Developer
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
Developer with mdr,ISO 13485,mdd
Job Summary
The Developer with expertise in mdr, ISO 13485, and MDD will be responsible for developing and maintaining software solutions in compliance with medical device regulations (mdr, ISO 13485, MDD). They will play a crucial role in ensuring that the software meets the required quality standards and regulatory requirements for medical devices. (1.) Key Responsibilities
1. Develop and implement software solutions adhering to mdr, iso 13485, and mdd regulations.
2. Collaborate within team to ensure software compliance with medical device regulatory standards.
3. Conduct thorough testing and validation of software to ensure it meets the required quality standards.
4. Maintain documentation related to software development processes in accordance with mdr, iso 13485, and mdd.
5. Stay updated on any changes or updates in the medical device regulations landscape and implement necessary changes in the software as required.
Skill Requirements
1. Knowledge and familiarity with mdr (medical device regulation).
2. Knowledge of understanding and implementing iso 13485 standards.
3. Familiarity with medical device directive (mdd) requirements.
4. Familiarity with developing software solutions for the healthcare or life sciences industry.
5. Attention to detail and analytical skills to ensure software compliance with regulatory standards.
6. Good communication skills to collaborate effectively with cross functional teams.
7. Ability to adapt to changing regulatory requirements and implement necessary changes in software development processes.
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
Developer with mdr,ISO 13485,mdd
Job Summary
The Developer with expertise in mdr, ISO 13485, and MDD will be responsible for developing and maintaining software solutions in compliance with medical device regulations (mdr, ISO 13485, MDD). They will play a crucial role in ensuring that the software meets the required quality standards and regulatory requirements for medical devices. (1.) Key Responsibilities
1. Develop and implement software solutions adhering to mdr, iso 13485, and mdd regulations.
2. Collaborate within team to ensure software compliance with medical device regulatory standards.
3. Conduct thorough testing and validation of software to ensure it meets the required quality standards.
4. Maintain documentation related to software development processes in accordance with mdr, iso 13485, and mdd.
5. Stay updated on any changes or updates in the medical device regulations landscape and implement necessary changes in the software as required.
Skill Requirements
1. Knowledge and familiarity with mdr (medical device regulation).
2. Knowledge of understanding and implementing iso 13485 standards.
3. Familiarity with medical device directive (mdd) requirements.
4. Familiarity with developing software solutions for the healthcare or life sciences industry.
5. Attention to detail and analytical skills to ensure software compliance with regulatory standards.
6. Good communication skills to collaborate effectively with cross functional teams.
7. Ability to adapt to changing regulatory requirements and implement necessary changes in software development processes.
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