Electronics Engineer PCB Must Innovations Pvt. Ltd.

1.0 - 5.0 years

0 Lacs

meerut, uttar pradesh

On-site

You will be responsible for creating schematics and PCB layouts, designing multi-layer and high-speed PCBs according to product requirements. You must ensure signal integrity, power integrity, and EMI/EMC compliance in the design process. Additionally, you will be required to generate Gerber files, BOM, Pick & Place files, and other manufacturing documents. Collaborating with vendors and fabrication houses for prototyping and production will be an essential part of your role. You will also need to review and troubleshoot PCB issues during prototyping and testing phases, while maintaining proper documentation for version control and design history. To excel in this role, you should have a good understanding of electronics components, circuit behavior, and layout best practices. Hands-on experience in 2-layer and multi-layer PCB design is crucial. The ability to work both independently and in a team environment, along with strong analytical and problem-solving skills, will be beneficial. Knowledge of high-speed, RF, or mixed-signal design is considered a plus. This is a full-time, permanent position with a flexible schedule. The job location is in Meerut, Uttar Pradesh, and the ability to commute or relocate to the specified location is required. A minimum of 1 year of experience in circuit design and PCB design is necessary for this role. If you are passionate about PCB design, have a keen eye for detail, and enjoy working on challenging projects, we encourage you to apply for this opportunity.,

Posted 4 weeks ago

Apply

Junior Design Engineer Chetan Meditech Pvt Ltd

0.0 - 2.0 years

3 - 4 Lacs

Sanand

Work from Office

Job Title: Senior Design Engineer Reports to: D&D Head Job Summary: The Senior Design Engineer will lead the design and development of innovative medical devices, ensuring compliance with regulatory and industry standards. This role involves mentoring junior team members, managing complex design projects, coordinating with cross-functional departments, and preparing comprehensive design documentation for regulatory submissions. The candidate must have a strong understanding of manufacturing processes, regulatory expectations, and design control principles. Key Responsibilities: 1. Design & Product Development Lead the design and development of new products and improvements to existing devices using SolidWorks and AutoCAD. Translate clinical and market requirements into functional designs while ensuring manufacturability and cost-effectiveness. Validate engineering calculations, tolerance stack-ups, and material selection for implantable devices and surgical instruments. 2. Project Leadership Plan and execute design activities in alignment with project timelines. Coordinate design reviews, risk analysis, and design verification/validation. Collaborate with the D&D Head to define design strategy and resource allocation. 3. Mentorship & Team Development Guide and mentor Junior Design Engineers in modeling, drafting, design analysis, and documentation. Review work submitted by junior staff and provide constructive feedback. 4. Manufacturing Integration Ensure designs are optimized for manufacturing processes such as CNC machining, laser marking, anodizing, and PEEK/titanium-specific considerations. Work closely with production, quality, and supply chain teams to ensure smooth handover from design to production. 5. Regulatory & Documentation Prepare and review Design History Files (DHF), Technical Files, Risk Management Reports, and Engineering Change Requests (ECRs). Ensure all designs and documentation meet CE MDR, US FDA, and CDSCO regulatory requirements. Support audits and regulatory submissions with accurate and complete documentation. 6. Design Evaluation & Predicate Comparison Conduct design benchmarking and engineering justification reports. Compare new designs against predicate or competitive devices for clinical and functional performance. 7. Innovation & Continuous Improvement Research new design trends, technologies, and surgical techniques in arthroscopy and orthopedics. Contribute to IP development, design patents, and publications where applicable. Qualifications: Education: Bachelors or Master’s degree in Mechanical, Biomedical, or Product Design Engineering. Experience: 3–6 years of experience in medical device design, preferably with exposure to orthopedic/arthroscopic implants and instruments. Skills: Advanced proficiency in SolidWorks and AutoCAD. Strong knowledge of GD&T, DFMA, FMEA, and design verification protocols. Familiarity with regulatory frameworks (CE MDR, US FDA 21 CFR 820, ISO 13485). Hands-on experience with prototype evaluation, testing fixtures, and validation tools. Good communication, leadership, and documentation skills.

Posted 1 month ago

Apply

Start Your Job Search Today

Browse through a variety of job opportunities tailored to your skills and preferences. Filter by location, experience, salary, and more to find your perfect fit.