TECHNICAL SPECIALIST
HCL
About HCLTech
HCLTech is a global technology company, spread across 60 countries, delivering industry-leading capabilities centered around digital, engineering, cloud and AI, powered by a broad portfolio of technology services and products. We work with clients across all major verticals, providing industry solutions for Financial Services, Manufacturing, Life Sciences and Healthcare, Technology and Services, Telecom and Media, Retail and CPG, and Public Services. We re powered by our people a global, diverse, multi-generational talent - representing 161 nationalities whose unique spark, perspective and boundless passion drive our culture of proactive value creation and problem-solving.
Our purpose is to bring together the best of technology and our people to supercharge progress for everyone, everywhere our clients, partners, their stakeholders, communities, and the planet. As a company, we are deeply focused on accelerating our ESG agenda. We are also creating technology-enabled sustainable solutions with and for our clients and partners. We embed ESG imperatives into every aspect of our business and ensure that the progress we supercharge is responsible, inclusive and beneficial to all our stakeholders in the long term. We have committed to achieving net zero by 2040.
To learn more about how we can supercharge progress for you, visit www.hcltech.com
Technical Specialist with mdr,ISO 13485,mdd
Job Summary
The Technical Specialist will be responsible for tasks related to mdr, ISO 13485, and MDD. The primary responsibilities include ensuring compliance with relevant regulations and standards in the medical device industry. (1.) Key Responsibilities
1. Implement and maintain processes to ensure compliance with medical device regulation (mdr), iso 13485, and medical device directive (mdd)
2. Provide expertise and guidance on regulatory requirements for medical devices
3. Collaborate with cross functional teams to assess and address regulatory compliance issues
4. Conduct internal audits to identify areas for improvement and ensure adherence to standards
5. Stay updated on changes in regulations and standards related to medical devices
Skill Requirements
1. Proficiency in medical device regulation (mdr), iso 13485, and medical device directive (mdd)
2. Strong understanding of regulatory requirements in the medical device industry
3. Excellent analytical and problem-solving skills
4. Effective communication and interpersonal abilities
5. Detail oriented with a focus on accuracy and compliance
Certifications: Relevant certifications in medical device regulations or ISO standards are a plus
HCLTech is a global technology company, spread across 60 countries, delivering industry-leading capabilities centered around digital, engineering, cloud and AI, powered by a broad portfolio of technology services and products. We work with clients across all major verticals, providing industry solutions for Financial Services, Manufacturing, Life Sciences and Healthcare, Technology and Services, Telecom and Media, Retail and CPG, and Public Services. We re powered by our people a global, diverse, multi-generational talent - representing 161 nationalities whose unique spark, perspective and boundless passion drive our culture of proactive value creation and problem-solving.
Our purpose is to bring together the best of technology and our people to supercharge progress for everyone, everywhere our clients, partners, their stakeholders, communities, and the planet. As a company, we are deeply focused on accelerating our ESG agenda. We are also creating technology-enabled sustainable solutions with and for our clients and partners. We embed ESG imperatives into every aspect of our business and ensure that the progress we supercharge is responsible, inclusive and beneficial to all our stakeholders in the long term. We have committed to achieving net zero by 2040.
To learn more about how we can supercharge progress for you, visit www.hcltech.com
Technical Specialist with mdr,ISO 13485,mdd
Job Summary
The Technical Specialist will be responsible for tasks related to mdr, ISO 13485, and MDD. The primary responsibilities include ensuring compliance with relevant regulations and standards in the medical device industry. (1.) Key Responsibilities
1. Implement and maintain processes to ensure compliance with medical device regulation (mdr), iso 13485, and medical device directive (mdd)
2. Provide expertise and guidance on regulatory requirements for medical devices
3. Collaborate with cross functional teams to assess and address regulatory compliance issues
4. Conduct internal audits to identify areas for improvement and ensure adherence to standards
5. Stay updated on changes in regulations and standards related to medical devices
Skill Requirements
1. Proficiency in medical device regulation (mdr), iso 13485, and medical device directive (mdd)
2. Strong understanding of regulatory requirements in the medical device industry
3. Excellent analytical and problem-solving skills
4. Effective communication and interpersonal abilities
5. Detail oriented with a focus on accuracy and compliance
Certifications: Relevant certifications in medical device regulations or ISO standards are a plus
Confirmar seu email: Enviar Email
Todos os Empregos de HCL