Quality control technician jobs in Clarkstown, NY

JOB TITLE: Quality Control Technician TYPE: Full time, regular COMPENSATION: $20.00/hr - $28.00/hr Clarapath is a medical robotics company based in Westchester County, NY. Our mission is to transform and modernize laboratory workflows with the goal of improving patient care, decreasing costs, and enhancing the quality and consistency of laboratory processes. SectionStar by Clarapath is a ground-breaking electro-mechanical system designed to elevate and automate the workflow in histology laboratories and provide pathologists with the tissue samples they need to make the most accurate diagnoses. Through the use of innovative technology, data, and precision analytics, Clarapath is paving the way for a new era of laboratory medicine. Role Summary: The Quality Control Technician will play a key role in ensuring the quality and reliability of Clarapath s advanced electro-mechanical medical device, SectionStar . This position is essential for inspecting components, assemblies, and finished products to verify conformance with specifications and quality standards. The ideal candidate will have a strong foundation in inspection methods, measurement techniques, and documentation practices, supporting both manufacturing and engineering teams to maintain consistency across production. We re looking for a hands-on, detail-oriented team player who thrives in a fast-paced environment and takes pride in upholding the precision and quality that define Clarapath s products. Responsibilities: Inspect incoming materials, in-process assemblies, and finished products using measurement tools and visual inspection techniques Interpret engineering drawings, specifications, and inspection procedures to verify conformance Record and maintain inspection data, generating non-conformance reports (NCRs) when necessary Collaborate with Quality, Manufacturing, and Engineering teams to identify and resolve quality issues Perform functional and dimensional testing using calipers, micrometers, gauges, CMMs, and other inspection tools Support calibration and maintenance of inspection equipment Assist in root cause analysis and corrective/preventive action (CAPA) activities Maintain cleanliness and organization in inspection and test areas Ensure compliance with ISO 13485, FDA, and internal quality system requirements Qualifications: High school diploma or equivalent required; associate degree or technical certification preferred 1 3 years of experience in quality inspection, preferably in medical devices, precision manufacturing, or electronics Proficient in the use of precision measurement instruments (calipers, micrometers, gauges, etc.) Ability to read and interpret mechanical drawings and technical specifications Strong attention to detail and documentation accuracy Familiarity with quality management systems (QMS) and manufacturing processes Basic computer skills (Microsoft Office, ERP systems experience, a plus) Team-oriented with strong communication and problem-solving skills Company Offers: Competitive salary will be commensurate with experience and education Comprehensive benefits package available: (healthcare, vision, dental and life insurances; 401k; PTO and holidays). A collaborative and diverse work environment where our teams thrive on solving complex challenges Ability to file IP with the company Connections with world class researchers and their laboratories Collaboration with strategic leaders in healthcare and pharmaceutical world A mission driven organization where every team member will be responsible for changing the standards of delivering healthcare Clarapath is proud to be an equal opportunity employer. We are committed to providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status. In addition to federal law requirements, Clarapath complies with applicable state and local laws governing nondiscrimination in employment. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

QC Technician oversees regulatory and quality compliance in bakeries, including QC monitoring and issue reporting. It also involves contributing to bakery R&D efforts, working with consultants to develop new products. JOB DUTIES (include but are not limited to the following): Monitor and support the implementation and maintenance of whole Quality Management System. Those programs are but not limited to: record keeping, allergen, pest control, temperature of coolers and freezers, pre-op, internal audit, and quality control. Monitoring the daily QC activities to ensure they are performed to the published procedures and are properly documented. Visit corporate and franchise stores to support and educate bakery teams/ kitchen managers. Regulate quality control of each bakery. Identification of any quality problems and recommend changes in quality standard where necessary. Working with consultants on innovating new potential products for the brand. Testing new recipes in the test kitchens. Data entry using common computer database software (Excel, Access or equivalent). QUALIFICATIONS & SKILLS: Prior bakery experience is required, with preferred experience in bakery industry research and development. Knowledge of baking various types of bread and baking and decorating cakes. Associate Degree, or Bachelors degree, or equivalent years of work experience 3-5 years of combined experience in food or ingredients and manufacturing. Knowledge of GMPs and HACCP. Basic understanding of food production fundamentals Proficiency in MS Office Products (Outlook, Word, Excel & PowerPoint) and basic computer skills. Excellent verbal and written communication skills. Ability to read and interpret procedure manuals and regulatory documents, and to write reports. Ability to effectively present information and respond to questions from management level. Demonstrate ability to manage and prioritize multiple tasks and demands working with minimum supervision. Detail oriented, excellent record keeping and documentation skills Employee Benefit Health Insurance options: PPO Medical, Dental, Vision covered (Company 100% paid) *insurance starts on the very 1st date. Life Insurance (Company 100% paid) Flexible Time (starting time can vary everyday) Short Term and Long-Term Disability Leave (short term 100% covered) Lifestyle Allowance (up to net $70 per Month) Cellphone reimbursement eligible Employee Discounts (40% off company products & services) 401(k) 5% Match (no vesting period!) from Day 1 Paid Time Off (generous and increases by tier!): Max ceiling of 180 hours PTO (15 days) the 1st year and increases by tier. Wellness Day: 40 Hours (Use it or Lose it System) Paid Maternity Leave (paid 100% for 12 weeks) Paid Secondary Caregiver Leave (up to 2 weeks) Paid Creative Leave Paid Holidays (11 days) Educational Benefit Employee Club Activities & Much More! Experience: Baking: 2 years (Required) Willingness to travel: 25% (Required)

IMMEDIATE QUALITY TECHNICIANS AVAILABLE! ($24-27/HR) Large company with opportunity for growth looking for QUALITY TECHNICIANS to join their team **Pay:** $24-27/hr **Shift:** 7am-5:30pm Monday-Friday **Job Description:** -Experience working within a manufacturing or production environment is a plus -Inspecting, Picking, packing and labeling products -Utilizing a computer and performing documentation -Experience tracking inventory -Ability to follow SOPs and GMPs -Experience with batch records is a plus *Position is a fulltime and permanent role *Company has great benefits and 401k plan *You can start work immediately as there is no interview PLEASE APPLY IMMEDIATELY TO BE CONSIDERED FOR THIS ROLE!! **Job Type & Location** This is a Permanent position based out of Fairfield, NJ. **Pay and Benefits** The pay range for this position is $25.00 - $27.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave) **Workplace Type** This is a fully onsite position in Fairfield,NJ. **Application Deadline** This position is anticipated to close on Dec 19, 2025. **About Aerotek:** We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry - from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies' construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow. Aerotek offers weekly pay, employee benefits including medical, dental & vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts. The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

Main responsibilities are line auditing for production of bread, environmental monitoring and air sampling, as well as a being involved in a monthly SQF audit Calibration and Verification of scales, monitors, and other basic instrumentation Utilizing MS Excel, Word, and Office for basic documentation practices Monitor and verify product quality throughout the manufacturing process following GMP Perform visual inspections, monitor product weights, codes, labeling, and other quality checks to ensure product quality Address all Food Safety issues and customer complaints with the help of QA Supervisors Other periodic tasks week to week Skills Quality control, Communication, adaptability to change, HS Diploma, Food safety, microsoft, bilingual, gmp environment, Environmental Monitoring, HACCP, SQF, Production, Air Sampling Top Skills Details Quality control,Communication,adaptability to change,HS Diploma,Food safety,microsoft Additional Skills & Qualifications Nice to be HACCP or SQF Certified Experience Level Entry Level Pay and Benefits The pay range for this position is $25.00 - $27.00/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 Paterson,NJ. Application Deadline This position is anticipated to close on May 9, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. 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.

Job Description : Freshline Produce LLC., a premium fresh fruit and vegetable processor based in Mahwah, NJ, is seeking a talented Quality Assurance Technician, for its 1st shift, to join its fast growing organization. This is perfect opportunity for a candidate looking to begin their QA career in the food industry. Responsibilities: Incoming Raw Materials/ Inspection/ Inform QA Manager and Operations Manager if there are quality issues. Fill out Receiving Log Identify, label, date, and make a daily inventory list of all WIP products in the coolers Production Line Quality Checks including product quality, case quality, Tsunami checks, Metal detector check and room temperature checks Practice and enforce GMP regulations - (Hand washing, no jewelry, no gum) Recognize and examine all inventory at all times Serve as member HACCP Team Requirements: Good communication, training and interpersonal skills Very detail oriented Strong problem solving skills Bi-lingual (English and Spanish) is preferred Experience in the food industry is a plus Effective organizational skill; Able to manage priorities and complexities Intermediate computer skills Proficiency with Microsoft Word, Excel and Outlook Strong multi-tasking skills

Job Title: Quality Technician/Inspector Type: Contract To Hire Compensation: $23-28 Contractor Work Model: Onsite Hours: 2 Shifts available - *Training will be on 1st Shift 7am to 3pm* + Second Shift: (3PM to 11PM) + Third Shift: (11PM to 7AM) DUTIES AND RESPONSIBILITIES: + Attentive inspection with note taking for mapping inspected rolls. + Label accuracy for rolls and packaging. + Process audits to ensure processing parameters are compliant. + Communication of findings to operators and supervisors. + Generation of Material Discrepancy Reports or Nonconforming Material + Reports to properly disposition defects or process deviations + Performs other related duties as assigned by management. QUALIFICATIONS: + Capable of performing repetitive work. + Perform basic mathematical calculations. + Able to work any shift as required. + Knowledge of coatings, mixers and, PPE. + High school diploma or general education degree (GED), or one to three months related experience and/or training, or equivalent combination of education and experience. Computer skills required: + Basic use of office/laboratory computer systems. System One, and its subsidiaries including Joulé, ALTA IT Services, and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. Ref: #562-Joule Staffing - Edison System One, and its subsidiaries including Joulé, ALTA IT Services, CM Access, TPGS, and MOUNTAIN, LTD., are leaders in delivering workforce solutions and integrated services across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible full-time employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

At Coco, we're revolutionizing last-mile delivery with autonomous robots, making deliveries faster, more efficient, and more sustainable. We're looking for a proactive and tech-savvy Office Manager to oversee our facility operations, ensuring our teams have the resources and environments needed to thrive. About the Role As a Fleet Quality Technician, you'll be the backbone of our robot operations, assembling, maintaining, and deploying delivery robots with precision while leading efforts to diagnose and resolve hardware, electrical, and IoT issues. You'll design repeatable solutions that scale, perform hands-on repairs and testing, and provide critical feedback that drives future hardware improvements. This role is fast-paced, technical, and highly dynamic-perfect for someone who thrives on problem-solving, takes pride in getting things right the first time. What You'll Do Serve as the technical lead during robot deployments, identifying and resolving mechanical, electrical, and software integration issues in real time Own the root-cause analysis and resolution process for fleet quality issues that impact launch success or fleet uptime Design and implement scalable SOPs, tools, and diagnostics for frontline teams to reduce downtime and improve serviceability Collaborate with Engineering, Supply Chain, and Field Operations to close the loop between product issues and fixes Provide structured feedback to Product & Engineering teams and help pilot new hardware, software, or process changes in the field Build lightweight dashboards, diagnostic logs, and technical documentation that can be adopted across teams About You 4-6+ years in hardware operations, fleet maintenance, or field engineering with a focus on mechanical and electrical systems Deep experience troubleshooting mechanical, electrical, and IoT (connectivity/sensor/data) issues Strong systems thinking mindset-you see the big picture and design processes to solve root causes, not just symptoms Independent, self-motivated, and solution-oriented-you don't wait to be told what's broken Excellent communicator with the ability to work fluidly across technical and non-technical stakeholders Familiarity with SQL, JIRA, inventory systems (e.g., Oracle ERP), and basic data analysis to spot trends and validate fixes Comfortable in fast-moving environments and field-based problem-solving scenarios Bonus Points Prior experience in robotics, micromobility, autonomous delivery, or connected fleet operations History of developing technical SOPs, diagnostic workflows, or cross-team enablement tools Experience working closely with Engineering and Product teams to iterate on hardware or firmware in production environments

Job DescriptionDescription: RK Pharma Inc, a vertically integrated pharmaceutical company with our main manufacturing site in Pearl River, NY, is seeking a Quality Control Chemist to work with our growing Quality Teams as we scale towards commercial manufacturing in the next upcoming months. As a company focused on the development, manufacturing and sale of high quality and affordable generic pharmaceutical products worldwide we are looking for sharp, driven, self-directed individuals to help us grow our mid-stage start-up team. Requirements: If this sounds interesting to you, it's probably because up to this point you have: Bachelor of Science of higher 0-3 years of quality Control experience, preferably in a pharmaceutical, manufacturing, or regulated environment. Familiarity with cGMP, GDP, and standards. Proficiency in Microsoft Office (Word, Excel, Outlook, PowerPoint) and experience with ERP or document management systems (e.g., SAP, Master Control). Excellent organization, time management, and communication skills. The main responsibilities for this position are: Perform daily verification /performance check of the QC analytical instruments such as Analytical balance, Microbalance, KF titrator, KF coulometer, Auto titrator etc., Perform calibrations of all the QC analytical instruments/equipment's as per the calibration calendar schedule or when required. Perform Instrument/ equipment performance qualification as and when required. Maintain inventories of chemicals, Standards, samples etc., Operation, calibration, maintenance and qualification of all analytical instruments such as HPLC, GC, TOC, UV, IR, automatic titrator, dissolution equipment, etc. Follow the procedures as per the SOP's/ guidelines. Perform Sampling of raw materials, drug substance, packaging components, stability samples, cleaning samples, In-process samples and finished products. Perform analytical tests and wet chemistry tests on raw materials, drug substance, packaging components, stability samples, cleaning samples, In- process samples and finished products in compliance with the STP and SOP's. Follow and document all test results under GLP, GDP, GMP and Lab Safety guidelines. Document test results, problems and other issues, perform troubleshooting of issues that arise during analysis. Logging various samples received to QC as per the SOP into their respective log books. Monitors Stability chambers, Photostability chamber, freezers, refrigerators etc. Performs Stability samples loading/charging and pull-out according to the stability calendar. Record the results and prepares CoA to be released in a timely manner. Perform analysis using various software's such as Empower, Tiamo, Spectrum two, Flex etc. Write and perform investigation of out of specification results. Train other QC chemists in a timely manner on all the general Laboratory SOPs and test methods. Preparation and review of Standard Operating Procedures, specifications and STP's for Raw materials, Packaging components, drug substances and finished products (based on ICH/Pharmacopeial reference). Preparation and execution of protocols for Method Validations, Method Transfers, Cleaning Validation, Raw material qualifications, Stability studies and any other studies. Maintains lab, instruments, logbooks and notebooks at all times. Maintains lab instruments and performs calibration/preventive maintenance to ensure proper working order and troubleshoot when necessary. Perform additional duties and responsibilities designated by the supervisor on the need basis after receiving the required training. RK Pharma Inc is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

Job Description BASIC FUNCTIONS Entry level position. Performs basic counterfeit lab testing and visual inspection of various commodities including, but not limited to, electromechanical and electrical devices, electronic components, aircraft parts and hardware. This individual has the responsibility and authority to carry out assigned tasks. SPECIFIC DUTIES Visual and dimensional inspection of all product, including corresponding documentation received into CTG facility Ability to complete a full analysis on all EEE Devices within the Laboratory Ability to learn and subsequently operate all test equipment within the Laboratory Department Prepare and complete all necessary documentation (records) for reporting acceptance/rejection of items inspected and/or tested. Identify nonconformity to provide data to Quality Manager. Ability to communicate, document and report all nonconformity within internal system and direct supervisor. Ability to conduct work as assigned by senior management. Ensure daily tasks and priority inspections are completed ensuring all stock sales are completed for the day. Ability to understand industry traceability and documentation requirement as required for each industry Ability to evaluate and differentiate between various commodity types. Review and implement detailed inspection reports to provide all information regarding product testing and inspection Ability to use general inspection gages, Ex. Calipers, Micrometers, etc. Ability to understand and decipher basic blueprint, data sheet, technical sheet requirements. Must possess the ability to verify products fit, form and function by utilizing the appropriate gages to identify conformity. Ensure First Article Inspection requirements are done in accordance with AS9102 and customer requirements. For source conducted first article inspection, utilized tools, equipment as appropriate to conduct GD&T for inspection reports. Complete AS9102 or equivalent or customer source designated reports for all First Articles and Source Inspections. STANDARD REQUIREMENTS Comply with all requirements of International Standard ISO9001 and ISO27001, NIST 800-171, CMMC - Cyber Security and Informational Data Security Requirements. Aerospace Management System Standards AS9100, AS9120, IDEA-QMS-9090, ASA-100 and supporting construct standards AS6081, IDEA-STD-1010, AC7402-CAAP, CCAP-101, FAA AC00-56, ANSI/ESD S20.20. All employees shall commit and comply with the requirements of AS5553 for Counterfeit Electrical, Electronic and Electromechanical (EEE) Parts - Avoidance, Detection, Mitigation and Disposition practices. METRICS AND MEASURABLES Daily throughput (inspections/Lab steps completed) Quality Issue detections (Incoming NCM ) Outgoing Quality (customer Escapes) IDEA Certification and knowledge implementation Use of GD&T and FAI knowledge for timely FAIR completion Issue communication Daily 6S/ESD/FOD policies followed Ability to find datasheets/drawings information on CTG Systems Diversity of inspections (EC/EM/HA/Hardware/etc) Achieving CQI certification EDUCATION / EXPERIENCE / COMPENTENCY High School Diploma or equivalent 1 year of manufacturing or quality experience is a plus but not required Must be proficient in English, both written and verbal communication skills Good arithmetic skills are required Mechanical aptitude desired Working knowledge of measurement instruments: i.e., calipers, etc. Basic proficiency of Microsoft Excel and Word Must complete IDEA-ICE-3000 Certification within 6 months of hire. Able to pass internal testing and training to meet internal requirements Must demonstrate acceptable vision requirement.

Job Description Job Title: Manufacturing Quality Technician II Job Duration: 6 Months Contract - W2 Note: Schedule and Shift: 9-80 A|1st Shift|07:30 AM This position will also support Saddle River NJ and Huntsville AL but will be based out of West Caldwell Description: Mercury Systems is seeking a talented individual to help drive cutting edge technology to mission critical aerospace and defense applications. As a Quality Technician, you will support our team of quality engineers by providing both technical and administrative assistance. You will be responsible for ensuring the accuracy of production records, discrepancy reports, and supplier documentation. Additionally, you will collaborate with operations, quality, purchasing, and stockroom to help achieve team objectives and drive continuous improvement. Job Responsibilities: Accurately completes AS9102 First Article Inspection Report (FAIR) and other dimensional inspection reports. Accurately reviews AS9102 First Article Inspection Report (FAIR) and other dimensional inspection reports from suppliers. Accurately compiles and completes End Item Data Packages (EIDP) Administrate and maintain calibration system complying to AS9100 and ISO 17025 for equipment. Updating calibration system cycle inventory across sites. Serve as the ESD coordinator for the site Perform comprehensive ESD program audits per ANSI/ESD S20.20 standards Inspect all grounding systems, flooring, and workstations, carts and shelving units Verify compliance with Mercury Systems' internal ESD policies Test equipment calibration & certification Data Review, Reporting & Corrective Actions Navigates internal company software and database systems to gather quality data information. Administrate and maintain calibration system to current updates. Create and submit Purchase Requisition (PR) to procurement department for Purchase Order release. Request quotes from external calibration houses. Coordinate with operations on site calibration schedule for stationary equipment. Support QA receiving inspection, in-process inspection and final inspection activities Interprets and understand drawings, specifications, customer requirements Works effectively with and communicates with various departments including operations, planning, quality, and QC inspection KPI/Metrics Review & Reporting Maintain and ensure accurate record-keeping of production documentation Collect and Index supplier-provided documentation for components and services Engagement with process audits, reviews, and revisions. Required Qualifications: Typically requires a minimum of three (3) years of quality assurance experience High School diploma or General Education Degree (GED) Previous AS9102 First article inspection experience Previous AS9100 Quality Management Standard experience. Previous IPC-A-610 and IPC-J-STD-001 training and/or certification. Familiar with GD&T terminologies print reading Experience with electrical and mechanical inspection tools. Strong PC skills with Microsoft Office - Excel, Word, Power Point, Minitab, JMP and database systems Must currently have or be eligible to obtain a DoD Secret clearance Preferred Qualifications: Experience in aerospace and defense industry Experience with any of the following business application systems - Oracle, Factory Logics, Power BI, Tableau, Agile, Net-Inspect -- Thanks and Regards, Jaswanth, Technical Recruiter *********************************** Phone- ************** | | | | Global Workforce Solutions | Certified MBE & EDGE Company | Microsoft Partner Direct Hire | Contingent Staffing | SOW Services | Clinical Staffing| IT Consulting | Payrolling You should be proficient in: IPC-A-610 IPC Joint Industry Standard (IPC-J-STD) AS9100 AS9102 High School / GED AS9100 Experience Machines & technologies you'll use: ERP Software (Oracle)

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

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. 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 Requirements:

Quality Control Microbiology Analytics I, II, III QC Microbiology Analyst I The Quality Control Microbiology Analyst I serves as a support role to clinical and/or commercial production. The QC Microbiology Analyst I will perform environmental monitoring activities including, but not limited to, non-viable particulate testing, active air viable, passive air viable, surface viable, and personnel monitoring. This position will report into the Manager of QC Microbiology. Environmental monitoring in controlled environments: Non-viable particulate monitoring; Active viable air monitoring, Personnel monitoring, Surface sampling, Passive air monitoring Equipment monitoring: Ensure equipment is in proper working conditions; Ensure all equipment is properly; maintained/calibrated; Assist with routine laboratory testing; Plate reads and incubations Shipping of test samples and equipment to contract laboratories for testing Complete all documentation according to written Standard Operating Procedures in accordance to Current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP). REQUIREMENTS Associates degree in a science or relevant field required; Minimum 0-2 years of experience or equivalent experience. Environmental monitoring or within the biopharmaceutical industry experience preferred. Proficient with computer software such as; Microsoft Office Strong written and oral communication skills Must be detail oriented, can multi-task, work in a team environment, and have the flexibility to adapt to company growth as well as its evolving responsibilities Trained in GxP/GDP, Safety The QC Microbiology Analyst I must be able to maintain aseptic behavior within a cleanroom environment for an extended period. Must have the ability to work in a team-oriented environment and with clients Must be able to work during the weekend, holidays and as required by the company Must be able to handle the standard/moderate noise of the manufacturing facility While performing the duties of this job, the employee may occasionally be exposed to infectious diseases transmittable through human blood, tissues, or bodily fluids and are expected to utilize universal precautions with all human specimens. QC Microbiology Analyst II The Quality Control Microbiology Analyst II serves as a support role to clinical and commercial production. Microbiology Analyst II will perform environmental monitoring activities including, but not limited to, non-viable particulate testing, active air viable, passive air viable, surface viable, and personnel monitoring. This position will report into the Manager of QC Microbiology. Environmental monitoring in controlled environments; Non-viable particulate monitoring, Active viable air monitoring Personnel monitoring, Surface sampling, Passive air monitoring Equipment monitoring; Ensure equipment is in proper working conditions, Ensure all equipment is properly maintained/calibrated, Program equipment with proper workflows, Assist with routine laboratory testing, Plate reads and incubations Shipping of test samples and equipment to contract laboratories for testing Produce documentation according to written Standard Operating Procedures in accordance to Current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP) Writing/conducting investigations pertaining to environmental monitoring and testing Develop and train QC Microbiology Analyst I personnel on relevant business processes. REQUIREMENTS BA/BS in a science or relevant field required or equivalent experience; Minimum 2-4 years of experience with environmental monitoring or within the biopharmaceutical industry. GxP/GDP, Safety Trained Proficient with computer software such as; Microsoft Office, MODA/LIMS Familiarity with ISO and EU standards Strong written and oral communication skills Technical training ability Must have the ability to work in a team-oriented environment and with clients Must be able to work during the weekend, holidays, and as required by the company Must be able to handle the standard/moderate noise of the manufacturing facility The QC Microbiology Analyst II must be able to maintain aseptic behavior within a cleanroom environment for an extended period. Must be detail oriented, can multi-task, work in a team environment, and have the flexibility to adapt to company growth as well as its evolving responsibilities While performing the duties of this job, the employee may occasionally be exposed to infectious diseases transmittable through human blood, tissues, or bodily fluids and are expected to utilize universal precautions with all human specimens. QC Microbiology Analyst III The Quality Control Microbiology Analyst III serves as a support role to clinical and/or commercial production. The QC Microbiology Analyst III will coordinate data for batch release, participate in project/client meetings, and author/revise environmental monitoring procedures. Additionally, the QC Microbiology Analyst will perform environmental monitoring activities including, but not limited to, non-viable particulate testing, active air viable, passive air viable, surface viable, and personnel monitoring. Documentation according to written Standard Operating Procedures in accordance to Current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP). Coordinates data for batch release Participation in project/client meetings and communications, providing scientific and technical expertise Authoring/revising Standard Operating Procedures, Work Instructions, Forms, and Protocols Review of investigations and documentation of non-confirming events and environmental excursions. Apply expertise of compliance requirements to maintain an inspection-ready state. Participate and act as subject matter expert during audits/inspections Develop and train QC Microbiology Analyst II on relevant business processes Processing of purchase orders for outsourced testing and lab supplies Coordinates work orders REQUIREMENTS BA/BS in a science or relevant field required or equivalent experience; Minimum 5-7 years of experience with environmental monitoring or within the biopharmaceutical industry GxP/GDP Trained Proficient with computer software such as; Microsoft Office, MODA/LIMS, Microsoft Visio (preferred), Netsuite (preferred), Maximo Asset Management System (preferred) Proficient knowledge of ISO and EU standards Strong knowledge of quality systems and ability to interpret Quality standards for implementation and review. Strong written and oral communication skills Strong technical writing skills Technical training experience Must be detail oriented, can multi-task, work in a team environment, and have the flexibility to adapt to company growth as well as its evolving responsibilities Must utilize proper personal protective equipment (PPE) when handling all human specimens, gases, corrosive chemicals, and liquid nitrogen. Must have the ability to work in a team-oriented environment and with clients Must be able to work during the weekend, holidays and as required by the company Must be able to handle the standard/moderate noise of the manufacturing facility Working Environment While performing the duties of this job, the employee may occasionally be exposed to infectious diseases transmittable through human blood, tissues, or bodily fluids and are expected to utilize universal precautions with all human specimens. Must utilize proper personal protective equipment (PPE) when handling all human specimens, gases, corrosive chemicals, and liquid nitrogen. Other exposures may include gases (nitrogen), or corrosive chemicals (Clorox, potassium hydroxide), or exposure to liquid nitrogen. The noise level in the work environment is moderately noisy. Must have the ability to work in a team-oriented environment and with clients Must be able to work during the weekend, holidays, and as required by the company Must be able to handle the standard/moderate noise of the manufacturing facility Physical Requirements The QC Microbiology Analyst II must be able to maintain aseptic behavior within a cleanroom environment for an extended period. Must be physically capable to stand; walk; site; bend; stretch; use hands to finger, handle or feel; reach with hands and arms; and talk or hear. Occasionally personal protective equipment may be required including lab coat, latex gloves, safety glasses and/or respirator. Please note these job descriptions are 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.

EP Tech / EP Lab Tech Location: Paramus, NJ Agency: Triage Staffing LLC Pay: $3,385 per week Shift Information: Days - 4 days x 10 hours Contract Duration: 13 Weeks Start Date: 1/12/2026 AlliedTravelCareers is working with Triage Staffing LLC to find a qualified Electrophysiology Tech in Paramus, New Jersey, 07652! Travel Radiology: EP Tech Paramus Location: Paramus Start Date: 1/12/2026 Shift Details: 10H Days (6:30 AM-4:30 PM) 40 hours per week Length: 13 WEEKS 13 weeks Apply for specific facility details.EP Tech About Triage Staffing LLC At Triage, we prefer to be real. Real about expectations--both ours and yours. Real about how a decision you make today could affect your tomorrows. Real about how compensation actually works. Real about how great-- or grating--your next supervisor may be. Being real allows everyone at Triage to be ready. Ready to serve you with real honesty. So if that gig near the ocean is really no day at the beach, or that third shift comes with a second-class rate, we tell you. So you can be ready, too. We staff all four major divisions of acute care - nursing, lab, radiology, and rehab therapy One point of contact for both travelers and facilities (per division) In-house compliance and accounting specialists On-staff clinical liaisons Mentoring program that is run and managed by actual clinicians - yeah, you read that right And more (because of course there's more) Are we the biggest? No. Are we the best? That's rather subjective, but we're trying to be. Will we work like hell to get you as close to your idea of heaven as possible? Yes. Yes, we will. In 2021, Triage and TaleMed merged to become better together under the Triage name. 11122777EXPPLAT

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.

Job Description JOB TITLE: Quality Control Technician TYPE: Full time, regular COMPENSATION: $20.00/hr - $28.00/hr Clarapath is a medical robotics company based in Westchester County, NY. Our mission is to transform and modernize laboratory workflows with the goal of improving patient care, decreasing costs, and enhancing the quality and consistency of laboratory processes. SectionStar™ by Clarapath is a ground-breaking electro-mechanical system designed to elevate and automate the workflow in histology laboratories and provide pathologists with the tissue samples they need to make the most accurate diagnoses. Through the use of innovative technology, data, and precision analytics, Clarapath is paving the way for a new era of laboratory medicine. Role Summary: The Quality Control Technician will play a key role in ensuring the quality and reliability of Clarapath's advanced electro-mechanical medical device, SectionStar™. This position is essential for inspecting components, assemblies, and finished products to verify conformance with specifications and quality standards. The ideal candidate will have a strong foundation in inspection methods, measurement techniques, and documentation practices, supporting both manufacturing and engineering teams to maintain consistency across production. We're looking for a hands-on, detail-oriented team player who thrives in a fast-paced environment and takes pride in upholding the precision and quality that define Clarapath's products. Responsibilities: Inspect incoming materials, in-process assemblies, and finished products using measurement tools and visual inspection techniques Interpret engineering drawings, specifications, and inspection procedures to verify conformance Record and maintain inspection data, generating non-conformance reports (NCRs) when necessary Collaborate with Quality, Manufacturing, and Engineering teams to identify and resolve quality issues Perform functional and dimensional testing using calipers, micrometers, gauges, CMMs, and other inspection tools Support calibration and maintenance of inspection equipment Assist in root cause analysis and corrective/preventive action (CAPA) activities Maintain cleanliness and organization in inspection and test areas Ensure compliance with ISO 13485, FDA, and internal quality system requirements Qualifications: High school diploma or equivalent required; associate degree or technical certification preferred 1-3 years of experience in quality inspection, preferably in medical devices, precision manufacturing, or electronics Proficient in the use of precision measurement instruments (calipers, micrometers, gauges, etc.) Ability to read and interpret mechanical drawings and technical specifications Strong attention to detail and documentation accuracy Familiarity with quality management systems (QMS) and manufacturing processes Basic computer skills (Microsoft Office, ERP systems experience, a plus) Team-oriented with strong communication and problem-solving skills Company Offers: Competitive salary will be commensurate with experience and education Comprehensive benefits package available: (healthcare, vision, dental and life insurances; 401k; PTO and holidays). A collaborative and diverse work environment where our teams thrive on solving complex challenges Ability to file IP with the company Connections with world class researchers and their laboratories Collaboration with strategic leaders in healthcare and pharmaceutical world A mission driven organization where every team member will be responsible for changing the standards of delivering healthcare Clarapath is proud to be an equal opportunity employer. We are committed to providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status. In addition to federal law requirements, Clarapath complies with applicable state and local laws governing nondiscrimination in employment. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

As a QC Technician, you will be a key player in ensuring product quality and safety throughout the production process of bread. Your role will encompass line auditing, environmental monitoring, air sampling, and participating in a monthly SQF audit. You will also be responsible for the calibration and verification of scales, monitors, and other basic instrumentation. Responsibilities * Conduct line auditing for bread production. * Perform environmental monitoring and air sampling. * Participate in monthly SQF audits. * Calibrate and verify scales, monitors, and other instrumentation. * Utilize MS Excel, Word, and Office for documentation. * Monitor and verify product quality following GMP. * Perform visual inspections and quality checks on product weights, codes, and labeling. * Address food safety issues and customer complaints with QA Supervisors. * Complete other periodic tasks as required. Essential Skills * Quality Control experience in the Food and Beverage industry. * High School Diploma. * Knowledge of Food Safety practices including SQF, FSMA, or HACCP. * Proficiency in Microsoft Word, PowerPoint, and Excel. * Ability to communicate effectively and work in a team. * Adaptability to change in a fast-paced production environment. Additional Skills & Qualifications * Bilingual proficiency is advantageous. * Experience in a GMP environment. * Familiarity with Environmental Monitoring, HACCP, SQF, Production, and Air Sampling. * HACCP or SQF Certification is a plus. * Passion for the food industry and a desire to grow in this field. Work Environment Join a thriving company known for its growth and expertise in the food industry. You will work in a dynamic Pastry Production facility, learning from leaders with over 20 years of experience in training technicians. The company imports and exports with European countries and distributes 300-500 additional items beyond their in-house manufacturing. This role offers an exceptional opportunity to expand your skills and contribute to a growing enterprise. Pay and Benefits The pay range for this position is $25.00 - $27.00/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 Paterson,NJ. Application Deadline This position is anticipated to close on May 13, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. 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.

Job Description BASIC FUNCTIONS Mid-level position. Performs counterfeit lab testing and visual inspection of various commodities including, but not limited to, electromechanical and electrical devices, electronic components, aircraft parts and hardware. This individual has the responsibility and authority to carry out assigned tasks. SPECIFIC DUTIES Visual and dimensional inspection of all product, including corresponding documentation received into CTG facility Prepare and complete all necessary documentation (records) for reporting acceptance/rejection of items inspected and/or tested. Ability to complete a full analysis on all EEE Devices within the Laboratory Ability to operate all test equipment within the Laboratory Department Identify nonconformity to provide data to Quality Manager. Ability to communicate, document and report all nonconformity within internal system and direct supervisor. Ability to conduct work as assigned by senior management. Ensure daily tasks and priority inspections are completed ensuring all stock sales are completed for the day. Ability to understand industry traceability and documentation requirement as required for each industry Ability to evaluate and differentiate between various commodity types. Review and implement detailed inspection reports to provide all information regarding product testing and inspection Compile, review data and complete test reports IAW CTG Standards Ability to use general inspection gages, Ex. Calipers, Micrometers, etc. Ability to understand and decipher basic blueprint, data sheet, technical sheet requirements. Must possess the ability to verify products fit, form and function by utilizing the appropriate gages to identify conformity. Ensure First Article Inspection requirements are done in accordance with AS9102 and customer requirements. For source conducted first article inspection, utilized tools, equipment as appropriate to conduct GD&T for inspection reports. Complete AS9102 or equivalent or customer source designated reports for all First Articles and Source Inspections. Comply with all requirements of the AS9120, ISO 9001, ASA-100, and IDEA QMS 9090 Quality Management System and criteria of CCAP-101, AS6081, AC7402 and ANSI/ESD-S20.20 STANDARD REQUIREMENTS Comply with all requirements of International Standard ISO9001 and ISO27001, NIST 800-171, CMMC - Cyber Security and Informational Data Security Requirements. Aerospace Management System Standards AS9100, AS9120, IDEA-QMS-9090, ASA-100 and supporting construct standards AS6081, IDEA-STD-1010, AC7402-CAAP, CCAP-101, FAA AC00-56, ANSI/ESD S20.20. All employees shall commit and comply with the requirements of AS5553 for Counterfeit Electrical, Electronic and Electromechanical (EEE) Parts - Avoidance, Detection, Mitigation and Disposition practices. METRICS AND MEASURABLES Daily throughput (inspections/Lab steps completed) Quality Issue detections (Incoming NCM ) Outgoing Quality (customer Escapes) IDEA Certification and knowledge implementation Use of GD&T and FAI knowledge for timely FAIR completion Issue communication Daily 6S/ESD/FOD policies followed Ability to find datasheets/drawings information on CTG Systems Diversity of inspections (EC/EM/HA/Hardware/etc) Achieving CQI certification EDUCATION / EXPERIENCE / COMPENTENCY High School Diploma or equivalent with a minimum of 2 years' experience performing in-process and final inspection preferably in a machining, automotive or aerospace business Must be proficient in English, both written and verbal communication skills Good arithmetic skills are required Mechanical aptitude desired Ability to correctly use and interpret basic measuring tools including weight gauge, micrometer, caliper scale (linear), gauge blocks, thread gauges, and comparative standards Basic proficiency of Microsoft Excel and Word Independent; can work with limited supervision and direction Must complete IDEA-ICE-3000 Certification within 6 months of hire. Able to pass internal testing and training to meet internal requirements ASQ CQI certified or must completed certification within 1 year of accepting position Strong Electronics inspection knowledge preferred Must demonstrate acceptable vision requirement.

Job Description **Job Title: Manufacturing Quality Technician II ** **Job Duration: 6 Months Contract - W2 ** 2 Henderson Dr, West Caldwell, NJ 07006 (Onsite) ** **Note: ** **Schedule and Shift: 9-80 A|1st Shift|07:30 AM ** **This position will also support Saddle River NJ and Huntsville AL but will be based out of West Caldwell ** **Description: ** Mercury Systems is seeking a talented individual to help drive cutting edge technology to mission critical aerospace and defense applications. As a Quality Technician, you will support our team of quality engineers by providing both technical and administrative assistance. You will be responsible for ensuring the accuracy of production records, discrepancy reports, and supplier documentation. Additionally, you will collaborate with operations, quality, purchasing, and stockroom to help achieve team objectives and drive continuous improvement. **Job Responsibilities: ** Accurately completes AS9102 First Article Inspection Report (FAIR) and other dimensional inspection reports. Accurately reviews AS9102 First Article Inspection Report (FAIR) and other dimensional inspection reports from suppliers. Accurately compiles and completes End Item Data Packages (EIDP) Administrate and maintain calibration system complying to AS9100 and ISO 17025 for equipment. Updating calibration system cycle inventory across sites. Serve as the ESD coordinator for the site Perform comprehensive ESD program audits per ANSI/ESD S20.20 standards Inspect all grounding systems, flooring, and workstations, carts and shelving units Verify compliance with Mercury Systems' internal ESD policies Test equipment calibration & certification Data Review, Reporting & Corrective Actions Navigates internal company software and database systems to gather quality data information. Administrate and maintain calibration system to current updates. Create and submit Purchase Requisition (PR) to procurement department for Purchase Order release. Request quotes from external calibration houses. Coordinate with operations on site calibration schedule for stationary equipment. Support QA receiving inspection, in-process inspection and final inspection activities Interprets and understand drawings, specifications, customer requirements Works effectively with and communicates with various departments including operations, planning, quality, and QC inspection KPI/Metrics Review & Reporting Maintain and ensure accurate record-keeping of production documentation Collect and Index supplier-provided documentation for components and services Engagement with process audits, reviews, and revisions. **Required Qualifications: ** **Typically requires a minimum of three (3) years of quality assurance experience ** **High School diploma or General Education Degree (GED) ** **Previous AS9102 First article inspection experience ** **Previous AS9100 Quality Management Standard experience. ** **Previous IPC-A-610 and IPC-J-STD-001 training and/or certification. ** **Familiar with GD&T terminologies print reading ** Experience with electrical and mechanical inspection tools. Strong PC skills with Microsoft Office - Excel, Word, Power Point, Minitab, JMP and database systems Must currently have or be eligible to obtain a DoD Secret clearance **Preferred Qualifications: ** **Experience in aerospace and defense industry ** **Experience with any of the following business application systems - Oracle, Factory Logics, Power BI, Tableau, Agile, Net-Inspect ** Salary info: $25 - $26 / hr