The Role
Sinclais is seeking a Hardware Technical Lead at their R&D department located in Esplugues del Llobregat.
The Hardware Technical Lead mission will be to provide with electronics and system designs that fullfills product requirements and regulatory standards following the quality standars set by the company.
About Sinclair
Description Essential:
• Bachelor's degree in electronic, telecommunicatios or a related field;
• 10 years of experience in electronic development
• Proven track record of successful electronic development projects in the medical device industry, from concept to commercialization.
• English Level: High.
• Spanish Level: High.
Desirable:
• Advanced degree in electronic, telecommunicatios or a related field
• 2 years of experience in a electronic development leadership role.
Role competencies:
• In-depth knowledge of hardware design principles, including analog and digital circuit design, PCB layout, and signal integrity.
• Experience with medical device regulations and standards, such as FDA QSR, ISO 13485, IEC 60601, and IEC 62304
• Strong leadership, communication, and interpersonal skills, with the ability to effectively collaborate with cross-functional teams
• Excellent problem-solving skills and attention to detail, with a commitment to quality and Compliance
• Experience with design control processes, risk management, and design for manufacturability and reliability
• Proficiency in CAD tools (e.g., Altium Designer, OrCAD) and simulation tools (e.g., SPICE, MATLAB).
General competencies:
• Achievement orientation.
• Adaptability and openness to change.
• Learning capacity.
• Integrity and professional ethics.
• Cross-cutting cooperation.
• Creativity, originality and innovation.
• Time management, organization and planning.
• Capacity for análisis and critical thinking.
• Team development and management.
If this sounds like you and you meet the requirements, please apply, we would love to hear from you.
Please note if we receive a high volume of applications, we may close the role before the closing date noted.
By making this application you give consent for personal information to be used in automated decision making processes relating to key job requirements which are stated in this ad.
If you have any questions, please email ****** .
Sinclair does not accept speculative or unsolicited CVs from Recruitment Agencies. Any unsolicited CVs received will be treated as property of Sinclair and Terms & Conditions associated with the use of such CVs will be considered null and void.
Key Responsibilities
Key Responsibilities • Lead a team of hardware engineers in the design, development, and testing of medical devices, including electromechanical systems, sensors, and embedded systems
• Define hardware requirements and specifications based on product requirements and regulatory standards
• Develop hardware architecture and design solutions that meet performance, reliability, and regulatory requirements.
• Lead the electrical saftey compliance testing in acordace with IEC 60601-1 and its collateral and particular standards.
• Lead the delivery of prototypes devices for V&V activities.
• Plan and execute hardware development projects, including resource allocation, scheduling, and risk management
• Collaborate with cross-functional teams to integrate hardware with software, firmware, and mechanical components
• Lead design reviews, risk assessments, and verification and validation activities to ensure product quality and compliance with regulatory standards.
• Follow the existing project management procedure within the company in accordance with ISO 13485 standard and the department's working methodology, and ensure that quality processes are followed and implemented on time.
• Drive continuous improvement in hardware design processes, tools, and methodologies.
• Provide technical guidance and mentorship to hardware engineers, fostering a culture of innovation, collaboration, and excellence.
• Lead the collaboration with new product introduction, manufacturing and quality departments for the industrialization of new designs providing support on the assembly and verification instructions, design of verification tools, trainings and parts homologations.
• Suport sustain activities for finding alternative components.
• Lead the collaboration with other departments such as Regulatory, Clinical, Quality, Service, Sustain Group, Operations, Sales, Manufacturing, NPI and MKT.
• Collaboration in the creation of "R&D&I" reports.
• Design of architectures, electronic parts, analog and digital circuits.
• Search, homologation, and management of suppliers of electronic components.
• Electronic assembly, integration, and verification testing.
Benefits We offer:
• Competitive fixed salary aligned with the market + variable.
• Medical + Dental Insurance.
• Hybrid work model.
• Flexible schedule + short Friday.
• Fruit at the office.
• Enjoyable, dynamic and international environment.
We have a real focus on developing our people, and by fostering an entrepreneurial culture, we encourage flexibility, accountability and autonomy. The company is full of opportunity for those who wish to grasp it. Our people thrive on engagement, development and a varied workload. You will often be included in projects that require you to collaborate cross-functionally.
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