6 Design Quality Jobs

Job Description: We are seeking a dedicated QA/QC Engineer to join our team at a cutting-edge marine robotics company. The ideal candidate will play a key role in ensuring quality assurance and quality control across both the electronics and mechanical departments, contributing to the development and maintenance of high-performance marine robotics systems. Key Responsibilities: Quality Assurance and Control (QA/QC): Develop and implement quality assurance protocols for electronics and mechanical components. Collaborate with design and production teams to establish testing criteria and standards. Conduct design reviews to ensure compliance with technical specifications and regulatory standards. Analyze defect trends and provide input for continuous improvement. Participate in the development of automated testing systems for ROV s. Perform inspections and testing of incoming components, in-process assemblies, and finished products. Use advanced tools such as oscilloscopes, multimeters (for electronics), and calipers, gauges (for mechanical) for quality assessment. Identify non-conformances, prepare detailed reports, and initiate corrective actions. Maintain detailed records of inspections and test data for traceability. Ensure the final product aligns with customer specifications and regulatory requirements. Knowledge of : QA/QC function set-up ISO/QMS process set-up Quality Audit Quality control and related activities in EMS or an equivalent company Experience: 5 to 7 years, out of which 2 to 3 years of experience as a QA/QC engineer role Qualification: BE/BTech in Electronics, Mechatronics, Electrical 5 to 7 years of Production Experience out of which 2 to 3 years of experience as a QA/QC engineer role Diploma in Electronics, Mechatronics, Electrical 8 years of Production Experience, out of which 3 to 5 years of experience as a QA/QC engineer role Added Advantage: Six Sigma certification ISO Process excellence certification Product/Project management certification

Responsibilities may include the following and other duties may be assigned. Qualify suppliers according to company standards & management of approved supplier list per purchasing control compliance. Initiate and drives SCAPA's/NCR's to suppliers not performing/or adhering to company standards. Manage supplier change requests . Assesssupplier performance on periodic basis & drive necessary action for continous improvement. Establish a process & ensures that suppliers deliver quality parts, materials, and services. LeadPPAP execution with supplier and ensure robust supplier process qualification/validation through IQ, OQ & PQ methodology. Monitors parts from acquisition through the manufacturing cycle and communicates and resolves supplier-related problems as they occur. Develops and prioritizes an auditing schedule to ensure that designated suppliers are audited on a regular basis to ensure good manufacturing practices (GMP) and quality standards are met. Provide pre-market quality engineering support to new product development (NPD) working in partnership with the component engineering and post-market supplier quality teams, to deliver quality parts, materials, and services, prevent defects, and allow company to provide customers with the highest quality and reliable products. Collaborates with component engineers to develop and deliver the product acceptance sampling strategy, approved supplier list coordination, supplier owned quality deployment, PFMEA,MSA, ,control plans andrelevant quality tools and methodologiesfor new products and legacy product. Define Receiving Inspection requirements as required and associated test method validation for all internal test methods. Conduct audits to qualify supplier's for intended use for the business as applicable. Must Have: Bachelors degree in Engineering, Science, or Technical Discipline required and Minimum of8+ years of quality systems experience. Experience in supplier management in medical domain is added advantage . Strong communication skills, both oral and written. Ability to comprehend principles of engineering, physiology and medical device use. Previous customer-facing and/or project management experience is a plus. Comfortable working with international and multi-cultural department and groups in different time zones . Accurate and delivers quality work, with a sense of urgency. Ability to work well under pressure and maintain positive, enthusiastic attitude. Ability to work in a fast-paced environment .Eagerness to learn and expand responsibilities & accountablity . Nice to Haves: Good interpersonal skills. Previous experience working with global team (Aerospace,Defence, Med device, automobile preferably). Ability to work effectively in a team environment and build strong working relationships. ASQ Quality certification CQE, CSQP, CQA. Working knowledge of Standard, Guidance, and Regulations. Hand on experience on Minitab tools . Exposure in auditing toFDA Quality System Regulation & ISO 13485. Lean Six Sigma Green Belt or Black Belt.

Design high-quality visual content for brochures, presentations, social media, websites, posters, infographics, and internal communications. Create graphics aligned with brand guidelines and business goals. Adapt existing designs for different platforms (digital, print, events, etc.). Support internal departments (e.g., HR for engagement activities, Manufacturing for factory displays, etc.) with creative assets. Collaborate with marketing and content teams to conceptualize campaigns. Take ownership of timelines, version control, and design quality. Basic video editing, motion graphics, or animation skills are a plus. Maintain and organize a visual asset library. Required Skills : Bachelor's degree/diploma in Graphic Design, Visual Communication, or a qualified course related field. Proficiency in Adobe Creative Suite (Illustrator, Photoshop, InDesign; After Effects is a bonus). Familiarity with tools like Canva, Figma, or CorelDraw (based on company usage). Strong sense of aesthetics, layout, typography, and color theory. Attention to detail and ability to handle multiple projects simultaneously. Good communication and collaboration skills. Prior experience in corporate/industrial sectors is a plus.

Verification and Validation R&D Primary responsibilities: Represent the Design Quality function on device development project teams and cross functional co-ordination with multiple departments including R&D, Quality Control, Manufacturing and Regulatory Affairs. Ensure that device development projects and changes to existing devices are conducted in compliance with the FDA 21CFR Part 820 Quality System Regulation, ISO 13485 Regulations, and other applicable standards like ISO 14971. Provide input to design and manufacturing documentation including material specifications, drawings, inspection procedures, and manufacturing procedures, to ensure that the resulting devices can be adequately manufactured and verified. Lead or support design activities including design verification, validation, test procedure development, usability engineering, and risk management. Generate or apply statistical methods with appropriate risk-based justification. Hands-on experience in Design History File compilation / Technical file documentation. Support internal and external inspections/ regulatory audits. Promote continuous improvement in design control activities and use of quality tools with design team. In-depth knowledge and understanding of 21 CFR Part 820 Quality System Regulation, ISO 13485 Quality Standard, 21 CFR 4 Regulation of Combination Products, 14971 Risk Management Standard, MDD, MDR, IEC/EN 62366 Application of Usability Engineering to Medical Devices, and ANSI HE75 Human Factors Engineering in Design of Medical Devices Secondary responsibilities (Wherever applicable): Experience interacting with regulatory agencies and notified bodies Experience with process improvements, process qualification and validation. Experience in complaint investigation, corrective action and preventive action system, statistical methods, quality risk management and Post Market Surveillance.

We are seeking a result-driven Assistant Manager / Manager – Design to lead product and order-based valve design activities. Must have expertise in SolidWorks, material science, and mechanical design principles, to work in a fast-paced,

We are hiring DQC for Pune and Bangalore location Min 3-5 years of Experience Immediate joiner preferred 6 Days of Working Bangalore-Kaikondrahalli Pune- Baner