Chemist Jobs in Wayne, NJ

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.

Chemist- South Plainfield, NJ Key Responsibilities: Prepare samples of OTC drug, pharmaceutical products per established methods. Conduct basic chemical analyses using laboratory instruments such as IR, UV, dissolution, viscosity, melting point, and other equipment. Perform HPLC and/or GC quantitative analysis Report data from methods and instruments, providing results ready for data review and QA. Assist in maintaining reagents and disposable supplies to ensure the lab operates efficiently. Perform raw materials, in process, finished products testing of solid dosage products. Qualifications: Life Sciences Bachelor's degree or Science-based Associate's degree (Chemistry preferred). 5-8 years of QC experience in a pharmaceutical or GMP environment. Experience with HPLC and/or GC quantitative analysis required Experience with Empower 3 software

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

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

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

About Us Imagine the innovation and expertise behind the world's leading cosmetic brands, brought to you by a distinguished Italian company with a legacy of excellence. Since 1972, Intercos Group has been at the forefront of color cosmetics, pencils, nail polish, skincare, and personal care products. We pride ourselves on being the only cosmetics manufacturer that combines top-tier quality and advanced technology with a global reach and a personalized touch. With 15 commercial offices and 15 production facilities across 12 countries, Intercos Group brings a local approach to a global stage. We continually set the standard for beauty, crafting exceptional product lines for brands worldwide. As one of the largest suppliers in the cosmetics industry, we are a leading force in the research, development, and production of beauty products, shaping the future of the industry with every season. Position Summary The Senior Chemist is responsible for all technical activities related to new/existing formulation, innovation and 1st production scale-up of new formulations in Congers, NY. Essential Functions Formulate and facilitate development of innovative colored cosmetic products, line extensions, and product improvements (i.e. Emulsion, Anhydrous, and Powder formulations). Leading a team of technicians/junior chemists to support with technical related activity Identify new/ improved formulation technologies and implement them to meet project needs, following different constraints (costs, regulatory, black lists, etc.) in collaboration with strategic marketing department. Interact with customers and provide technical support via oral, presentation and written venues. Work directly with clients in order to achieve the desired formulation when necessary. Proactively scan and research new concepts, materials, technical opportunities and partnerships. Interface with all departments throughout the company and interact with material suppliers. Monitor preliminary product stability for new/ existing formulations. Effectively manage projects and provide status reports to group leader/ manager. Execute all formula customization work in DEVEX and follow all SOP's with regards to development and formula creation. Ensure that all projects are done through the use of the BPM when communicating about projects and/or reporting results. To work with the Corporate Applied Research in order to standardize technical information and processes on a global basis for all new formulas. Work with Corporate Applied Research in the technical transfer arena of commercialized and non-commercialized formulations. Record and review all activity with the direct supervisor. Other duties as assigned. Job Qualifications Bachelor's Degree in Scientific Discipline, such as Chemistry, Biology, Physics, etc. 2-4 years in Cosmetic Formulation Cosmetic Formulation, color perception, raw material knowledge, regulatory knowledge, GLPs, GMPs, FDA guidelines Computer Skill (Word, Excel, SAP, Devex), Good Communication Skills, Math Skills, Professional, Courteous, Able to travel if needed 10% of the time Job Benefits Health Insurance: Comprehensive medical, dental, and vision coverage Retirement Plans: 401(k) plan, often with company matching Life Insurance: Coverage for employees in the event of death or disability Paid Time Off (PTO): Vacation days, sick leave, and personal days Holidays: Paid company holidays and floating holidays Professional Development: Training programs and opportunities for career advancement Performance Bonuses: Annual merit increase and/or bonus based on individual performance Company Events: Team-building activities, social events, and company outings Employee Assistance Programs (EAPs): Confidential counseling and support services for personal and professional issues. EEO Intercos Group is committed to creating a diverse and inclusive workplace where everyone is valued and respected. We believe that a wide range of perspectives and experiences enhances our innovation and success. We are an Equal Opportunity Employer and do not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or any other legally protected status. All qualified applicants are encouraged to apply and will receive consideration for employment without regard to any of these characteristics. We are dedicated to providing a work environment that is free from discrimination and harassment and promotes equal opportunity for all.

Title: Associate Scientist - II :: Ligand Binding Duration: 06 months (Extendable) Pay Rate: $50 - 53.45/hr on W2 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. MRL 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. To achieve all of the highlighted activities, our team combines state-of-the-art capabilities and expertise in 4 key areas. We collaborate closely with project teams to craft a holistic approach appropriate for each program & question at hand: • Protein Biochemistry. We provide carefully designed, high-quality and thoroughly characterized proteins for screening and assay development. Leveraging our expertise across target classes (including integral membrane proteins & multi-subunit complexes) and utilizing both internal & external resources we partner directly with teams to produce proteins that are qualified for even the most challenging applications. • Biophysics & Biochemistry. Using a toolbox of techniques including SPR, fluorescence/CD spectroscopy, calorimetry, nano-DSF & radioligand binding we perform detailed thermodynamic & kinetic profiling of protein-ligand interactions across all modalities. • BioNMR. Our capabilities in high-resolution NMR spectroscopy enable us to rigorously study the solution behavior of proteins (including excipient and self-association effects) and to conduct detailed experiments probing molecular interactions using both ligand- and protein-detected techniques. • Mass Spectrometry. We specialize in biophysical mass spectrometry including HDX-MS for protein characterization, binding site mapping and epitope/paratope determination; metabolic flux as a readout for pharmacodynamics and pathway engagement in physiologically relevant settings (both in vitro and in vivo); and ultrahigh-throughput mass spectrometry where we have partnered with groups across the network to enable screening, chemical reaction profiling and protein engineering. • Our overarching goal is to work directly with teams to accelerate the discovery and characterization of molecules on the path to delivering meaningful therapies to patients. 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. Quals-- 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. Personality: Team oriented, detail oriented, highly collaborative, joyful, and understands timelines.

We are seeking an Analytical Scientist to join a reputable pharmaceutical manufacturing company to conduct routine and non-routine analyses of in-process materials, raw materials, environmental samples, finished goods, or stability samples. ** No Relocation, No C2C Candidates** Pay: Up to $50/hour. 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. QUALIFICATIONS: 2 years hands-on method development experience (HPLC) Knowledge of cGMPs, pharmacopeia (USP, EP), and regulatory standards (21 CFR Part 210/211/820, ISO). Bachelor's in Chemistry-related discipline with 2+ years of analytical lab experience. 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!

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

**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.

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

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.

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.

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!

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

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