Chemist jobs in New Jersey - 203 jobs

Exemplify BioPharma, Inc. a Symeres Company, is a global partner research organization (PRO) based in New Jersey, USA. We are a team of biopharma industry experts focused on delivering end-to-end Chemistry, Manufacturing and Controls (CMC) throughout the drug development and regulatory market application processes. Using a unique combination of program management, coupled with our New Jersey based process development laboratories we are ideally positioned to deliver CMC success to partner organizations. We are talent based team and our key asset is our experience, multidisciplinary expertise and proven track record. We strive to bring tangible value to our partners through provision of strategic, tactical and technical leadership to solve complex problems focused on reducing program timelines and costs. Position & Responsibilities Exemplify BioPharma is seeking a scientific leader to serve as Senior Analytical Chemist at our R&D laboratory located in Cranbury, New Jersey. The ideal candidate will have 0-3 years' experience and a proven record of sustained laboratory achievement and innovation. The professional in this position will lead analytical development for high priority drug candidates. You will identify and characterize key physical and chemical properties of pharmaceutical materials (e.g., active drug substances) and/or formulated drug products (e.g. tablets, injectable solutions). As an innovator, you will develop, validate and implement new analytical methods to guide product development and solve challenging technical problems related to purity, stability, packaging, and manufacturing. You will define strategies to address quality-related objectives, and will recommend the methods and specifications used to monitor pharmaceutical materials and/or the formulated product. You will then lead the transfer of these technologies to CRO, CMO manufacturing sites. This professional will lead and/or participate on multi-disciplinary product development teams and will supervise the studies and professional development of one or more laboratory professionals. You will develop new scientific ideas, methods and technologies that contribute to the responsibilities described above. Other responsibilities include statistical data analysis, compliance with pharmaceutical good manufacturing practices and the completion of technical reports and external publications (as appropriate). This visible and business-critical role demands excellent oral and written communication skills. This is an exceptional opportunity for motivated candidates who wish to be exposed to all aspects of CMC drug development in a fast moving, collaborative and learning environment. Qualifications A Ph.D. degree in analytical chemistry or a related discipline is preferred. The candidate must have a demonstrated ability to conduct independent research, solve scientific problems, and lead other professionals in a highly collaborative environment. Application If you are interested in applying for this exciting opportunity at Exemplify BioPharma please e-mail a cover letter and resume to ******************************.

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 or C2C available ** Type: Contract Pay: Up to $40/hr Location: Middlesex County, NJ 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: Bachelor's in chemistry-related discipline with 2+ years of analytical lab experience. Strong technical proficiency with HPLC/UPLC, GC, UV, FTIR, Karl Fischer, and particle size analysis. Hands-on background in method transfer and method verification; method validation experience is a strong plus (HPLC). 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!

Are you an experienced Biochemist - High-Throughput Screening with a desire to excel? If so, then Talent Software Services may have the job for you! Our client is seeking an experienced Biochemist - High-Throughput Screening to work at their company in Rahway, NJ. Primary Responsibilities/Accountabilities: The Chemical Biotechnologies Group at the client is seeking an experienced researcher to support our high-throughput capabilities. The mission of the group is to invent, develop, and implement biomolecules and biocatalytic processes to advance the client's pipeline and our impact on the scientific community. This position in our biochemistry team is responsible for lysing E. coli cell pellets to liberate enzyme in solution or generate enzyme from in vitro transcription translation (iv TT) mix, setting up reactions using this solution as a catalyst solution, quenching reactions and prep them for HPLC analysis, running the HPLC, and analyzing the data generated in support of our protein directed evolution workflow. The candidate will perform high throughput workflows with 96 or 384 well formats using various automation instruments. The candidate will have hands-on, extensive experience with instrumentation essential for monitoring substrates and products profiles for reactions, especially Agilent UPLC systems. In this position, the candidate will have the opportunity to work with a diverse group of team members to effectively coordinate efforts and operate multiple projects. The candidate ensures activities of assignments are executed such that project deliverables and timelines are met. The candidate is responsible for good housekeeping and performing work in a safe manner in the work area by applicable safety equipment and personnel protective equipment (PPE). Qualifications: Bachelor's degree in Molecular Biology, Synthetic Biology, Bioengineering, Biochemistry or related field with +5 years' of experience, or MS with +2 years of experience, or PhD. Experienced in high-throughput screening and automated liquid handling (Biomek or Tecan liquid handling systems) and various analytical methods (HPLC, LC-MS, spectrophotometry, gel electrophoresis, FPLC). Proficient in preparing chemical and biochemical reactions Experience with protein handling and biochemical, biophysical, and/or phenotypic protein characterization techniques (e.g., activity assays, SDS-PAGE, UV-Vis spectrophotometry). Understanding of experimental design and data analysis principles Strong organizational skills and attention to detail Excellent teamwork and multitasking Good documentation of experimental reports Software Skills: MS office (Word/Excel) Preferred: Experience with one or more of the following: next-generation sequencing, directed evolution, protein expression or microfluidics Experience in protein characterization and purification Experience in protein expression platforms (yeast, bacillus, mammalian) is a plus Experience with data analysis using Python, R, Excel, or similar tools Industry experience is preferred.

Source One is a consulting services company and we're currently looking for the following individual to work as a consultant with our direct client, a global pharmaceutical manufacturing client in Summit, NJ . No Third-Party, No Corp to Corp, No Sponsorship Now or Future Title: Product Development Scientist - Formulation Location: Skillman NJ Hybrid Work Locations; Skillman, NJ 4 days/week then in Summit, NJ 1 day per week. Hours: 8:30am to 5:00pm (Monday through Friday). May fluctuate based on needs. Contract Duration: 10 months, with likely extension Pay Rate: $43.28 per hour (w2) *PLEASE NOTE: Apply only if you have FORMULATION Experience this is required Job Description: Consumer Products - Skin Health A Product Development Scientist role involves a wide range of activities, including developing and optimizing new product formulations and processes, conducting laboratory testing and evaluations. Key responsibilities include batching several iterations, ensuring technical accuracy in product development through stability studies, and documentation. Working with the team, time management, attention to detail, strong analytical skills, strong communication, following the timeline. FORMULATION Experience is required BA Degree 2 to 4 years' experience

The purpose of this position is to provide analytical chemistry subject matter expertise to one or more chemistry-based applied research projects. Essential Duties and Responsibilities: Develops and validates analytical methods using thermal desorption (TD), gas chromatography (GC), liquid chromatography (LC), ion chromatography (IC), mass spectrometry (MS), and microscopy. Performs troubleshooting and non-routine maintenance on TD, GC, LC, IC, MS, and microscopy instrumentation. Ensures the readiness of TD, GC, LC, IC, MS, and microscopy instrumentation Facilitates the stand-up of new analytical instrumentation Leads meetings with company clients by preparing and presenting meeting materials in meetings Develops innovative solutions to complex problems Develops improvements to currently used processes and analysis methods Trains, leads, and mentors junior level scientists to execute analytical chemistry tasks Performs wet chemistry (dilutions, extractions, etc.) Composes, reviews, and executes test plans and standard operating procedures Composes and reviews technical reports Performs literature reviews Safely handles explosives and other hazardous materials Sources materials and submits purchase requests Other duties as assigned Required Knowledge, Skills & Abilities: Positive attitude with a willingness to learn new things Previous experience with TD, GC, LC, IC, or MS Excellent working knowledge of TD, GC, LC, IC, and MS Technical writing, presentation, verbal communication, and listening skills Education/Experience: Incumbent professional should have a minimum of a bachelor's degree in chemistry with five to ten years of analytical chemistry experience or a graduate degree (masters or PhD) chemistry with up to five years of experience. Certificates and Licenses: None Clearance: The ability to obtain a Secret clearance and Department of Homeland Security suitability is required for this position. Supervisory Responsibilities: The incumbent professional has little to no supervisory responsibilities. Working Conditions/ Equipment: The incumbent professional is expected to work and/or be available during regular business hours. He/she should also generally be available via e-mail or phone during non-business hours as needed to address critical issues or emergencies. He/she may be required to travel on behalf of the company up to 25%. The above job description is not intended to be an all-inclusive list of duties and standards of the position. Incumbents will follow any other instructions and perform any other related duties, as assigned by their supervisor. Powered by ExactHire:160577

Piper Health and Sciences is actively seeking a Scientist - Analytical Chemist to work in the Titusville area. Responsibilities for Scientist - Analytical Chemist: * Oversee method development and method validation for HPLC, UPLC, and GC * Develop and train junior staff on analytical techniques and methods * Review, revise and rewrite SOPs in the analytical development department * Identify deviations, conduct investigations, determine root cause analysis and implement CAPAs * Collect data from studies to interpret findings, write summary reports, and analyze data for accuracy Technical Requirements for Scientist - Analytical Chemist: * Bachelor's or Master's Degree in Chemistry, Chemical Engineering or similar field * 5 years of experience in a fast-paced medical, pharmaceutical, biotechnology, or other regulated environment * Minimum 3 years of experience with analytical chemistry techniques and equipment including pipetting, pH meters, UV-Vis, Karl Fischer, FTIR, etc * Experience with mass spectrometry including LC-MS and GC-MS preferable * Strong organizational and written communication skills Compensation & Benefits for Scientist - Analytical Chemist: * Compensation: $55-60/hr, based on experience * Full Benefits: Medical, Dental, Vision, 401k, PTO, etc #LI-NW1 #LI-ONSITE

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

Analytical Chemist-Florham Park, NJ Arxada is a global leader in innovative solutions that protect our world. Our groundbreaking technologies, in-depth regulatory know-how, manufacturing and process development help our customers to safeguard nutrition, health and infrastructure efficiently through chemistry and biotechnology that enhance sustainability. We offer a broad portfolio of ingredients and services for multiple end-markets that include Human Health & Nutrition, Home & Personal Care, Professional Hygiene, Paints & Coatings and Wood Protection. With customers in more than 100 countries, the company achieved sales of CHF 2 billion in 2024. Headquartered in Basel (Switzerland), Arxada employs 3,200 associates across 24 production sites and 14 R&D centers, all committed to our customers' success. As a member of the Analytical Chemistry team, the candidate has an important role to play in support of a wide range of tasks including the analysis of R&D and customer samples, as well as troubleshooting issues related to manufacturing and customer complaints. The incumbent will utilize a variety of analytical techniques to deliver accurate and timely results in a dynamic, fast-paced environment Essential Job Functions: Perform analytical testing on R&D, customer and production samples using chromatographic, spectroscopic, wet chemistry, and other techniques. Develop, validate, and optimize analytical methods for both new and existing products and raw materials as needed. Ensure analytical results are accurate, reliable, and delivered within required timelines, following proper documentation protocols. Prepare technical reports and data summaries for internal use and customer reporting. Collaborate with R&D, manufacturing, and quality teams to support product development, resolve manufacturing issues etc. Adhere strictly to company policies, health and safety guidelines, and ISO Quality Management procedures. Perform additional duties and special projects as assigned. Qualifications & Experience: Bachelor's or master's degree require in preferred areas of study: General or Analytical Chemistry 5 years analytical professional experience with bachelor's degree or 2 years' experience with Masters degree Proficient in HPLC (UPLC), GC, spectroscopy ( UV-Vis, FT-IR), wet chemistry, and other modern techniques as well as sample preparation techniques Proficient with common software, including MS Office Effective written and verbal communication skills The expected salary range for this role is 75-92k annually, but specific employee compensation may vary depending on factors including experience, education, training, licensure, certification, location and other job-related, non-discriminatory factors permitted by law. This role is also eligible to earn a short-term incentive bonus and the following benefits: 401(k) plan, medical, dental, vision, life, and disability insurance, paid time off, paid holidays and paid sick leave. Arxada has world class offering in two distinct areas: Microbial Control Solutions (MCS) focuses on threats posed by microorganisms to people and planet through five distinct business lines including Professional Hygiene, Home & Personal Care, Wood Protection, Paints & Coatings and Material Protection. Nutrition, Care & Environmental (NCE), meanwhile, provides materials used to manufacture composites for electronics, aerospace and other markets, as well as vitamins and nutritional ingredients, chemicals and performance intermediates, and raw materials for a wide range of high-performance applications. Arxada is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law. #LI-BR1 US41

About Us: Shamrock Technologies is a family-owned business which prides itself on its enterprising spirit. This atmosphere inspires associates to pursue their ambitions without the boundaries of classic organizational structure. Headquartered in Newark, New Jersey, Shamrock Technologies is one of the world's largest processors of micronized polytetrafluoroethylene (PTFE), as well as a leading worldwide manufacturer and supplier of a broad line of specialty products. Our materials are found in Inks and Coatings, Lubricants, Grease, Thermoplastics, and more. Using advanced technology and sophisticated production equipment, combined with our state-of-the-art Application and R&D laboratory facilities, Shamrock creates products to help customers meet their challenging formulation needs. Shamrock differentiates itself by hiring associates with an approach to thinking that actively seeks change rather than waiting to adapt to it. Our business embraces originality, curiosity, critical questioning, service, and continuous improvement, while creating a work culture that values cooperation. Summary: We are seeking a hands-on, innovative Research Chemist to support product development and applications research within the Wax Additives business. This role focuses on designing and conducting laboratory experiments, characterizing materials, and generating data that help bring new wax powders, dispersions, emulsions, and surface-modified products to market. The Research Chemist will work closely with the Technical Director and cross-functional teams to translate customer needs into technical solutions. Primary Responsibilities Plan, execute, and document lab experiments to develop new wax additives and improve existing products. Formulate and test emulsions, dispersions, blends, and surface-modified waxes for coatings, inks, and plastic applications. Operate and maintain laboratory equipment such as mills, mixers, particle size analyzers, DSC, FTIR, and rheometers. Collect, interpret, and summarize experimental data to guide decision-making. Prepare technical reports and communicate findings to the technical teams. Screen new raw materials and evaluate competitive technologies. Support scale-up trials by providing lab-to-pilot correlations and data. Assist in preparing technical presentations and samples for customer trials. Follow established safety protocols and maintain a clean, organized lab environment. Ensure accurate documentation and compliance with internal and external standards. Qualifications Education and Experience Bachelor's degree in Chemistry, Polymer Science, Materials Science, or Chemical Engineering. 0-5 years of experience in a chemical, polymer, or coatings laboratory (industrial or academic research). Hands-on experience with emulsions, dispersions, or polymer/wax formulations is highly preferred. Experience with polyamide chemistry or related polymer modification techniques is a plus. Professional Skills Strong experimental design and data analysis skills. Proficiency with common lab instrumentation (particle size, DSC, FTIR, rheology). Creative problem-solver with curiosity and initiative. Effective communicator with ability to work cross-functionally. Comfortable with multitasking in a fast-paced environment. Work Environment & Physical Requirements: Laboratory-based position with occasional pilot plant and production floor exposure. Required to wear PPE and complete safety training. Able to stand/sit for extended periods of time, may include bending/stooping. Prepared for prolonged periods sitting at a desk and working on a computer. Compensation package We offer a competitive salary complemented by an annual performance-based bonus. Our comprehensive benefits package includes generous paid time off hours, a 401(k) plan with employer matching, comprehensive healthcare coverage, employer-sponsored life insurance, and additional benefits designed to support your well-being and financial security. Equal Opportunity Statement Shamrock Technologies provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. Request for Assistance If you are a qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation if you are unable or limited in your ability to access job openings or apply for a job on this site as a result of your disability. You can request reasonable accommodations by contacting Human Resources via email at ***************************. Reasonable Accommodation Applicants with disabilities may contact Shamrock Technologies via telephone, e-mail, and other means to request and arrange accommodation. If you need assistance to accommodate the disability, you may request accommodation at any time. Please contact the Shamrock Technologies Human Resources department at ***************************.

Voyant Beauty believes our people are more than just employees; they're the driving force behind everything we achieve. Our culture fosters teamwork, respect, and camaraderie, ensuring that every individual's contribution is valued and celebrated. We invest in their growth, providing opportunities for development and advancement within our dynamic team. Voyant Beauty is a company that specializes in the development and manufacturing, of beauty, personal and home care products. We work with various brands, retailers, and businesses to create customer formulations and products tailored to their needs. This can include skincare, haircare, bath and body products, fragrances, and more. Essentially, Voyant Beauty serves as a one-stop-shop for companies looking to bring their beauty and personal care product ideas to life. Safety is a core value at Voyant Beauty. We prioritize the well-being of our team members, ensuring a safe and secure environment where everyone can thrive and excel. If you're seeking to be part of a team where your talents are valued, your safety is paramount, and your efforts contribute to meaningful change, then Voyant Beauty is the place for you. Come join us and be a part of our journey. A Brief Overview Ensures accuracy and reliability in laboratory testing and analysis. The QC Analytical Chemist is responsible for conducting quantitative and qualitative analysis of raw materials and products, developing analytical methods, and ensuring compliance with industry standards. What you will do · Conduct quantitative and qualitative analysis of raw materials and products. · Collaborate with production teams to troubleshoot production issues. · Ensure compliance with industry standards and regulations. · Prepare technical documents and reports. · Develop and validate analytical methods. · Calibrate and maintain analytical instrumentation. · Manage standard chemical inventory and safety protocols. · Some duties may vary slightly by location. Education Qualifications · Bachelor's Degree in Chemistry or related scientific discipline (Preferred) Experience Qualifications · 1-3 years Analytical chemistry in a manufacturing environment (Preferred) · 1-3 years Method development and validation (Preferred) Skills and Abilities · Analytical Chemistry (High proficiency) · Quality Control (Medium proficiency) · Laboratory Safety (Medium proficiency) · Technical Documentation (Medium proficiency) · Regulatory Compliance (Medium proficiency) · Data Analysis (Low proficiency) · Instrumentation Calibration (Low proficiency) · Method Validation (Low proficiency) · Chemical Handling (Low proficiency) · Collaboration (Low proficiency) To Staffing and Recruiting Agencies: Our company does not accept unsolicited curriculum vitae's or applications from agencies. We are not responsible for any fees related to unsolicited curriculum vitae's or applications and explicitly reserve its right to contact candidates presented in such unsolicited curriculum vitae's or application. Our company provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, religion, sex, color, national origin, sexual orientation, age, disability or veteran status. Voyant Beauty will consider requests for accommodations due to a disability impacting a qualified employee's ability to perform the essential functions of their position consistent with applicable laws. In addition to federal law requirements, Voyant Beauty complies with applicable provincial and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

Join a Fortune 500 leader in the personal care industry, dedicated to delivering innovative, high-quality products that inspire confidence and wellness. We are seeking a Formulation Chemist to contribute to the development of cutting-edge consumer health and personal care solutions. Position Summary The Formulation Chemist will play a key role in designing, optimizing, and testing formulations for personal care products. This role requires hands-on laboratory experience, scientific curiosity, and a strong commitment to product quality and compliance. Key Responsibilities Formulate prototypes to support formula optimization and innovation initiatives Assess physical and clinical properties of formulations in alignment with project requirements Design and optimize formulas for performance, stability, and consumer appeal Select and evaluate raw materials and ingredients for efficacy and safety Conduct laboratory stability testing and monitor product performance over time Perform lab aesthetics assessments to ensure consumer-preferred sensory attributes Prepare formulas for internal and external testing, including clinical evaluations Ensure compliance with Good Manufacturing Practices (GMP) during formulation activities Qualifications Bachelor s degree in Chemistry or a related scientific discipline (required) 1 5 years of laboratory and formulation experience within consumer health, hair care, skin care or personal care industries Strong knowledge of formulation principles, raw material functionality, and product development processes Experience with stability testing, sensory evaluation, and GMP practices Excellent problem-solving skills and ability to work collaboratively in cross-functional teams Strong communication and documentation skills Preferred Attributes Experience in hair care formulation strongly preferred Familiarity with regulatory and safety requirements for consumer health products Ability to balance technical rigor with creativity in product design What We Offer Competitive compensation and benefits package Opportunity to work with a Fortune 100 organization at the forefront of consumer health innovation Collaborative, science-driven environment with career growth potential Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws. By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.

The Quality Control Chemist-II is responsible for performing a variety of complex analytical testing, ensuring the quality of dietary supplements and OTC products through testing, documentation, and compliance with regulatory standards. This position also involves reviewing and maintaining SOPs, Testing Procedures, calibrations, and other controlled documents to support quality assurance activities. Additionally, the Chemist-II will assist with troubleshooting and minor repairs of laboratory equipment and support stability testing and documentation. This mid-level position will require more independent work, the ability to mentor QC chemist-I and Lab Tech personnel, and involvement in process improvements and corrective actions. ESSENTIAL FUNCTIONS ( Essential functions, as defined under the Americans with Disabilities Act, may include the following tasks, knowledge, skills and other characteristics. This list of tasks is illustrative ONLY and is not a comprehensive listing of all functions and tasks performed by positions in this class. It does not imply that all positions within the class perform all of the duties listed, nor does it necessarily list all possible duties that may be assigned.) Coordinates with other QC Supervisors and laboratory management so that the shared resources such as laboratory instruments, reagents, etc. are available for assigned staff to perform their job duties effectively and efficiently. Performs the pharmaceutical OTC & Dietary supplement analysis to support OTC & Dietary Supplement manufacturing which includes assay, impurity, dissolution testing, content uniformity, and physical testing. Conduct Analysis in compliance with cGMP requirements, compendia standards, and internal procedures. Maintain accurate record of analysis and perform documentation to company standards Perform laboratory analysis right first time, contemporaneous documentation, analyze and document the results. Notify manager immediately of nonconforming data or unexpected occurrences. Reviews and analyzes the stability samples and associated analytical data, prepares or assists in preparing Stability Summary Reports for Annual Product Review Reports. Reviews/Checks of analytical data by following test methods/SOPs. Performs operational qualification on analytical instruments, analytical method verification/validations, validation protocols and reports for analytical methods. Conducts laboratory investigation (OOS/OOT) under the supervision of laboratory management. Organize work schedule to complete assigned tasks efficiently and on schedule. Work under direction provided by supervisor and other duties as assigned Assist in Training and monitoring of the new hires (trainees) in learning or performing basic skills and assists in evaluating the need of any potential equipment for laboratory. Ensures the laboratory is kept in a safe working environment and in compliance with OSHA and other laboratory safety standards. Maintains knowledge of the latest guidelines of regulatory requirements of International Conference of Harmonization, USP, USFDA and OSHA. Complies with all regulatory/ in-house requirements may include but not be limited to safety, housekeeping, laboratory chemical waste, cGMP, cGLP, documentation. Assists in compilation of regulatory documents. Managing the Pharmacopeia changes and up gradation and implementing the same after upgrading the change repeated documents through proper channels of change control and training to all concerned. EXPERIENCE AND QUALIFICATIONS T o perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the experience and education required : EDUCATION & EXPERIENCE o Bachelors degree in Chemistry or related science field with eight (8) to ten (10) years lab experience in a pharmaceutical chemical or related industrial experience; preferably solid dosage forms manufacturing. Method Development experience is preferred. o Masters degree or higher with six (6) to eight (8) years of progressive lab experience in a pharmaceutical chemical or related industry; preferably generic pharmaceuticals. Method Development experience is preferred. o Demonstrated skills and experience in leading a group of QC Chemists. COMPUTER SKILLS o Basic knowledge of computers using MS Office, MS Outlook and business software systems commonly used in the pharmaceutical industry required. MATHEMATICAL SKILLS o Requires a strong knowledge of algebra, calculus and statistics and how they are applied. o Math skills commensurate with scientific background are required. KNOWLEDGE, SKILLS AND ABILITIES To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills and abilities required : INDUSTRY KNOWLEDGE: Knowledge and experience of applicable FDA regulatory standards and requirements for the solid oral dosage manufacturing required. Knowledge of analysis of pharmaceutical dosage forms and raw materials utilizing HPLC, GC, ICP-MS, UV, TLC, dissolution testing, spectroscopic and wet chemistry techniques is a plus. COMMUNICATION SKILLS: Advance level of written and verbal communication skills with the ability to read, technical procedures or governmental regulations. Ability to write reports, and required documentations. REASONING ABILITY: Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. Ability to interpret a variety of instructions furnished in written, oral, diagram or schedule form. Must possess initiative and trouble shooting ability.

Job Title: Quality Control ChemistJob Description We are seeking a dedicated Quality Control Chemist to join our team. The ideal candidate will conduct quality control testing of raw materials and finished products using various analytical techniques. This role requires a strong understanding of chromatography, spectroscopy, and other analytical methods to ensure regulatory compliance and product quality. Responsibilities * Conduct quality control testing on raw materials and finished products using analytical techniques such as HPLC, UPLC, GC, UV-Vis, FT-IR, and dissolution apparatus. * Interpret and report analytical results, maintaining accurate laboratory records, and ensuring compliance with regulatory requirements. * Collaborate with the quality assurance team to ensure products meet in-house and regulatory quality specifications. * Operate, maintain, and calibrate analytical instruments, ensuring they are functioning properly. * Adhere to health and safety guidelines, ensuring a safe working environment in the laboratory. * Ensure compliance with international regulations such as FDA and EMA. * Work collaboratively with R&D and production teams to support product development and release. * Provide technical support and training to junior team members or other departments. Essential Skills * 3-7 years of routine testing experience using HPLC and dissolution techniques. * Proficiency in working with solid oral dosage forms, raw materials, and finished products. * Experience with analytical instruments such as GC, FTIR, KF, and UV-VIS. * Strong understanding of Pharma GMP practices. * Competence in laboratory applications including wet chemistry, titration, and chromatography. * Basic computer skills in MS Word, Excel, and Outlook. Additional Skills & Qualifications * Bachelor's degree in Chemistry, Analytical Chemistry, Biochemistry, Biology, or a related field. * Proven hands-on experience in a pharmaceutical analytical laboratory. * Ability to document and record analytical experiments and results as per cGMP guidelines. * Strong problem-solving skills and attention to detail. * Knowledge of regulatory guidelines such as GMP and GLP. Work Environment The role is based in a laboratory setting, involving exposure to chemicals, reagents, and specialized equipment. The position may require standing for extended periods and the ability to lift moderate weight, approximately 25 pounds. A team of 10 professionals works collaboratively in this environment. Overtime may be required to meet project deadlines. Job Type & Location This is a Contract to Hire position based out of East Windsor, NJ. Pay and Benefits The pay range for this position is $35.00 - $35.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in East Windsor,NJ. Application Deadline This position is anticipated to close on Jan 19, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

About Atrium: What you do matters. As a people-centric organization, we foster an environment of collaboration, high performance, and innovation where your talents are valued, and your achievements are celebrated. Join us and become part of an inclusive team. Client Overview: Our client specializes in the development and manufacturing of commercial products used for various industries. They are looking to add an Associate Chemist to their team. Salary/Hourly Rate: $20/hr - $21/hr (Based on experience) Position Overview: The Associate Chemist will assist with essential laboratory tasks, with a primary focus on wet chemistry, inventory management, and sample preparation. Responsibilities of the Associate Chemist: * Evaluate product properties using established test methods. * Perform application testing of product prototypes. * Generate samples as needed from product formulations. * Record observations and test results clearly and accurately. * Independently execute work assignments. * Maintain laboratory equipment and supplies. * Adhere to all laboratory safety rules and guidelines. * Clean and maintain the laboratory and equipment to support a safe working environment. Required Experience/Skills for the Associate Chemist: * 0 - 3 years of experience in a laboratory setting. * Proficient in Microsoft Word, Excel, and PowerPoint. * Ability to understand written instructions, test procedures, and Safety Data Sheets (SDS). Preferred Experience/Skills for the Associate Chemist: * Basic knowledge of coatings, test methods, or application techniques is a plus. Education Requirements: * Bachelor's degree in Chemistry or a related field is required. Benefits: * Atrium Care Package available, upon eligibility (including healthcare plans, discount programs, and paid time off).

Quality Control Chemist Apex Systems has an immediate opening for a Chemist to join a Pharma company in the Southern New Jersey area. The incumbent demonstrates proficiency through a wide exposure to pharmaceutical analyses and has a firm grasp of scientific principles and skill in applying this knowledge. The incumbent has practical experience in pharmaceutical analyses and routinely performs analysis in two of the functional areas (HPLC, GC, or Wet Chemistry). The incumbent performs and trains on routine chromatographic analyses. The incumbent works independently. ESSENTIAL DUTIES AND RESPONSIBILITIES: * Provides analytical support for production. * Performs GC, HPLC and/or Wet chemistry analyses on Raw Material, In-process and Finished Lot samples. * Supports Analytical and Chemical Development by testing samples. * Provides quick turnaround of In-process samples to production. * Thoroughly documents all results in a laboratory notebook as well as compile all data into an ancillary. * Empties HPLC and Organic waste containers. * Discards completed samples. * Makes retains of all production samples and maintains the inventory of retain samples. * Calibrates production pH meters. * Support Laboratory Investigation through testing. * Performs all tasks in accordance with cGMP compliance. * Assists in writing of SOPs, testing standards, protocols and reports. * Assists in training of lab personnel on instrumentation, methods, and cGMP. * Shares in the responsibilities of housekeeping (i.e. Glassware, waste, retains, etc.) * Provides ideas/feedback for areas where efficiency can improve. * Has in-depth understanding of most analytical methods. * Ability to troubleshoot most methods and equipment. * Reviews and releases analytical results. * Performs any other laboratory tasks deemed necessary by the QC Production Support Manager. * Adheres to personal moral, ethical, legal, and behavioral conduct that is in compliance with the Siegfried Code of Conduct. * Adheres to all applicable SHE and cGMP regulations. Requirements: * Bachelor degree in Chemistry or other science related field. Please send all resumes to David Neto [email protected] EEO Employer Apex Systems is an equal opportunity employer. We do not discriminate or allow discrimination on the basis of race, color, religion, creed, sex (including pregnancy, childbirth, breastfeeding, or related medical conditions), age, sexual orientation, gender identity, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, disability, status as a crime victim, protected veteran status, political affiliation, union membership, or any other characteristic protected by law. Apex will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law. If you have visited our website in search of information on employment opportunities or to apply for a position, and you require an accommodation in using our website for a search or application, please contact our Employee Services Department at [email protected] or ************. Apex Systems is a world-class IT services company that serves thousands of clients across the globe. When you join Apex, you become part of a team that values innovation, collaboration, and continuous learning. We offer quality career resources, training, certifications, development opportunities, and a comprehensive benefits package. Our commitment to excellence is reflected in many awards, including ClearlyRated's Best of Staffing in Talent Satisfaction in the United States and Great Place to Work in the United Kingdom and Mexico. Apex uses a virtual recruiter as part of the application process. Click here for more details. Apex Benefits Overview: Apex offers a range of supplemental benefits, including medical, dental, vision, life, disability, and other insurance plans that offer an optional layer of financial protection. We offer an ESPP (employee stock purchase program) and a 401K program which allows you to contribute typically within 30 days of starting, with a company match after 12 months of tenure. Apex also offers a HSA (Health Savings Account on the HDHP plan), a SupportLinc Employee Assistance Program (EAP) with up to 8 free counseling sessions, a corporate discount savings program and other discounts. In terms of professional development, Apex hosts an on-demand training program, provides access to certification prep and a library of technical and leadership courses/books/seminars once you have 6+ months of tenure, and certification discounts and other perks to associations that include CompTIA and IIBA. Apex has a dedicated customer service team for our Consultants that can address questions around benefits and other resources, as well as a certified Career Coach. You can access a full list of our benefits, programs, support teams and resources within our 'Welcome Packet' as well, which an Apex team member can provide. Employee Type: Contract Location: Pennsville Township, NJ, US Job Type: Date Posted: December 15, 2025 Pay Range: $36 - $39 per hour Similar Jobs * QC Specialist * Sr R&D Chemist - (Polymer Chemist) * Research Chemist Technician * QC Analyst II * Lab Technician

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 $45/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!

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

Voyant Beauty believes our people are more than just employees; they're the driving force behind everything we achieve. Our culture fosters teamwork, respect, and camaraderie, ensuring that every individual's contribution is valued and celebrated. We invest in their growth, providing opportunities for development and advancement within our dynamic team. Voyant Beauty is a company that specializes in the development and manufacturing, of beauty, personal and home care products. We work with various brands, retailers, and businesses to create customer formulations and products tailored to their needs. This can include skincare, haircare, bath and body products, fragrances, and more. Essentially, Voyant Beauty serves as a one-stop-shop for companies looking to bring their beauty and personal care product ideas to life. Safety is a core value at Voyant Beauty. We prioritize the well-being of our team members, ensuring a safe and secure environment where everyone can thrive and excel. If you're seeking to be part of a team where your talents are valued, your safety is paramount, and your efforts contribute to meaningful change, then Voyant Beauty is the place for you. Come join us and be a part of our journey. A Brief Overview Ensures accuracy and reliability in laboratory testing and analysis. The QC Analytical Chemist is responsible for conducting quantitative and qualitative analysis of raw materials and products, developing analytical methods, and ensuring compliance with industry standards. What you will do * Conduct quantitative and qualitative analysis of raw materials and products. * Collaborate with production teams to troubleshoot production issues. * Ensure compliance with industry standards and regulations. * Prepare technical documents and reports. * Develop and validate analytical methods. * Calibrate and maintain analytical instrumentation. * Manage standard chemical inventory and safety protocols. * Some duties may vary slightly by location. Education Qualifications * Bachelor's Degree in Chemistry or related scientific discipline (Preferred) Experience Qualifications * 1-3 years Analytical chemistry in a manufacturing environment (Preferred) * 1-3 years Method development and validation (Preferred) Skills and Abilities * Analytical Chemistry (High proficiency) * Quality Control (Medium proficiency) * Laboratory Safety (Medium proficiency) * Technical Documentation (Medium proficiency) * Regulatory Compliance (Medium proficiency) * Data Analysis (Low proficiency) * Instrumentation Calibration (Low proficiency) * Method Validation (Low proficiency) * Chemical Handling (Low proficiency) * Collaboration (Low proficiency) To Staffing and Recruiting Agencies: Our company does not accept unsolicited curriculum vitae's or applications from agencies. We are not responsible for any fees related to unsolicited curriculum vitae's or applications and explicitly reserve its right to contact candidates presented in such unsolicited curriculum vitae's or application. Our company provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, religion, sex, color, national origin, sexual orientation, age, disability or veteran status. Voyant Beauty will consider requests for accommodations due to a disability impacting a qualified employee's ability to perform the essential functions of their position consistent with applicable laws. In addition to federal law requirements, Voyant Beauty complies with applicable provincial and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

Our client is a consumer products company specializing in cosmetics and personal care products and operating in a very fast-paced environment. They are now seeking a Formulations Chemist to support formulation innovation and product development initiatives. Salary/Hourly Rate: $60k - $75k Position Overview: The Formulations Chemist will lead technical formulation efforts for powder-based cosmetic products, with occasional support for emulsion and anhydrous formulations. This role requires close cross-functional collaboration and the ability to thrive in a fast-paced, deadline-driven environment. Responsibilities of the Formulations Chemist: * Develop and improve powder cosmetic formulations, including new product development and reformulations. * Assist with emulsion and anhydrous product development as needed. * Evaluate and incorporate new raw materials and technologies to enhance performance while meeting cost and regulatory requirements. * Collaborate directly with clients to define formulation objectives, troubleshoot issues, and deliver solutions. * Provide technical support through clear documentation and communication. * Research emerging trends, ingredients, and technologies relevant to powder and cosmetic formulations. * Work cross-functionally with Marketing, Manufacturing, Quality, Regulatory, Packaging, and Research teams. * Monitor product stability and manage multiple formulation projects simultaneously. * Maintain accurate documentation of formulations and processes in compliance with internal and regulatory standards. * Support global standardization initiatives related to formulation and testing. Required Experience/Skills for the Formulations Chemist: * At least 6 months of hands-on powder formulation experience and 2+ years of cosmetic formulation experience. * Practical formulation experience in a fast-paced laboratory or R&D environment. * Strong understanding of powder technologies and basic emulsion and anhydrous formulation principles. * Knowledge of cosmetic raw materials, regulatory guidelines, and industry standards. * Ability to adapt quickly to changing priorities and manage multiple projects effectively. * Proficiency in Microsoft Word, Excel, SAP, DEVEX, or similar systems. * Strong communication, analytical, and problem-solving skills. * Highly organized, detail-oriented, and collaborative. Preferred Experience/Skills for the Formulations Chemist: * Prior experience working in a fast-paced product development environment. Education Requirements: * Bachelor's degree in Chemistry, Biology, Biochemistry, or a related scientific discipline required. Benefits: * Medical, dental, and vision coverage. * 401(k) plan. * Paid time off and paid holidays.