Cyient is a global engineering and technology solutions company. As a Design, Build, and Maintain partner for leading organizations worldwide, we take solution ownership across the value chain to help clients focus on their core, innovate, and stay ahead of the curve. We leverage digital technologies, advanced analytics capabilities, and our domain knowledge and technical expertise, to solve complex business problems.
With over 15,000 employees globally, we partner with clients to operate as part of their extended team in ways that best suit their organization’s culture and requirements. Our industry focus includes aerospace and defence, healthcare, telecommunications, rail transportation, semiconductor, geospatial, industrial, and energy.
Job Description
A 10+ years of experience in product QA lifecycle , Sustenance product design LCM in medical device industry
Competency :
Quality Management ISO 1485
Risk Management
Design Controls and change Management
Quality Assurance
Quality Engineering
Design Transfer / Supplier quality engineering
Hands on experience in Medical Device design and development projects per Quality
Management Systems (ISO 13485), Design controls (US FDA 21CFR 820. Part 30), and Risk
Management (per ISO 14971).
Coordinating with manufacturing team to develop the Process Validation testing (IQ,
OQ, PQ).
Application of ISO 14971, Medical Device-Application of Risk Management for the
various product families belonging to Hypo Disposable Medical Devices.
Updated Risk Management documents for the stand-alone products.
Interaction with Cross function teams regularly over the globe.
Skills & Experience
Customer Quality, Design Quality, ISO 13485:2003- Quality in Medical Devices, Management of Product & Facility quality systems, Medical Device Product Development Experience, Medical Technology & Healthcare, Quality Assurance, Quality Checking, Quality Complaints, Quality Consulting, Quality Control, Quality Management system, Quality Monitoring, Quality Services, Quality Training, Statistical Quality Control, Supplier Quality, • Clinical/ medical writing /regulatory writing experience • FDA (510K) submissions • Excellent communication skills both written and verbal, • Working experience in both Assay and Medical devices • Would have working experience in IVD industries
Cyient is an Equal Opportunity Employer.
Cyient recruits, employs, trains, compensates, and promotes regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender, gender identity or expression, veteran status, and other protected status as required by applicable law. We are proud to be a diverse and inclusive company where our people can focus their whole self on solving problems that matter.
At Cyient, we work towards improving the daily lives of people with unwavering focus. From a quieter flight to a safer train journey, a more reliable energy supply, or a faster internet connection, we provide engineering, manufacturing, geospatial, network and operations management services to industry leaders across the globe.
Our 15,000 associates are located in more than 21 countries, supporting 12 industries, including aerospace, rail transportation, power generation, telecommunications and medical technology.
With a sound track record of growth and profitability, we are committed to developing a sustainable society and actively promoting education and inclusive growth initiatives in our local communities.
We have established deep-rooted, enduring relationships with global industry leaders, by understanding their business needs, goals, culture, and core values. As part of our strong corporate ethos, co-creating business and public value is important to us. In this direction, the Cyient Foundation has developed a framework that unifies our diverse corporate social responsibility initiatives, such as government school adoptions, digital literacy programs, and social innovation technology projects.
Or, as we like to call it, Designing Tomorrow Together.
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