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...
ASQ Certified Quality Manager – CQM, ASQ Certified Quality Auditor – CQA, and/or ASQ Certified Quality Engineer – CQE, NQA1 Certified Manager, operating knowledge of GMP / GDP. Deploy the Strategic Quality Plan at the operational level in conjunction with the Regional Quality Assur...
Under general supervision of the Quality Engineering Supervisor, the Quality Engineer I establishes and maintains quality requirements and relevant inspection standards for all products, to ensure all design and performance requirements are achieved. Education: Bachelor’s Degree in Industrial ...
Under general supervision of the Quality Engineering Supervisor, the Quality Engineer II establishes and maintains quality requirements and relevant inspection standards for all products, to ensure all design and performance requirements are achieved. Education: Bachelor’s Degree in Industrial...
Overseeing all managerial and technical operations of quality engineering department; providing leadership and coaching to assigned individuals; participating in long- and short-term planning and goal setting for group; operating department in a safe, efficient, and quality-oriented manner according...
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...
We are seeking a Quality Assurance Analyst to join our team. As a QA Engineer at SmartCOP, you will be placed into a small development team for our Records Management System software used by law enforcement and conservation enforcement agencies nationwide. Bachelor’s degree in Computer Science or En...
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...
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. ...
Interfaces heavily with Technical Antennas, manufacturing hourly and salaried support personnel, and external corporate engineering, quality, and supplier quality resources. Quality Engineering role supporting Columbia Manufacturing operations. Experience within manufacturing Quality, Manufacturing ...
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...
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,...
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 ...
Manages data accuracy for all deliverables within the QA test repository. Strong understanding of QA's lifecycle requirements. ...
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...
Designs and implements quality control training programs to key personnel in conjunction with managers. Plan, coordinate, and direct a quality control program designed to ensure continuous production of products consistent. Formulates and maintains quality control objectives. Interpret quality contr...
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...
Quality Systems team located in Columbia, Missouri. The Validation Specialist Iwill 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, ...
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...