Chemist Jobs in Elizabeth, NJ

Job Title: Chemist Department: Quality Control This position is responsible for performing various laboratory tests to determine chemical and physical characteristics or composition of solid or liquid materials. Laboratory tests will primarily include wet chemistry and may include basic use of instrumentation such as Gas Chromatography and High Pressure Liquid Chromatography. The Chemist I will also be responsible for supporting the Quality Control laboratory through reagent compounding. This position will also be responsible for performing identification testing using wet chemistry or instrumentation analysis, physical property testing and general laboratory upkeep. The individual will also be responsible for maintaining a laboratory notebook in accordance with Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP). ESSENTIAL DUTIES AND RESPONSIBILITIES: Performs tests on a wide variety of samples of manufactured products to verify their conformity to defined specifications. Such products may be regulated under Good Manufacturing Practices and regulated by government regulatory agencies like FDA. As such the individual is required to have a basic knowledge of GMPs and other pertinent government regulations. Operates basic laboratory equipment such as analytical balances, pH meters, volumetric glassware, and spectrophotometers. Basic operation of advanced instrumentation such as Gas Chromatography and High Pressure Liquid Chromatography may also be required. Responsible for performing tests on a wide variety of materials comprised of powders, granules, gases and liquids to confirm quality attributes such as purity, stability, viscosity, density, absorption, and melting point. Records test results on standardized forms and laboratory notebooks. Writes test reports describing procedures used and uses basic mathematical analysis following Good Documentation Practices. Understands basic statistical concepts that may be required to reach sound scientific conclusions. Participates in Out of Specification investigations to resolve scientific issues in a timely manner. Maintains workspace and common areas for tidiness and cleanliness. SUPERVISORY RESPONSIBILITIES: This position has no supervisory responsibilities. QUALIFICATIONS: To perform this job successfully, the individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. EDUCATION and EXPERIENCE: A Bachelor's Degree from an accredited four year college or university in chemistry, biochemistry or related scientific field with 3 plus years experience working in a laboratory in a cGMP setting. Or, a Master's Degree from an accredited four year college or university with 3 year's experience MATHEMATICAL SKILLS: The individual is required to have the ability to work with mathematical concepts such as unit conversion, stoichiometry, and basic chemistry formulas. The individual must also be able to apply basic mathematical skills such as fractions, percentages, ratios, and proportions to basic problem solving techniques. Some knowledge of basic statistical techniques is recommended. CERTIFICATES, LICENSES, REGISTRATIONS: None required for this position. PHYSICAL DEMANDS: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to use hands to finger, handle, feel or reach with hands and arms. The employee frequently is required to stand, walk, sit, talk or hear, and taste or smell. The employee is occasionally required to climb or balance and stoop, kneel, crouch, or crawl. The employee may be required to lift and/or move up to 10 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus. Must pass respiratory fitness test as position requires employee to wear a respirator. WORK ENVIRONMENT: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee may be frequently exposed to fumes or airborne particles and toxic or caustic chemicals. The noise level in the work environment is usually moderate.

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

Insight Global is looking for an Analytical Chemist to join the R&D organization of a large animal health pharmaceutical company. This individual will be supporting the small molecule portfolio specifically for a liquid formulation project. The Chemist will be responsible for hands on laboratory activities including executing analytical tests and techniques. On a daily basis, they will be utilizing HPLC, UPLC, Density Meters, and Karl Fisher instrumentation. 90% of the role will be based within the laboratory and the other 10% will be dedicated to documentation within the Electronic Laboratory Notebook. The idea candidate will have 3+ years of industry experience within an analytical lab REQUIRED SKILLS AND EXPERIENCE - Bachelor's Degree in Chemistry, Biology, or Scientific Field - 3+ years experience within pharmaceutical industry - Experience with UPLC or HPLC instrumentation - Empower software experience - Strong communication and collaboration skills NICE TO HAVE SKILLS AND EXPERIENCE - Experience with liquid product formulations

Opportunity for an experienced Upstream Manufacturing Scientist (multiple levels) to continue their career in downstream/upstream manufacturing. This role will be with our client who has a global footprint in both R&D and manufacturing within the biopharma industry. Location- Middlesex County, NJ Terms: Direct Hire Salary: $80-100k/yr. What you will be doing: Work closely with manufacturing associates and engineers to execute upstream batch processes. Perform cell culture and bioreactor operations (single-use fed-batch bioreactors) across various scales. Carry out harvest clarification processes using centrifuges and depth filters at multiple scales. Ensure timely execution of engineering and clinical batches. Develop equipment specifications and optimize manufacturing techniques. Leverage programs to collect and analyze operational data, making real-time adjustments to products, instruments, and equipment. Interpret and follow instructions in written, oral, diagrammatic, or scheduled formats. Adhere to GMP standards in the manufacturing area and lead compliance with environmental health and safety regulations. Review completed manufacturing and packaging batch records and supporting documentation. Coordinate investigations and implement corrective actions for any issues identified during batch execution. Perform additional duties as assigned. Comply with all company policies and standards. What you bring to the company: Bachelor's or Master's degree in Chemical, Biological, or Biochemical Sciences, with at least 3 years of relevant experience in the biopharmaceutical industry. Proven expertise in independently designing, executing, analyzing, and documenting all phases of process development. Strong foundational knowledge and subject matter expertise in executing both engineering and clinical batches. Hands-on experience in GMP and aseptic manufacturing environments. Familiarity with single-use manufacturing consumables, such as bags, tube sets, columns, and process manifolds. Proven ability to work both independently and collaboratively within a team; excellent interpersonal skills. Strong verbal and written communication skills, with advanced computer and organizational abilities. High attention to detail and proficiency in basic software, including Word, Excel, and spreadsheets. In-depth understanding of GMP batch manufacturing and packaging documentation, including audit and review procedures. Knowledge of cleaning verification and validation processes. ** This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you**

OLI is pioneering kidney care with our backpack-sized, portable hemodialysis systems. As we expand our R&D capabilities, we're seeking a talented Research Chemist (polymer chemistry / material science) to play a critical role in the development and optimization of materials essential to our product's success. Role Description We are seeking a (Full-Time) Research Chemist with deep expertise in polymer synthesis and characterization. The ideal candidate will leverage their understanding of polymer chemistry to develop and optimize advanced materials that meet the performance, safety, and regulatory requirements for portable hemodialysis prototypes. This role will involve collaborating with cross-functional teams-engineering, pre-clinical, quality, and regulatory-to ensure our solutions remain at the forefront of kidney care innovation. Key Responsibilities Polymer Science: Synthesize, process, and characterize polymers and related materials used in hemodialysis devices. Process Development: Establish and refine scalable processes for polymer synthesis. Polymer Testing & Optimization: Design and conduct experiments to synthesis polymer derivatives and evaluate their chemical and physical properties, such as loading capacities, porosity, particle size, biocompatibility, and sterilization stability. Data Analysis & Reporting: Maintain detailed records of experimental work, analyze findings, and present statistically-sound results to internal stakeholders. Cross-Functional Collaboration: Collaborate with engineering and clinical teams to integrate polymer solutions into product design and manufacturing processes. Qualifications PhD in Polymer Chemistry, Materials Science, or a related field (Master's candidates with significant polymer experience will be considered). Hands-on experience in polymer synthesis, characterization, and processing techniques. Demonstrated problem-solving skills with the ability to interpret data, propose experiments, and drive solutions independently. Excellent communication and teamwork capabilities, with a proactive approach to cross-departmental collaboration. Familiarity with medical device or life sciences development, particularly dialysis or other fluid-based systems, is a plus. Strong knowledge of regulatory requirements (FDA, ISO) in the context of materials development and testing is a plus. If you're excited about innovating in chemistry to advance healthcare, we'd love to hear from you!

What we're looking for: We're seeking a dedicated and detail-oriented Analytical Chemist to join our dynamic team, supporting both Production and R&D operations. In this role, you will perform critical analyses using HPLC, GC-MS, NMR, and other analytical techniques, ensuring the success of kilo-scale production and small molecule development. This position provides an exceptional opportunity to leverage your expertise in analytical chemistry to support the production and development of high-quality materials. Join our team and take a pivotal role in shaping innovation, advancing precision, and driving excellence in our laboratory operations. About Us: Mironova Labs, Inc. is a small, fast-paced, manufacturing company with a successful history in the discovery and development of specialty ingredient technologies. With a thirty-year heritage in process innovation, our research and development capabilities deliver process technologies for breakthrough ingredients used in the cosmetic industry. Responsibilities Analytical: Update and optimize methods for HPLC/MS analysis, ensuring accuracy and compliance with established protocols. Perform routine and advanced analyses using HPLC-MS, NMR, GC-MS, and other analytical instruments as required. Maintain, calibrate, and troubleshoot analytical equipment to ensure operational efficiency and reliability. Ensure the analytical laboratory remains clean, organized, and fully operational. Accurately document all analysis results in logbooks, laboratory notebooks, and digital systems. Troubleshoot and resolve issues with analytical methods or equipment to minimize downtime. Production: Support kilo production processes by assisting with chemical reactions, distillation, extraction, filtration, chromatography, crystallization, and related tasks. Help maintain cleanliness and organization of work areas while ensuring all documentation and logbooks are accurately completed and up-to-date. Research and Development: Conduct laboratory experiments (wet chemistry) to support process chemists in method development and process optimization. Maintain accurate and detailed experimental records and laboratory notebooks. Qualifications: Education: Minimum of Bachelor's Degree (required) in Chemistry, Biochemistry, or a related scientific field. Preferred Masters or Ph.D. in Analytical Chemistry or related field. Skills: Proficiency in using analytical instruments (e.g., HPLC-MS, GC-MS, NMR, UV-Vis, FTIR, etc.). Strong communication, time management, organizational skills, and attention to detail. Experience: 3-7 years of experience in a laboratory environment, preferably in a regulated industry. Experience managing multiple projects and ensuring timely delivery of results. Compliance: Familiarity with industry-standard EHS protocols and regulatory requirements (FDA, ISO, GMP).

QC Analyst 3 Job Title: Quality Control Laboratory Analyst 3 - Radiopharmaceuticals About Us Evergreen Theragnostics, Inc. is a radiopharmaceutical company beginning operations in Springfield, NJ. The state-of-the-art facility will provide contract development and manufacturing services for radiopharmaceutical companies, including therapeutics and centrally distributed diagnostics. Evergreen is a small team, where all team members support each other in a variety of activities. Job Description: We are looking for an experienced and proactive Quality Control Laboratory Analyst 3 to join our team. 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.

To be considered for this position, you must be authorized to work for any US employer without sponsorship now or in the future. will be working the overnight shift, Mon-Fri from 10PM to 6:30AM. The Opportunity: A New Jersey-based flavor and fragrance company is seeking an experienced Chemist with a strong background in organic and process chemistry to develop new products and processes for flavor and fragrance ingredients for the food and cosmetics industry. Successful applicant will have excellent theoretical and practical knowledge as well as experience in organic synthesis including synthetic methodology, catalysis, upstream and downstream processing. The position also requires conceptual design and experimental validation of designed processes. Qualifications: Bachelor or Master Degree in organic chemistry or related field Experience in distillation, re-crystallization, sublimation, deposition and extractions, synthesis Two years of industrial experience or related Knowledge of various lab equipment Ability to design, execute and troubleshoot experiments and processes Capacity to work independently Possess strong written and oral communication skills Ability to work effectively in a team environment and individually Physical fitness is required

Responsible for performing the day-to-day activities in the laboratory working under prescribed procedures (protocols, standard operating procedures, methods, etc.) Performs qualitative and quantitative analysis, prepares solutions, performs calibration, qualification, and maintenance of laboratory instrumentation, conducts environmental monitoring, assists with technical writing, and performs administrative tasks. Assists the department in areas including but not limited to solving problems, reviewing experimental data, writing protocol/SOP/validation reports and assist with training support staff as necessary. Monitors study procedures to ensure data accuracy and report quality. Maintains a GMP/GLP Laboratory. Evaluates the chemical and physical properties of various organic and inorganic substances. Utilizes established methods, procedures, and laboratory equipment to perform analytical testing of substances. Prepares compounds, reagents, and solutions. Develops and writes technical reports of testing results. Has gained exposure to some of the complex tasks within the job function. Works under the moderate supervision of senior personnel in the functional area. Gained or has attained full proficiency in a specific area of analysis. Responsibilities Include Conduct Analysis in compliance with cGMP requirements, compendia standards, and internal procedures. Maintain accurate record of analysis and perform documentation to company standards. Prepare test solutions, volumetric solutions, and samples used in analysis Performs assigned sampling, physical, chemical tests and assay on raw materials, active pharmaceutical ingredients, in-process, finished bulk, finished product, and stability products analysis in an FDA regulated lab environment. Uses a variety of analytical instruments such as HPLC, GC, Dissolution, Malvern particle size analyzer, IR, Auto Titrator, UV Spectrophotometer, Karl Fisher (KF), Potentiometer etc. Perform analysis with a practical understanding of the test procedure and instrument operation. Perform laboratory analysis right first time, contemporaneous documentation, analyze and document the results. Conducts laboratory investigation under the supervision of laboratory manager. Performs maintenance and calibrations of laboratory instruments /equipment. Complies with all regulatory/ in-house requirements may include but not be limited to safety, housekeeping, laboratory chemical waste, cGMP, cGLP, documentation. Perform analysis with a practical understanding of the test procedure and instrument operation. Maintain required level of training needed to perform a GMP task. Prepares and/or Reviews Test Procedures, SOP's and Protocols as assigned. Qualifications Education & Experience - Bachelor degree or master degree in a Pharmaceutical, Biological, Chemical science or related field. 5-6 years of experience of related laboratory work experience; minimum of 5 years of experience as a QC Chemist in a GMP environment. Knowledge/Skills - The ability to work successfully in both a team/matrix environment as well as independently. The ability to work in a fast-paced environment, manage priorities and maintain timelines for multiple projects. The ability to work safely in a chemical laboratory. Cognitive Requirements - Ability to perform basic calculations, read, writes, communicate and handle stress produced by time pressure, customer demands, etc.

Outlier helps the world's most innovative companies improve their AI models by providing human feedback. Are you an experienced Expert who would like to lend your expertise to train AI models? About the opportunity: Outlier is looking for talented Chemistry Experts to help train generative artificial intelligence models This freelance opportunity is remote and hours are flexible, so you can work whenever is best for you You may contribute your expertise by… Assessing the factuality and relevance of domain-specific text produced by AI models Crafting and answering questions related to ChemistryEvaluating and ranking domain-specific responses generated by AI models Examples of desirable expertise: A bachelor's or higher degree in Chemistry or a related subject Experience working as a Chemistry professional Ability to write clearly about concepts related to Chemistry in fluent English Payment:Currently, pay rates for core project work by Chemistry experts range from $30 to $50 per hour USD. Rates vary based on expertise, skills assessment, location, project need, and other factors. For example, higher rates may be offered to PhDs. For non-core work, such as during initial project onboarding or project overtime phases, lower rates may apply. Certain projects offer incentive payments. Please review the payment terms for each project.

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

Base Pay Range: $100,100.00 - $170,200.00 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 identified below. Interns are eligible for some of the benefits identified below. Our pay ranges are determined by role, level, and location. The range displayed above reflects the minimum and maximum pay for this position in the primary location identified in this posting. Actual pay depends on several factors, including location, job-related skills, experience, and relevant education level or training. If applicable, your recruiter can share more about the specific pay range for your preferred location during the hiring process. Company Overview 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 Responsibilities Perform daily R&D work activities in the field of analytical chemistry and electrochemistry. Possess ability to work independently and with a team of colleagues. Prepare and plan the experiments, and compile comprehensive daily reports on R&D work. Demonstrate knowledge in lab safety. Participate in preparation of scientific articles and perform oral presentations of R&D work. Visit customer sites as part of a team and independently. Preferred Qualifications Advanced analytical electrochemistry experience with your OWN and NEW ideas on how to perform analysis using electrochemical methods. Experience in semiconductor industry is desired Laboratory work experience is necessary Minimum Qualifications Doctorate (Academic) Degree OR Master's Level Degree and related work experience of 3 years OR Bachelor's Level Degree and related work experience of 5 years The company offers a total rewards package that is competitive and comprehensive including but not limited to the following: 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. 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.

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

Job Title: Analytical ChemistJob Description We are seeking a dedicated and detail-oriented Analytical Chemist to join our dynamic team, supporting both Production and R&D operations. This role involves performing critical analyses using HPLC, GC-MS, NMR, and other analytical techniques, ensuring the success of kilo-scale production and small molecule development. This position offers an exceptional opportunity to leverage your expertise in analytical chemistry to support the production and development of high-quality materials. Join us and take a pivotal role in shaping innovation, advancing precision, and driving excellence in laboratory operations. Responsibilities + Update and optimize methods for HPLC/MS analysis, ensuring accuracy and compliance with established protocols. + Perform routine and advanced analyses using HPLC-MS, NMR, GC-MS, and other analytical instruments as required. + Maintain, calibrate, and troubleshoot analytical equipment to ensure operational efficiency and reliability. + Ensure the analytical laboratory remains clean, organized, and fully operational. + Accurately document all analysis results in logbooks, laboratory notebooks, and digital systems. + Troubleshoot and resolve issues with analytical methods or equipment to minimize downtime. + Support kilo production processes by assisting with chemical reactions, distillation, extraction, filtration, chromatography, crystallization, and related tasks. + Help maintain cleanliness and organization of work areas while ensuring all documentation and logbooks are accurately completed and up-to-date. + Conduct laboratory experiments (wet chemistry) to support process chemists in method development and process optimization. + Maintain accurate and detailed experimental records and laboratory notebooks. Essential Skills + Proficiency in using analytical instruments (e.g., HPLC-MS, GC-MS, NMR, UV-Vis, FTIR, etc.). + Strong communication, time management, organizational skills, and attention to detail. + 3-7 years of experience in a laboratory environment, preferably in a regulated industry. + Experience managing multiple projects and ensuring timely delivery of results. + Familiarity with industry-standard EHS protocols and regulatory requirements (FDA, ISO, GMP). Additional Skills & Qualifications + Minimum of a bachelor's degree in Chemistry, Biochemistry, or a related scientific field (required). + Master's or Ph.D. in Analytical Chemistry or a related field (preferred). Work Environment Work in a small, fast-paced manufacturing company with a successful history in the discovery and development of specialty ingredient technologies. The facility includes a large lab space, despite having a 10-person worksite team. You will have the opportunity to work on cosmetics for big brand names, contributing to stable revenue and innovation, including the launch of an innovative skincare product by 2026. The team is very willing to train and develop people long-term as long as they are motivated and driven. Pay and Benefits The pay range for this position is $38.00 - $49.00/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 Fairfield,NJ. Application Deadline This position is anticipated to close on Mar 18, 2025. 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. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: + Hiring diverse talent + Maintaining an inclusive environment through persistent self-reflection + Building a culture of care, engagement, and recognition with clear outcomes + Ensuring growth opportunities for our people 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 process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

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

Symrise is a global supplier of fragrances, flavors, food, nutrition, and cosmetic ingredients. Its clients include manufacturers of perfumes, cosmetics, food and beverages, pharmaceuticals and producers of nutritional supplements and pet food. Its sales of € 4.7 billion in the 2023 fiscal year make Symrise a leading global provider. Headquartered in Holzminden, Germany, the Group is represented by more than 100 locations in Europe, Africa, the Middle East, Asia, the United States and Latin America. Symrise works with its clients to develop new ideas and market-ready concepts for products that form an integral part of everyday life. Economic success and corporate responsibility are inextricably linked as part of this process. Symrise - always inspiring more… * Performs sample preparation for GC(-MS), HPLC(-MS) analysis. Operates GC(-MS), HPLC, and FTIR instrumentation and interprets data using company specific evaluation and reporting software, reporting results in a timely fashion. Make entries & updates to laboratory sample database. * Maintaining, troubleshooting, and sometimes repairing GC(-MS), HPLC, FTIR, other lab equipment and instruments. * Participation within the global analytical team on cross-regional projects. * Maintain contact with analytical personnel in GmbH and other Symrise subsidiaries worldwide to keep appraised of new technology and developments within within TN&H. * Provide technical support as requested to creative, flavor ingredients research team, applications, sales, QC, affiliates, and to outside customers. * As a project team member, participate with flavorists and applications personnel in evaluation of flavors and flavored products. Present test results and provide suggestions to improve flavor systems to meet customer requirements. Knowledge and Experience Requirements: * MS in Food Science, Chemistry, or a related field with 3-5 years of experience & training or PhD in Food Science, Chemistry, or a related field. * Interest in data analysis is a plus. * Thorough knowledge of flavor and food chemistry and ingredients and extensive experience in flavor analysis. * Demonstrated success in working on analytical teams and analytical research projects. Skills & Abilities: * Must be skilled in operating, troubleshooting, and maintaining GC(-MS) instruments, preferably also HPLC(-MS) instruments. Some basic instrument repair experience is a plus. * Must be a team player, able to work effectively and coordinate with scientists, flavorists, business managers and customers. * Accuracy and attention to detail in documentation, in operating analytical instruments, sample preparation and product testing. * Able to plan, organize, and execute the testing & analysis of a high volume of varied sample types, producing consistently high-quality results. * Possess good organizational and communication skills. Able to write clear, concise reports and effectively present and discuss results to all audiences, including customers. * Formal project management training will be provided. Safety/Regulatory Training Requirements * OSHA HAZCOM, CHP & lab safety, DOT awareness, RCRA waste management, ISO 9000 training per company policy. Working Conditions: * Normal laboratory/ office environment Become part of our open and transparent culture. It will give you the opportunity to flourish and to develop inspiring experiences that contribute to the health and well-being of consumers in 160 countries around the world. Putting our employees in focus fuels our strong company growth above market rates and makes us an excellent place to develop your career. Come join us and embark on a fascinating journey with Symrise. If you feel that you fit the above criteria, then please apply by using our online application system. Your application will be treated confidentially. We are an Equal Opportunity Employer. We do not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need.

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.

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