Quality control analyst jobs in Randolph, NJ - 132 jobs

Primary Duties & Responsibilities Member of prototype fabrication team: Project planning, execution, tracking and reporting Develop and improve processing methods for inorganic composite materials (preform fabrication, metal casting, mold production and assembly, programming and operation of advanced furnaces, programming and operation of CNC machining centers, precision finishing/lapping of hard materials, and other associated activities) Characterization of materials properties Measurement of dimensions, both manually and via computer controlled CMMs Interface with outside entities (raw materials suppliers, equipment vendors, toll manufacturers, machine shops, and test labs) Transfer successful products to manufacturing, including documentation and training Education & Experience New AAS in Engineering or Science fields (or equivalent training and experience) Relevant certifications a strong plus, such as CAM, CAD, ISO, Lean, CMM, others Skills Familiarity with manufacturing and/or lab environment Experience with advanced equipment (materials processing, furnaces, CNC machining centers, CMMs, etc.) Knowledge of assembly operations Strong mechanical aptitude Strong computer aptitude (data summaries, programmable furnaces and machining centers, etc.) Working Conditions Position requires on-site activities for prototype fabrication. Work schedule is 5 days, 40 hrs per week, first shift. Working in lab, production and office Physical Requirements Hands-on, lab-based job environment: Required to frequently lift/push/pull a minimum of 35 lbs Must be able to sit, bend, squat and walk about facility Depending on project assignment, may be required to walk/stand for entire 8 hour day Safety Requirements All employees are required to attend scheduled training, follow the site EHS procedures and Corporate EHS standards. This includes the use of proper protective equipment (PPE) as required by the job responsibilities. Managers will ensure that all safety and environmental procedures are followed consistently. They will ensure that risk assessments are performed, proper training, work instructions, required PPE is available, and will monitor compliance. Quality and Environmental Responsibilities Depending on location, this position may be responsible for the execution and maintenance of the ISO 9000, 9001, 14001 and/or other applicable standards that may apply to the relevant roles and responsibilities within the Quality Management System and Environmental Management System. Culture Commitment Ensure adherence to company's values (ICARE) in all aspects of your position at Coherent Corp.: Integrity - Create an Environment of Trust Collaboration - Innovate Through the Sharing of Ideas Accountability - Own the Process and the Outcome Respect - Recognize the Value in Everyone Enthusiasm - Find a Sense of Purpose in Work Coherent Corp. is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. If you need assistance or an accommodation due to a disability, you may contact us at ****************************** .

At Corbion, we exist to champion preservation in all its forms, preserving food and food production, health, and our planet. The Quality Control Technician is a 2nd shift position based at the Totowa, NJ plant reporting to the Quality Control Supervisor. This role is responsible for performing daily analytical tests, pre-operation and line audits, and ensuring production procedures and systems are followed. The position ensures that all quality standards are consistently met while supporting the development of QC team members. Essential Functions * Follow all GMP's (Good Manufacturing Practices), FSMA, Safety, and Environmental regulations as well as company policies. * Maintain positive attitude. Focus on the customer, teamwork, and quality productivity. * Give recommendations to improve workplace safety, efficiency, and to better serve the customer. * Analyze finished product for various analytical testing including redox, Chittick, pH, %moisture, color, titratable acid (TA), enzymes, vitamins, proteins, etc., on a daily basis. * Daily verification/calibration of lab equipment prior to testing finished product to ensure product quality. * Maintain the cleanliness of the lab making sure that the areas are clean after testing. * Ensure that lot codes and finished products package is correct and legible. * Product that has been analyzed and does not meet specification, must be re-sampled and re-analyzed immediately. If product is not in compliance, HOLD stickers must be applied immediately and system hold activated. * Participate in and successfully complete all required laboratory training classes. * Complete the picking, testing and approval of raw materials, issuing deviation when the material is out of specification and reporting to the supervisor/manager. * Keeping record of the materials that need to be tested for micro and send the samples on time. * Duties, responsibilities and activities may change or new ones may be assigned at any time with or without notice. Education & Experience * Bachelor's Degree in Chemistry, Bio-Chemistry, Chemical Engineering, Biology or Microbiology. * Experience in a laboratory environment within a related industry is required. * SAP/Sample Manager experience preferred. Knowledge, Skills and Abilities * Strong analytical and problem-solving skills. * Knowledge of laboratory testing procedures and equipment calibration. * Ability to maintain compliance with GMPs, FSMA, HACCP, and company policies. * Strong communication and teamwork skills. Working Environment * Manufacturing plant with large open floor areas and loud machinery. * Exposure to high temperatures in summer and cold environments in winter. * Dusty environment due to raw materials. * Exposure to allergens including eggs, soy, sesame seeds, milk, and wheat. Physical Demands * Must wear GMP-compliant hair and beard nets, company-provided uniforms, gloves, and, in some areas, respirators. * Ability to stand for long periods and perform repetitive laboratory or line auditing tasks. * Must be able to lift up to 55 lbs. Our offer The below reflects the range of possible compensation for this role at the time of this posting. This range may be modified in the future. An employee's position within the salary range will be based on several factors including, but not limited to, relevant education, qualifications, certifications, experience, skills, seniority, performance, location and business or organizational needs. The base salary range for this role is $24.00 to $25.00 per hour. In addition, we offer: * Variable bonus potential * Paid time off, including company holidays * Medical, dental and vision coverage * 401K with company match * Education assistance * Short- and long-term disability * Employee Assistance Program (EAP) About Corbion Corbion is the global market leader in lactic acid and its derivatives, and a leading supplier of emulsifiers, functional enzyme blends, minerals, vitamins, and algae ingredients. We use our unique expertise in fermentation and other processes to deliver sustainable solutions for the preservation of food and food production, health, and our planet. For over 100 years, we have been uncompromising in our commitment to safety, quality, innovation and performance. Drawing on our deep application and product knowledge, we work side-by-side with customers to make our cutting-edge technologies work for them. Our solutions help differentiate products in markets such as food, home & personal care, animal nutrition, pharmaceuticals, medical devices, and bioplastics. In 2024, Corbion generated annual sales of €1,288.1 million and had a workforce of 2,399 FTE. Corbion is listed on Euronext Amsterdam. For more information: *************** Corbion is an equal opportunity employer and committed to a diverse workplace. All applicants will be considered equally without regard to race, color, ethnicity, veteran status, religion, national origin, marital status, political affiliation, age, sex, sexual orientation, handicapping condition, membership in an organization or any other non-merit factors. Corbion provides reasonable accommodation to applicants. EOE/M/F/Vet/Disabled Corbion does not accept unsolicited resumes from individual recruiters or third party recruiting agencies in response to job postings. No fee will be paid to third parties who submit unsolicited candidates directly to our hiring managers. All candidates must be submitted by approved Corbion vendors who have been expressly requested to make a submission by our Talent Acquisition team for a specific job opening. No placement fees will be paid to any firm unless such a request has been made by the Corbion Talent Acquisition team and such candidate was submitted to the Corbion Talent Acquisition Team.

We are seeking an innovative, creative, and detail-oriented Quality Control Sample Coordinator to join our team in Bridgewater, New Jersey. This individual will play a critical role in ensuring the seamless handling, tracking, and shipping of analytical samples in support of assay execution for the Quality Control (QC) teams. This position acts as the central point of contact between Manufacturing, Analytical teams (multi-site), and other cross-functional stakeholders in managing sample logistics and documentation. All activities are performed in accordance with cGMP guidelines and are supported by departmental and inter-departmental policies and standard operating procedures. Candidates should enjoy working in a fast-paced, mission-driven environment, and be prepared to tackle a broad selection of challenges as the company grows.Responsibilities Create and maintain sample schedule, from sample creation through QC testing Track sample shipments between internal and external sites Receive samples from clients or other Cellares sites and ensure proper logging, handling, & reconciliation Maintain visibility into sample storage locations, including LN2 and -80°C freezers Manage documentation related to the shipping and receiving of samples Document sharing & coordinate ordering cryoports/cryopods with the Warehouse team and coordinate shipment/reshipment logistics for analytical samples Be comfortable working with LN2 systems Work with QC teams in developing and managing sample batching approaches Deliver required samples to the QC team in real time Monitor for and address discrepancies (labels not accurate, vial missing, wrong concentration, etc) proactively Be available to support unplanned analytical re-executions Review the assay execution schedule and monitor turnaround times for data release to ensure alignment with project timelines Ensure sample retains are shipped to appropriate long-term storage locations after assay execution Assist in general upkeep of the laboratory and maintain a clean work environment Perform other duties as assigned Requirements Bachelor's degree in a science discipline required, or comparable experience 2+ years of experience in cGMP or cGxP at an operational level supporting manufacturing in a pharmaceutical or biotech environment is preferred Prior experience related to LN2 sample handling is preferred Prior experience with scheduling/planning tools (e.g Binocs) is preferred Knowledge of pharmaceutical cGMP (US and EU) is preferred Must have excellent verbal, written, interpersonal, and organizational and communication skills Must be able to commute to Bridgewater, New Jersey Self-awareness, integrity, authenticity, and a growth mindset This is Cellares Cellares is the first Integrated Development and Manufacturing Organization (IDMO) and takes an Industry 4.0 approach to mass manufacturing the living drugs of the 21st century. The company is both developing and operating integrated technologies for cell therapy manufacturing to accelerate access to life-saving cell therapies. The company's Cell Shuttle integrates all the technologies required for the entire manufacturing process in a flexible and high-throughput platform that delivers true walk-away, end-to-end automation. Cell Shuttles will be deployed in Cellares' Smart Factories around the world to meet total patient demand for cell therapies at global scale. Partnering with Cellares enables academics, biotechs, and pharma companies to accelerate drug development and scale out manufacturing, lower process failure rates, lower manufacturing costs, and meet global patient demand.The company is headquartered in South San Francisco, California with its commercial-scale IDMO Smart Factory in Bridgewater, New Jersey. The company is backed by world-class investors and has raised over $355 million in financing. Leveling will be based on overall experience, education, and demonstration of knowledge throughout the interview process.

The QC Analyst II will be responsible for analytical testing and data verification supporting both late-stage clinical and commercial small molecule and biosimilar products in cGMP-compliant laboratories. A strong background in protein chemistry will be essential to perform and troubleshoot techniques such as HPLC, SDS-PAGE, cell-based bioassays, capillary electrophoresis, SDS-PAGE, ELISA, and standard compendial assays. A demonstrated ability to collaborate across multiple departments to drive timely resolution of projects, laboratory investigations, and process improvements is required. Essential Duties & Responsibilities · Analytical testing to support product in-process, release, Raw materials and stability programs. · Strong knowledge of cGMP, Quality Systems, and ICH / regulatory guidance. · Conduct, compile, and/or review Out of Specification lab investigations, deviations, and corrective and preventative actions plans. · Work with cross-functional teams to advance projects, maintain equipment, and authoring of documents and reports. Performs other functions as required or assigned Complies with all company policies and standards Perform the investigation analysis during the non-conformance. Conduct the investigation process as a part of Quality Event and work with supervisor to close the investigation. Requirements Position Requirements and Qualifications Education: · Bachelor's degree in biotechnology, biochemistry, chemistry, or related field with a minimum of 8 years of experience in a pharmaceutical/biotech QC laboratory. Alternatively, Master's degree in above areas with 6 years of experience in a pharmaceutical/biotech QC laboratory. Experience: · Previous experience in a cGMP laboratory. · Strong background in small molecule and protein chemistry and experience troubleshooting analytical results. · Demonstrated success at writing, revising, and complying with SOPs, policies, and QC methods. Specialized Knowledge and Skills: · Demonstrated success working with techniques such as HPLC, SDS-PAGE, cell-based bioassays, capillary electrophoresis, SDS-PAGE, ELISA, and standard compendial assays. · Previous experience supporting regulatory inspections (e.g. PAI). · Familiarity with preparing regulatory dossiers and data packages for interactions between Kashiv and regulatory agencies. Work Environment & Physical Demands: General Working Environment: · Some time spent in an office doing office work (reading, writing, reviewing, and editing documents). · Significant amount of time spent in the laboratory. · Must be able to work extended hours or weekend hours, as may be required. Noise: · No extraordinary noise levels. Standing/Lifting: · Must be able to lift at least 25 lbs. Visual: · No extraordinary requirements. Stress: · High-paced demanding environment to meet ambitious project goals. Travel: · No travel required. Supervisory Responsibility, if any: No This position description is not a complete list of all responsibilities, duties or skill required for the job and is subject to review and change at any time, with or without notice, in accordance with the needs of the organization.

A Few Words About Us 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. Job Description Job Responsibilities • Analyze laboratory samples (raw material, in-process, finished product, stability, etc.) • legibly document the data and report the results associated with each analysis • Participate in laboratory investigations when required • Service laboratory equipment (calibrations, preventative maintenances, etc.) • Laboratory responsibilities can be assigned as deemed necessary • actively participates in the development of lower level Chemists (train, mentor & guide) • Comply with all applicable OSHA Safety and Health Programs • Adhere to all applicable cGXP regulations • Follow protocols, guidelines, procedures and methods as written • Obey all corporate systems and policies • Initiate and takes the lead role in Out-of-Specifications and Analytical Deviations of Quality Control Laboratory Investigations. • Ensure that products are being tested strictly under cGMP conditions and disposition is taken on time as per the committed Production Plan of every month (C to A, > 95%) and or procedural requirements • Troubleshoot laboratory equipment and methods • Helping to the Group Leaders in various aspects as and when needed. • Order and maintain all the Laboratory Chemicals and other needs of the Laboratory. • Hands on experience in handling analytical instruments like HPLC, GC, IR, UV, AAS, DSC, TGA, Malvern particle size • Knowledge on trouble shooting the Analytical Equipment • Performance of laboratory analyses correctly at the first time • Maintenance of the Analytical Equipment, the Analytical Columns and all other necessary things. Qualifications EDUCATION & EXPERIENCE: • 2- 4 years analytical experience in Pharmaceutical companies within the Quality Control / Quality Assurance environment • BS/MS in Chemistry, Pharmacy, Biochemistry or related field. • Experience in Generic Pharma. And Solid oral Dosage tablets / capsule highly desirable. Additional Information For more information contact me at 732-429-1921

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.

Quality Control Analytical ScientistAllendale, NJ Lynkx Staffing LLC specializes in placing talented professionals in the Biotechnology, Pharmaceutical and Medical Devices industries in New Jersey. The QC Analytical Scientist will be a member of the Quality Control Department. As a Senior Member of the team the QC Analytical Scientist will be involved in various QC projects and should have a deep understanding of general QC flow and the Product Cycle. Support internal and external customers to ensure that proper and timely execution of all aspects of the clinical analytical method life cycle across clients. Support routine GMP testing as assigned. Mentor and train team members Evaluate corporate and regulatory requirements along with coordination of activities for implementation of these requirements. Write the contents of Analytical Method Transfer and Validation life cycle documentation including master plans, protocols, test methods, and reports. Create validation project plan i.e., timelines and resources and provides status updates to management. Utilize statistical tools for evaluation of method validation and trending data. Identify, evaluate, and implement continuous business process improvements. Perform troubleshooting activities with respect to methods/assays, equipment malfunctions and investigations (Deviations and OOS). Provide support during laboratory investigations. Train QC personnel during method transfer and validation. Provide support during equipment qualification. Consistently produce elevated level of documentation accuracy and clarity according to cGMP documentation practices. Ability to set deadlines and prioritize work for self, group members, and support groups involved. Ability to review/approve work performed by coworkers for accuracy and alignment with procedures. Indirectly may supervise cross functional teams including product development, QA, PMP, and Manufacturing. REQUIREMENT B.S Analytical Chemistry or other scientific field or MS/Ph.D. in Analytical Chemistry or other scientific field with demonstrated experience in Quality Control laboratories for biotechnology products. 8-10 years of experience in the areas of method development, validation, and transfer. Direct GMP Experience. Proficiency in project management skills and tools. Strong background and in-depth knowledge in analytical chemistry e.g. Flow Cytometry, ELISA, HPLC, CE, PCR, etc. Extensive knowledge and experience of QC assay development, transfer and validation, along with cGMPs. Strong Quality orientation with attention to detail required. Analytical and problem-solving skills required. Excellent communication skills, both written and verbal, with all levels of the organization, including the ability to state opinions clearly, ask questions, seek clarification, communicate facts objectively, challenge when appropriate, and pursue issues to resolution. Excellent presentation skills. Ability to communicate to upper management, across departments and within the immediate QC team. Ability to create and manage work plans and timelines and independently manage competing priorities with limited instruction. Highly motivated individual with good interpersonal skills that have proven effective in managing relationships and negotiating solutions while maintaining a level of approachability with colleagues both internal and external. Must be familiar with GMP lab environment and Aseptic techniques. Working EnvironmentMust have the ability to work in a team-oriented environment and with clients Must be able to work during the weekend, holidays, or overtime and as required by the company May be exposed to infectious diseases transmittable through human blood, tissues, or bodily fluids Must utilize proper personal protective equipment (PPE) when handling all human specimens, gases, corrosive chemicals, and liquid nitrogen Must have the ability to work with specialized equipment Must be able to handle the standard/moderate noise of the manufacturing facility May work with hazardous materials and chemicals Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.

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.

Quality Inspector - 3rd Shift Join a quality‑driven manufacturing and laboratory environment where your attention to detail directly impacts product integrity and customer satisfaction. As a Quality Inspector, you'll play a key role in verifying incoming materials, supporting lab operations, and ensuring compliance with cGMP and QA standards. What You'll Do * Inspect incoming components and lab‑prepared samples to verify compliance with specifications, including appearance, dimensions, and overall integrity. * Perform sampling and submission activities, including pulling samples from multiple pallets, completing submission forms, and making pass/reject decisions based on lab test results. * Document all inspection activities accurately and consistently in alignment with SOPs, QA requirements, and audit expectations. * Maintain compliance within the lab, ensuring proper labeling, cleanliness, and adherence to cGMP protocols. * Assist with investigations related to out‑of‑spec results and support corrective and preventive action (CAPA) efforts. * Collaborate with QC team members to uphold a strong culture of safety, accuracy, and continuous improvement. Top Skills & Experience * Component and material inspection * Quality Control / Quality Assurance * Laboratory environment experience * GMP knowledge and compliance * Strong documentation and organizational skills Additional Qualifications * Ability to work independently while maintaining high attention to detail * Experience with component‑level inspections and lab‑based quality systems * Strong communication skills and a commitment to accuracy and consistency Experience Level * Intermediate level; prior QC or inspection experience preferred This position is moving fast! If interested please send over your updated resume to carendas @actalentservices.com with your availability for a 5 minute phone screen. Job Type & Location This is a Contract to Hire position based out of Wharton, NJ. Pay and Benefits The pay range for this position is $23.00 - $25.00/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 Wharton,NJ. Application Deadline This position is anticipated to close on Jan 20, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

**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.

1. Quality control system construction and process optimization: Develop warehouse quality control strategies and standardized procedures, overseeing operational compliance in warehousing, outbound storage, sorting, and other processes. Optimize warehousing workflows to enhance efficiency, minimize losses, and ensure operations meet industry standards and business requirements. 2. Quality monitoring and risk control: Monitor warehousing operations in real time to assess quality performance, analyzing inventory data and operational records to identify potential risks (e.g., errors, losses, safety hazards). Formulate and implement corrective actions to maintain product safety and quality consistency. 3. Team collaboration and capability building: Collaborate closely with warehousing, logistics, and other teams to facilitate cross-departmental resolution of quality issues. Organize quality control training and evaluations to strengthen team members' quality awareness and operational proficiency, ensuring effective execution of quality objectives. 4. Data-driven continuous improvement: Perform statistical analysis on quality metrics (e.g., error rates, customer complaints, inventory accuracy), generate quality reports, and propose actionable recommendations. Drive innovation in warehousing processes and management practices through intelligent solutions, continuously elevating service quality and customer satisfaction. 【About JD.com】 JD.com (NASDAQ: JD and HKEX: 9618), also known as JINGDONG, is a leading supply chain-based technology and service provider. The company's cutting-edge retail infrastructure seeks to enable consumers to buy whatever they want, whenever and wherever they want it. The company has opened its technology and infrastructure to partners, brands and other sectors, as part of its "Retail as a Service" offering to help drive productivity and innovation across a range of industries. JD.com's business has expanded across retail, technology, logistics, health, industrials, property development and international business. JD.com is ranked 44th on the Fortune Global 500 list and is China's largest retailer by revenue, serving over 600 million annual active customers. The company has been listed on NASDAQ since 2014, and on the Hong Kong Stock Exchange since 2020. Committed to the principles of customer first, innovation, dedication, ownership, gratitude, and integrity, the company's mission is to make lives better through technology, striving to be the most trusted company in the world. 【Our Global Business】 We are dedicated to building a digitally intelligent, cross-border supply chain and global retail infrastructure. Leveraging our global supply chain capabilities, JD.com continues to expand in markets where our competitive strengths shine. Currently, JD.com's operations span China, the U.K., the Netherlands, France, Germany, Spain, Brazil, Hungary, Japan, South Korea, Australia, Thailand, Vietnam, Malaysia, Indonesia, Saudi Arabia, the UAE, the U.S., and many others, serving customers worldwide. Key International Business Segments: Joybuy (online retail business in Europe), International Logistics, Cross-border Import Business, JD Industrials International, JD Property International 【International Logistics】 JINGDONG Logistics (HKEX: 2618), also known as JD Logistics, is a leading technology-driven supply chain solutions and logistics services provider. JINGDONG Logistics has established six integrated logistics networks: warehouse managment, line-haul freight transportation, last-mile delivery network, bulky items logistics, cold chain logistics, and cross-border logistics networks. As of June 30, 2025, JINGDONG Logistics manages over 3,600 warehouses (third-party-operated cloud warehouses included), with a total area exceeding 34 million square meters. JINGDONG Logistics has strategically built a Global Smart Supply Chain Network, featuring highly automated warehousing systems and reliable international transportation solutions. The company currently operates over 130 bonded, direct mail and overseas warehouses, with a total GFA exceeding 1.3 million square meters, spanning 23 countries and regions worldwide. “JoyLogistics” and “JoyExpress” are JINGDONG Logistics' international business brands.

QUALITY CONTROL - WALDWICK NEW JERSEY START NOW !!!!!!!!!!!!!!!!!! ** We are looking for reliable and responsible candidate for warehouse associate in Waldwick. Pay rate: $13.50 (NEGOTIABLE DEPENDING ON EXPERIENCE) 2nd shift QA( Quality Assurance) Train for 2 weeks on 1st shift MONDAY - FRIDAY ( 7am-3:30pm) Regular hours MONDAY - FRIDAY 3pm-11:30pm OVERTIME AVAILABLE Must work weekends.( rotate) Requirements: Computer Knowledge, Inspecting Materials, Test Samples Able to stand all day performing this job. Bilingual is a plus Must have transportation Benefits offered - Health Care Sick Pay 401 k offered in 2021 MUST HAVE TRANSPORTATION!!!!!!!!!!!!!!!! Start now! Vaccinated

Full-time Description About Generant: Initially founded in the early 1930's, Generant designs and manufactures valves and pressure regulators for a wide variety of industries with a strong position in the Industrial Gases and Cryogenics, Medical Gases and Equipment, Energy, and Chemicals markets. Generant is 100% employee-owned and is headquartered in Butler, NJ where most valve and regulator products are manufactured. We look for dedicated and talented people who accept the responsibilities of thinking like owners and embrace our mission as stated in our Quality Policy: “Our Goal is to provide our customers, suppliers and employees true value. We believe this can only be accomplished through a strong commitment to continuous improvement in the quality of our products, services and working environment.” Our ideal candidates: Are people who are personally motivated to produce high-quality work Are lifelong learners - driven to continually improve Are well organized Enjoy working in a team environment Join our growing team and be a part of our journey! Generant is looking for a 3rd shift Quality Control Inspector Join our growing company! 3rd shift is Monday - Friday. 11:00pm - 07:30am Job Summary: The primary function of the Quality Control Inspector is to help assure the quality of finished goods and conformance to product requirements. This is accomplished by inspecting parts, checking calibration status of measurement devices, and documenting inspections and nonconformance. Essential Functions: · Conduct First Article Inspection and in-process inspections of products to ensure compliance with quality standards and specifications. · Maintain Calibration of Metrology Tools · Perform In-Process inspections, Final Inspection, Raw Material Inspection - Bar Stock, Inspection of Incoming Purchased Parts, and Outside Process Inspection · Data Entry into Quality Databases · Interpret mechanical drawings · Communicate product and material nonconformances to management. · Identify and report any deviations from quality standards to the appropriate personnel · Collaborate with production teams to resolve quality issues and implement corrective actions · Conduct root cause analysis and implement preventive measures to minimize defects and improve product quality · Maintain accurate records of inspections, test results, and quality documentation. · Assist in the development and implementation of quality control procedures and processes · Other duties as assigned Requirements Qualifications: Education/Experience/Skills: · High School Diploma or equivalent · 2+ years as a Quality Control Inspector in a manufacturing environment that produces metal pieces · Able to read and interpret engineering drawings · Must have a complete knowledge of metrology equipment and their uses including micrometers, calipers, indicators, depth micrometers, gauge pins, thread gauges and optical comparators · Advanced Math Skills · Strong knowledge of Statistical Process Control (SPC) techniques and tools · Familiarity with quality control standards and regulations · Must be able to work in a fast-paced environment · Excellent attention to detail and analytical skills · Ability to work independently and as part of a team · Fluent in English (Good Verbal and Written Communication Skills) · Ability to carryout detailed, written and verbal instructions Physical Demands: · Must frequently lift up to 25 pounds and occasionally lift up to 75 pounds · When performing the duties of this job, the employee is regularly required to sit, use hands to finger or handle or feel objects and tools or controls and talk or hear · Employee is frequently required to reach with hands and arms · Employee is occasionally required to stand, walk, stoop, kneel, crouch, or crawl · Specific vision abilities require close vision, distant vision, color vision, peripheral vision, depth perception and the ability to adjust focus. Work Environment: · Inspector works near moving mechanical parts and is occasionally exposed to vibration · Noise level is usually moderate for a manufacturing plant Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions Benefits: Medical, Dental, Vision, Employee Stock Ownership Plan (ESOP), 401k, Life and AD&D Insurance Please note that this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.

: Fly Alliance is a Part 135 and Part 145 industry leading private aviation group specializing in private jet charter, jet card memberships, aircraft sales, management, parts, and MRO. Dedicated to providing unparalleled luxury, safety, and efficiency in air travel, the company has over 30 aircraft, 6 offices across the country, and over 200 employees supporting a global operation. Three consecutive years as a top 20 U.S. operator, Fly Alliance continues to redefine the private aviation landscape. Role Objective: Responsible for the return to service of all assigned articles to include completion of all work orders and all other required documentation from pre-planning to delivery of the aircraft. Physically inspect aircraft, aircraft components, and review paperwork to ensure that workmanship meets acceptable standards of quality, and that customer aircraft are returned to service in an airworthy condition with all required documentation properly completed and filed. Major Duties and Responsibilities: Determine inspection status of aircraft in for scheduled inspection, as assigned. Audit of inspection and maintenance work packages generated by the repair station during the performance of maintenance and repair. Work with production personnel, Team Leaders, Lead Technicians and Technicians to ensure accurate and complete documentation of work performed in company work order packages. Generation of maintenance record entries for aircraft, engines, propellers, and accessories maintained by the repair station in accordance with 14 CFR Part 43 and the requirements of this repair station manual. Includes completion of FAA forms 337 and 8130-3 as required. Assist in surveillance of the repair station facilities and procedures and report results to the Chief Inspector. Assist the Quality Assurance Manager and Chief Inspector in the development of improved methods and procedures for the performance of quality assurance functions. Assist the Quality Assurance Manager and Chief Inspector in the maintenance of the technical publication libraries throughout the repair station. Assist the Quality Assurance Manager and Chief Inspector in the tracking and calibration of inspection and test equipment used by the repair station for the purpose of product acceptance. The proper execution of Malfunction or Defect Reports, FAA Form 8010-4 when required. This report will be submitted to the FAA within 96 hours after the malfunction or defect has been discovered in accordance with 14 CFR§145.221. Assist the Quality Assurance Manager and Chief Inspector as necessary in the receiving inspection of parts or material forwarded to him by the receiving inspector. 1 Assuring proper documentation of the preliminary inspection, hidden damage inspection, and final inspections of all items processed as assigned. Make entries into maintenance logs & work orders IAW 14 CFR Part 43 and Operator/Air Carrier manuals. Maintaining Quality Department work areas in a clean and orderly manner. Assist the Quality Assurance Manager and Chief Inspector as dire Knowledge, Skills and Abilities: Knowledge of inspection techniques and tools within an FAA 145 repair station. Thorough understanding of FAR's and regulations pertaining to aircraft maintenance part 145. High mechanical aptitude. Ability to read schematics and blueprints. Be proficient with PC and be familiar with MS office. Knowledge of quality control. Ability to interact with a group of coworkers. Ability to work with complex equipment. Ability to establish procedures. Ability to work in a production-oriented environment. Ability to work under frequent changing priorities. Ability to select and evaluate priorities. Ability to read and comprehend documentation written in the English language. Problem-solving and decision-making skills. Good written and verbal communication skills. Self-starter with the ability to multi-task and prioritize workday/projects independently. Ability to travel. Work Conditions & Physical Requirements: The employee must occasionally lift and/or move up to 50 pounds Stands at least 75% of each workday. Other motions: standing; walking; repetitive motion hand - wrist; fingering; grasping; feeling; handling; hearing; talking; seeing; eye-hand coordination. High organizational, time management and logic skills required Ability to work at a desk in an office environment for extended periods of time Availability during nights, weekends, & holidays as needed. Must be capable of maintaining a flexible schedule, including the willingness to occasionally work extended hours as per project demands and organizational needs. Travel: Some travel is required. Required Education/Experience: Minimum ten years of experience in maintaining aircraft with verifiable practical experience as an active aircraft mechanic in a maintenance organization. Minimum of five years of experience in a supervisory position in a maintenance organization. Minimum of ten years of experience in a Part 145 environment. Must have a thorough working knowledge and understanding of FARs, aircraft technical bulletins, service bulletins, airworthiness directives, aircraft systems, and the ability to communicate this knowledge to the required persons. Previous Director of Maintenance or Chief Inspector experience preferred. FAA Airframe and Power Plant Certification or license (A&P) Must have and maintain a valid driver license and must meet the company's vehicle insurance requirements. Subject to pre-employment and random drug testing. Must pass a background check. Direct Reports: This role has direct reports. Work Authorization: Must be authorized to work in the United States of America. Compensation: Competitive pay based on experience Medical including Health, Dental and Vision Short-Term and Long-Term Disability Insurance Paid Holidays Paid Vacation Profit Share Program

Job DescriptionDescription: : Fly Alliance is a Part 135 and Part 145 industry leading private aviation group specializing in private jet charter, jet card memberships, aircraft sales, management, parts, and MRO. Dedicated to providing unparalleled luxury, safety, and efficiency in air travel, the company has over 30 aircraft, 6 offices across the country, and over 200 employees supporting a global operation. Three consecutive years as a top 20 U.S. operator, Fly Alliance continues to redefine the private aviation landscape. Role Objective: Responsible for the return to service of all assigned articles to include completion of all work orders and all other required documentation from pre-planning to delivery of the aircraft. Physically inspect aircraft, aircraft components, and review paperwork to ensure that workmanship meets acceptable standards of quality, and that customer aircraft are returned to service in an airworthy condition with all required documentation properly completed and filed. Major Duties and Responsibilities: Determine inspection status of aircraft in for scheduled inspection, as assigned. Audit of inspection and maintenance work packages generated by the repair station during the performance of maintenance and repair. Work with production personnel, Team Leaders, Lead Technicians and Technicians to ensure accurate and complete documentation of work performed in company work order packages. Generation of maintenance record entries for aircraft, engines, propellers, and accessories maintained by the repair station in accordance with 14 CFR Part 43 and the requirements of this repair station manual. Includes completion of FAA forms 337 and 8130-3 as required. Assist in surveillance of the repair station facilities and procedures and report results to the Chief Inspector. Assist the Quality Assurance Manager and Chief Inspector in the development of improved methods and procedures for the performance of quality assurance functions. Assist the Quality Assurance Manager and Chief Inspector in the maintenance of the technical publication libraries throughout the repair station. Assist the Quality Assurance Manager and Chief Inspector in the tracking and calibration of inspection and test equipment used by the repair station for the purpose of product acceptance. The proper execution of Malfunction or Defect Reports, FAA Form 8010-4 when required. This report will be submitted to the FAA within 96 hours after the malfunction or defect has been discovered in accordance with 14 CFR§145.221. Assist the Quality Assurance Manager and Chief Inspector as necessary in the receiving inspection of parts or material forwarded to him by the receiving inspector. 1 Assuring proper documentation of the preliminary inspection, hidden damage inspection, and final inspections of all items processed as assigned. Make entries into maintenance logs & work orders IAW 14 CFR Part 43 and Operator/Air Carrier manuals. Maintaining Quality Department work areas in a clean and orderly manner. Assist the Quality Assurance Manager and Chief Inspector as dire Knowledge, Skills and Abilities: Knowledge of inspection techniques and tools within an FAA 145 repair station. Thorough understanding of FAR's and regulations pertaining to aircraft maintenance part 145. High mechanical aptitude. Ability to read schematics and blueprints. Be proficient with PC and be familiar with MS office. Knowledge of quality control. Ability to interact with a group of coworkers. Ability to work with complex equipment. Ability to establish procedures. Ability to work in a production-oriented environment. Ability to work under frequent changing priorities. Ability to select and evaluate priorities. Ability to read and comprehend documentation written in the English language. Problem-solving and decision-making skills. Good written and verbal communication skills. Self-starter with the ability to multi-task and prioritize workday/projects independently. Ability to travel. Work Conditions & Physical Requirements: The employee must occasionally lift and/or move up to 50 pounds Stands at least 75% of each workday. Other motions: standing; walking; repetitive motion hand - wrist; fingering; grasping; feeling; handling; hearing; talking; seeing; eye-hand coordination. High organizational, time management and logic skills required Ability to work at a desk in an office environment for extended periods of time Availability during nights, weekends, & holidays as needed. Must be capable of maintaining a flexible schedule, including the willingness to occasionally work extended hours as per project demands and organizational needs. Travel: Some travel is required. Required Education/Experience: Minimum ten years of experience in maintaining aircraft with verifiable practical experience as an active aircraft mechanic in a maintenance organization. Minimum of five years of experience in a supervisory position in a maintenance organization. Minimum of ten years of experience in a Part 145 environment. Must have a thorough working knowledge and understanding of FARs, aircraft technical bulletins, service bulletins, airworthiness directives, aircraft systems, and the ability to communicate this knowledge to the required persons. Previous Director of Maintenance or Chief Inspector experience preferred. FAA Airframe and Power Plant Certification or license (A&P) Must have and maintain a valid driver license and must meet the company's vehicle insurance requirements. Subject to pre-employment and random drug testing. "Offer of employment is contingent upon successfully completing DOT background check screening and drug testing required by federal regulation for this role." Direct Reports: This role has direct reports. Work Authorization: Must be authorized to work in the United States of America. Compensation: Competitive pay based on experience Medical including Health, Dental and Vision Short-Term and Long-Term Disability Insurance Paid Holidays Paid Vacation Profit Share Program Requirements:

Job Description Goodwill NYNJ Ecommerce Quality Control - Part time Job Position To receive merchandise and sort & separate items based on quality standards for listing. • Receive incoming totes from stores & record seal information as directed. • Research items online for matching descriptions and value by using different market places. • Accept and reject items based on quality standards. • Use provided manifesting software to print SKUs and safely apply them to a variety of items. • Comply with production expectation. • May need to lift up to 50lbs. • Additional duties as required. • Minimum high school diploma. • Ability to read and write English. • Basic computer & internet research skills. • Ability to deal with change and work in a dynamic environment. • Able to work under minimal supervision and process the expected number totes per day. • Able to work as part of a team involved in the quality control of items for Goodwill's E-Commerce (Online) department. Duties will be performed in an industrial warehouse environment. This job requires you to stand/move for long periods of time. Covid-19 Update - In alignment with New York City's decision to lift the private employer vaccination requirements, effective November 1, 2022, Retail Employees in NYC are now exempt from submitting vaccination proof and/or no longer required of submitting proof of weekly PCR/Antigen(Rapid) testing if they have requested medical/ religious accommodation. Retail stores in NJ and Upstate continue to be exempt as per New Jersey and New York State Guidelines.

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 an established consumer goods company and is looking to add a Chemistry Lab Technician to their team Salary/Hourly Rate: $20/hr Position Overview: The Chemistry Lab Technician will work in the lab formulating products and assisting with testing samples. The ideal candidate should have strong attention to detail and organization skills, and the ability to work well individually as well as in a team environment. Responsibilities of the Chemistry Lab Technician: * Formulate and perform testing on products using established formulas and protocols. * Conduct testing on samples, including pH, viscosity, and color. * Calibrate and maintain lab equipment and instrumentation. * The Chemistry Lab Technician will maintain accurate test results and lab data. * Follow all SOPs and company rules and regulations. Required Experience/Skills for the Chemistry Lab Technician: * Knowledge of basic lab equipment. * Familiarity with Microsoft Office Suite. * Work well in a fast-paced environment. * Good written and oral communication skills. Education Requirements: * Associate's or Bachelor's degree in Chemistry, Biochemistry, Biology, or a related science is preferred. Benefits: * Atrium Care Package available, upon eligibility (including healthcare plans, discount programs, and paid time off).

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.