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

Job Title: Application Technician Duration:6+ Month Pay Rate:$25- 40/H Shift Time:1ST Shift What will you do? Your key responsibilities • Prepare and deliver complex application samples for internal/external clients using our CLASS sampling system while adhering to delivery due dates and applying good laboratory practices • Ensures all samples produced meet the quality standards as per the global SOPs before releasing the samples and identifies/flags any technical sampling issues • Keeps and maintains application bases up to date and aligned with the collection in digital systems • Keeps the personal workbench clean and organized as per the best practices • Operates with a team spirit mindset and supports their colleagues under high workload situations What qualifications will make you successful? Qualifications for this role are as follows: • Bachelor's degree or equivalent degree/experience preferably in a concentration of Science along with a minimum of 1 year of practical laboratory experience. • Previous experience in the fragrance industry strongly preferred • Strong communication skills, attention to detail, and proactivity • Excellent planning, organizational and time management skills with proficiency in MS Office Applications such as Word, Excel • Self-starter, with strong sense of ownership, assertive and passionate for high level of client satisfaction • Ability to work comfortably in a very fast paced environment with short project deadlines

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

The Analytical Scientist is responsible for performing a wide range of tests to assess the quality of raw materials, in-process materials, finished products, and cleaning verification/validation samples to ensure compliance with established regulatory and company standards. This role leads analytical method development and validation activities, conducts both routine and non-routine testing, and plays a key role in laboratory investigations, documentation, and reporting. The position also serves as a technical liaison with clients, supporting method development, data interpretation, and investigative efforts. Key Responsibilities: Conduct and validate analytical testing of raw materials, intermediates, finished products, environmental samples, and stability batches. Develop, validate, and implement new analytical methods, including those for cleaning verification (e.g., via HPLC). Author detailed analytical protocols, validation reports, and Certificates of Analysis. Troubleshoot analytical methods and laboratory equipment. Compile, interpret, and document analytical data following cGMP standards. Maintain accurate laboratory records including notebooks, worksheets, and batch records. Review and peer-check laboratory documentation for accuracy and compliance. Lead investigations into Out-of-Specification (OOS) and Out-of-Tolerance (OOT) results, and communicate findings per SOPs. Support environmental monitoring efforts as needed. Train and lead a team of analytical scientists and technicians. Ensure adherence to SOPs, cGMP, ICH, USP/EP, ISO, and regulatory guidelines (21 CFR Parts 210, 211, and 820). Interact with clients regarding laboratory activities, including method development and investigation outcomes. Perform other related duties as assigned. Qualifications: Bachelor's degree in Chemistry or a related scientific field. 2-4 years of analytical laboratory experience. Extensive knowledge of cGMP, FDA (21 CFR Parts 210, 211, 820), ICH, EU, and ISO standards. Strong expertise in pharmacopeial requirements (USP, EP, etc.). Experience in specialized testing such as dissolution or aerosol analysis is preferred. Proven ability to develop and validate complex analytical methods. Excellent written and verbal communication skills, including the ability to present findings internally and externally. Highly skilled in Microsoft Office (Word, Excel, PowerPoint, Outlook). Strong organizational skills, attention to detail, and manual dexterity. Ability to interpret and follow complex documents such as SOPs, protocols, and regulatory guidelines. Capable of clear and effective communication with internal teams and external clients. Proficient in applying arithmetic and basic statistical concepts to analytical processes.

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.

Job Title: QC Scientist - Cell & Gene Therapy Industry: Biotechnology / Pharmaceutical We are seeking a highly motivated and detail-oriented Quality Control (QC) Scientist to support our growing Cell & Gene Therapy operations. The ideal candidate will have hands-on experience in aseptic techniques, microbiology, QC microbiology, and QC chemistry in a GMP-regulated environment. This role is critical to ensuring the quality and safety of our innovative cell and gene therapy products. Key Responsibilities: Perform microbiological and chemical testing of raw materials, in-process samples, and final drug products. Execute environmental monitoring (EM) and aseptic process simulation (APS) in classified cleanroom areas. Support QC Microbiology and QC Chemistry functions, including sterility testing, endotoxin testing, bioburden, and pH/conductivity testing. Ensure all testing is performed in compliance with GMP, GLP, and regulatory requirements. Maintain accurate and complete laboratory documentation according to Good Documentation Practices (GDP). Participate in investigations, deviations, and CAPAs related to QC activities. Assist in method qualification, validation, and transfer for cell and gene therapy products. Collaborate with manufacturing, quality assurance, and R&D teams to support product release and continuous improvement efforts. Qualifications: Bachelor's or Master's degree in Microbiology, Chemistry, Biotechnology, or a related life sciences field. 2+ years of experience in a QC laboratory environment within the biologics or advanced therapy medicinal products (ATMPs) industry. Solid knowledge of aseptic techniques and cleanroom practices. Experience with cell therapy and/or gene therapy products strongly preferred. Familiarity with USP, EP, FDA, and ICH guidelines. Excellent documentation and communication skills. Ability to work independently and collaboratively in a fast-paced environment. Preferred Skills: Experience with rapid micro methods and advanced QC analytical platforms. Knowledge of GMP regulations applicable to cell and gene therapy manufacturing. Comfortable working in a regulated cleanroom environment.

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

Now hiring! Associate Chemist - Technical Support (ECT-Chemetall) We are looking for an Associate Chemist-Technical Service to join our team in New Providence, NJ. Come create chemistry with us! BASF/Chemetall, is the Surface Treatment global business unit of BASF's Coatings division, operating under the Chemetall brand, and a leading supplier of applied surface treatments worldwide. At BASF/Chemetall, we develop and manufacture tailor-made technology and system solutions for applied surface technology. Our products protect metals from corrosion, facilitate forming and treatment, prepare parts optimally for the painting process and ensure excellent coating adhesion. Our technologies and products are used in a variety of industries and end markets such as automotive, aerospace, aluminum finishing and metal forming. The chemical treatment of metal surfaces is BASF/Chemetall core competence. The focus of our worldwide activities is on the development and implementation of customized technology and system solutions for surface treatment The Associate Chemist - Technical Service will perform routine testing and reports results. Processes project requests from customers and the field sales force. Recommends appropriate products for customers' operations. Provides technical consultation/advice to the Field Sales force. As a Associate Chemist - Technical Support (ECT-Chemetall), you create chemistry by... * Providing Technical Support/Technical Service. Runing laboratory evaluation of Customers' Tech Service Jobs. Selecting and recommending appropriate products for customers' applications. * Developing optimum operating parameters for Chemetall/BASF products. * Providing technical advice to the sales force, field engineers and customers such as troubleshooting assistance in the field. * Providing technical information for Profiles, Process Instructions and other technical literature when necessary. * Writing reports on lab results and field visits and informing on project status. Maintaining Technical Service Worksheet for each project * Assisting in telephone support for sales/customers as required. * Continuously upgradeding technical skills and staying abreast of technical developments in the field. * Working with Chemetall/BASF's Equipment Engineering group as required to better understand dispensing and control equipment. * Working in the field with Chemetall/BASF TSRs at customers to deepen and broaden knowledge of the products and applications. * Attending industry seminars and in-house seminars . * Ensuring work area is maintained in a safe manner and operating in the lab environment according to Health and Safety Policies. * Maintaining laboratory equipment in peak operating condition in accordance with Chemetall/BASF quality system. * Checking inventory level sufficiency of supplies. If you... * Have a BS Degree in Chemistry or Chemical Engineering required; bachelor's degree in a related physical science is acceptable * Have a minimum of 2 years prior experience is required. * Possess excellent communication skills, both verbal and written. * Have excellent problem-solving abilities and interpersonal skills. * Are able to sit, walk, stand, alternate sit/stand and viewing monitor, simple grasp, power grasp, and fine manipulate with hands, push and pull with hands, reaching above shoulder level, and lift and carry up to 20lbs., occasional lift and carrying of up to 50 lbs. Create your own chemistry with you@BASF At BASF, you will have the chance to do meaningful work towards building a more sustainable future. In addition to competitive compensation and benefits, BASF provides you with access to a wide range of elements to help you be your best. It's what we call you@BASF. We are committed to providing benefits, programs, and opportunities that support our employees' overall well-being, personal growth, and a safe, collaborative, and inclusive work environment. Just some of the many benefits we offer include: * Flexible work arrangements whenever possible * Highly competitive retirement savings plan with company match and investment options * Well-being programs that include comprehensive mental health support for you and your household family members * Family forming benefits (fertility, adoption and surrogacy reimbursement, maternity/parental leave, and more) * Back-up child and elder care with discount programs for families of all ages and stages * Mentoring and career development opportunities that allow you to share, learn, and thrive * Matching gifts program that allows you to deepen the impact of your contributions to qualified charities. * Employee crisis support for when the unexpected happens * Access to our BASF wine cellar, employee discounts, and much more! Job details Organization: G-ECT/NTS Technical Support North America Number of Openings: 1 Locations: New Providence, NJ Incentive Plan: PIC - 5% Hiring Manager: Khalid M Rana Recruiter: Lucia Bouzout Posting End Date: Privacy statement BASF takes security & data privacy very seriously. We will never request financial information of any kind via email, private text message or direct message on any social medial platform or job board. Furthermore, we will never send a candidate a check for equipment or request any type of payment during the job application process. If you have experienced any of the above, please contact ************* to report fraud. Equal employment opportunities We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, age, citizenship, color, religion, sex, marital status, national origin, disability status, gender identity or expression, protected veteran status, or any other characteristic protected by law. Applicants must be currently authorized to work in the United States on a full-time basis.

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

We are 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

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 GenScript GenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy. GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology. About ProBio ProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy (CGT), vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio's total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing. In terms of plasmid service, ProBio supports the most clinical approvals for CGT drugs including mRNA vaccines, CAR-T in China. It is also the first GMP manufacturing platform to provide in vitro transcription (IVT) template linearized plasmids for mRNA vaccines and has supported several mRNA vaccine global enterprises to obtain clinical approvals. In terms of viral vector service, ProBio has a stable and high-yield viral vector platform. Position: Associate Production Scientist Location: Piscataway, New Jersey Report to: Production Manager, Integrated DNA Chip Role Description: We are looking for a dedicated and hardworking associate scientist to join a cross-disciplinary team to help us develop and support advanced oligonucleotide synthesis technologies and applications. The candidate will play a key role in our production team providing support to both routine and investigatory laboratory activities. Knowledge of oligonucleotide synthesis chemistry, hybridization assays, PCR and qPCR techniques, and next-generation sequencing are desirable, but training will be provided as well. Position will also include primary responsibility over maintaining critical inventory by monitoring usage rates and actively producing inventory using proprietary technology and methodology. Level of the position will be commensurate with the qualifications of the final candidate. Key Responsibilities: Perform array-based oligonucleotide synthesis on GenScript's CMOS semi-conductor synthesis platform. Perform QC operations on GenScript products including PCR and hybridization assays. Perform additional pre and post synthesis operations associated with the production of GenScript products. Follow and update key SOP documents as needed. Maintain production records. Conduct routine lab maintenance procedures. Contribute observations and experience to production team to optimize and improve processes. Manage critical inventory levels and proactively schedule and conduct production of critical materials Produce and maintain manufacturing records according to ISO9001 regulations and as per QMS Provide additional support as we expand the scope of our technology. Qualifications: Bachelor's degree in Biology or Chemistry related field with 2 years of hands-on experience. Master's degree a plus. Working knowledge of oligonucleotide synthesis Experience with surface chemistry techniques and electrochemistry desirable Good grasp of basic molecular biology techniques including PCR, qPCR, array-based hybridization assays, and NGS. Familiarity with vacuum instrumentation and surface coating/modification techniques highly desirable Ability to work as part of a small cross-disciplinary team to accomplish both short term and long term goals. #LI-EB1 #GS GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law. GenScript USA Inc./ProBio Inc. maintains a drug-free workplace.

Microsoft Research (MSR) AI Frontiers lab is seeking applications for the position of Senior Principal Researcher to join their team. This role can be located in any one of our 3 labs: New York City, NY, Cambridge, MA, and Redmond, WA. The mission of the AI Frontiers lab is to expand the pareto frontier of Artficial Intelligence (AI) capabilities, efficiency, and safety through innovations in foundation models and learning agent platforms. Some of our projects include work on Small Language Models (e.g. Phi, Orca), foundation models for actions (e.g., in gaming, robotics, and Office productivity tools) and Multi-Agent AI (e.g. AutoGen). We are seeking a Senior Principal Researcher to join our team and contribute to the advancement of Large Action Model (LAM) and Large Language Model (LLM) technologies. As a Senior Principal Researcher, you will play a crucial role in developing, improving, and exploring the capabilities of AI models. Your work will have a significant impact on the development of cutting-edge technologies, advancing state-of-the-art and providing practical solutions to real-world problems. Our ongoing research areas encompass but are not limited to: Pre-training: especially of language models, action models and multimodal models Alignment and Post-training: e.g., Instruction tuning and reinforcement learning from feedback Continual Learning: Enabling LLMs to evolve and adapt over time and learn from previous experiences human interactions Specialization: Tailoring models to meet application-specific requirements Orchestration and multi-agent systems: automated orchestration between multiple agents incorporating human feedback and oversight Microsoft Research (MSR) offers a vibrant environment for cutting-edge, multidisciplinary, research, including access to diverse, real-world problems and data, opportunities for experimentation and real-world impact, an open publication policy, and close links to top academic institutions around the world. Microsoft's mission is to empower every person and every organization on the planet to achieve more. As employees we come together with a growth mindset, innovate to empower others, and collaborate to realize our shared goals. Each day we build on our values of respect, integrity, and accountability to create a culture of inclusion where everyone can thrive at work and beyond. In alignment with our Microsoft values, we are committed to cultivating an inclusive work environment for all employees to positively impact our culture every day. As a Senior Principal Researcher in AI Frontiers, you will design, develop, execute, and implement technology research projects in collaboration with other researchers, engineers, and product groups. As a member of a world-class research organization, you will be a part of research breakthroughs in the field and will be given an opportunity to realize your ideas in products and services used worldwide. Embody our culture and values. Required Qualifications

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

Job Description: Contract 10Months Worker will need steel toe shoes and safety glasses 2nd shift This is a 2nd shift position: 2:00PM - 10:30PM with overtime availability Long assignment with goal to convert right candidate to FTE The Senior Finishing Technician performs visual quality inspections and modifies rolls of indicators according to customer specifications. How you will do it Independently set up and operate equipment in accordance with current good manufacturing practices and standard operating procedures Responsible to finish operations on the appropriate jobs in the order needed to meet production schedules Follow the Finishing work instructions and other instructions as trained Maintains rewind tables calibrated Basic understanding in the use of conventional measuring tools and techniques to assure compliance with specification Inspect the product for defects and any non-conforming material Repair and splice Time Temperature Indicator rolls Ensure the products are properly stored (freezer, chilled enclosure, room temperature - per produce specification) Number Time Temperature Indicators Performs periodic preventive and maintenance activities. Manages and operates ink jet equipment. Tracks modifications performed to the Finished Label Inventory Maintains and adheres to all company safety policies and procedures. Maintains work area organization and documentation to satisfy ISO and GMP standards. Maintains good communication and working relationships with all departments and effectively functions within a team environment. Exhibits professional etiquette that exemplifies the values of the organization. Attendance at the worksite is required on a regular and on-going basis. What we look for High School Diploma or GED At least 2 years of experience Key Skills & Competencies: Ability to read and interpret documents such as work instructions, safety rules, operating and maintenance work instructions, procedure manuals and MSDS sheets. Must have sufficient English reading, writing and speaking skills to review work instructions and communicate effectively throughout the organization. Must be able to perform basic arithmetic using units of measure, whole numbers, common fractions and decimals. Must understand and be able to convert measurement units to/from Imperial to Metric. Ability to maintain quality and safety control standards. Knowledge of light equipment operation in the performance of job responsibilities. Ability to prepare routine administrative paperwork. Ability to read, sort, check, count, and verify numbers. Ability to lift and manipulate heavy objects. Ability to detect problems and report information to appropriate personnel. Ability to read, analyze and interpret complex written and verbal information. Must have the ability to effectively communicate orally and in written form both internally and externally. Must be familiar with and be able to communicate via e-mail. Must be familiar with and be able to use computer software including word processing & spreadsheets (Microsoft products preferred), and ERP System.

Key Responsibilities Conduct routine analysis of finished products and raw materials. Operate and troubleshoot laboratory instruments: HPLC, UPLC, GC, Karl Fischer, FTIR, visualization testers, and pH meters. Experience with chromatography software specifically Empower 3 for HPLC and UPLC analysis. Perform a range of tests, including assay, identity, content uniformity, blending uniformity, impurity testing, water content determination, content resolution, disintegration, and hardness testing, Follow approved testing procedures and methods according to internal SOPs and USP monographs. Report data accurately and promptly. Conduct peer data reviews and analyze data trends to ensure consistent results. Participate in laboratory investigations using TrackWise software Support routine lab activities such as balance calibration, pH calculations Perform stability testing of pharmaceutical products and excipients under ICH conditions, and assist with medical testing as necessary Position Requirement 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 Strong working knowledge of pharmaceutical testing, including stability testing, dissolution testing and compliance with USP standard Experience with laboratory instrumentation: HPLC, UPLC, GC, Karl Fischer, FTIR, and pH meter Prior experience with Empower 3 software

QC Analyst 2 Job Title: Quality Control Laboratory Analyst 2 - Radiopharmaceuticals About Us Evergreen Theragnostics, Inc. is a radiopharmaceutical company beginning operations in Springfield, NJ. The state-of-the-art facility will provide contract development and manufacturing services for radiopharmaceutical companies, including therapeutics and centrally distributed diagnostics. The company expects rapid growth in the next few years. Evergreen is a small team, where all team members support each other in a variety of activities. Job Description: We are seeking a highly motivated and detail-oriented Quality Control Laboratory Analyst 2 to join our team. This individual will play a key role in ensuring the highest standards of quality and compliance in our radiopharmaceutical release processes. The ideal candidate will have a background in pharmaceutical or life sciences, and hands-on experience with analytical techniques such as GC (Gas Chromatography), TLC (Thin Layer Chromatography), and HPLC (High-Performance Liquid Chromatography). Key Responsibilities: Perform quality control testing and analysis release testing of radiopharmaceutical products to ensure compliance with internal and external specifications and regulatory standards. Independently operate and maintain laboratory equipment, ensuring calibration and proper functionality. Maintain a clean, safe, and organized lab environment, adhering to all safety and pharmaceutical regulations, including radiation safety protocols. Perform daily lab tasks, including solution preparation, drug product analysis, and documentation of all testing. Utilize laboratory techniques including GC, TLC, and HPLC to perform a variety of testing procedures. Maintain thorough and accurate documentation of testing activities, results, and reports in accordance with SOPs (Standard Operating Procedures). Train and mentor new team members, offering support and guidance to ensure smooth onboarding and integration into laboratory operations. Maintain strict attention to detail while working with hazardous materials and ensure proper handling of radioactive substances as per safety guidelines. Qualifications: 2-5 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. Proficiency and hands-on experience with laboratory techniques such as GC, TLC, and HPLC. Ability to work independently and as part of a team, managing multiple tasks and priorities. Strong problem-solving skills and attention to detail, with an understanding of GMP, GLP, and other regulatory requirements. Previous experience in training or mentoring new staff members is a plus. Working Environment: Laboratory setting with exposure to radiation and other chemical hazards. Required to wear personal protective equipment (PPE) such as lab coats, gloves, and safety goggles. Fast-paced laboratory setting with occasional lifting and movement of materials. Commitment to maintaining a clean, organized, and safe working environment.