Quality control technician jobs in Somerville, NJ - 751 jobs

This position is for a Travel Cardiac Cath Lab Technologist to work a 12-week assignment in Pompton Plains, New Jersey, providing specialized cardiac catheterization procedures. The role requires an Allied Health Professional with 40-hour weeks on day shifts and offers various travel healthcare benefits including housing support, medical coverage, and reimbursement programs. Host Healthcare facilitates travel assignments with comprehensive support and premium benefits for allied health professionals seeking flexible work opportunities nationwide. Host Healthcare is seeking a travel Cath Lab Technologist for a travel job in Pompton Plains, New Jersey. Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Start Date: Duration: 12 weeks 40 hours per week Shift: 8 hours, days Employment Type: Travel Host Healthcare Job ID #a1fVJ000007dsJ3YAI. Pay package is based on 8 hour shifts and 40 hours per week (subject to confirmation) with tax-free stipend amount to be determined. Posted job title: Cath Lab Tech About Host Healthcare At Host Healthcare, we provide a truly comfortable experience as you explore your travel nursing, therapy, or allied career. We make your travel healthcare journey easy by taking care of all the details, so you don't have to. We are on a mission to help others live better and we do this by helping the healers of the world be as comfortable as possible. With access to tens of thousands of travel nursing, therapy, and allied jobs in all 50 states, our responsive and friendly recruiters find your dream position based on what's important to you. During your assignment, get access to premium benefits, including Day 1 medical that continues up to 30 days between assignments, 401K matching, travel reimbursements, dedicated housing support, and more. We also offer 24/7 support from our team and access to our on-staff clinicians so you can feel comfortable and confident throughout your entire assignment. Travel comfortably with Host Healthcare. Benefits Referral bonus School loan reimbursement Vision benefits Wellness and fitness programs Company provided housing options License and certification reimbursement Life insurance Medical benefits Mileage reimbursement Pet insurance Discount program Employee assistance programs Guaranteed Hours Health savings account Holiday Pay 401k retirement plan Continuing Education Dental benefits Keywords: travel cath lab technologist, cardiac catheterization, travel healthcare jobs, allied health professional, medical travel nursing, cath lab technician, cardiovascular technologist, travel medical benefits, healthcare travel assignment, host healthcare

We are seeking a dedicated and detail-oriented Tissue Culture Laboratory Technician to join our team. This role involves ensuring the timely production of kits in accordance with Good Manufacturing Procedures, as well as maintaining high standards of quality and consistency in our products. Responsibilities + Ensure that all kits are produced in a timely fashion in accordance with Good Manufacturing Procedures. + Ensure that all raw materials, including chemicals, antigens, serums, and plasmas, are available for production. + Carefully follow and accurately complete all procedures in accordance with FDA requirements, ensuring all documents are up to date. + Participate in cycle counts and review kit data to ensure product quality and consistency. + Assist Technical Services in troubleshooting any problems, facilitating sample and kit testing in response to customer complaints or requirements. + Interact with all other departments as needed to fulfill job responsibilities. Essential Skills + Academic biology lab experience. + Experience with sample preparation and pipetting. + Proficiency in using laboratory glassware and lab equipment. + Ability to read and follow written directions. + Basic working knowledge of Biology, Microbiology, Immunology, and aseptic technique. + Ability to perform basic mathematical calculations, including the creation of dilutions. + Ability to operate and maintain machines such as the automated plate washer, reader, and pH meter. + Basic computer skills. Additional Skills & Qualifications + Associates or Bachelor's degree in Biology preferred. + Science experience background, lab experience required. Work Environment The work schedule is Monday to Thursday from 6:30 am to 4:30 pm and Friday from 7:15 am to 11:15 am, totaling a 35-hour work week. The work environment requires adherence to good laboratory practices to maintain a safe and efficient workspace. Job Type & Location This is a Contract to Hire position based out of Branchburg, NJ. Pay and Benefits The pay range for this position is $25.00 - $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 Branchburg,NJ. Application Deadline This position is anticipated to close on Jan 26, 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.

The Travel Cardiac Cath Lab Technologist provides specialized support in cardiac catheterization and interventional procedures, assisting physicians pre-, intra-, and post-procedure. This travel position requires licensure as a Radiologic Technologist with experience in cardiac catheterization, along with certifications such as BLS and ACLS. The role offers flexible shifts, on-call duties, and comprehensive benefits through a healthcare staffing agency. ARMStaffing is seeking a travel Cath Lab Technologist for a travel job in Pompton Plains, New Jersey. & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Start Date: Duration: 12 weeks 36 hours per week Shift: 12 hours, flexible Employment Type: Travel Cardiac Catheterization Technologist Location Not specified Assignment Duration This is a 13-week contract position. Schedule 4, 10-hour shifts per week, with options for 7 AM - 5 PM or 8 AM - 6 PM, Monday through Friday. On call for 8-10 shifts a month, including one full weekend. Job Description The Cardiac Catheterization Technologist is responsible for preparing and assisting in cardiac catheterization procedures, including PCI (STEMI), peripheral vascular procedures, pacemaker placements, and interventional radiology procedures. The technologist will help monitor, document, and calculate hemodynamic data while providing procedural assistance to the physician before, during, and after procedures. This role involves assessing and managing the access site and informing the physician as necessary while adhering to on-call protocols for the catheterization lab. Responsibilities Prepare and prep for cardiac catheterizations and other interventional procedures. Monitor, document, and calculate hemodynamic data. Provide procedural assistance to the physician pre, intra, and post procedure. Assess and manage the access site, informing the physician as needed. Ensure adherence to on-call protocol for the catheterization lab. Prepare patients for procedures. Required Experience / Certifications / Licensure Licensed Radiologic Technologist. RCIS certification preferred. BLS, ACLS & IABP experience required. Cardiac catheterization lab experience required. Why ARMStaffing? At ARMStaffing, we take care of our employees! We offer: Health Benefits: Day-1 access to Medical, Vision, Dental, Life, and more Onboarding Made Easy: We handle physicals, titers, and more so you can focus on care Clinical Support: In-house clinical team available to assist and advocate 401k Retirement Plan: Eligible after waiting period; 4% match with 5% contribution Recruiter Matching: Get paired with a recruiter based on your location and specialty Extras: Travel reimbursement, housing allowance, meals, referral bonuses, and more We're not the only ones who think ARMStaffing should be your first choice. Here's why: SIA's Top-50 Fastest Growing Healthcare Staffing Firms - 2019 SIA's Largest Healthcare Staffing Agencies in the U.S. - 2023 Top Workplace in the Lehigh Valley - 2022, 2023 Perfect scores for 'Name, Not a Number' and 'Recruiters' Personalities' on Highway Hypodermics We've earned The Joint Commission's Gold Seal of Approval for healthcare staffing 15 years strong and counting! Contract & local rates may vary based on location and applicant residency. Ask your ARMStaffing recruiter for details! ARMStaffing Job ID #. Pay package is based on 12 hour shifts and 36.0 hours per week (subject to confirmation) with tax-free stipend amount to be determined. Posted job title: Cath Lab Tech:Cath Lab Tech,19:00:00-07:00:00 About ARMStaffing Allied Resources Medical Staffing (ARMStaffing) places the most qualified medical professionals in the industry, including: local and travel contract, temp-to-perm, per diem, and direct-hire personnel. As a leader in medical staffing, we cover every segment of the healthcare market and take pride in our ability to exceed our clients' expectations. We accomplish this through our total dedication to our clients and field associates, our over 15 years of experience, a strong and diverse poor of medical professionals, and the high level of loyalty of our internal staff. We also make it a point to develop and maintain close relationships with staffing and office managers to ensure clear communication and proper placements based on the client's criteria. This allows us to tailor our services to best suit the staffing needs of our clients, while placing our employees in positions that match their abilities and preferences. Our goal is to offer unparalleled service to our valued healthcare clients, regardless of facility size or location, and to maintain a top-notch workforce of qualified, dedicated and medical professionals. The Experts in Healthcare Recruiting Local and travel contracts Temp-to-perm employment Direct-hire personnel Per Diem Staffing for every segment of the healthcare industry including, RNs, LPNs, and CNAs, and Allied Health Professionals Long-term contracts, block scheduling and per diem staffing options 24-Hour customer service and on-call support 365 days a year Full-time, registered nurse on staff to provide screening, background, and reference checks Long-term and temporary career options with outstanding employee benefits Medical Benefits Company-matched 401K Keywords: Cardiac Catheterization, Cath Lab Technologist, Travel Healthcare Job, Interventional Radiology, PCI Procedures, RCIS Certified, BLS ACLS Certified, Cardiovascular Technician, Healthcare Staffing, Cardiac Cath Lab

A Travel Cardiac Cath Lab Technologist assists with cardiac catheterization and electrophysiology procedures in healthcare settings, preparing equipment, supporting surgeons, and monitoring patients. The role requires certifications such as ARRT and BLS, a current state license, and at least one year of acute care experience. This is a travel position offering competitive pay, comprehensive benefits, and a temporary 12-week assignment in Pompton Plains, NJ. Cross Country Allied is seeking a travel Cath Lab Technologist for a travel job in Pompton Plains, New Jersey. & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Start Date: Duration: 12 weeks 40 hours per week Shift: 8 hours, days Employment Type: Travel Job Description As a cardiac cath lab technologist, you'll assist with catheterization of the heart and other electrophysiology procedures. Working in an operating room, cardiac cath lab or similar healthcare facility, you'll prepare equipment, assist surgeons, monitor patient vitals, help maintain sterile conditions and more. You might care for patients undergoing angioplasty, stent implantation, ablation, fluoroscopy or other procedures. Minimum Requirements • At least 1 year of recent acute care experience as a cardiac cath lab technologist • ARRT Certification • BLS Certification (AHA) • Current state license Benefits The benefits of taking a travel allied job with Cross Country include: Private housing or generous housing allowance Comprehensive health insurance with prescription coverage Dependent health insurance with prescription coverage Competitive salaries Referral bonuses Travel reimbursement 401(k) retirement plan Direct deposit/free checking Unlimited free CE credits Cross Country Allied Job ID #. Pay package is based on 8 hour shifts and 40 hours per week (subject to confirmation) with tax-free stipend amount to be determined. Posted job title: RAD - CCL TECH Cardiac Cath Lab Technologist. About Cross Country Allied You bring the expertise. We bring the support you deserve. At Cross Country, we connect allied professionals with flexible opportunities designed around what matters most - your goals, your growth, and your wellbeing. Whether you specialize in imaging, respiratory, surgical, or lab work, we're here to champion your success with nationwide roles, hands-on support, and a team that sees you as essential. Because this isn't just work. It's your purpose. Benefits • 401k retirement plan • Referral bonus Keywords: Cardiac Cath Lab Technologist, Cardiovascular Technology, Cath Lab Technician, Electrophysiology Procedures, ARRT Certification, BLS Certification, Travel Healthcare Job, Acute Care Technician, Patient Monitoring, Cardiac Catheterization

JobID: 210690782 JobSchedule: Full time JobShift: Base Pay/Salary: Jersey City,NJ $142,500.00-$200,000.00 Join our team to play a pivotal role in mitigating tech risks and upholding operational excellence, driving innovation in risk management. As a Tech Risk & Controls Lead in the Cybersecurity and Technology Controls organization, you will be responsible for identifying, and mitigating compliance and operational risks in line with the firm's standards. You will also provide subject matter expertise and technical guidance to technology-aligned process owners, ensuring that implemented controls are operating effectively and in compliance with regulatory, legal, and industry standards. By partnering with various stakeholders, including Product Owners, Business Control Managers, and Regulators, you will contribute to the reporting of a comprehensive view of technology risk posture and its impact on the business. Your advanced knowledge of risk management principles, practices, and theories will enable you to drive innovative solutions and effectively manage a diverse team in a dynamic and evolving risk landscape. Job responsibilities * Ensure effective identification, quantification, communication, and management of technology risk, focusing on root cause analysis and resolution recommendations * Develop and maintain robust relationships, becoming a trusted partner with LOB technologists, assessments teams, and data officers to facilitate cross-functional collaboration and progress toward shared goals * Execute reporting and governance of controls, policies, issue management, and measurements, offering senior management insights into control effectiveness and inform governance work * Proactively monitor and evaluate control effectiveness, identify gaps, and recommend enhancements to strengthen risk posture and regulatory compliance Required qualifications, capabilities, and skills * Formal training or 5+ years of experience or equivalent expertise in technology risk management, information security, or related field, emphasizing risk identification, assessment, and mitigation * Familiarity with risk management frameworks, industry standards, and financial industry regulatory requirements * Proficient knowledge and expertise in data security, risk assessment & reporting, control evaluation, design, and governance, with a proven record of implementing effective risk mitigation strategies * Demonstrated ability to influence executive-level strategic decision-making and translating technology insights into business strategies for senior executives * Experience in various Technology and Cyber domains such as Data Management, Vulnerability Management, or Cloud * Risk management experience in AWS or AI/ML Preferred qualifications, capabilities, and skills * CISM, CRISC, CISSP, or other industry-recognized risk certifications #CTC

Become a Resiliency Technology Risk and Controls Lead Are you ready to lead and innovate in the realm of technology resiliency? Join our Employee Platforms Resiliency Technology team as a Resiliency Technology Risk and Controls Lead, where your expertise will drive our resiliency strategy forward. In this pivotal role, you will be a key point of contact for the resiliency team, managing multiple workstreams within our firmwide resiliency program. As a Resiliency Technology Risk and Controls Lead within the Employee Platforms Resiliency Technology team, you will be key leader with collaborating on our resiliency strategy. Your role will involve being a key point of contact for the resiliency team on multiple workstreams of the firmwide resiliency program. You will be instrumental in promoting the continuous improvement of our Resiliency Operating Framework, ensuring it aligns with our firmwide and regulatory obligations. Job responsibilities Supports the resiliency operating model framework, providing resiliency domain expertise as guidance to application and product owner. Ensuring all resiliency related compliance objective are met on time. Collaborates with Stakeholders, including Application Owners, Product Owners, Engineers, Tech and Business Control Managers, and Software Reliability Engineers to ensure alignment and integration of resiliency practices across the firm. Achieves risk and performance measures to continuously validate and assess the effectiveness of resiliency controls, incorporating them into reporting and escalation processes. Participates in post incident response, planning and root cause analysis to ensure quick lessons learned from disruptions and establish action items for resiliency gap remediation. Supports the development and implementation of our comprehensive resiliency strategy that integrates business and technology risk management to mitigate risks associated with disruptive events. Required qualifications, capabilities, and skills 5+ years of extensive experience focusing on resiliency, program management, or controls. Proficient knowledge in core infrastructure technologies and experience with cloud provider products and services. Strong ability to influence and drive change, with a proactive approach to identifying potential issues and implementing practical solutions. Excellent verbal and written communication skills, with the ability to lead discussions with cross lines of business team at multiple levels. Strong analytical and problem-solving skills with attention to detail and accuracy. Expert in managing relationships, partnering with stakeholders, and resolving conflict to deliver solutions that meet the needs of the business. Excellence in High-Pressure Environments: Demonstrated leadership in crisis management, strategic stress management, task prioritization, and sound decision-making, with the ability to excel in problem-solving. Demonstrated domain expertise in crisis management, strategic stress management, task prioritization. Preferred qualifications, capabilities, and skills Financial industry exeperince Knowledge of the JPMC Business and Technology Resiliency Framework Familiar with JPMC CORE Objectives and Procedures Strong data analytics skills

Job DescriptionOVERVIEW: Quality Control Technician:The Quality Control Technician will play a critical role in ensuring products are packaged correctly and meet quality standards before they are shipped to customers. The primary objective of the Quality Control Technician - Manufacturing is to identify and rectify defects or deviations from established quality criteria to maintain high product quality. This position runs Monday - Friday, with the following shifts: 2nd Shift: 2:00 PM - 10:30 PM 3rd Shift: 10:00 PM - 6:30 AM QUALIFICATIONS: Quality Control Technician: High school diploma or equivalent qualification. Certification in quality control is preferred. Must have food manufacturing experience. A minimum of 2 years' experience in a similar role. Excellent knowledge of MS Office. Good math, technical, and communication skills. Strong understanding of quality control standards and testing techniques. KEY RESPONSIBILITIES: Quality Control Technician: Perform thorough inspections of raw materials, components, and finished products to check for defects, non-conformities, and deviations from quality standards. Work closely with production teams to ensure that manufacturing processes are in compliance with quality standards and are carried out correctly. Inspect finished produced goods to ensure their quality and adherence are up to specifications. Keep detailed records of inspections, testing results, and any deviations from the quality standards up-to-date and maintained. Reject all products and materials that fail to meet quality expectations. Collect and take samples of production batch to ensure products are meeting standards. Identify opportunities for process improvement and suggestions on changes to enhance efficiency and product quality. Ensure that inspection and testing equipment are regularly calibrated to maintain accuracy and reliability. Investigate the root causes of quality issues, collaborate with cross-functional teams, and recommend corrective and preventive actions to prevent future occurrences. Conduct internal audits of manufacturing processes and procedures to ensure ongoing compliance with quality standards and regulations. Maintain open and effective communication with production staff, quality assurance teams, and management to ensure everyone is aligned on quality goals and expectations. Prioritize safety in the manufacturing environment, ensuring that quality control activities are carried out safely and in accordance with safety protocols. Other duties as assigned. Onsite Personnel is an equal opportunity employer committed to hiring a diverse workforce in an inclusive culture environment. Onsite Personnel does not discriminate based on disability, veteran status or any other basis protected under federal, state, or local laws

Job DescriptionWe 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°ree;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 Cellares total compensation package contains competitive base salaries, highly subsidized Medical, Dental, and Vision Plans, 401(k) Matching, Onsite lunches, and Stock options. All displayed pay ranges are approximate, negotiable, and location dependent.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. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

The Role As a Production Tech, you'll be an essential part of the process of turning raw cannabis flower into our beautiful line of medicated products. Under the guidance of the management team, you will produce, package, and handle products, perform inventory duties, adhere to compliance requirements, and keep safety as your top priority while working daily in our facility. Here at GTI, we are looking for true team players who are the perfect hybrid between precision and energy. Responsibilities Deliver on production goals, while focused on safety and quality Produce product per recipes and SOP's, maintaining high quality standards Package product into proper containers with proper labeling to ensure compliance with state regulations Ensure all standards for processing procedures and laboratory protocols are followed Compliance with local and state regulations Adherence to quality control methods throughout entire process Documentation of manufacturing methods are created and maintained Electronically convert packaged products in the state traceability system Manage time efficiently to meet goals while consistently producing quality product Practice good housekeeping habits throughout the facility with focus and personal contributions towards a clean and organized assigned work area at the end of the assigned shift Exhibit competency in basic organizational skills, communication skills and Windows based operating software Use independent judgment regarding product processing, keeping quality and goals in mind Help create a positive environment by having a positive attitude and by being self-motivated Other duties as assigned Qualifications High School Education or GED graduate; some college or college graduate preferred 1-2 years' experience in manufacturing, food processing, warehousing, and/or inventory preferred Equivalent combinations of education and experience may be considered Must be able to work well in a group and independently; demonstrate self-motivation and initiative Must be able to adapt quickly to changes in policy, procedure, and technique Employee must exhibit personal hygiene and follow the health guidelines set forth by GTI Ability to listen well and communicate effectively with various audiences Ability to perform monotonous tasks with great efficiency without losing qualities Must be able to follow basic instructions and accept constructive criticism Prior cannabis experience not required Additional Requirements Must have a valid driver's license or State ID card Must be a minimum of 21 years of age Must pass all required background checks Must be and remain compliant with all legal and company regulations for working in the industry Must be approved by the Cannabis Compliance Board to receive an Agent Card Working Conditions While performing the duties of this job, the employee is regularly required to perform reaching, grasping, bending, stooping, talking, hearing, seeing and repetitive motions. Must be able to sit and/or stand for extended periods of time while maintaining focus. PHYSICAL DEMANDS: Must be able to lift, carry, and balance up to 50 pounds AND must be able to do so with extreme care and caution when working with product. Work involves daily exposure to allergens (such as cannabis, tree nuts, and coconut oil). The pay range is competitive and based on experience, qualifications, and/or location of the role. Positions may be eligible for a discretionary annual incentive program driven by organization and individual performance. Green Thumb Pay Range$18-$18 USD

**Technician, Quality Control** **Princeton NJ, US** **On-Site** The QC Technician is responsible for maintaining conducting analyses, results entry and reporting and processing of quality related deviations, to ensure products meet specified standards defined, to help ensure that the products manufactured are safe, reliable, and meet both internal and external requirements, promoting customer satisfaction and trust in the business. **Your key responsibilities** + Perform Lab Tests: Independently carry out routine quality control analyses following set procedures. + Data Integrity & Documentation: : Confidently handle all steps of testing, including preparation, execution, and accurate documentation. + Check Results: Review test results for accuracy and consistency before submission. + Initial OOS Testing: Conduct first-level tests for out-of-spec results as per procedures. + Escalate Issues: Identify recurring problems and escalate them to the appropriate person or team. + Maintain Equipment: Take care of assigned lab equipment, including calibration and basic maintenance, following GMP and safety standards. **We bring** + Empowerment to make meaningful contributions while upholding ethical standards. + Recognition and celebration of your efforts and accomplishments. + Opportunities for growth and advancement for those who embrace innovation and take initiative. + Collaboration with experts in health, nutrition, and beauty to drive progress. + Customer-first approach, working with world-renowned brands to turn ideas into impactful solutions. + Opportunity to build a career making a significant impact on billions of lives, with the freedom to shape your own path. + Dedication to creating better futures for customers, communities, people, and the planet. + Responsibility and accountability in living company values and driving sustainable solutions. + Supportive environment where individuals are empowered to progress and contribute to meaningful change. **You bring** + Education: Bachelor's degree in Science, or a related field preferred. + Experience: Minimum of 2 years of experience in quality control. + Fluency in local language a requirement, other languages encouraged. The salary provided reflects the pay range dsm-firmenich expects to pay the successful candidate for the position. Individual pay offered will be based on the applicant's job-related skills, experience, relevant education, or training, and primary work location. $47,000 - $68,000 In addition to base salary, we also offer a comprehensive total rewards package, inclusive of annual incentive pay, a retirement savings plan, health care coverage, paid time off, recognition programs and a broad range of other benefits. All benefits and incentives are subject to eligibility requirements. **About dsm-firmenich** At dsm-firmenich, we don't just meet expectations - we go beyond them. Join our global team powered by science, creativity, and a shared purpose: to bring progress to life. From elevating health to making fortified food and sustainable skincare, the impact of your work here will be felt by millions - every single day. Whether it's fragrance that helps you focus, alternative meat that's better for the planet, or reducing sugar without losing flavor, this is where you help shape the future of nutrition, health, and beauty for everyone, everywhere. And while you're making a difference, we'll make sure you're growing too. With learning that never stops, a culture that lifts you up and the freedom to move across businesses, teams, and borders. Your voice matters here. And your ideas? They're essential to our future. Because real progress only happens when we **go beyond, together** . **Inclusion, belonging and equal opportunity statement** At dsm-firmenich, we believe being a force for good starts with the way we treat each other. When people feel supported, included, and free to be themselves, they do their best work - and that's exactly the kind of culture we're building. A place where opportunity is truly equal, authenticity is celebrated, and everyone has the chance to grow, contribute, and feel they belong. We're proud to be an equal opportunity employer, and we're serious about making our hiring process as fair and inclusive as possible. From inclusive language and diverse interview panels to thoughtful sourcing, we're committed to reflecting the world we serve. We welcome candidates from all backgrounds - no matter your gender, ethnicity, sexual orientation, or anything else that makes you, you. And if you have a disability or need any support through the application process, we're here to help - just let us know what you need, and we'll do everything we can to make it work. **Agency statement** _We're managing this search directly at dsm-firmenich. If you're applying as an individual, we'd love to hear from you. We're not accepting agency submissions or proposals involving fees or commissions for this role._

The QA Technician is responsible for reviewing customer documentation and specifications to ensure compliance with contractual, regulatory, and quality requirements. This role prepares and maintains certification packages, supports customer and government source inspections, and administers quality documentation throughout the part lifecycle. GENERAL FUNCTIONS: -Work in accordance with work instructions, safety procedures, and quality procedures - Process, prepare and analyze inspection reports - Review customer purchase orders, specifications, and quality requirements for accuracy and completeness - Compile, prepare, and maintain certification packages to support customer deliveries and regulatory compliance - Coordinate and support customers - Maintain customer accreditation and approval programs - Assign and track heat codes for saw shed work orders - Prepare certification, shipping, and export documentation - Administer and maintain documentation for returned material and nonconforming product - Schedule and coordinate required eye exams for inspectors - Ensure quality records are accurate, complete, and properly retained per internal and customer requirements - Communicate quality‑related information with Quality, Production, Engineering, and Shipping to support on‑time delivery - Other duties as assigned Training and Experience: - Completion of all general company training as outlined in the Orientation program - Ongoing quality, compliance, and system training as required - Minimum of 2 years experience in a quality, inspection, or manufacturing support role - Strong understanding of shop traveler operations and associated inspection and test reports - Ability to interpret customer purchase orders and quality requirements - Effective time management, organizational, and interpersonal skills - Working days will be Thursday-Sunday with the possibility of workday flexibility depending on production demands.

The Production Technician - Chemical Reagents and Kit Assembly will be responsible for manually building and assembling chemical reagents and kits. This role requires a hands-on, detail-oriented individual capable of following precise production protocols to ensure product quality and consistency. Key Responsibilities: Kit Assembly: Manually assemble chemical reagent kits according to detailed instructions and quality standards. Preparation of Reagents: Measure, mix, and prepare chemical reagents, adhering to all safety and quality procedures. Quality Control: Perform routine checks to ensure that products meet specified quality standards and report any inconsistencies. Inventory Management: Track inventory levels of materials, report shortages, and assist in ordering supplies as needed. Documentation: Maintain accurate records of production processes, quality control checks, and inventory use. Safety Compliance: Follow safety protocols for handling and storage of chemicals; participate in safety training. Continuous Improvement: Identify opportunities to streamline and improve assembly processes. About Us: ENG Scientific is dedicated to providing high-quality laboratory solutions, including the manufacture of chemical reagents and kits. We are seeking a meticulous and motivated individual to join our team in the production of these kits. If you have a keen attention to detail, can quickly learn new processes, and are committed to quality, we encourage you to apply. Skills Required: Excellent attention to detail and manual dexterity. Ability to follow precise instructions and adapt quickly to new processes. Strong organizational skills and ability to work in a structured, process-oriented environment. Other Requirements: Must be comfortable working with chemicals and handling materials according to safety protocols. Why Join Us? Competitive salary and benefits package. Opportunity to work in a growing company with a collaborative team. Hands-on experience in a specialized production environment. ENG Scientific is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Job Description The Production Technician - Chemical Reagents and Kit Assembly will be responsible for manually building and assembling chemical reagents and kits. This role requires a hands-on, detail-oriented individual capable of following precise production protocols to ensure product quality and consistency. Key Responsibilities: Kit Assembly: Manually assemble chemical reagent kits according to detailed instructions and quality standards. Preparation of Reagents: Measure, mix, and prepare chemical reagents, adhering to all safety and quality procedures. Quality Control: Perform routine checks to ensure that products meet specified quality standards and report any inconsistencies. Inventory Management: Track inventory levels of materials, report shortages, and assist in ordering supplies as needed. Documentation: Maintain accurate records of production processes, quality control checks, and inventory use. Safety Compliance: Follow safety protocols for handling and storage of chemicals; participate in safety training. Continuous Improvement: Identify opportunities to streamline and improve assembly processes. About Us: ENG Scientific is dedicated to providing high-quality laboratory solutions, including the manufacture of chemical reagents and kits. We are seeking a meticulous and motivated individual to join our team in the production of these kits. If you have a keen attention to detail, can quickly learn new processes, and are committed to quality, we encourage you to apply. Skills Required: Excellent attention to detail and manual dexterity. Ability to follow precise instructions and adapt quickly to new processes. Strong organizational skills and ability to work in a structured, process-oriented environment. Other Requirements: Must be comfortable working with chemicals and handling materials according to safety protocols. Why Join Us? Competitive salary and benefits package. Opportunity to work in a growing company with a collaborative team. Hands-on experience in a specialized production environment. ENG Scientific is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Quality Assurance Technician- 3rd (11:30pm-8:00am) Pay Range: $25-$28/hr. Your Role at Prestone Our Freehold, NJ Plant is looking for a self-motivated, reliable, and detail-oriented Quality Assurance Technician to be part of our growing team. People that take the initiative and action to pursue production line goals and complete tasks. People that are thorough and accurate in accomplishing tasks. People that hold a high standard for safety, quality, production, and teamwork. If you are this person, we encourage you to apply! What You'll Be Doing Review of production line parameters and performance for adherence to Company Standard Operating Procedures, Quality Guidelines and Facility Procedures Testing samples for physical and chemical properties for adherence to Quality Specifications Include raw materials and Finished Products Generating and shipping samples for outside analytical testing Maintenance of the Quality Retain Program Responsible for laboratory cleanliness and organization Responsible for documentation of testing, holding product, internal investigations and root cause analysis Ordering lab supplies Maintenance of Instrument Calibration Program Other duties as assigned What You'll Bring High school diploma or equivalent 2-3 years of hands on Quality Systems experience, manufacturing preferred Must be able to work 3rd shift Ability to work in a fast paced, time sensitive environment Able to lift to 50 pounds periodically throughout the manufacturing shift and meet physical requirements of position including lifting, bending, standing for extended periods, reaching with both hands/arms, ability to visually inspect product Excellent math and problem solving skills Excellent communication skill set (verbal, written, etc.) Bilingual English/Spanish preferred What You Will Get PRESTONE offers a competitive salary and comprehensive benefits including health, wellness, dental, vision, life, and disability insurance. You can plan for your future with PRESTONE's retirement savings options including employer match. PRESTONE also recognizes the importance of continuing education and offers Education Assistance to our employees to encourage continued personal development and growth.

Quality Assurance Technician Objective: Inspects and tests materials and products for form, fit, and functions at various stages of production, including incoming, in-process, and final. Compiles and evaluates data to determine and maintain quality and reliability of products. Essential Duties Performs receiving inspection of incoming material using various measuring devices such as comparators, Calipers, micrometers, meters, etc. Verifies documentation such as picking lists, vendor supplied test data, purchase orders, etc. Interprets and utilizes inspection procedures, blueprints, schematics, assembly drawings, work orders, specifications, and process documentation to perform quality tasks Confers with management, engineering, and production to determine quality and reliability standards. Selects appropriate inspection sample and performs appropriate inspections based on established inspection procedures or creates new procedures if necessary. Prepares charts, graphs, reports, and other documentation using various software applications. Work closely with production departments to assure manufactured products maintain conformance. Practices good housekeeping and safety procedures and adheres to all company policies. Knowledge, Skills and Abilities: To perform the job successfully, an individual should demonstrate the following knowledge, skills and abilities: Ability to verify parts meet specifications, visual inspection, confirm color codes. Ability to interpret drawings, ECN's, sketches, schematics, etc. Tools: micrometers, calipers, CMM's, depth mic's, etc. PC software knowledge ( Microsoft Office Suite) Able to analysis problems and provide solutions. Ability to work close with production personnel provide guidance and possibly training to enhance quality. Qualifications Education/ Experience: 5+ years QA experience. Or 3 years + Associates degree in related field Or 1 year + Bachelors degree in related field Additional Information All your information will be kept confidential according to EEO guidelines.

Job Description Are you ready to join our team at C&L Auto Body, an esteemed family-owned MSO in Plainfield, NJ? We are in search of a talented and devoted Quality Control Technician to uphold our dedication to business expansion and client contentment. Your precision and proficiency will be pivotal in reducing customer inconvenience following accidents. This position is a great jumping-off point for higher-paying jobs such as estimating & production management. Compensation: $18 - $30 hourly Responsibilities: 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, skill, and/or ability required: Assure that C&L QC procedures are being followed by all departments Solely responsible for final quality inspections Assure that all repairs to the vehicle match the final invoice Perform other related duties as assigned to ensure an efficient and effective repair Meet & greet customers Review repairs of all vehicles & sign off on ready-for-delivery Deliver vehicles to customers, reviewing repairs & answering any questions Perform ADAS on all vehicles that need scanning or calibrations fill out appropriate paperwork & check in requirements for each vehicle Qualifications: The ideal candidate should have the following experience: Experience working in a Team Environment Prior working knowledge of body repairs and parts Prior experience in multi-tasking, prioritizing, and organizing Ability to effectively communicate Technical knowledge for automotives Ability to learn & adapt quickly customer service experience Quality control experience About Company C&L Autobody is a regional Multiple-Shop Organization (MSO) with 11 body shops throughout Morris, Essex, Sussex, Warren, Union, and Middlesex counties in Northern NJ. We also manage one of the largest towing fleets in the state. As one of NJ's largest family-owned MSOs, we pride ourselves on delivering an unmatched level of customer service and craftsmanship for all your collision repair needs. We offer full benefits (medical, dental, and vision), paid time off, paid holidays, and a 401(k) with a company match. Work hours are Monday through Friday, 8 am to 5 pm, with occasional Saturdays.

Product chemistry Development Tech needs 3 years or more related experience in the Rubber, Plastics Compounding or Coatings Industry Product chemistry Development Tech requires: Bachelors degree (B.A.) in a Chemistry related or Material Science field from a four-year college or university with 3 years or more related experience in the Rubber, Plastics Compounding or Coatings Industry; or Associates Degree (A.A.) in Chemistry related or Material Science field with five or more years related experience and / or extensive training in the Rubber, Plastics Compounding or Coatings Industry; or equivalent combination of education and experience. Product chemistry Development Tech duties: Work with multiple chemistry adhesive type products Develop tests and reports on formulations Independently works to perform tests needed per product. Performs gauge R&R on batches produced in lab Executes lab testing and generates test data and documentation necessary Ensures SHE and compliance is met with lab safety and hygiene Communicate with various internal functions Comfortable lifting items and utilizing equipment for lab procedures.

Our QC Laboratory Technician plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training, your responsibilities will include performing basic laboratory support functions related to the management of laboratory samples, materials, and testing supplies. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US. This is a full-time role working Monday through Friday from 8:00 AM to 4:30 PM. This is a set, consistent schedule with minimum overtime requirements and based on site in our Bloomsbury, NJ location. This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws. What the QC Laboratory Technician Does Each Day: * Verifies information on incoming lab samples and enters sample information into the laboratory database * Place orders and stock laboratory supplies * Light housekeeping, including operation of glassware washer * Ensures all work is performed and documented in a timely manner and according to approved standard operating procedures and in general compliance with cGMPs Our Most Successful QC Laboratory Technicians: * Are accurate and well organized, with strong attention to detail * Express energy, show accountability, can multi-task and work in a fast-paced, quality-rich environment * Fulfill expectations, establish sustainable relationships with team members, maintain effective and meaningful communication channels * Have good interpersonal skills and work effectively and efficiently in a team environment to accomplish goals * Have strong verbal and written communications skills Minimum Requirements for this Role: * A High School diploma or equivalent * Able to successfully complete a drug and background check * Proficient in Microsoft Office, Word and Excel * Able and willing to walk, stoop, stand, bend, and lift up to 50 lbs. throughout each shift, with or without reasonable accommodation * Must be currently authorized to work in the United States on a full-time basis; Quva will not sponsor applicants for work visas Any of the Following Will Give You an Edge: * Bachelor's Degree in life science or related field * 1 to 2 years' experience in data entry/clerical, or related responsibilities Benefits of Working at Quva: * Set, full-time, consistent work schedule * Comprehensive health and wellness benefits including medical, dental and vision * 401k retirement program with company match * 17 paid days off plus 8 paid holidays per year * Occasional weekend and overtime opportunities with advance notice * National, industry-leading high growth company with future career advancement opportunities * Salary Range: $18.85-27.34/hour About Quva: Quva is a national, industry-leading provider of compounded injectable medicines and software solutions that help power the business of hospital and health-system pharmacy. Quva Pharma produces and distributes injectable medicines required by health care providers and critical to patient care. Quva BrightStream partners with health-systems to analyze large amounts of data and through AI and machine learning, develops software solutions that turns the data into insights that are used to better run their pharmacy operation. Quva's overall product and technology offerings help health-systems achieve greater value and deliver the highest-quality patient care. Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is "at will." California Consumer Privacy Act (CCPA) Notice for Applicants and Employees

Date 05/2025 Title Technician, QC Analytical Department Quality Control Reports to Manager, Chemistry Laboratory FLSA (Exempt or Non-Exempt Non-Exempt We are seeking a detail-oriented and skilled Laboratory Technician to join our Chemistry Lab division. The successful candidate will support physical and chemical testing of raw materials, R&D, Method development / Stability and finished products using various analytical instruments / Equipment's and techniques to ensure compliance with internal specifications. Areas of Responsibility Prepare samples, Mobile Phase, Buffer solution, Dissolution Media, Sample digestion etc. for analysis according to standard operating procedures (SOPs) or as per suitable method provided by senior management. Perform chemical analyses using techniques such as UV-Vis, Dissolution, FTIR, titration, Microwave Digestion system, TOC water sample and physical testing using apparatus and equipment's' such as Disintegration, Bulk Density, Tap Density, Loss on Drying, Karl Fisher, etc. Accurately record, and report test results in compliance with GLP/GMP standards. Calibrate, maintain, and troubleshoot laboratory instruments and equipment. Example-pH meter, Weighing Balance, etc. Maintain a clean, organized, and safe work environment. Assist in the development and validation of analytical methods under supervision. Document laboratory activities and results in lab notebooks, Raw Datasheets, and on computer system with validated excel. Dispose of chemical waste properly and follow all environmental, health, and safety (EHS) protocols. Participate in quality audits and continuous improvement initiatives. Must be able to work extended hours as needed and occasional weekends. Other duties and responsibilities as assigned. Other Responsibilities Including Safety: Works in a safe and responsible manner to create an injury-free and incident-free workplace. Complies with all job-related safety and other training requirements. Keeps management informed of area activities and of any significant problems. Requirements Education & Qualification: Associate's or Bachelor's degree in Chemistry, Biochemistry, or related scientific field. 0-3 years of hands-on experience in an analytical chemistry lab (academic or industrial). Strong understanding of laboratory safety and quality standards (e.g., GMP, GLP, ISO). Good problem-solving and organizational skills with attention to detail. Ability to work independently and collaboratively within a team. Certifications, Licenses, Credentials: N/A Skills & Ability Ability to maintain integrity and honesty at all times and to communicate with transparency. Ability to work independently or as part of a team. Solid understanding of cGMP's and GLP and is familiar with 21 CFR Part 11 Strong working knowledge of Microsoft Word, Excel. Good documentation practices and able to write simple, clear reports Meets commitments on time and practices time-management skills Seeks to identify continuous improvement needs Experience with Shimadzu LC2010, Nexera, GC2010, Thermo ICP-MS, Labsolution and Waters Empower Lab Software a plus. Physical Requirements (lifting, etc.): May execute 90%-100% of their work at the bench level either standing or sitting on a stool. Uses hands to finger, handle, feel, or operate objects or controls, lifting to waist height and/or above shoulder height, frequent bending from the waist, or squatting, walking short distances and leaning over equipment as well as kneeling on the floor to clean under the equipment. Must be able to wear all PPE including a lab coat, face mask, booties, gloves, safety glasses/goggles, and respirators. On occasion may need to lift up to 35 lbs. Ability to navigate office, lab, and/or plant floor working environments. Work Environment (Office, Warehouse, temperature extremes, etc.): Approximately 80% of work performed in a laboratory environment which may have unpleasant odors or hazardous conditions. Temperatures can be moderate, exposure to dust, odors, noise, and fumes. The noise level is usually moderate. Employees can be exposed daily to chemicals and cleaning agents. The above statements are intended to describe the general nature and level of work being performed by people assigned to this job. They are not intended to be an exhaustive list of all the job responsibilities, duties, skill, or working conditions. In addition, this document does not create an employment contract, implied or otherwise, other than an "at will" relationship. USPL is proud to be an Equal Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy), sexual orientation, gender identity or expression, national origin, age, genetic information, disability, protected veteran status, or any other characteristic protected by applicable local, state, or federal law. Benefits And Compensation: Our benefits are designed to help you move forward in your career, and in areas of your life outside of USPL. From health and wellness benefit options including: medical, dental, vision, short and long term disability, basic life insurance, supplemental life insurance, AD&D insurance. We also offer a matched 401(k) savings plan. Employees have the opportunity to receive compensation in the form of premium pay such as overtime, shift differential, holiday pay, sick time, etc. Newly hired employees receive up to 10 days of vacation the first year, which grows to 12 days starting the second year of employment. Office Hours: 8:30 AM - 5:00 PM 9:00 AM - 5:30PM