15.0 - 17.0 years

0 Lacs

Bengaluru, Karnataka, India

On-site

Job Description We are seeking an experienced EMC Systems Engineer to join our IGT Systems team. This role is ideal for a compliance-focused professional with a strong background in medical device safety, EMC/EMI testing, and regulatory standards. You will lead EMC strategy development, risk management, and compliance activities, ensuring our products meet global regulatory requirements and maintain the highest standards of safety and performance. Job Responsibilities: Collaboratively co-create, define, execute, and maintain the EMC System strategy for IGT-S Systems as a part of the Norm Compliance Team IGT-S. Co-ownership of the System-level EMC Risk Management file, crafting and maintaining system-level EMC & Radio compliance evidence. Develop EMC processes, tools, and provide training for EMC engineers. Develop and own EMC-related renewal projects and ensure alignment with internal and external certifying bodies. Work closely with stakeholders such as the MDC team, EMC LAB , and internal and external certifying bodies to optimize the usability of created evidence. Foster successful cooperation within your team and with stakeholders. Qualifications: Bacheloru2019s or Masteru2019s degree in Electronics, Electrical Engineering, Mechanical or a related field. 15+ years of experience in product safety and compliance engineering, with at least 5 years in EMC/EMI testing and certification. Proven experience with medical device standards including IEC 60601-1, IEC 60601-1-2 Hands-on experience with product certification processes (CB, NRTL, CSA). Strong understanding of risk management and EMC/Safety engineering. Experience in product development, lifecycle management, and regulatory audits. Excellent communication, coordination, and stakeholder management skills. Ability to work independently and collaboratively in a global, cross-functional environment. Preferred Attributes: Experience working or collaborating with certifying bodies and regulatory agencies. Strong focus on patient safety and product quality. Ability to lead and influence in a matrixed organization. Green belt certification How we work together We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week. Onsite roles require full-time presence in the companyu2019s facilities. Field roles are most effectively done outside of the companyu2019s main facilities, generally at the customersu2019 or suppliersu2019 locations. Indicate if this role is an office/field/onsite role. About Philips We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others. u2022 Learn more about . u2022 Discover . u2022 Learn more about . If youu2019re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our culture of impact with care .

Posted 2 weeks ago

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IT - Risk Management Systechcorp Private Limited

2.0 - 6.0 years

2 - 6 Lacs

Bengaluru / Bangalore, Karnataka, India

On-site

Responsibilities Collaborate with cross functional teams (engineering, manufacturing, regulatory, sourcing, etc.) to lead or support compliance activities to medical device regulations. Review regulatory compliance change notifications and drive associated actions to be compliant by the effective date Lead compliance efforts to various global regulations (E.g. REACH, ROHS, etc.) in alignment with the quality management system Lead or support product regulatory documentation updates (e.g. NRTL reports, tech file, etc.) Support regulatory audits and inspections to ensure post-market surveillance compliance. Qualifications we seek in you! Minimum Qualifications Knowledge of medical regulations including FDA, EU MDR, NMPA/CFDA, and other applicable international regulations Knowledge of regulatory standards such as IEC 60601, ISO13485, 14971 and other applicable standards and substandard. Proficiency in interpreting, applying complex regulations, and preparing associated documentation. Excellent interpersonal communication and collaboration skills Bachelor s degree in engineering, Science or related area Minimum of 2 years of experience working with medical devices regulations and quality management system. proficiency with written English and with neutral English accent Preferred Qualifications/ Skills Strong technical knowledge Effective probing skills and analyzing / understanding skills

Posted 1 month ago

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IT - Risk Management Systechcorp Private Limited

2.0 - 6.0 years

2 - 6 Lacs

Delhi, India

On-site

Posted 1 month ago

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