87 quality-assurance-control jobs found in Mahwah, NJ

Senior Quality Assurance Engineer Location: Mahwah, NJ Duration: 6 months with a possible extension  Pay Terms: up to $72/hour on W-2 Description/Comment: Develops and implements methods and procedures for process control and process improvement. Analyzes reports on defective products to determine trends and recommend corrective actions. Collaborates with post market representatives on quality problems, ensures that effective corrective actions are implemented and contributes to quality improvement programs. This is an individual contributor role that requires the use of judgement in applying professional expertise and is expected to work independently with minimal supervision. Roles typically require a university degree or an extensive amount of practical knowledge gained through experience. Job requires an understanding and application of procedures and concepts of own discipline. The job requires attention to detail in making evaluative judgements based on the analysis of...

Title: Senior Quality Assurance Engineer Location: Mahwah, NJ Start date: ASAP Responsibilities: Develops and implements methods and procedures for process control and process improvement. Analyzes reports on defective products to determine trends and recommend corrective actions. Collaborates with post market representatives on quality problems, ensures that effective corrective actions are implemented and contributes to quality improvement programs. EUMDR contract position; would be authoring and approving post market safety reports as well as trend reports. Requirements: Bachelor’s Degree or equivalent and a minimum of 2 or more years’ experience. Use of judgement in applying professional expertise and is expected to work independently with minimal supervision. An understanding and application of procedures and concepts of own discipline. Attention to detail in making evaluative judgements based on the analysis of factual information....

Company Description Veolia Group aims to be the benchmark company for ecological transformation. With nearly 220,000 employees worldwide, the Group designs and provides game-changing solutions that are both useful and practical for water, waste and energy management. Through its three complementary business activities, Veolia helps to develop access to resources, preserve available resources and replenish them. In 2021, the Veolia group provided 79 million inhabitants with drinking water and 61 million with sanitation, produced nearly 48 million megawatt hours and recovered 48 million tons of waste. Veolia Environnement (Paris Euronext: VIE) achieved consolidated revenue of 28,508 billion euros in 2021. www.veolia.com   Job Description You’ll be part of a specialized team working closely with project managers and other technical groups to set up and run data-driven environmental compliance programs that contribute to a cleaner, more sustainable planet. The position will...

Our client in Paterson, NJ is looking for hardworking, motivated talent to join their team. Don't wait… apply today! What's in it for you? Payrate $19.50 Shift 6am to 6:30pm, 12 hour shifts (facility is 24/7) Paid training Full time hours Clean and safe work environment What will you be doing? Testing Chemical Samples Inspecting Quality of products Are you Interested? Stop your job search and apply today! A recruiter will be in touch within 24 hours. Share this job with friends and family and earn dollars with every successful hire. ManpowerGroup recognizes the importance of providing an accessible and barrier-free environment. We are committed to creating a welcoming, fair and inclusive environment by offering equal opportunity to access our services. At ManpowerGroup, we are committed to providing accommodations, and will work with you to meet your needs.

Key Responsibilities: Develop and build Supplier Quality Requirements Manual, Product Specifications, Inspection and Testing plan and ongoing monitor supplier compliance.  Create standardized procedures to manage supplier quality performance of incidents and defective rates.  Implement “Supplier Corrective Action Plan”, “Supplier Recovery Plan” and “Supplier Improvement Program” Develop and implement Supplier Score card program.   Ongoing monitor supplier KPI and drive continuous improvement Develop and lead Supplier On-site quality audit guidelines and provide direction and requirements to the agent and 3rd. party inspection firm to assure satisfactory results Provide all aspects of quality inspection requirements, manage inspection results and compliance from factory pre-shipment inspection, to Warehouse incoming inspection, to customer field complaints.  Investigate issues and provide...

Spec Quality Assurance - Clifton, NJ - Monday - Friday JOB SUMMARY Support and coordinate efforts that foster quality and ensure that all pre-analytical, analytical and post-analytical processes are consistent with our company values and mission. JOB RESPONSIBILITIES : Licensing and Accreditation Support the internal inspection process of the business unit, associated laboratories and specimen collection sites to ensure compliance with applicable federal, state, and local regulations, College of American Pathologists (CAP) accreditation requirements and Quest Diagnostics standards. Serve as a resource regarding Clinical Laboratory Improvement Amendments of 1988 (CLIA '88) regulations and CAP accreditation standards. Proficiency Testing Assist and ensure enrollment and participation in proficiency testing for each test to include Corrective Action when necessary. Coordinate the Validity Check program and Blind Samples resubmission program, if applicable. Assist in...

Job Description: Responsible for the identification and documentation of quality discrepancies related to assembly, process, mechanical, electrical, and electro-mechanical systems. Facilitates the implementation of standards, methods and procedures for inspecting, testing and evaluating the precision, accuracy and reliability of company products. Leads the preparation and execution of internal audits within established manufacturing and production controls to ensure compliance with internal and external specifications and standards. Liaises with auditing groups and inspectors to develop formal written reports, and recommend corrective actions. Identifies trends in discrepancies and collaborates with process owners on the refinement and optimization of business processes. Oversees testing department activities and work of inspectors. Reviews, approves, and controls work order flow tags. Develops inspection techniques, tools, and supplemental...

Manager Electronics Quality Passiac, New Jersey Full time direct hire Full benefits Relocation package US Citizen Only Job Description: The Quality Manager will lead the program quality engineering team and be responsible for program and product Quality Assurance efforts on the site. The Manager will create strategic partnership with cross-functional leadership to ensure product and process integrity, leading to customer satisfaction, overall mission success while supporting division quality, delivery and cost targets. This role will work closely with the sector quality director to drive strategic initiatives across the sector. Essential Functions: Hands on leader with responsibility for resolving technical challenges, ensuring successful tactical execution, as well as creating and implementing the strategic vision for the Quality department. Work closely with the program teams and the functional organizations to ensure that all phases of the...

Company Description   SGS is the world’s leading inspection, verification, testing and certification company. SGS is recognized as the global benchmark for quality and integrity. With more than 94,000 employees, SGS operates a network of over 2,600 offices and laboratories around the world. Job Description   Data Review, Quality Control is responsible for the second person review of selected data generated in the laboratory.  You must be sensitive to the demanding regulatory compliance requirements attending to the operation of a pharmaceutical testing laboratory.  This job also requires the ability to demonstrate a high commitment to interpersonal relations. Perform data review following staff performance of customer test requests in a timely and effective manner. Customer test requests include wet chemistry, instrumentation, and/or microbiological data reviews Perform reviews for reagent and standard preparations and their assays or suitability testing and/or media...

Title:  Quality Auditor Location:  Fairfield, NJ Duration:  Contract to hire  Schedule:  M-F Full Time Target Start Date:  ASAP Responsibilities: Transitioning to corporate quality management system creating a backlog of quality events, deviations, and unexpected test results. Will receive a data packet with quality issue- will need to look into why?  What caused this event?   Will be required to detail out in standard format and translate raw data from the investigations into reports (report writing skills needed) Good communication skills to work with lab analysts, study managers, and quality departments required. Requirements: BS Micro preferred, will consider related science 3-5 years’ QA, Micro, or Regulatory experience from pharma Risk assessment, investigations, and auditing experience Experience with quality management systems General Microsoft Office computer skills

A hospital in Westchester County is currently seeking a licensed professional to join their staff as their new Quality Systems Laboratory Manager. In this role, the Quality Systems Laboratory Manager will be responsible for the overall management of the Quality Management, Licensure/Accreditation and Performance Improvement Programs for the Medical Center Laboratory. Responsibilities The Quality Systems Laboratory Manager will: Oversee and manage the quality, regulatory compliance, and safety operations of the Clinical and Pathology Laboratories Work closely with Laboratory Leadership and staff and the hospital’s Compliance department to coordinate and standardize quality, compliance and safety practices across the health system to provide excellent patient care Act as a liaison and link between the laboratory and the hospital quality plans Function as an in-house surveyor of laboratory services to assure that the laboratories remain in a ready survey state....

Top-tier Aerospace Manufacturer - Experienced Quality Engineer - Growth Opportunity This Jobot Job is hosted by: David Six Are you a fit? Easy Apply now by clicking the "Apply Now" button and sending us your resume. Salary: $80,000 - $110,000 per year A bit about us: Are you looking to join a Top-tier Aerospace Manufacturer of precision components? We are looking for a highly motivated individual to join Quality Engineering team as the organization continues to experience progressive growth. In this role, you will communicate product issues, concerns, and specifications with customers and other members of the quality and internal teams. You will be responsible for Root Cause and Corrective Action. Work to develop, coordinate, implement, monitor, and evaluate quality activities and systems to improve customer satisfaction. Why join us? Amazing benefits Professional growth Work with products from diverse industries Supportive, friendly, and dynamic team...

Overview POSITION SUMMARY The Manager, Quality Control will oversee and coordinate the daily activities of the Quality Control Laboratory, while ensuring compliance with protocols, company procedure and cGMP standards   The Manager will lead a group of approximately 12 employees in the Quality Control laboratory and interact with other functional departments to ensure QC services are provided timely, efficiently and in a compliant manner. Responsibilities ESSENTIAL FUNCTIONS - Directs the work activities of the Quality Control group to ensure that testing is executed in a timely and compliant manner. Maintain the necessary organizational and planning skills to effectively assign work schedules to ensure timely completion of all tasks necessary to provide responsive delivery of quality services to other functional areas.  - Conduct, review and/or approve laboratory investigations of product, equipment and analytical method issues. Act as primary point of contact for QC team...

Summary/objective The Quality Assurance Manager will own the responsibility of developing/building, implementing, and managing the quality management system (QMS) and all quality areas within company, including but not limited to Distribution and Service of medical devices and products. Essential functions Develop, implement, manage, document and maintain the quality management system in conjunction with FDA requirements under CFR 21 Part 820 Establish and execute internal quality audit processes Develop, document and institute recall procedures Conduct Document Control within the document management system (DMS) and work with HR & IT to maintain the learning management system (LMS) Train staff on SOP compliance as required Handle both customer and supplier complaints and reporting, including CAPA and SCAR documentation Develop and continuously report on Quality Objectives & Metrics & KPIs Conduct annual Management Reviews with Senior Leadership Conduct...

Senior Quality Assurance role - Onsirte - Jersey city NJ or Phoenix AZ Qualifications: * Able to analyze and understand business requirement to develop and execute manual Testcases and there by create automation scripts if applicable. * Significant exposure to and demonstrated proficiency in all aspects of testing and analysis, including software requirements, systems facilities, and execution protocols. * Experience with Architecture design of multi-tiered client/server applications. * Must be well organized and self-motivated and be able to work with minimal supervision. * Excellent problem solving, analytical and communication skills (both oral and written). * Ability to work with others in a team environment. * Ability to work on aggressive schedules. May require work beyond normal hours (weekends or evenings). * Working knowledge of SQL- create queries to verify test results or Troubleshoot issues. * Experience in test automation tools preferably in Selenium,...

The following are essential duties and responsibilities for this position: Responsible for direct management of all Quality Assurance associates. Responsible for ensuring Food Safety and Food Quality policies and procedures are adhered to including but not limited by SQF Code, CFIA, HACCP, Refresco Quality and any customer quality requirements. Responsible for direct management and utilization of laboratory (analytical and microbiology), water treatment, syrup blending, sanitation, microbiological equipment, raw materials, and all quality processes. Optimize resources while ensuring raw materials and finished product meet specifications and manufacturing standards and in accordance with FDA, CFIA, GMP's, HACCP, and all other governmental policies, procedures, and regulations. Oversee daily Quality Assurance inspections to ensure all products are meeting compliance. Write, update, and maintain SOP's (Standard Operating Procedures) for the Quality Assurance Program....

Location: Morristown, NJ Description: Our client is currently seeking a Quality Director, Steriles Description: Title:   The Director, Quality – Steriles Location: Morristown, NJ (1-2 days onsite/week)- Remote-Hybrid Job Type: Perm RESPONSIBILITIES: Primary responsibilities of this role include the following: 1. Leadership: Provides guidance and supervision to a team of Quality Associates, Sr. Associates and Managers who work with Contract Manufacturers and partners which manufacture and/or supply injectable/combination products for Company. 2. Third-Party Support: a. Ensures all injectable/combination products manufactured for or on behalf of Company by third party suppliers are manufactured, packaged, and tested in compliance with cGMPs, the approved ANDA/NDA, applicable regulatory requirements, and Company policies and procedures. b. Manages the batch release process for all third party manufactured injectable/combination products....

Title:  Quality Specialist Location:  Morristown, NJ (ON SITE DAILY)  Schedule:  Mon-Fri 8:30AM-5PM Type:  Contract to Hire Start date:  ASAP Responsibilities: Write and/or revise Standard Operating Procedures (SOPs) (*off of templates) Lead investigations into consumer complaints and make recommendations for product improvements Review and release products for commercial distribution Coordinate stability and other quality testing programs "reach out to clients contract manufacturers to review stability protocols)" Address and escalate, if needed quality issues that arise Assist in Quality Audits of manufacturing facilities, if required Develop and implement Corrective/Preventive Actions (CAPA) And other quality related projects as required by client Requirements: 4 Year degree in a life science or related field 3-5 years in QA regulated GMP Quality from Pharma, OTC, Nutraceuticals or Medical Device (NO  FOOD) Experience with...

RESPONSIBILITIES: Kforce's client, a leading National CPA firm is seeking a Quality Control Partner in New York, NY. Summary: The Quality Control Partner will be responsible for leading review of financial statements, work papers, and related audited and reviewed work product, to ensure compliance with regulatory standards and requirements (PCAOB, AICPA) and Firm policies. Responsibilities: In this role, the Quality Control Partner leads the QC group in the review of financial statements, work papers, and related audited and reviewed work product, to ensure compliance with all requirements Assist with internal quality programs to achieve strategic objectives through initiatives designed to meet Firm goals The Quality Control Partner leads the QC group regarding internal inspections of issuers and non-issuers, providing assistance to engagement teams undergoing PCAOB and other external inspections, coaching of engagement teams in the identification of and...

Optum is a company that's on the rise. We're expanding in multiple directions, across borders and, most of all, in the way we think. Here, innovation isn't about another gadget, it's about transforming the health care industry. Ready to make a difference? Make yourself at home with us and start doing your life's best work.(sm)   You’ll enjoy the flexibility to telecommute* from anywhere within the U.S. as you take on some tough challenges. Primary Responsibilities: Perform audits of designated workers compensation and auto medical bills to ensure accurate coding/billing practices by the provider Monitors bill aging for bills held to specified queue to ensure held age does not exceed 4 days Stays updated in state regulated rule changes Handles and assists in reconsideration issues, discusses payment disputes with provider when necessary Maintains professional knowledge by attending educational workshops, reviewing professional publications, maintains...