HCL Technologies
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.
Senior Designer - MDR Job Summary The Senior Designer - MDR plays a pivotal role in creating high-quality designs that align with the overall project vision and meet customer requirements. This role focuses on leveraging extensive knowledge in Medical Device Regulations (MDR) to ensure designs are compliant, innovative, and effective. The designer will collaborate with various stakeholders, mentor junior team members, and validate design concepts through practical implementations, significantly impacting the organization’s success in delivering exceptional products.
Key Responsibilities
Collaborate with stakeholders to gather and refine design requirements, ensuring alignment with MDR compliance standards and customer expectations.
Develop prototypes and proof‑of‑concept implementations using design tools and methodologies to validate design decisions and facilitate feedback.
Mentor junior designers by sharing knowledge and expertise through structured training sessions and comprehensive documentation, fostering skill development within the team.
Work with cross‑functional teams to ensure software design aligns with overall project goals and adheres to MDR guidelines.
Collaborate with quality assurance teams to establish and uphold high‑quality design processes and methodologies that ensure regulatory compliance.
Skill Requirements
Strong understanding of Medical Device Regulations (MDR) and related compliance standards.
Proficiency in design tools and methodologies, with experience in creating prototypes and proof‑of‑concept implementations.
Familiarity with stakeholder engagement and requirement gathering techniques.
Solid knowledge of quality assurance processes and practices in design.
Certification
Optional but valuable: Certification in ISO 13485 or relevant medical device design certifications.
Employee Group
Business Line FT
City
Boone
Entity
CSW
Auto req ID
1635526BR
Expected Date of Closure
08-Dec-2025
Pay Range Minimum
68000
Pay Range Maximum
105000
Skill (Primary)
Tools and Standards (ERS)-Standards - Medical-MDR
Skill Level 3 (Secondary Skill 1)
Technical Skills (ERS)-Other Technical Skills-Remediation
Skill Level 3 (Secondary Skill 2)
Technical Skills (ERS)-Other Technical Skills-IVDR
Skill Level 3 (Secondary Skill 3)
Technical Skills (ERS)-Other Technical Skills-DHF
Skill Level 3 (Secondary Skill 4)
Tools and Standards (ERS)-Medical-ISO 13485
Skill Level 3 (Secondary Skill 5)
Domain Competencies (ERS)-Medical Devices-Regulatory-510(k)
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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.
Senior Designer - MDR Job Summary The Senior Designer - MDR plays a pivotal role in creating high-quality designs that align with the overall project vision and meet customer requirements. This role focuses on leveraging extensive knowledge in Medical Device Regulations (MDR) to ensure designs are compliant, innovative, and effective. The designer will collaborate with various stakeholders, mentor junior team members, and validate design concepts through practical implementations, significantly impacting the organization’s success in delivering exceptional products.
Key Responsibilities
Collaborate with stakeholders to gather and refine design requirements, ensuring alignment with MDR compliance standards and customer expectations.
Develop prototypes and proof‑of‑concept implementations using design tools and methodologies to validate design decisions and facilitate feedback.
Mentor junior designers by sharing knowledge and expertise through structured training sessions and comprehensive documentation, fostering skill development within the team.
Work with cross‑functional teams to ensure software design aligns with overall project goals and adheres to MDR guidelines.
Collaborate with quality assurance teams to establish and uphold high‑quality design processes and methodologies that ensure regulatory compliance.
Skill Requirements
Strong understanding of Medical Device Regulations (MDR) and related compliance standards.
Proficiency in design tools and methodologies, with experience in creating prototypes and proof‑of‑concept implementations.
Familiarity with stakeholder engagement and requirement gathering techniques.
Solid knowledge of quality assurance processes and practices in design.
Certification
Optional but valuable: Certification in ISO 13485 or relevant medical device design certifications.
Employee Group
Business Line FT
City
Boone
Entity
CSW
Auto req ID
1635526BR
Expected Date of Closure
08-Dec-2025
Pay Range Minimum
68000
Pay Range Maximum
105000
Skill (Primary)
Tools and Standards (ERS)-Standards - Medical-MDR
Skill Level 3 (Secondary Skill 1)
Technical Skills (ERS)-Other Technical Skills-Remediation
Skill Level 3 (Secondary Skill 2)
Technical Skills (ERS)-Other Technical Skills-IVDR
Skill Level 3 (Secondary Skill 3)
Technical Skills (ERS)-Other Technical Skills-DHF
Skill Level 3 (Secondary Skill 4)
Tools and Standards (ERS)-Medical-ISO 13485
Skill Level 3 (Secondary Skill 5)
Domain Competencies (ERS)-Medical Devices-Regulatory-510(k)
#J-18808-Ljbffr