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0.0 - 4.0 years
0 Lacs
palwal, haryana
On-site
As a Quality Assurance Coordinator at WIKA Group, you will be responsible for coordinating with Sales & Design to ensure the submission of QA Procedures in compliance with Project requirements within a timeframe of less than 15 Days. You will be tasked with the preparation of Quality Docs Dossier in accordance with customer specifications and participating in Certification and Recertification processes. Additionally, you will maintain a tracker of Quality Docs and be involved in updating and amending Procedures & Documents as necessary. Your role will also involve reviewing MTC's to ensure alignment with Project requirements. To qualify for this position, you should hold a Diploma in Mechanical Engineering and demonstrate proficiency in MS Excel. WIKA Group offers a range of benefits including work-life integration, employee discounts, an attractive remuneration system, flexible working hours, good development opportunities, health initiatives, and the option for mobile working. The WIKA Group is a global leader in measurement technology, providing innovative sensing solutions to enable safe, efficient, and sustainable processes for over 75 years. With a team of more than 11,000 dedicated employees, we are committed to meeting the challenges and opportunities presented by megatrends such as demographic change, digitalization, and sustainability. Embrace this opportunity to contribute your perspectives and ideas towards driving innovation and growth for a better future. Join us on this journey by applying now.,
Posted 12 hours ago
4.0 - 9.0 years
4 - 9 Lacs
Mumbai, Maharashtra, India
On-site
Role & Responsibilities Lead and support a team of globally located Product Assessors Conduct in-depth technical documentation reviews for Active Medical Devices Ensure compliance with EU medical device regulations and standards Collaborate with cross-functional teams to improve efficiency and service quality Monitor team performance, technical skills, KPIs, and wellbeing Handle recruitment, including CV review, interviews, and onboarding Develop and deliver technical training sessions internally and externally Provide expert support on technical and sales-related queries in Active Medical Devices Ensure top-tier service delivery within the SGS medical device certification network Preferred Candidate Profile Strong experience in Active Medical Devices or regulatory affairs Proven leadership and mentoring abilities Excellent communication and cross-functional collaboration skills Familiarity with EU MDR and quality compliance processes Experience in technical assessments and certification services
Posted 2 weeks ago
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