Quality assurance manager jobs in Orange, New Jersey - Page 3Create job alerts

Supported by more than 40 manufacturing facilities, we provide high-quality, affordable medicines, trusted by healthcare professionals and patients, to more than 100 countries across the globe including the United States.

Job Responsibilities * Ensure the team is informed of and adhering to the policy throughout assigned area(s) * Risk assessment of incidents involving alcohol * Review and complete incident reports * Coordinate with management and event security to report and intervene when necessary * Maintain a sa

Senior Data Platform Compliance Manager Job Summary The Senior Data Platform Compliance Manager will be responsible for leading and accomplishing compliance initiatives across BD's global data platforms, ensuring alignment to data privacy regulations (e.

We are seeking a detail-oriented Quality Assurance (QA) Specialist with strong expertise in Power BI testing and Microsoft Fabric migrations. Establish repeatable testing processes to validate data quality, consistency, and accuracy across Power BI reports and semantic models. Track and report quali

Job Title Regulatory Compliance Manager About your role: The Compliance Manager is responsible for managing compliance risk and executing the regulatory compliance goals for a prepaid debit portfolio. Advanced proficiency Microsoft Excel and PowerPoint * Bachelor's Degree What would be great to

ADDITIONAL EEO INFORMATION (Click link below) Know your Rights: Workplace Discrimination is Illegal Nearest Major Market: Newark Nearest Secondary Market: New York City Job Segment: Compliance, Computer Science, Project Manager, Engineer, Legal, Technology, Engineering.

Responsibilities Safety Manager As a Safety Manager in Rahway, NJ, you'll lead the charge in building a culture where safety is more than a priority - it's a core value. HazTek is seeking an experienced Safety Manager to oversee safety operations on our commercial construction projects.

At Blue Foundry Bank we invest in the well-being of our most prized asset…our employees! We provide a robust array of programs and benefits to help employees advance their careers and enhance the quality of their lives.

Compliance Analyst Req number: R6660 Employment type: Full time Worksite flexibility: Onsite Who we are CAI is a global technology services firm with over 8,500 associates worldwide and a yearly revenue of $1 billion+.We have over 40 years of excellence in uniting talent and technology to po

Investigates and verifies customer complaints and works with the Area and Regional Quality Managers including finalizing credits as required, appropriate disposition of any returned product and management of internal and customer requested RCCA. Plans, promotes, and organizes training activities rel

Develop and write high quality coding that meets customer requirements. Work closely with peer developers and QA team members to ensure overall quality of solutions.

You will earn real world experience by working directly with clients and receiving structured feedback from managers.

How would you like to join one of the most highly regarded financial institutions in New Jersey with deep roots in the community? Provident is a successful and highly regarded multi-billion dollar bank that continues to grow with branches in New Jersey, Eastern Pennsylvania and New York.Our longevit

We are looking for a Senior QA Engineer who will be an integral part of a cross-functional Agile product development group, responsible for ensuring the quality, reliability and usability of the HR/cloud solution. You will collaborate closely with Product Owners, Developers, UX/Design, DevOps and ot

Location: Berkeley Heights, NJ (Onsite) Type: Contract (Automation, Selenium, Mobile, Web Testing).Analyze Business Requirements Documents to get better understanding of the system both on technical and business perspectives.Postman, pipeline testing with various tools and knowledge on Node-based au

Quality Engineer is accountable for supporting new product development and product maintenance through the application of Quality Engineering skills for medical devices. Assists with supplier and internal quality system audits as a means of evaluating the effectiveness of the established Quality Sys

Quality Engineer is accountable for supporting new product development and product maintenance through the application of Quality Engineering skills for medical devices. Assists with supplier and internal quality system audits as a means of evaluating the effectiveness of the established Quality Sys

Applied knowledge of the FDA medical device quality system regulations and international quality system standards/regulations (e. Quality Engineer is accountable for supporting new product development and product maintenance through the application of Quality Engineering skills for medical devices.

Experience with Advanced Quality Management and knowledge of various quality systems, especially ISO 9001, and IATF 16949. Able to think critically and able to improve elements of the Automotive Quality System to remove waste of time and dollars, while increasing quality performance. Quality and Env

Collaborates with the Patient Safety and Quality Department as well as with the VP, Chief Quality/Safety to ensure that organizational wide safety and quality initiatives are implemented effectively and risk reduction strategies implemented wherever appropriate. Oversees various activities of the Pa

Ensure compliance with aerospace quality management standards, industry regulations, and IAQG requirements. Stay current with aerospace quality standards and contribute to continuous improvement and impartiality in certification activities. Bachelor's degree in Engineering, Quality, Aerospace, or a

Job Title: Quality Coordinator. Department Name: Quality Resource Services. Performs chart audits, workflow analysis and other activities to measure and monitor clinical quality.

Minimum of three (3) years of experience in quality control or similar quality assurance activities. Investigate quality issues, report findings to the Quality Manager or Supervisor, and ensure that corrective actions are implemented. Maintain ongoing communication with Line Leaders, keeping them in

Statistical methods for Quality Assurance. As a Staff Quality Engineer II, you'll play a vital role in our Wearable Injector platform, contributing to new product development and maintenance. Evaluate customer requirements and identify quality standards.

This person will assist in organization-wide quality activities under the direction of the Director of Quality Services within the Quality Assurance & Research Team. Supports the Quality Assurance & Research department with other organization-wide activities including but not limited to internal aud

This person will assist in organization-wide quality activities under the direction of the Director of Quality Services within the Quality Assurance & Research Team. Supports the Quality Assurance & Research department with other organization-wide activities including but not limited to internal aud

Hybrid flexible are roles that can be performed remotely but require some level of onsite work/in-person interactions on a regular basis, require employees to live within a commutable distance and, since business needs vary by position and may change over time, managers will set expectations and fle

Familiar with construction management software (CapEx, Site Manager, eBuilder, BIM 360).

Preparing Suggestion Documents to improve the quality of the application. Communication with the Test Lead Test Manager Onsite Team Onsite Client BAs.

Senior level onshore tester with AWS, IVR, and Automation testing experience-using Playright.Senior level onshore tester with AWS, IVR, and Automation testing experience-using Playright.The resource should be able to develop test plans and scenarios without much guidance.

My client is a leading contract manufacturer and is growing! They are looking to add a Quality Engineer focused on supplier quality to their team. Quality Assurance & Compliance. Develop and implement supplier quality requirements, including incoming inspection processes, supplier scorecards, and co

Possess a keen understanding of hardware manufacturing processes and quality assurance methodologies. The Supplier Quality Engineer will be responsible for ensuring the quality and reliability of our vendors (GPU/CPU, Thermal & Cooling system, Network). This role requires a deep understanding of com

Compliance Risk Management (CRM) delivers a compliance risk framework that enables the businesses and functions to comply with applicable internal and external rules and regulations, maintain risk levels within MetLife's risk appetite, and integrate ethics and compliance principles across MetLife.Wi

The Validation Engineer III performs validation and engineering activities; conducts development studies; and monitors, analyzes and assists in improving pharmaceutical systems and processes.Provides detailed reports to management.Design, develop and execute validation documents, define validation s

Ensure customer/3d party agreements/ documentation meets internal (Arxada Quality Management System) and external compliance standards.

Experience with drafting and executing IQ/OQ/PQ.CAD proficiency to support the update of various P&IDs.Problem solving and troubleshooting skills to be able to identify and resolve issues through the validations.Good Communication and documentation Skills.Generation of qualification / validation doc

Management of significant quality events within WSR through investigation and CAPA plan Transition of Hospira CAPA plans to Pharmaceutical systems. Knowledge of Quality Systems, management of Corrective and Preventative Action plans, Knowledge of Trackwise CAPA systems, QTS, GEMs etc.

Are you the "snack-obsessed" person in your friend group? Do you dream of turning your passion for snacks into something bigger… like a career? If you're a college student looking for a paid Summer 2026 internship, PIM Brands might just be your perfect match.Our 10-week immersive summer internship

A bachelor's degree with at least 5+ years of experience working in the pharmaceutical industry in Quality/Regulatory Compliance, Quality Assurance, Quality Management Systems or associated pharmaceutical manufacturing related functions. Associate degree or High School Diploma with 10+ years of expe

Senior Data Platform Compliance Manager. The Senior Data Platform Compliance Manager will be responsible for leading and accomplishing compliance initiatives across BD's global data platforms, ensuring alignment to data privacy regulations (e.

HSE Staffing: The Corporate Safety Director is responsible, in cooperation with the Company's Human Resources Department (with approval by Executive Management), for staffing the appropriate number of experienced/qualified job site HSE Managers and Technicians for projects, and managing the career d

Comply with all embecta quality policies, procedures, and practices through consistent application of sound quality engineering/assurance principles. Maintain alignment to company quality policies, procedures, and practices through consistent application of sound quality assurance principles. Mainta

Responsible for Validation/PPAP Packages on new customer programs, as well as ensuring compliance is applicable regulatory bodies and standards (ISO13485, 21 CFR 820, GMP).Requires a 4-yr engineering degree or substitute experience; a graduate degree in engineering, technical, or management discipli

Responsible for preparing and executing test documentation for GMP computerized systems as well as providing support in the troubleshooting of issues during test execution.You should have excellent understanding of 21 CFR Part 11, ICH standards, EMA and FDA (GxP) regulations, and GAMP methodologies.

Job Description: 50% onsite required.Work schedule - M- F(Should be flexible on timings based on business needs).PURPOSE AND SCOPE OF POSITION:.The CSV Engineer supports the successful implementation of manufacturing and laboratory equipment, and computerized systems at multi-use sites through inter

Job Title: Validation Engineer.Job Location: Summit, NJ (Hybrid Role).Job Duration: 12 Months (possibility of extension).The CSV Engineer supports the successful implementation of manufacturing and laboratory equipment and computerized systems at multi-use sites through interaction with internal cus

Develop and execute validation protocols for computer systemsEnsure compliance with regulatory requirements and industry standardsCreate detailed validation documentation including plans, reports, and scriptsConduct risk assessments and impact analyses related to computer systemsCoordinate and super

Ability to participate in product design (R&D) meetings with Medical Customers in relationship with understanding key quality deliverables. Lead-in customer, internal and registrar quality system audits. Knowledge of quality inspection tools and methods required.