepare comprehensive reports to communicate results and findings to key stakeholders. Work Hours: 8 AM - 5 PM Location: Piscataway, New Jersey PPE and Dress Code: Business Casual, work-appropriate attire. Benefit offerings include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and 401K plan. Our program provides employees the flexibility to choose the type of coverage that meets their individual needs. Available paid leave may include Paid Sick Leave, where required by law; any other paid leave required by Federal, State, or local law; and Holiday pay upon meeting eligibility

Our client develops, manufactures, and commercializes a wide range of generic pharmaceuticals, active pharmaceutical ingredients (API) and injectables globally. They are seeking a Chemist to join their team on a 6-month contract. Responsibilities: 100% benchwork min of BS and hopefully 6 mon-1 yr exp. Need HPLC dissolution, typically working up to 10 samples/batches daily generic solid oral dosage a must

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

Veggies Made Great is a leading food manufacturing company specializing in creating delicious and nutritious vegetable-forward products. Our mission is to make it easier for people to incorporate vegetables into their daily diet without compromising on taste. We are committed to producing high-quality, convenient, and innovative products that cater to the evolving needs of health-conscious consumers. Scope: The Food Scientist will help shape the future of the R&D department at New Classic Cooking. This role will work cross functionally to build a culture of innovation while enhancing our technical expertise and maintaining an environment where quality and food safety is paramount. This team member will drive projects forward and assist other team members to do the same to ensure flawless execution. Responsibilities Lead innovation and some renovation projects from bench top formulation, commercialization and scale up, plant trials, 1st production and other support as needed. Deliver recipes, internal specifications, documentation, nutrition panel labeling, and ingredient declarations to meet regulatory guidelines and quality food safety requirements. Enhance our technical body of knowledge by working with internal and external resources to ensure VMG produces the highest quality products; this includes ingredients as well supplier research and competitive benchmarking. Participate in innovation sessions and ongoing work to build and strengthen pipelines. Develop an understanding of the voice of our consumer with insights from customer service and marketing. Partner with operations and QA to better understand how R&D can improve operational efficiencies. Collaborate with QA on SQF initiatives as needed. Perform operational tasks and other projects and activities as needed. Requirements: · BS in Food science or chemistry or food engineering. Masters degree is preferred. · 5+ years experience in the food/ingredient manufacturing industry required. · Ability to work in a fast-paced environment. · Basic skills related to chemical analysis, food processing and project management are a must. · Knowledge of raw materials and ingredient functionality are essential. · Proficient in office software (Excel, Word, Office) and Genesis software. · Excellent, effective communication skills are required as well as effective presentation skills. · Demonstrated proficiency in supporting and communicating technical information to all technical, production and marketing staff. · Bi-lingual (English/Spanish) language skills a plus.

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.

QC Cell Therapy Scientist - Contract - Cranbury, NJ Proclinical is on the hunt for a bold, innovative thinker who is ready to help push the boundaries of science and make a tangible difference in the world. Primary Responsibilities: The successful candidate will be required to support the clinical and commercial manufacturing of gene therapy products. This role focuses on AAV and LVV gene therapies, requiring strong technical expertise in CGT analytical methodologies and excellent communication and collaboration skills. Skills & Requirements: Background in Biology, Molecular Biology, or Immunology. Experience in QC/GMP environments, preferably with gene/cell therapy products. Understanding of cGMPs and international regulations. Proficiency in cell and gene therapy assays and analytical characterization of viral vectors. Experience with mammalian cell culture and related activities. Ability to create, revise, and approve SOPs and reports. Experience in authoring and approving investigations for IA, OOS, and OOT results. Knowledge of method transfer, qualification, and validation. Strong analytical and problem-solving skills. Ability to work independently and make decisions. Effective in a fast-paced environment with a proactive attitude. The QC Cell Therapy Scientist's responsibilities will be: Conduct laboratory techniques such as q-PCR, dd PCR, ELISAs, Western Blot, and Infectivity assays in compliance with cGMPs. Perform routine testing for sample release and stability, ensuring timely reporting. Manage stability data mining and prepare data summaries. Review QC stability data and generate Certificates of Compliance. Execute laboratory protocols and prepare reports. Sub-culture mammalian cell lines and perform cell counts. Maintain laboratory reagents, supplies, and equipment. Qualify reagents, reference materials, and analytical techniques. Assist in planning and executing stability studies. Perform QC data review and generate CoAs for product release. Enhance knowledge of analytical techniques and procedures. Liaise with functional groups to progress projects and plans. If you are having difficulty in applying or if you have any questions, please contact Mike Raletz at m.raletz@proclinical.com Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.

Iselin, NJ Engineering - Chemical EXP 1-2 yrs DEG Doctorate Relo Job Description The Analytics and Materials Characterization group in Iselin, NJ is part of the Catalyst Research and Development department. We provide direct analytical support to catalyst research and manufacturing platforms, including environmental, refining, chemical, solar cell and battery materials. This position is for a highly motivated Microscopist/Material Scientist to work as part of an electron microscopy group involving the characterization of catalysts, their precursors, associated assembly components and related materials. The successful candidate will have a strong materials science, analytical and catalyst background with an emphasis on microscopic evaluations, and thrive on leadership roles in multi-disciplinary catalyst research teams. Responsibilities include but are not limited to: -Operating and maintaining Microscopy instrumentation including HR FE-SEM (High Resolution Field Emission Scanning Electron Microscopy) and VP-SEM (Variable Pressure Scanning Electron Microscopy) with ancillary attachments: EDS (Energy Dispersive X-ray Spectroscopy), WDS (Wavelength-Dispersive X-Ray Spectroscopy) and STEM (Scanning and Transmission Electron Microscopy) and image analyses software suite -Supporting other microscopy areas like EPMA (Electron Probe Microanalyzer) or TEM (Transmission electron microscopy) -Collaborating with research scientists, engineers, and manufacturing associates on new-product development, fundamentals understanding and manufacturing support, with strong catalyst chemistry knowledge -Interpreting results, writing reports and sharing information with a high degree of accuracy in a fast paced analytical chemistry laboratory -Developing new microscopy capabilities, investigative strategies, and innovative microscopy methods to support knowledge and product development -Preparing a wide variety of sample types for SEM/STEM analyses using vacuum evaporation systems, microtome and trimmer; knowledge of ion-milling, FIB (Focused Ion Beam), tripod polishing, etching, and electro-polishing a plus Qualifications -PhD in materials science, physics, engineering, chemistry or related degree with 1+ years related analysis and laboratory experience preferably in industry, OR a MS degree in materials science, physics, engineering, chemistry or related degree with 3+ years of relevant industrial experience or BS degree with a minimum of 5+ years of relevant industrial experience -Strong theoretical and practical understanding of EM technologies with extensive hands on experience in solving complex materials problems using primarily FE-SEM and other technologies like VP-SEM, STEM, TEM or EPMA Solid materials characterization and heterogeneous catalysis knowledge Ability to participate at a leadership level within multi-disciplinary teams Hands-on experience in experimental design using EM and methods development for EM Knowledge of crystallography and diffraction techniques (EBSD, electron backscatter diffraction) a plus Knowledge of related AEM (Analytical Electron Microscopy) equipment and methodologies a plus Expected to work independently with minimum supervision as well as part of a team Strong organizational, time management and multi-tasking skills Demonstrated track record of a systematic approach to problem solving critical thinking skills SKILLS AND CERTIFICATIONS Does this candidate have heterogeneous catalysis and microscopy experience? IDEAL CANDIDATE Heterogeneous catalysis and microscopy experience REQUIRED Additional Information All your information will be kept confidential according to EEO guidelines. Direct Staffing Inc

About the Team The R&D Soft Product Innovation Team at Harry's is responsible for all personal care category launches from concept to market. We are a team of researchers, developers, and formulators who are on a mission to create things people like more. As our brands continue to grow, the Soft Product Laboratory will be a key driver for both new product innovation and continuous improvement, raising the bar for product excellence. About the Role The Soft Product Formulation Chemist will support the global development of new products and enhance our existing personal care portfolio for the Harry's and Flamingo brands. In close collaboration with Product, Quality, and Sourcing teams, you'll help bring performance-driven, consumer-loved products to market while maintaining and improving our current formulations. We seek a hands-on, detail-oriented chemist with 2+ years of experience in personal care formulation. You'll thrive in our fast-paced, creative environment, where innovation, problem-solving, and cross-functional collaboration are key. What You'll Do: Develop and optimize formulations across skincare, bodycare, haircare, hairstyling, and suncare categories, balancing performance, aesthetics, cost, and timeline requirements. Identify opportunities to enhance existing formulas, including root-cause analysis, cost-saving initiatives, and technical transfers. Demonstrate creativity and resourcefulness in proactively identifying and proposing solutions to issues that may arise during product development or in transfer to manufacturing. Work closely with cross-functional teams and external partners to execute improvement strategies efficiently. Lead formulation testing, ensuring stability, compliance, and precise record-keeping. Manage raw material stocks, packaging inventory, and maintain traceability of formulation data. Support pilot runs and first production batches as needed. Stay ahead of scientific advancements, ingredient innovations, and market trends to drive innovation. Who You Are: Product Developer at Heart - Excited by new products, technologies, formats, and how they interact with one another to create the ultimate user experience, down to the last detail, have pride in the work and development of creating things. Creative Problem Solver - Energized by challenges and can't sleep until a solution is found. Lifelong Learner - Hunger for knowledge, admits when they don't know the answer and diligently works to find it. Proactive doer: Takes initiative, thrives in a “no task too small” environment with an eagerness to learn and address any issue that may arise. Execution-Focused - Gets things done, creates efficient systems for tracking, testing, and reporting. Results-Driven - Relentlessly committed to achieving goals while fostering strong internal and external relationships. Collaborative & Adaptable - Works well in cross-functional teams, embraces change, and pivots with shifting business needs. Communicative & Team-Oriented - You thrive on direct, honest, and constructive communication. Sense of Humor - We take our work seriously, but not ourselves too seriously! Requirements: Bachelor's degree in Chemistry, Biology, or a related science. 2+ years of formulation experience in cosmetics, personal care, or health & beauty. Experience in fast-paced product development, working with cross-functional teams, raw material suppliers, and third-party manufacturers. Strong analytical, organizational, and project management skills. Ability to juggle multiple projects and pivot as business needs evolve. Willingness to travel domestically and internationally as needed. Benefits and perks Medical, dental, and vision coverage 401k match Equity in Harry's Flexible time off and working hours Wellness and L&D stipends 4 weeks sabbatical after 5 years, 6 weeks after 10 years, and 8 weeks after 15 years Up to 20 weeks of pregnancy leave and up to 16 weeks of parental leave Fun IRL and virtual events including happy hours, team building events, and parties on our rooftop Free products from all of our brands Harry's is committed to bringing together individuals from different backgrounds and perspectives. We strive to create an inclusive environment where everyone can thrive, feel a sense of belonging, and do great work together. Harry's is an Equal Opportunity Employer, providing equal employment and advancement opportunities to all individuals. We recruit, hire and promote into all job levels the most qualified applicants without regard to race, color, creed, national origin, religion, sex (including pregnancy, childbirth and related medical conditions), parental status, age, disability, genetic information, citizenship status, veteran status, gender identity or expression, transgender status, sexual orientation, marital, family or partnership status, political affiliation or activities, military service, domestic violence victim status, arrest/conviction record, sexual or reproductive health decisions, caregiver status, credit history immigration status, unemployment status, traits historically associated with race, including but not limited to hair texture and protective hairstyles or any other status protected under applicable federal, state and local laws. Harry's commitment to providing equal employment opportunities extends to all aspects of employment, including job assignment, compensation, discipline and access to benefits and training. We respect the laws enforced by the EEOC and are dedicated to going above and beyond in fostering diversity across our company. We can't quantify all of the intangible things we think you'll love about working at Harry's, like the exciting challenges we tackle, the smart and humble team you'll get to work with, and our supportive and inclusive culture. That said, our salary ranges are based on paying competitively for our size and industry, and are one part of our total rewards package, which also includes a comprehensive set of benefits and our equity program. The base salary hiring range for this position is $90,800-$124,850, but the final compensation offer will ultimately be based on the candidate's location, skill level and experience.