The Quality Assurance Specialist is responsible for the completion and submission of various quality assurance reviews pertaining to phone and written communications. Work with the Quality Assurance Supervisor to administer new and existing quality assurance programs for each area (including Contact...
Oversee Product Quality Engineering in the Medical Equipment department. Report quality system performance to site management. Drive CAPA activities using quality data analysis. Develop and maintain quality assurance procedures and work instructions. ...
As the Quality Leader for Supplier Management, you will oversee the Supplier Quality function at our St. This role includes supervising the Supplier Quality and Receiving Inspection teams, managing supplier audits, and leading quality improvement initiatives. Quality experience in Medical Device or ...
Relevant certifications such as Certified Quality Inspector (CQI) or similar are a plus. Perform visual and measurement inspections of metal-plated components to ensure adherence to specifications and quality standards. Monitor plating processes to ensure compliance with established procedures and q...
We are now hiring a Manager Quality Laboratory on our Westport site for a fixed term contract of 12 months. The Manager, Quality Laboratory, is responsible for the planning, supervision and control of the testing schedule for all Westport manufactured product and all product included in the global s...
This is a non-exhaustive overview of the job duties for this position.Visually analyze computer data for extended periods of time daily .Perform field equipment audits .Generate reports based on results .Occasional travel may be required .Regular and consistent engagement, participation and promotio...
Quality Program Management: Lead relevant quality programs and methods such as 8D, Lean Six Sigma, Quality Fundamentals, Digital Quality, and customer interaction to ensure continuous improvement. What do you get to do in this position? Job Responsibilities Transformative Leadership: The Quality Eng...
The Validation Manager will be responsible to provide quality support and oversight for GMP software validation activities and to maintain data integrity standards as per 21CFR Parts 210, 211, 11, and ensuring compliance with relevant regulatory requirements and industry standards/best practices. Th...
The service portfolio supports all stages of the drug development process and all functional areas of bio/pharmaceutical manufacturing, including method development, microbiology, process validation and quality control. Quality Systems team located in Columbia, Missouri. The Validation Specialist Iw...
Quality Systems team located in Columbia, Missouri. The Validation Specialist I will have responsibility for computer system validation activities. This will include working closely with the Part 11 Team, QA, the validation teams, and Quality Engineering to assure compliance with US FDA regulations,...
We are seeking a Quality Assurance Analyst to join our team. Knowledgeable of concept practices and procedures commonly used in software quality assurance. Effective testing skills:proficient in test planning and execution and using test methodologies to identify software defects, applying software ...
Drive the process robustness of the production lines leveraging digital quality • Collaborate with LOB and CSQ central team for quality improvement • Up to 50% travel to US Plants What qualifications will make you successful? • Bachelor’s Degree (or higher) in Supply Chain, Management, Engineering o...
Quality & Regulatory Manager - Medical Device/Equipment (Remote with travel). Quality and Regulatory Manager. Implement the worldwide Belimed Quality Policy and derive appropriate programs and systems to support strategic direction and conduct training on those systems. Analyze quality/regulatory in...
Participate in the continuous improvement of QA processes and methodologies, contributing to the overall quality assurance strategy. We are currently seeking an experienced and passionate QA Analyst to join our dynamic team. As a QA Analyst you will play a critical role in the design, development, a...
Quality Systems team located in Columbia, Missouri. The Validation Specialist I will have responsibility for computer system validation activities. This will include working closely with the Part 11 Team, QA, the validation teams, and Quality Engineering to assure compliance with US FDA regulat...
Manages data accuracy for all deliverables within the QA test repository. Strong understanding of QA's lifecycle requirements. ...
The Validation Manager will be responsible to provide quality support and oversight for GMP software validation activities and to maintain data integrity standards as per 21CFR Parts 210, 211, 11, and ensuring compliance with relevant regulatory requirements and industry standards/best practices. Th...
Lead Time, Order Quantity, stock, forecast) o Schneider Electric specific Upstream tools and data base usage o Coordinating and working with suppliers on any applicable plant rejections o Coordinating with quality department for appropriate feedback o Working with engineering on any PPAP related qua...