Quality control analyst jobs in Clinton, NJ - 144 jobs

MACOM designs andmanufactures semiconductor products for Data Center, Telecommunication, and Industrial and Defense applications. Headquartered in Lowell, Massachusetts,MACOM has design centers and sales offices throughout North America, Europe,and Asia. MACOM is certified to the ISO9001 international quality standard and ISO14001 environmental management standard. MACOM has more than 65years of application expertise with multiple design centers, Si, GaAs and InPfabrication, manufacturing, assembly and test, and operational facilitiesthroughout North America, Europe, and Asia. In addition, MACOM offers foundry servicesthat represents a key core competency within our business. MACOM sells anddistributes products globally via a sales channel comprised of a direct fieldsales force, authorized sales representatives, and leading industrydistributors. Our sales team is trained across all of our products to give ourcustomers insights into our entire portfolio. Title: Quality ControlInspector Asa Quality Inspector, you will be responsible for verifying all requireddocuments that are involved/required with the parts/products you areinspecting. Document any non-conformances in detail on the Company's Q-notesystem. This includes all areas of quality control, incoming inspection, in-processinspection and final inspection. When not working with the microscope, you willbe verifying measurements with handheld measuring tools. Key Responsibilities: Perform incoming inspection, in-process inspection, first article inspection and final inspection of electronic and mechanical components with little to no assistance. Schedule source inspections as required. Generate internal and external reports. Generate and maintain data for the control of documentation, effectively report information, and accurately respond to questions from team members, internal suppliers, and customers. Communicate non-conformances and work with Quality and Manufacturing to drive corrective actions. Ensure all incoming, in-process and final materials meet specifications. Perform routine SAP transactions to move, disposition, and route material. Key Competencies & Skills Required: Safe handling of ESD sensitive materials. Working knowledge of SAP, Agile, Excel, MSWord and Outlook. Ability to prepare oral and written reports clearly and concisely. Excellent internal and external communication skills. Advanced understanding of quality control standards and testing techniques. Knowledge of statistical sampling techniques. Able to lift up to 20 pounds. Able to sit for periods of time working with a microscope. Required Qualifications and Experience: High School diploma (or equivalent) or AS degree (preferred). Minimum 2 years Quality Control inspection experience (preferred). Self-motivated with the ability to evaluate complex issues in a high-pressure environment. Knowledge of all aspects of inspection and testing. Experience with Mil-PRF-38534, class H & K; Hybrids, Mil-STD-883; methods 2008, 2009, 2010, 2017 Semiconductors and Passive devices. Knowledge of IPC-600 and 610, J-STD-001. Knowledge and experience in performing mechanical and electronic inspections. Ability to work from technical drawings, sketches and specifications. Due to ITAR regulations, U.S. citizenship or permanent residency required. The Salary Range for this position is $25.00-$28.00.Actual salary offered to candidate will depend on several factors, includingbut not limited to, work location, relevant candidates' experience, education,and specific knowledge, skills, and abilities. Benefits: This position offers a comprehensive benefits packageincluding: Health, dental, and vision insurance. Employer-sponsored 401(k) plan. Potential for performance-based bonus. Paid time off. Professional development opportunities. EEO: MACOM is an EqualOpportunity Employer committed to a diverse workforce. MACOM will not discriminateagainst any worker or job applicant on the basis of race, color, religion, sex,gender identity, sexual orientation, national origin, age, disability, geneticinformation, veteran status, military service, marital status, or any othercategory protected under applicable law. Reasonable Accommodation: Reasonable Accommodation. MACOM is committed to working with and providingreasonable accommodations to qualified individuals with physical and mentaldisabilities. If you have a disability and are in need of a reasonableaccommodation with respect to any part of the application process, please call+1-978-###-#### or email [email protected]. Provide your name, phone number andthe position title and location in which you are interested, and nature ofaccommodation needed, and we will get back to you. We also work with currentemployees who request or need reasonable accommodation in order to perform theessential functions of their 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 ******************************.

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Title: Scientist I Duration: 6 Months (Possibility of Extension) Location: Ewing NJ 08628 Shift - Can be flexible, can start as early as 7:30 AM (end at 4 PM), up to 9 AM (end at 5:30 PM) Job Description The Analytical Scientist will be involved in the design, planning, organization and evaluation of drug product and combination drug/device product development. They will perform analytical testing on formulation and manufacturing intermediate dosage forms as well as inhalation devices (aerosol performance testing) as part of a project team within Analytical Chemistry. The position requires use and application of analytical chemistry principles, theories, and concepts. Work is directly supervised. The Analytical Scientist will follow established procedures and methodologies and contributes to completion of routine scientific/technical tasks and has limited discretion to vary from established procedures. Ability to work both closely with other team members from various disciplines as well as the ability to work independently when needed. The Analytical Scientist will assist with the development of new procedures and methodologies (based on prior established techniques at this site) to develop solutions to solve scientific/technical problems of limited scope. Qualifications Mandatory and/or minimum requirements: Prior experience with aerosol performance testing of inhalation dosage forms is required - (1 year or more of experience is required) Prior experience with aerosol performance testing in a pharmaceutical environment (R&D preferred but QC setting acceptable) Ability to work in a team-based / collaborative environment Excellent documentation skills Desirable attributes/qualifications: Prior experience with Waters Alliance HPLCs and Empower Prior experience creating technical documents including standard operating procedures and reports Prior experience with MS Word, Excel, and PowerPoint for presenting data Attention to detail in execution and documentation Required levels experience and/or education: BS/MS in Chemistry or a related field, 3-7 yrs of experience (1-3 years could be considered depending upon relevance of experience to our needs) Additional Information Feel free to forward my email to your friends/colleagues who might be available. We do offer referral bonus Thank you for your time and consideration. I look forward to hearing from you! Kind Regards Ruchi Kumari Clinical Recruiter Integrated Resources, Inc. IT Life Sciences Allied Healthcare CRO Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I (DIRECT BOARD) # 732-844-8716 (F) 732-549-5549 LinkedIn: https://www.linkedin.com/in/ruchi-kumari Gold Seal JCAHO Certified ™ for Health Care Staffing “INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)

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.

**General Description:** Perform QC Chemistry laboratory activities with a primary focus on capillary electrophoresis techniques to support GMP manufacturing, testing, and release of material, intermediates and finished biological products (monoclonal antibodies) under FDA/EU regulations, applicable International Regulations, and BeOne Medicines' processes and procedures. **Essential Functions of the job:** + Perform routine and non-routine testing using capillary electrophoresis techniques (e.g., CE-SDS, CZE, ic IEF) in the QC Chemistry laboratory to ensure timely and compliant generation and reporting of in-process, release, and stability test results in support of manufacturing operations. + Review, interpret, and report analytical data in accordance with GMP regulations and internal procedures. + Lead troubleshooting efforts for analytical methods and instrumentation related to CE. + Conduct laboratory investigations, including OOS, Out of Trend, deviations, and invalid assays. + Implement corrective actions and preventive actions (CAPAs). + Participate in transfer and method validation activities, including protocol preparation, protocol execution, and report preparation. + Support routine operations, including but not limited to instrument qualification and maintenance, SOP generation and revision, test record keeping, etc. + Maintain equipment in a qualified and calibrated state, coordinating with metrology or vendors as needed. + Manage inventory of reagents and supplies for the laboratory. + Participate in internal and external GMP audits, as needed. + Train other junior level analysts and new hires on CE instrumentation, GMP practices, and data analysis. + Serving as subject matter expert in one or more areas of required testing. + Interacts with all levels of BeOne employees. + Undertake other duties as required. **Education/Experience Required:** + Bachelor's or above in Chemistry, Biochemistry, or Biotechnology related scientific discipline. + Minimum of 4+ years of working experience in an FDA-regulated biotechnology, pharmaceutical company are required. + Familiar with Waters Empower Chromatography Data System. + Familiar with instrument and equipment validation. Impressive, demonstrable track record and skills/experience gained within a similar position(s), at a similar level. Working knowledge with USP/EP and cGMP/EU GMP regulations. + Impressive, demonstrable track record and skills/experience gained within a similar position(s), at a similar level. + Credible and confident communicator (written and verbal) at all levels. + Strong analytical and problem-solving ability. + Hands-on approach, with a 'can do' attitude. + Ability to prioritize, demonstrating good time management skills. + Excellent attention to detail, with the ability to work accurately in a busy and demanding environment. + Self-motivated, with the ability to work proactively using own initiative. + Committed to learning and development. **Computer Skills:** + Strong PC literacy required; MS Office skills (Outlook, Word, Excel, PowerPoint). **Travel:** + Must be willing to travel approximately 10%. + Ability to work on a computer for extended periods of time. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

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 is a Consumer Products/Personal Care company and they are now looking for a QC Chemist. Salary/Hourly Rate: $25/hr - $30/hr Position Overview: They are looking for an experienced QC Chemist to join their team. This role involves performing analytical testing and quality control in a regulated laboratory setting, ensuring products meet quality and regulatory standards. The ideal candidate is detail-oriented, collaborative, and committed to meeting deadlines. Responsibilities of the QC Chemist: * Perform quality control testing on raw materials and finished products using analytical techniques such as HPLC, UPLC, GC, UV-Vis, FT-IR, dissolution testing, and particle size analysis. * Process, analyze, and accurately report analytical data while maintaining detailed laboratory documentation in compliance with cGMP requirements. * Troubleshoot analytical methods and laboratory instruments to ensure consistent and reliable test results. * Ensure products meet internal quality standards and regulatory requirements while collaborating with QA to maintain GMP compliance. * Operate, calibrate, maintain, and perform routine troubleshooting on laboratory instruments. * Work closely with R&D and production teams to support product development, investigations, and product release. * Provide guidance and technical support to junior laboratory staff when needed. Required Experience/Skills for the QC Chemist: * 3 - 7 years of experience working in an analytical laboratory environment. * Hands-on experience with HPLC/UPLC, GC, UV-Vis, FT-IR, and dissolution testing. * Strong knowledge of GMP, GLP, and regulatory standards. * Excellent documentation practices and strong data interpretation skills. Preferred Experience/Skills for the QC Chemist: * Strong attention to detail with effective problem-solving abilities. * Clear written and verbal communication skills in English. Education Requirements: * Bachelor's degree in Chemistry, Analytical Chemistry, Biochemistry, Biology, or a related field. Benefits: * Medical, Vision, and Dental options, 401K, Life Insurance, Short & Long Term Disability, PTO reimbursement, and more through Atrium Staffing.

As a QC Chemist, you will be responsible for performing day-to-day laboratory activities under prescribed procedures, including qualitative and quantitative analysis, solution preparation, calibration, qualification, and maintenance of laboratory instrumentation. You will also conduct environmental monitoring, assist with technical writing, and perform administrative tasks. Additionally, you will contribute to solving problems, reviewing experimental data, writing protocols/SOPs/validation reports, and training support staff as necessary. You will monitor study procedures to ensure data accuracy and report quality while maintaining a GMP/GLP laboratory. Responsibilities * Conduct analysis in compliance with cGMP requirements, compendia standards, and internal procedures. * Maintain accurate records of analysis and perform documentation to company standards. * Prepare test solutions, volumetric solutions, and samples used in analysis. * Perform assigned sampling, physical, chemical tests and assays on raw materials, active pharmaceutical ingredients, in-process, finished bulk, finished product, and stability products analysis in an FDA regulated lab environment. * Use a variety of analytical instruments such as HPLC, GC, Dissolution, Malvern particle size analyzer, IR, Auto Titrator, UV Spectrophotometer, KF, Potentiometer, etc. * Perform analysis with a practical understanding of the test procedure and instrument operation. * Conduct laboratory investigations under the supervision of the laboratory manager. * Perform maintenance and calibrations of laboratory instruments/equipment. * Comply with all regulatory and in-house requirements including safety, housekeeping, laboratory chemical waste, cGMP, cGLP, and documentation. * Maintain the required level of training needed to perform GMP tasks. * Prepare and/or review test procedures, SOPs, and protocols as assigned. Essential Skills * Proficiency in current Good Manufacturing Practices (cGMP), FDA, and other regulatory requirements. * Experience with analytical techniques such as Dissolution, FT-IR, GC, UV-VIS, KF, TLC. * Knowledge of computer applications and programs related to laboratory applications such as HPLC, FTIR, TOC. * Familiarity with sampling methods and quality control systems. * Understanding of mathematics including statistics. * Proficiency in sample preparation techniques, spectroscopic techniques, and chromatographic systems. * Basic computer knowledge including MS Word, Excel, and Outlook. * 3-5 years of routine testing using HPLC and Dissolution. * Experience with solid oral dosage and focus on raw material, finished product. * Pharma GMP experience, laboratory, wet chemistry, titration, chromatography. Additional Skills & Qualifications * Bachelor's or master's degree in Pharmaceutical, Biological, Chemical science or related field. * 5-6 years of related laboratory work experience; minimum of 5 years as a QC Chemist in a GMP environment. * Ability to work successfully in both a team/matrix environment and independently. * Ability to work in a fast-paced environment, manage priorities and maintain timelines for multiple projects. * Ability to work safely in a chemical laboratory. * Ability to perform basic calculations, read, write, communicate, and handle stress produced by time pressure, customer demands, etc. * Must be able to access all laboratory, manufacturing, and office areas. * Must be able to wear the required PPE for entering laboratory and processing areas. * Specific vision requirements include reading written documents and using a computer. * Ability to sit or stand for prolonged periods and occasionally lift up to 25 lbs. with or without assistance. Work Environment You will be working in a laboratory setting with approximately 10 people. The laboratory is equipped with modern instrumentation and follows strict safety and regulatory protocols. The work environment requires wearing personal protective equipment (PPE) and involves standing or sitting for prolonged periods. The laboratory operates under a fast-paced and dynamic atmosphere, providing an excellent opportunity for growth and development. Pay and Benefits The pay range for this position is $30.00 - $40.00/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 Cranbury,NJ. Application Deadline This position is anticipated to close on Apr 30, 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 for other accommodation options.

Gelest, Inc., part of the Mitsubishi Chemical Group, is hiring a Development Chemist to join our team in Morrisville, PA. This role offers the opportunity to contribute to our mission of delivering innovative specialty chemical solutions to customers worldwide. The Development Chemist will play a key role in designing, developing, and optimizing chemical processes for specialty chemical products. This hands-on role involves synthetic organic chemistry, process development from lab to pilot scale, and data acquisition and analysis to ensure safe, reliable, and cost-effective manufacturing. The Development Chemist will collaborate closely with Product Development, Engineering, Production, and Quality teams to translate laboratory discoveries into scalable processes that meet business and regulatory requirements. **PRINCIPAL ACCOUNTABILITIES:** + Design and perform laboratory experiments involving synthetic organic reactions, route evaluation, optimization, and troubleshooting. + Generate and analyze process data to identify improvement opportunities. + Scale laboratory processes to pilot and full production, ensuring robust transfer of technology and clear documentation. + Utilize analytical techniques (GC, NMR, FTIR, MS) to characterize materials, monitor reactions, and assess process performance. + Document experiments, observations, and recommended improvements in lab notebooks and technical reports. + Support process hazard assessments, safety reviews, and compliance with environmental, health, and safety regulations. + Maintain awareness of industry developments, new technologies, and specialty chemical manufacturing best practices. + Perform other duties as assigned. **KNOWLEDGE/ EXPERIENCE/SKILLS:** To perform the job successfully, an individual should demonstrate the following competencies: + Bachelor's degree in Chemistry, Chemical Engineering, or a related field. Master's degree preferred. + 1-3+ years of experience in specialty chemical synthesis, chemical process development, or scale-up preferred. + Hands-on experience with laboratory techniques and equipment preferred. + Background in synthetic organic chemistry, including multi-step synthesis and reaction mechanism understanding is preferred. + Experience with process development, including reaction kinetics, heat, and mass transfer, mixing, and scale-up considerations is preferred. + Hands-on experience with analytical instrumentation (GC, NMR, FTIR, MS) is preferred. + Excellent written and verbal communication, including technical reporting. + Commitment to maintaining a safe and compliant work environment. + Must be able to wear required PPE (safety shoes, glasses, gloves, hard hat; respirators as needed). + Must be able to climb ladders and stairs to collect samples and observe processes. + Must be able to lift up to 50 pounds and operate a forklift. + **Must be able to work 2nd shift:** Four (4) 10-hour shifts, Monday-Thursday, 12:30 PM - 11:00 PM **Supplemental Company Information:** Gelest, located in Morrisville, PA-conveniently accessible from Interstate 95, Route 1, and the PA/NJ Turnpikes-offers a rewarding career with competitive pay and a comprehensive benefits package, including: + Generous paid time off + Medical, Dental, Vision, and optional supplemental plans for employees and their families + 401(k) with a competitive company match + Company-paid Life Insurance, AD&D, Short-Term Disability, and Long-Term Disability + Eligibility for an annual performance bonus + Company-provided uniforms, work boots, and PPE The salary range for this position is $27.00 (entry level) - $35.00 per hour. Factors such as scope and responsibilities of the position, candidate's work experience, education/training, job-related skills, internal peer equity, as well as market and business considerations may influence base pay offered. This salary will be subject to a geographic adjustment (according to a specific city and state), if an authorization is granted to work outside of the location listed in this posting.

Now Hiring! Analytical Associate Chemist (ECT-Chemetall) Come create chemistry with us! BASF/Chemetall, is the Surface Treatment global business unit of BASF's Coatings division, operating under the Chemetall brand, and a leading supplier of applied surface treatments worldwide. At BASF/Chemetall, we develop and manufacture tailor-made technology and system solutions for applied surface technology. Our products protect metals from corrosion, facilitate forming and treatment, prepare parts optimally for the painting process and ensure excellent coating adhesion. Our technologies and products are used in a variety of industries and end markets such as automotive, aerospace, aluminum finishing and metal forming. The chemical treatment of metal surfaces is BASF/Chemetall core competence. The focus of our worldwide activities is on the development and implementation of customized technology and system solutions for surface treatment. We are looking for a Analytical Associate Chemist to join our Technical Service team in New Providence, NJ. This position will perform routine testing and provide analytical support for the Corporation. The ideal candidate will complete any special projects as requested by the Analytical Specialist. As a Analytical Associate Chemist (ECT-Chemetall), you create chemistry by... * Performs required analytical tests on customer's samples from the field and on samples submitted by team leaders. * Writes clear, concise lab reports on work completed, making appropriate recommendations with the assistance of the Analytical Specialist and other technical resources. * Learns operation and maintenance of all analytical instrumentation; assists in troubleshooting problems. * Maintains supplies for all analytical requirements in accordance with Chemetalls quality system. * Maintains calibration and validation equipment log for lab instrumentation. * Works with Technical Service and support manager to log in solution analysis projects daily and maintaining these logs for the New Providence Lab. * Prepares and presents seminars/lectures to the department on analytical topics. * Works with analytical team members to develop new test procedures as required. * Continuously upgrade technical skills by working in the laboratories with other technical personnel, staying abreast of technical developments, reading journals, and learning new methods of analysis. * Attend industry seminars and in-house seminars to keep current with new technologies. * Polish written and verbal communication with technical and business stakeholders; continue to improve computer skills and learn new digitalization tools. * Works in the analytical laboratory in a safe and clean manner. * Maintain laboratory equipment in accordance with Chemetall/BASF's quality system; maintain appropriate inventory levels of analytical supplies. If you have... * Bachelor's Degree in Chemistry or Chemical Engineering is required * 3-5 years' industrial experience. * Prior lab experience is required (understanding of lab procedures, use of chemicals, importance of safety) * Prior lab testing experience is required. * Prior experience with analytical equiptment. * Experience is data science is preferred. * Strong analytical/computer skills required. * Excellent communication skills, both verbal and written. * Ability to maintain lab supplies, manage inventory, and order lab supplies. * Travel: 10% as needed. Create your own chemistry with you@BASF At BASF, you will have the chance to do meaningful work towards building a more sustainable future. In addition to competitive compensation and benefits, BASF provides you with access to a wide range of elements to help you be your best. It's what we call you@BASF. We are committed to providing benefits, programs, and opportunities that support our employees' overall well-being, personal growth, and a safe, collaborative, and inclusive work environment. Just some of the many benefits we offer include: * Flexible work arrangements whenever possible * Highly competitive retirement savings plan with company match and investment options * Well-being programs that include comprehensive mental health support for you and your household family members * Family forming benefits (fertility, adoption and surrogacy reimbursement, maternity/parental leave, and more) * Back-up child and elder care with discount programs for families of all ages and stages * Mentoring and career development opportunities that allow you to share, learn, and thrive * Matching gifts program that allows you to deepen the impact of your contributions to qualified charities. * Employee crisis support for when the unexpected happens * Access to our BASF wine cellar, employee discounts, and much more! About us As one of the largest chemical companies in North America we have been finding solutions for your everyday needs and addressing the most complex economic, environmental, and sustainability challenges for more than 150 years! At BASF we empower our employees with the tools, guidance and opportunities they need to advance and succeed in work and life. Giving you the support you need to be your best and fulfill your personal ambitions is what helps us create chemistry. After all, our success is linked to yours. Whatever path you envision, BASF is a great place to build a rewarding, successful career. Belong to Something Bigger. #belongat BASF Privacy statement BASF takes security & data privacy very seriously. We will never request financial information of any kind via email, private text message or direct message on any social medial platform or job board. Furthermore, we will never send a candidate a check for equipment or request any type of payment during the job application process. If you have experienced any of the above, please contact ***************************** to report fraud. Pay transparency BASF is committed to pay transparency practices. The competitive Pay Range for this role is $65,000-$70,000. Actual pay will be determined based on education, certifications, experience, and other job-related factors permitted by law. Equal employment opportunities We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, age, citizenship, color, religion, sex, marital status, national origin, disability status, gender identity or expression, protected veteran status, or any other characteristic protected by law. Applicants must be currently authorized to work in the United States on a full-time basis.

A primary focus of this role is creating and modifying LIMS test plans to support QC activities while adhering to regulatory and data integrity guidelines. The LIMS Coordinator is responsible for tracking and managing laboratory inventories within the LIMS system and to perform and verify daily verification of laboratory data for accuracy and completeness, ensuring compliance with GxP standards before submission for review. Essential Functions: Register samples and input relevant test results, instrument data, and laboratory information into the LIMS system as per QC procedures. Manage laboratory inventories, ensuring timely replenishment and accurate record-keeping within the LIMS system as well as generate and run standard reports from the LIMS system for Laboratory Resource tracking. Perform and verify daily verification data for accuracy and completeness before submitting it for review. Create, troubleshoot and modify LIMS Test, worksheets, and test plans as needed to support QC activities. Train new peers in LIMS operations, including sample manager and resource modules. Assist QC personnel with sample registration and label generation using the LIMS software Additional Responsibilities: Performs other functions as required or assigned. Hands on to follow compendial (USP/EP/BP/JP) procedures for wet chemical tests. Must understand and apply cGMP requirements applicable to quality control laboratory. Follow up on sample status and testing progress within the LIMS system. Participate in continuous improvement initiatives to optimize LIMS functionality and workflows. Education: Associate Degree - Required Bachelors Degree (BA/BS) Chemistry or related field - Preferred Experience: 1 year or more in Pharmaceutical/manutfacturing Skills: Proficient in laboratory informatics - Intermediate Strong understanding of regulatory compliance (FDA, GMP). - Intermediate Proficiency in inventory management systems and data analysis tools. - Intermediate Excellent organizational, communication, and problem-solving skills. - Intermediate The hourly rate for this position ranges from $22.00 to $26.00 per hour. In addition, Amneal offers a short-term incentive opportunity, such as a bonus or performance-based award, with this position within the first 12 months. Amneal ranges reflect the Company's good faith estimate of what Amneal reasonably believes that it will pay for said position at the time of the posting. Individual compensation will ultimately be determined based on a variety of relevant factors, including but not limited to, qualifications, experience, geographic location and other relevant skills. At the heart of our Total Rewards commitment is a comprehensive, flexible and competitive benefits program for eligible positions that enables you to choose the plans and coverage that meet your personal needs. This includes above-market, diverse and robust health and insurance benefits to meet the varied needs of our employees as well as a significant 401(k) matching contribution to help our employees save for retirement. We also promote employee well-being with programs that help you enjoy your career alongside life's many other commitments and opportunities.

SGS is the world's leading Testing, Inspection and Certification company. We operate a network of over 2,700 laboratories and business facilities across 119 countries, supported by a team of 99,250 dedicated professionals. With over 145 years of service excellence, we combine the precision and accuracy that define Swiss companies to help organizations achieve the highest standards of quality, safety and compliance. Our brand promise, when you need to be sure , underscores our commitment to reliability, integrity and trust - enabling businesses to thrive with confidence. We proudly deliver our expert services through the SGS name and trusted specialized brands, including Brightsight, Bluesign, Maine Pointe and Nutrasource. SGS is publicly traded on the SIX Swiss Exchange under the ticker symbol SGSN (ISIN CH0002497458, Reuters SGSN.S, Bloomberg SGSN:SW). Our Dayton, NJ laboratory is looking for a Laboratory Analyst to join their AIR team! The Laboratory Analyst prepares and analyzes samples with accuracy and precision in accordance to SGS' analytical SOPs. The Laboratory Analyst works independently and as part of a team to meet daily production targets and ensure hold times and turnaround times are met. The Laboratory Analyst understands and applies basic analytical chemistry principles. The Laboratory Analyst always follows safe laboratory practices and maintains a safe working environment. Job functions: After appropriate training independently prepares and analyzes samples according to SGS' analytical SOPs using instrumentation specific to the department and analytical methodologies Performs routine operation, maintenance, calibration of laboratory instruments/equipment May assist with validation and MDL studies. Assists with investigation, and preparation of responses to client inquiries and CARs. Inputs and maintains technical information as needed to support the laboratory functions/operations. Maintains Laboratory Notebook where applicable. Adheres to internal standards, policies and procedures. Performs other duties as assigned. Qualifications Associate Degree in a Chemistry or similar scientific discipline and 0-2 years of experience in Analytical Chemistry Laboratories OR 3 years of relevant experience (i.e. Sample Prep) (Required) Bachelor's Degree in a Chemistry or similar scientific discipline and 1-2 years of years' relevant experience in Analytical Chemistry Laboratories (Preferred) Basic mathematical and reasoning skills (Required) Experience with Microsoft Office (Excel, Outlook, Word) (Required) Experience with LIMS (Preferred) Ability to lift/carry/push and/or pull upwards of 25 lbs on a frequent basis (Required) Additional Information SGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, color, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression, genetics, status as a protected veteran, or any other characteristics protected by law. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skills, and/or abilities required. This job description should not be construed as an exhaustive statement of duties, responsibilities or requirements, but a general description of the job. Nothing contained herein restricts the company's rights to assign or reassign duties and responsibilities to this job at any time. If you are applying for a position within the United States and you have difficulty completing the on-line employment application because of a disability, please call ************ for assistance and leave a message. You will receive a call back. Please note, this phone number is not for general employment information, but is only for individuals who are experiencing difficulty applying for a position due to a disability.

Are you looking for a job that's both challenging and fun? US Cannalytics is looking for a candidate that seeks a challenging Chemistry Laboratory Technician position in the exciting and ever-evolving medical cannabis industry. The successful candidate will be reliable, exhibit strong attention to detail and thrive in a fast-paced laboratory environment LABORATORY TECHNICIAN QUALIFICATIONS, must: Have a valid driver's license and high school diploma or equivalent. 21+ years old and subject to applicable employment requirements for the state of Pennsylvania for cannabis businesses including criminal background check. 2 years of relevant, professional (non-academic) laboratory experience or 1 year of laboratory experience plus a skills assessment. LABORATORY TECHNICIAN RESPONSIBILITIES: The laboratory technician is responsible and accountable for the testing, quality control, and tracking of cannabis material. The laboratory technician will ensure the safe, accurate, and timely testing of cannabis products. ESSENTIAL DUTIES: Proficiently utilize Microsoft Word and Excel, and other laboratory information management systems. Work in a timely manner, while striving to improve quality and maintain accuracy during all laboratory activities. Follow organizational policies and procedures for laboratory operations and comply with all state-specified rules and regulations for cannabis licenses, cannabis transport and cannabis testing, as applicable. Responsible for accurate measurements and documentation of all cannabis and cannabis materials, including sample weights/volumes, compliant cannabis tracking and destruction, and completion of supporting laboratory documentation. Adhere to Good Documentation Practices (GDP) for the completion of laboratory logs, forms, worksheets, or other documentation. Maintain laboratory reagent and supply inventory, including compliant documentation. Assists with the performance of sample intake and accessioning, and non-analytical test methods (foreign material, water activity, moisture content, etc.), as needed. Participate in and endeavor to complete training and be determined competent for assigned test methodologies including the following steps: a. Sample collection, intake and homogeneity. b. Sample preparation across all applicable matrices. c. Reagent preparation, including safe handling, storage and disposal. d. Sample loading and initial data analysis performed under the technical supervision of a Laboratory Chemist. e. Daily performance checks of applicable analytical equipment and method test parameters. f. Regular instrument cleaning and preventative maintenance for applicable analytical equipment. g. Basic troubleshooting of testing methodologies including all items listed within this sub-section. For test methods the employee has been trained and determined competent for: a. Independently prepare samples using aseptic techniques, including compliant documentation and necessary updates to laboratory workflow. b. Independently prepare reagents, solutions, and substrates for the equipment necessary for testing, including compliant documentation and necessary updates to laboratory workflow. c. Perform initial data analysis under the technical supervision of a Laboratory Chemist or Microbiologist. d. Assist in equipment and method validations or verifications, including compliant documentation and necessary updates to laboratory workflow. e. Successful completion of proficiency testing samples, completed as part of ongoing competency within the test method. Perform all other tasks and duties as assigned by Management, which may include cannabis sampling and transport. WORK ENVIRONMENT: The work environment characteristics described below 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. Work is performed in a production laboratory environment and requires use of personal protection equipment to limit exposure to chemicals or other hazards found within a laboratory environment. Work environment is fast-paced and will require frequent pivoting and multitasking, as well as the reprioritization of tasks based on demand/urgency. The work environment may expose employee to fumes or airborne particles, moving mechanical parts and vibration. The noise level in the work environment may be loud. Per state requirements for this industry, the facility is secured by user-specific access and is surveillance by cameras located throughout the laboratory except in restrooms. PHYSICAL DEMANDS: The physical demands described 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. Ability to concentrate and consistently produce accurate work. Frequent standing, walking, sitting, and use hands. Occasionally lift and/or move up to 40 pounds. Visual requirements to include close vision, color vision and ability to adjust focus. WORK HOURS: Wednesday - Saturday (training and competency determined on a Monday-Friday schedule) Job Type: Full-time, 10-hour shifts Benefits: Dental insurance Health insurance Paid time off Vision insurance Schedule: Tuesday-Saturday 10 hour shifts Overtime available Work Location: In person Job Type: Full-time Compensation: $20-$22 / hour Expected hours: 40 - 45 per week Education: High school or equivalent (required) BS in a natural science (preferred) Experience: Laboratory: 1 year (required) Analytical chemistry in a high-volume laboratory setting: 2 years (preferred) Laboratory sample extractions: 2 years (preferred) Agilent HPLC and/or GC: 2 years (preferred) Cannabis: 1 year (preferred)

Inspection and Testing: Perform routine inspections and tests on finished goods and/or components according to established procedures and specifications. This may involve physical inspections, physiochemical analyses, or using specialized functionality testing equipment. Documentation and Record Keeping: Maintain accurate and complete records of all inspections, tests, and results. This includes entering data into databases, filing reports, and maintaining laboratory inspection plan. Equipment Maintenance and Calibration: Assist in the routine maintenance and calibration of laboratory equipment. Ensure that all equipment is in good working order and meets required standards.

MACOM designs and manufactures semiconductor products for Data Center, Telecommunication, and Industrial and Defense applications. Headquartered in Lowell, Massachusetts, MACOM has design centers and sales offices throughout North America, Europe, and Asia. MACOM is certified to the ISO9001 international quality standard and ISO14001 environmental management standard. MACOM has more than 65 years of application expertise with multiple design centers, Si, GaAs and InP fabrication, manufacturing, assembly and test, and operational facilities throughout North America, Europe, and Asia. In addition, MACOM offers foundry services that represents a key core competency within our business. MACOM sells and distributes products globally via a sales channel comprised of a direct field sales force, authorized sales representatives, and leading industry distributors. Our sales team is trained across all of our products to give our customers insights into our entire portfolio. Title: Quality Control Inspector As a Quality Inspector, you will be responsible for verifying all required documents that are involved/required with the parts/products you are inspecting. Document any non-conformances in detail on the Company's Q-note system. This includes all areas of quality control, incoming inspection, in-process inspection and final inspection. When not working with the microscope, you will be verifying measurements with handheld measuring tools. Key Responsibilities: * Perform incoming inspection, in-process inspection, first article inspection and final inspection of electronic and mechanical components with little to no assistance. * Schedule source inspections as required. * Generate internal and external reports. * Generate and maintain data for the control of documentation, effectively report information, and accurately respond to questions from team members, internal suppliers, and customers. * Communicate non-conformances and work with Quality and Manufacturing to drive corrective actions. Ensure all incoming, in-process and final materials meet specifications. * Perform routine SAP transactions to move, disposition, and route material. Key Competencies & Skills Required: * Safe handling of ESD sensitive materials. * Working knowledge of SAP, Agile, Excel, MSWord and Outlook. * Ability to prepare oral and written reports clearly and concisely. * Excellent internal and external communication skills. * Advanced understanding of quality control standards and testing techniques. * Knowledge of statistical sampling techniques. * Able to lift up to 20 pounds. * Able to sit for periods of time working with a microscope. Required Qualifications and Experience: * High School diploma (or equivalent) or AS degree (preferred). * Minimum 2 years Quality Control inspection experience (preferred). * Self-motivated with the ability to evaluate complex issues in a high-pressure environment. * Knowledge of all aspects of inspection and testing. * Experience with Mil-PRF-38534, class H & K; Hybrids, Mil-STD-883; methods 2008, 2009, 2010, 2017 Semiconductors and Passive devices. * Knowledge of IPC-600 and 610, J-STD-001. * Knowledge and experience in performing mechanical and electronic inspections. * Ability to work from technical drawings, sketches and specifications. * Due to ITAR regulations, U.S. citizenship or permanent residency required. The Salary Range for this position is $25.00-$28.00. Actual salary offered to candidate will depend on several factors, including but not limited to, work location, relevant candidates' experience, education, and specific knowledge, skills, and abilities. Benefits: This position offers a comprehensive benefits package including: Health, dental, and vision insurance. Employer-sponsored 401(k) plan. Potential for performance-based bonus. Paid time off. Professional development opportunities. EEO: MACOM is an Equal Opportunity Employer committed to a diverse workforce. MACOM will not discriminate against any worker or job applicant on the basis of race, color, religion, sex, gender identity, sexual orientation, national origin, age, disability, genetic information, veteran status, military service, marital status, or any other category protected under applicable law. Reasonable Accommodation: Reasonable Accommodation. MACOM is committed to working with and providing reasonable accommodations to qualified individuals with physical and mental disabilities. If you have a disability and are in need of a reasonable accommodation with respect to any part of the application process, please call *************** or email HR_*************. Provide your name, phone number and the position title and location in which you are interested, and nature of accommodation needed, and we will get back to you. We also work with current employees who request or need reasonable accommodation in order to perform the essential functions of their jobs.

**General Description:** Perform QC Chemistry laboratory activities to support GMP manufacturing, testing and release of materials, intermediates and finished products under FDA/EU regulations, applicable International Regulations, BeOne processes and procedures. Establishes and implements QC Chemistry procedures and supports regulatory compliance inspections. Ensures efficient and effective day to day operations of the Chemistry laboratory. This position reports to the QC Manager and is located full time at the Hopewell, NJ site. **Essential Functions of the Job:** + Perform routine and non-routine testing using HPLC, UPLC, UV-Vis, capillary electrophoresis, and other techniques (PS-20, HPLC-SEC, TOC, Conductivity, CZE, etc.) in the QC Chemistry and Raw Materials laboratory to ensure timely and compliant generation and reporting of in-process, release, and stability test results in support of manufacturing operations. + Review, interpret, and report analytical data in accordance with GMP regulations and internal procedures. + Ensure appropriate investigation of OOS events, discrepancies, lab errors, and equipment failures. + Implement corrective actions and preventive actions (CAPAs). + Participate in transfer and method validation activities, including protocol preparation, protocol execution, and report preparation. + Support routine operations, including but not limited to instrument qualification and maintenance, SOP generation and revision, test record keeping, etc. + Maintain equipment in a qualified and calibrated state, coordinating with metrology or + vendors as needed. + Manage inventory of reagents and supplies for the laboratory. + Participate in internal and external GMP audits, as needed. + Train other junior level analysts and new hires on instrumentation, GMP practices, and data analysis. + Serving as subject matter expert in one or more areas of required testing. Undertake other duties as required. + Ensure timely completion of testing (e.g., In-process control, DS release, DP release, and stability testing) to ensure timely generation and reporting of test results in support of manufacturing operations. + Review of laboratory test results, ensuring adherence to Good Documentation Practices. + Expertise in Quality Control (QC) within a Good Manufacturing Practice (GMP) environment, ensuring compliance with industry standards and regulations through hands-on laboratory experience. + Working knowledge and experience with analytical methods such as GC, HPLC, UPLC, IEF, TOC, UV, FTIR, etc. + Knowledgeable with USP/EP and cGMP/EU GMP regulations. + Familiar with instrument and equipment validation. + Expert knowledge of quality control principles, practices and standards for the biopharmaceutical industry. + Impressive, demonstrable track record and skills/experience gained within a similar position(s), at a similar level. + Credible and confident communicator (written and verbal) at all levels. + Strong analytical, problem-solving ability, with excellent attention to detail, with the ability to work accurately in a busy and demanding environment. + Hands-on approach, with a 'can do' attitude. + Ability to prioritize, demonstrating good time management skills. + Self-motivated, with the ability to work proactively using own initiative. + Committed to learning and development. + Interacts with all levels of BeOne employees + Undertake any other duties as required. **Education/Experience Required:** + Bachelor's or above in Chemistry, Biochemistry, or Biotechnology related scientific discipline. + Minimum of 4+ years of working experience in an FDA-regulated biotechnology, pharmaceutical company are required. + Familiar with Waters Empower Chromatography Data System. + Familiar with instrument and equipment validation. Impressive, demonstrable track record and skills/experience gained within a similar position(s), at a similar level. Working knowledge with USP/EP and cGMP/EU GMP regulations. + Impressive, demonstrable track record and skills/experience gained within a similar position(s), at a similar level. + Strong leadership/team management skills and experience. + Credible and confident communicator (written and verbal) at all levels. + Strong analytical and problem-solving ability. + Hands-on approach, with a 'can do' attitude. + Ability to prioritize, demonstrating good time management skills. + Excellent attention to detail, with the ability to work accurately in a busy and demanding environment. + Self-motivated, with the ability to work proactively using own initiative. + Committed to learning and development. **Computer Skills:** + Strong PC literacy required; MS Office skills (Outlook, Word, Excel, PowerPoint). + Ability to work on a computer for extended periods of time **Travel:** Must be willing to travel approximately 10% All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

Job Title: QC ChemistJob Description We are seeking a highly skilled QC Chemist to join our dynamic team. In this role, you will conduct comprehensive testing of raw materials and finished products using a range of advanced analytical techniques. You will ensure the highest quality standards and regulatory compliance in a fast-paced pharmaceutical environment. Responsibilities + Conduct raw material and finished product testing using chromatography (HPLC, UPLC, GC), spectroscopy (UV-Vis, FT-IR), dissolution apparatus, and other analytical techniques. + Independently process and report analytical results, ensuring clear documentation of findings. + Maintain accurate laboratory records and follow methods, specifications, and protocols to ensure reproducibility and compliance with regulatory requirements. + Identify and troubleshoot issues with analytical instruments and techniques. + Ensure products meet regulatory standards, in-house, and regulatory quality specifications. + Collaborate with the quality assurance team to ensure compliance with Good Manufacturing Practices (GMP) or other industry standards. + Operate analytical instruments and equipment, ensuring they are calibrated and functioning properly. + Perform routine maintenance, troubleshooting, and calibration of laboratory instruments. + Adhere to health and safety guidelines, ensuring a safe working environment in the laboratory. + Ensure all work is compliant with international regulations, such as FDA and EMA. + Work with R&D and production teams to support product development, scale-up, and product release. + Provide technical support and training to junior team members or other departments when necessary. Essential Skills + Proven hands-on experience in a pharmaceutical analytical laboratory. + 3-7 years of experience with analytical instruments (HPLC/UPLC, GC, Dissolution apparatus, UV-Vis spectrometer, FT-IR) is highly preferred. + Current Good Manufacturing Practices (cGMP), FDA, and other regulatory requirements knowledge. + Proficiency in dissolution, FT-IR, GC, UV-VIS, KF, TLC, and other analytical techniques. + Basic computer knowledge including MS Word, Excel, and Outlook. Additional Skills & Qualifications + Bachelor's degree (minimum) in Chemistry, Analytical Chemistry, Biochemistry, Biology, or a related field. + Ability to document and record analytical experiments and results in detail as per cGMP guidelines. + Excellent attention to detail and problem-solving skills. + Ability to interpret and report complex data clearly. + Knowledge of regulatory guidelines (e.g., GMP, GLP). Work Environment The role is based in a laboratory setting with exposure to chemicals, reagents, and specialized equipment. The team consists of approximately 10 people. This position may require standing for extended periods and the ability to lift moderate weights (about 25 lbs). Willingness to work overtime may be necessary depending on project deadlines. The workplace fosters growth with new leadership and offers a collaborative atmosphere. Job Type & Location This is a Contract to Hire position based out of Cranbury, 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 Cranbury,NJ. Application Deadline This position is anticipated to close on Jan 16, 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 (%20actalentaccommodation@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 is a leading pharmaceutical contract development and manufacturing organization (CDMO), specializing in oral solid dosage and ingestible powder products. They partner with pharmaceutical companies to support drug development and manufacturing needs with a strong focus on quality, compliance, and innovation. They are now looking for a Quality Control Chemist - Pharmaceutical. Salary/Hourly Rate: $34/hr - $36/hr Position Overview: Our client is seeking a skilled Quality Control Chemist - Pharmaceutical to join their onsite team. The Quality Control Chemist will play a critical role in quality control testing, data interpretation, and regulatory compliance within a fast-paced pharmaceutical CDMO environment. This position is ideal for candidates with hands-on experience in analytical instrumentation and a strong understanding of GMP standards. Responsibilities of the Quality Control Chemist - Pharmaceutical: * Perform QC testing of raw materials and finished products, including tablets, capsules, and other dosage forms, using analytical techniques such as HPLC, UPLC, GC, UV-Vis, FT-IR, dissolution apparatus, and particle size analysis. * Independently interpret and report analytical results while maintaining detailed and accurate laboratory records. * Ensure compliance with regulatory standards, including FDA and EMA guidelines. * Operate, calibrate, and maintain analytical instruments and laboratory equipment. * Collaborate with cross-functional teams, including R&D and production, to support product development and release. * Provide technical support and training to junior staff as needed. Required Experience/Skills for the Quality Control Chemist - Pharmaceutical: * 3-7 years of hands-on experience in a pharmaceutical analytical laboratory. * Proficiency with analytical instruments such as HPLC/UPLC, GC, UV-Vis, FT-IR, and dissolution apparatus. * Strong documentation skills aligned with cGMP guidelines. * Ability to troubleshoot analytical techniques and instrumentation. * Excellent attention to detail and strong problem-solving capabilities. Preferred Experience/Skills for the Quality Control Chemist - Pharmaceutical: * Experience working in a CDMO environment. * Familiarity with ingestible powder and oral solid dosage product testing. * Knowledge of international regulatory standards and quality systems. Education Requirements: * Bachelor's degree in Chemistry, Analytical Chemistry, Biochemistry, Biology, or a related scientific field. Benefits: * Atrium Care Package available, upon eligibility (including healthcare plans, discount programs, and paid time off).

We are SGS - the world's leading testing, inspection and certification company. We are recognized as the global benchmark for sustainability, quality and integrity. Our 99,600 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer and more interconnected world. Our Dayton, NJ laboratory is seeking an entry-level Lab Technician I to join their General Chemistry team! The Lab Technician I will prepare samples with accuracy and precision in accordance to SGS' analytical SOPs. Work independently and as part of a team to meet daily production targets and ensure hold times and turnaround times are met. Always follow safe laboratory practices and maintain a safe working environment. Job Functions * After appropriate training independently prepare samples for analysis according to SGS' analytical SOPs using basic instrumentation specific to the department and analytical methodologies * Performs routine operation, maintenance, calibration of prep instruments/equipment * May assist with validation and MDL studies. * Inputs and maintains technical information as needed to support the laboratory functions/operations. * Maintains Laboratory Notebook where applicable. * Adheres to internal standards, policies, and procedures. * Performs other duties as required. Qualifications * High school diploma (Required) * 0-2 years of experience in Analytical Chemistry Laboratories or prior experience working with one's hands (Required) * Associates Degree in a Chemistry or similar scientific discipline (Preferred) * 1-2 years of years' relevant experience in Analytical Chemistry Laboratories (Preferred) * Language Skills: English (Required) * Mathematical Skills: Basic (Required) * Reasoning Skills/Abilities: Basic (Required) * Computer Skills: Basic (Required) * Ability to lift/carry/push and/or pull upwards of 25 lbs on a frequent basis (Required) Additional Information SGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, color, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression, genetics, status as a protected veteran, or any other characteristics protected by law. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skills, and/or abilities required. This job description should not be construed as an exhaustive statement of duties, responsibilities or requirements, but a general description of the job. Nothing contained herein restricts the company's rights to assign or reassign duties and responsibilities to this job at any time. If you are applying for a position within the United States and you have difficulty completing the on-line employment application because of a disability, please call ************ for assistance and leave a message. You will receive a call back. Please note, this phone number is not for general employment information, but is only for individuals who are experiencing difficulty applying for a position due to a disability.

**General Description:** Perform QC Biochemistry laboratory activities with a primary focus on capillary electrophoresis techniques to support GMP manufacturing, testing, and release of material, intermediates and finished biological products (monoclonal antibodies) under FDA/EU regulations, applicable International Regulations, and BeOne Medicines' processes and procedures. **Essential Functions of the job:** + Perform routine and non-routine testing using capillary electrophoresis techniques (e.g., CE-SDS, CZE, ic IEF) in the QC biochemistry laboratory to ensure timely and compliant generation and reporting of in-process, release, and stability test results in support of manufacturing operations. + Review, interpret, and report analytical data in accordance with GMP regulations and internal procedures. + Lead troubleshooting efforts for analytical methods and instrumentation related to CE. + Conduct laboratory investigations, including OOS, Out of Trend, deviations, and invalid assays. + Implement corrective actions and preventive actions (CAPAs). + Participate in transfer and method validation activities, including protocol preparation, protocol execution, and report preparation. + Support routine operations, including but not limited to instrument qualification and maintenance, SOP generation and revision, test record keeping, etc. + Maintain equipment in a qualified and calibrated state, coordinating with metrology or vendors as needed. + Manage inventory of reagents and supplies for the laboratory. + Participate in internal and external GMP audits, as needed. + Train other junior level analysts and new hires on CE instrumentation, GMP practices, and data analysis. + Serving as subject matter expert in one or more areas of required testing. + Undertake other duties as required. **Core** **Competencies** **, Knowledge, and Skill Requirements** + Bachelor's or above in Chemistry, Biochemistry, or Biotechnology related scientific discipline. + Minimum of 4+ years of GMP testing using capillary electrophoresis techniques in an FDA-regulated biotechnology, pharmaceutical company is required. + Working knowledge and experience with biochemistry analytical methods such as residual DNA by qPCR, host cell protein ELISA, Residual Protein A ELISA, binding activity ELISA, Capillary Electrophoresis (CE), capillary isoelectric focusing (cIEF), etc. + Familiar with Waters Empower Chromatography Data System. + Working knowledge with USP/EP and cGMP/EU GMP regulations. + Familiar with instrument and equipment validation. + Impressive, demonstrable track record and skills/experience gained within a similar position(s), at a similar level. + Strong leadership/team management skills and experience. + Credible and confident communicator (written and verbal) at all levels. + Strong analytical and problem-solving ability. + Hands-on approach, with a 'can do' attitude. + Ability to prioritize, demonstrating good time management skills. + Excellent attention to detail, with the ability to work accurately in a busy and demanding environment. + Self-motivated, with the ability to work proactively using own initiative. + Committed to learning and development. **Significant Contacts** + Interacts with all levels of BeOne employees. **Supervisory Responsibilities:** + N/A All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.