Key Responsibilities: • Review existing design to identify CTQs (critical to Quality) from Product Requirements • Review & update the subassy/component specifications, aligning with CTQs • Review the component level DFMEA and ensure the subassy/component specifications have listed sampling plans, based on risk levels • Provide Sustenance support for existing products such as design changes, component obsolescence etc • Component redesign & Component qualification • Collaborate with cross-functional teams to optimize design and performance. • Communicate effectively with suppliers and vendors to ensure timely and cost-effective procurement of components. • Ensure compliance with industry standards and regulations, particularly in the medical domain.
Qualifications: • Bachelor's degree in electrical engineering, Electronics Engineering, or a related field. • Proven hands-on experience in analog, digital, and power electronics. • Extensive experience in the product development lifecycle. • Strong requirement analysis skills. • Preference for candidates with experience in the medical domain. • Excellent communication skills for effective interaction with suppliers and vendors. • Demonstrated ability to optimize designs to meet specific requirements. • Strong problem-solving skills and attention to detail.
Preferred Skills: • Experience with medical device regulations and standards. • Proficiency in relevant software tools and simulation programs. • Ability to work independently and as part of a team.
Strong organizational and project management skills