Quality Engineer Salary at Williams Controls Inc BETA

Quality Engineer Overview: The Quality Engineer is tasked with ensuring that pharmaceutical manufacturing processes comply with regulatory standards set by the United States Pharmacopeia (USP), Food and Drug Administration (FDA), and Current Good Manufacturing Practices (cGMP). This role involves conducting thorough audits, inspections, and evaluations, leading investigations into quality issues, implementing corrective actions, and collaborating with various teams to enhance overall quality systems and drive continuous improvement. Responsibilities: Conduct audits, inspections, and evaluations to ensure compliance with USP, FDA, and cGMP standards in compounding practices. Develop and review processes and documentation in line with cGMP requirements, including change controls and quality records. Lead investigations into deviations and complaints, utilizing root cause analysis to implement corrective actions (CAPAs). Collaborate with cross-functional teams to improve quality systems a

Build your Career with an Industry Leader As the global leader of premium labels, MCC helps brands stand out in competitive markets and inspire positive consumer experiences. Backed by over a century of printing experience, MCC is focused on the future by developing consumer-driven innovations and sustainable packaging solutions. Working for our team, you can truly make a difference. The objective of the Quality Engineer is to develop and implement procedures to maintain and continually improve product and process quality. Be a change agent for process improvement and standardization efforts. Lead efforts to maintain certifications for ISO and Food Safety as well as relevant customer qualifications. Provide support for other Quality and Manufacturing efforts that pertain to customer quality and satisfaction. Why work at MCC: Compensation: $95,000.00 annually Generous benefits package including medical, dental, vision, disability, life insurance and 401(k) Paid Holidays: New Years, Memo

R&D Circuits, a member company of Advantest America, Inc., is wholly owned by Advantest Corporation (a Tokyo Stock Exchange listed company). For over 50 years, R&D Circuits has been a leader in the printed circuit board industry. The Quality Engineer (QE) will be responsible for supporting site Key Performance Indicator (KPI's) metrics through use of continuous improvement and process improvement methodologies. Candidates shall have knowledge of Quality Engineering, or Process Engineering, or Industrial Engineering skills with a basic knowledge of project management. This engineer shall be comfortable managing projects of importance to the organization with some oversight. Work is guided by individual annual goals and objectives with some management oversight to deliver mission success and excellence throughout the integrated product lifecycle resulting in defect-free work products and delighted customers. Duties and Responsibilities include: Primary Tasks: Hands-on go-getter comfortab

Our client is actively looking for a seasoned Quality Engineering Manager. This is an on-site position in the Cranbury NJ area. You should apply if you have: Bachelor's degree with 2+ years of Quality Engineering management experience within pharma/biotech Experience leading and training a team of 5+ Experience with aseptic filling

Responsibilities: Monitors, inspects, and evaluates products to ensure predetermined quality standards are met. Develops and updates testing-related documentation, including test cases, plans, and flaw-reporting procedures. Performs Quality and technical review of Nonconformance investigations (Company) and CAPAs within defined timeframes. Ensures investigations and root cause analysis are accurate and complete. Maintain an accurate log of Non-Conformances and CAPAs activities. Tracks, follows-up and assists in the timely closure of Company/CAPAs. Provides hands-on guidance and training to all personnel performing activities within the Quality system. Ensure documentation is complete before closure. Assist Quality Systems team as needed to investigate Nonconformances and ensure proper implementation of CAPAs. Prepare monthly and quarterly metrics to present at Quality Review meetings. Requirements: CAPA and non-conformance experience required. Investigation experience required. Managin

Changing lives. Building Careers. Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging whats possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care. This position is for a Staff Quality Engineer, Global Supplier Process Validation with hands-on experience and proven success in Process Validation and driving continuous improvement with suppliers. This position will be primarily engaged to ensure timely completion of process validation requirements of new products and life cycle change management (LCM) projects with suppliers to the required quality standard in accordance with defined program and company requirements. The ideal candidate should demonstrate proficient experience with quality management concepts, IQ/OQ/PQ process validation, and manufacturing eng

#x 9; Leverage your expertise in manufacturing engineering to ensure product quality and compliance with industry standards. Prepare and maintain technical files, ensuring adherence to ISO 13485 and EUMDR standards Write and update quality documentat Quality Engineer, Manufacturing Engineer, Engineer, Technology, Staffing, Quality

The Quality Engineer will apply engineering knowledge, problem solving skills and ingenuity to resolve quality issues for all Humanscale Products. They will also drive continuous improvement for product and process performance. Responsibilities Essen Quality Engineer, Continuous Improvement, Electrical Engineer, Engineer, Mechanical, Manufacturing, Technology, Quality