12607 Drawing Jobs - Page 27

In the minute it takes you to read this job description, Bluecore has launched over 100,000 individually personalized marketing campaigns for our retail ecommerce customers! The Engineering team’s Technical Services arm at Bluecore is committed to delivering quality products and services by holding each other accountable and always being open and honest. We use curiosity and creativity to drive ourselves and our customers towards higher levels of success while fostering a fun and collaborative environment. Bluecore’s Forward Deployed Engineer (FDE) unit is a software engineering team dedicated to helping Bluecore customers extract maximum value from the Bluecore Retail Data Platform. As FDE , you will bring your technical know-how to the main connections of the Bluecore engine to our clients - drawing meaningful intelligence from their websites and implementing marketing solutions that map to the customer’s vertical, audience behavior and product mix. As a Forward Deployed Engineer, your principal responsibilities will lie in (1) writing JavaScript integrations that live on client websites, (2) configuring and maintaining the intake and manipulation of client data across multiple channels including websites, SFTP clients, and Google Cloud Functions, (3) utilizing internal infrastructure and tooling to solve complex, often-unique, client-specific problems, and (4) interfacing with clients to help them understand and best utilize our array of products and services. Besides raw intellect and the ability to not take yourself too seriously, it is important to be detail-oriented in your work, as we work closely with a multitude of the industry’s top online retailers, all of which have very stringent requirements around the look and feel of their strategic communications. You Are A Perfect Fit If You Love Interfacing with Clients: You are someone who loves chatting with clients and figuring out how to push the limits of Bluecore’s technology for them. You are an equal parts engineer, consultant, and subject matter expert with distinct gravitas. Our customers are often non-technical and are responsible for choosing and buying technically sophisticated products. The better we are at helping them understand and use our product, the more successful they will be and the more they will appreciate Bluecore. Solving unique, complex problems: You are someone who can think critically, often on the fly, about nuanced technical problems to devise a scalable, maintainable solution. You enjoy the puzzle and the process of iterating and ideating before implementing a solution, and you are able to break complex problems into simple components for better analysis and digestion. Metrics and Data: You are someone who finds yourself consumed by daily, weekly and monthly metrics and loves turning those into best practices. Seriously, you will advise executive-level decision-makers at industry-leading brands on best business practices. Teaching Others: You are someone who actually believes that diversity in thought and skills makes for a better workplace and a better you. Responsibilities Write client-side JavaScript to be run on clients' websites and configure custom recommendation logic using domain-specific tooling. Serve as the technical point-of-contact for clients both pre- and post-launch: working with them to integrate their website and databases with Bluecore, as well as helping establish and maintain a strong, long-term technical relationship between their systems and Bluecore. Working closely with clients and with our Customer Success team to think creatively and strategically about ways to extract maximum value from the Bluecore platform, designing and implementing custom technical solutions as needed. Develop the best technical solution possible for the toughest challenges that our customers will throw at you. Ideate, develop, and improve upon internal tooling, procedures, and processes that facilitate the work of the Technical Services team. Monitor the overall health and uptime of our most critical connections to clients Work as a liaison between clients, Customer Success, and the product development team to improve Bluecore’s product offering. Requirements Experience 2- 5 years into Solutions Engineering. Successful completion of a reputable Coding Bootcamp or similar level of programming knowledge. Current or past professional experience in a client-facing role, working and communicating directly with customers. Fluent in JavaScript and familiar with various other web development technologies. Ability to take ambiguous workflows and turn them into structured processes. Nice to have Expose to (interested in learning) in SQL, Python, or Google Cloud functions. Familiarity with Marketing, Advertising, eCommerce, or other Emerging Technology (Artificial Intelligence, etc.) platforms. Ability to grow into a client-facing technical resource as career progresses in Bluecore. Shift Timings - 6:30 PM IST - 2:30 AM IST More About Us Bluecore is a multi-channel personalization platform that gives retailers a competitive advantage in a digital-first world. Unlike systems built for mass marketing and a physical-first world, Bluecore unifies shopper and product data in a single platform, and using easy-to-deploy predictive models, activates welcomed one-to-one experiences at the speed and scale of digital. Through Bluecore’s dynamic shopper and product matching, brands can personalize 100% of communications delivered to consumers through their shopping experiences, anywhere . This Comes To Life In Three Core Product Lines Bluecore Communicate™ a modern email service provider (ESP) + SMS Bluecore Site™ an onsite capture and personalization product Bluecore Advertise™ a paid media product At Bluecore we believe in encouraging an inclusive environment in which employees feel encouraged to share their unique perspectives, demonstrate their strengths, and act authentically. We know that diverse teams are strong teams, and welcome those from all backgrounds and varying experiences. Bluecore is a proud equal opportunity employer. We are committed to fair hiring practices and to building a welcoming environment for all team members. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, disability, age, familial status or veteran status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Job Title: Trainee Project Engineer – AutoCAD 2D Design Location: MAS Industries Pvt. Ltd. – Turbhe MIDC Reporting To: Senior Project Engineer Job Brief: We are looking for a highly motivated Trainee Project Engineer to join our Design department. This role is ideal for fresh graduates who are eager to begin their careers in mechanical design and project engineering. The candidate will work primarily with AutoCAD 2D and assist in preparing and modifying technical drawings as per client requirements. Roles and Responsibilities: Prepare shaft plans and layout drawings in accordance with client specifications Make modifications to existing drawings based on client feedback or project changes Support the design team in the creation and documentation of engineering drawings Maintain drawing accuracy and follow internal documentation standards Collaborate with project managers and engineers to ensure timely and precise execution of designs Assist in preparing reports, documentation, and presentations as needed Educational Qualification: Degree in Mechanical OR Automobile Engineering or a related field Required Freshers with Good 2D Drafting Skills If Experienced then 1 years experience with Elevator background preferred Certifications (Preferred): AutoCAD (2D Design specialization) Basic knowledge Salary & Benefits : Salary + PF, ESIC, Yearly Bonus Pick Up and Drop Facility Contact Details : Interested candidates can share their updated CV and 2D AutoCAD Draft Samples via: Call/WhatsApp: +91 86556 58105 Email: hrrecruiter1@masind.net Job Types: Full-time, Fresher Pay: ₹18,000.00 - ₹25,000.00 per month Benefits: Commuter assistance Provident Fund Application Question(s): Can you join immediately? Education: Bachelor's (Preferred) License/Certification: AutoCAD Certification (Preferred) Location: Navi Mumbai, Maharashtra (Preferred) Work Location: In person

Hi Connections!! Livspace #hiringalert About Livspace : Livspace is Building the world's first end-to-end interior design platform out of India. We’re India's top online home improvement & interior destination for consumers and the world & first design automation platform for designers. Profile: Interior Designer Location: Trivandrum Years of Experience: 1 -2 years About the Role As an Interior Designer, you should have excellent creative thinking skills and be able to create Modular designs based on conversations with a client. You should be confident communicating regularly with clients in order to assess their needs and be able to adjust a given approach based on feedback. You should maintain familiarity with the Interior Design landscape and trends in order to provide the best idea for the Renovation client. To own the Sales funnel & drive Sales Closure. To own Customer Experience during a project. To lead and own the quality & accuracy of design deliverables. To own an end-to-end Project lifecycle. Graduation / relevant Diploma. Minimum Experience 1 year as an Interior Designer. Led and delivered a minimum of 2 to 4 Residential Modular KWS projects and Renovation projects. Holds excellent knowledge of design tools, PPT presentation, and AutoCAD. Holds design expertise in Conceptual design (Layout, Style, Moodboard) Technical design (Material knowledge, Execution, and Drawing Preparation) Modular design (Material knowledge, aesthetics & functionality, module planning) Civil works & Services (specifications & installation details) Holds project expertise in Creating BoQ for customers, Coordinating with internal & external agencies. Holds sales expertise in Sales Closure by way of logical & trusted Sales pitches, Driving and leading the Design meetings with the customers. Holds behavioral attributes of Result oriented, Teamwork, Integrity & Ethics, Crisp & meaningful communication. Holds a high degree of willingness to learn, and ability to drive performance among independent team members.

Position Title: Quality Inspector Department: Quality Control / Inspection Location: Bhiwadi, Rajasthan We are seeking a male diploma holder with experience in quality inspection and the ability to read and interpret 2D engineering drawings. The Quality Inspector will be responsible for inspecting raw materials, in-process components, and finished products to ensure they meet specified quality standards and drawing requirements. Key Responsibilities: Quality Inspection: Perform incoming, in-process, and final inspections of materials and components as per 2D drawings and specifications. Use precision measuring instruments (Vernier calipers, micrometers, height gauges, etc.) to verify dimensions. Conduct visual and dimensional checks to identify defects, deviations, or non-conformities. Drawing Interpretation: Read and understand 2D engineering drawings, including tolerances, GD&T (Geometric Dimensioning & Tolerancing), and surface finish requirements. Ensure all inspected parts comply with the given drawings and quality standards. Documentation & Reporting: Prepare inspection reports and maintain records of approved/rejected materials. Raise Non-Conformance Reports (NCR) for defective parts and follow up on corrective actions. Coordination with Production & Vendors: Communicate with production teams and suppliers regarding quality issues. Assist in resolving quality-related concerns with vendors and internal departments. Compliance & Continuous Improvement: Follow company quality policies and industry standards (ISO, ASTM, etc.). Participate in root cause analysis for recurring defects. Qualifications & Skills: Education: Diploma in Mechanical/Production/Manufacturing Engineering ( Mandatory ). Experience: 0 -2 years in quality inspection in a manufacturing/factory environment. Technical Skills: Must be able to read and interpret 2D engineering drawings. Hands-on experience with measuring instruments (Vernier, micrometer, plug gauges, etc.). Basic knowledge of quality standards. Soft Skills: Strong attention to detail. Good communication skills (to interact with vendors and production teams). Ability to work in a fast-paced environment. Additional Requirements: Only male candidates will be considered due to work environment requirements. Willingness to work in shifts if required. Work Conditions: Shop floor / factory environment. May involve standing for long hours and handling inspection tools. How to Apply: Interested candidates meeting the above criteria may send their resumes to hr1@silcoautomotive.in with the subject line "Application for QC – [Your Name]." Job Types: Full-time, Permanent, Fresher Pay: ₹15,000.00 - ₹20,000.00 per month Benefits: Health insurance Paid sick time Paid time off Location: Bhiwadi, Rajasthan (Preferred) Work Location: In person

Company Description Dawn Digital Studio is a leading 3D architectural visualization company based in Delhi, India. The studio specializes in creating stunning 3D visualizations and architectural walkthroughs for various sectors using cutting-edge techniques. With a team of creative professionals, Dawn Digital offers comprehensive solutions to clients worldwide. Role Description This is a full-time on-site role for a 3D Architectural Visualizer at Dawn Digital Pvt. Ltd in Delhi, India. The role involves creating visualizations, graphics, graphic design, lighting, and drawing for architectural projects on a daily basis. Qualifications Visualization and Graphics skills Graphic Design expertise Proficiency in Lighting techniques Drawing capabilities Strong attention to detail Excellent communication and teamwork skills Proficiency in 3D modeling software such as AutoCAD, SketchUp, or 3ds Max Degree in Architecture, Design, or related field is a plus Job Type: Full-time Pay: ₹30,000.00 - ₹50,000.00 per month Application Question(s): What is your current salary? What is your expected salary? How soon can you join us (Days)? Are you comfortable with the location of Okhla Phase 2 New Delhi? Work Location: In person

About Us We are the independent expert in assurance and risk management. Driven by our purpose, to safeguard life, property, and the environment, we empower our customers and their stakeholders with facts and reliable insights so that critical decisions can be made with confidence. As a trusted voice for many of the world’s most successful organizations, we use our knowledge to advance safety and performance, set industry benchmarks, and inspire and invent solutions to tackle global transformations. About SCPA We help our customers respond to the increased demand for trust and transparency around products, assets, supply chains, and ecosystems, driving the transformation of the assurance industry. Whether certifying products, sharing claims or optimizing and decarbonizing supply chains, DNV helps companies manage risks and realize their long-term strategic goals, improving ESG performance and generating lasting, sustainable results. Drawing on our wide technical and industry expertise, we work with companies worldwide to bridge trust gaps among consumers, producers and suppliers. About The Role As part of our continued growth, we are looking to recruit technical and experienced In-Vitro Diagnostic Medical Device Assessors and Lead Auditors. The successful candidates will be responsible for planning and conducting audits / assessments against the manufacturing of medical devices, in accordance with ISO 13485, IVDR 2017/746 and MDSAP standards, enabling the delivery of assessment and certification services that meet customer requirements and appropriate accreditation standards. Key Accountabilities: Assessor Conduct assessments (either desk-based or on client’s sites) in accordance with established procedures, maintaining a high standard of service delivery that ensures effective customer communication. Conduct Technical File reviews specific for products being authorized. Complete all chargeable work within the required timeframes to ensure customer satisfaction and efficiency of the business. Complete specific projects in relation to IVDR procedures, processes, systems and documentation as requested by the Operations Manager. If required, undertake reviews of files and make certification decisions within target timescales and in line with DNV policies and accreditation/approval requirements. Key Accountabilities: Auditor Responsible to carry out audits of the manufacturer's quality management system (QMS) and of its suppliers and/or subcontractors when appropriate and to draw up records and reports on the corresponding audits. Conduct surveillance audits including follow-up activities in accordance with established procedures, maintaining a high standard of service delivery that ensures effective customer relationships. Complete all chargeable work within the required timeframes to ensure customer satisfaction and efficiency of the business. Complete projects in relation to IVDR procedures, processes, systems and documentation as requested by the Operations Manager. If required, undertake reviews of files and make certification recommendations within target timescales and in line with DNV policies and accreditation/approval requirements. Project manage auditing teams, as appropriate, to maximize efficiencies, enhance client satisfaction and ensure compliance with standards. What we offer Flexible work arrangements for better work-life balance Generous Paid Leaves (Annual, Sick, Compassionate, Local Public, Marriage, Maternity, Paternity, Medical leave) Medical benefits ( Insurance and Annual Health Check-up) Pension and Insurance Policies (Group Term Life Insurance, Group Personal Accident Insurance, Travel Insurance) Training and Development Assistance (Training Sponsorship, On-The-Job Training, Training Programme) Additional Benefits (Long Service Awards, Mobile Phone Reimbursement) Company bonus/Profit share. *Benefits may vary based on position, tenure/contract/grade level* DNV is an Equal Opportunity Employer and gives consideration for employment to qualified applicants without regard to gender, religion, race, national or ethnic origin, cultural background, social group, disability, sexual orientation, gender identity, marital status, age or political opinion. Diversity is fundamental to our culture and we invite you to be part of this diversity. About You Assessors and Auditors shall have a technical college degree in a relevant product or medical area, as described below. In-Vitro Diagnostic devices: Biology or Microbiology Chemistry or Biochemistry Human Physiology Medical Technology or Biotechnology Medicine, Veterinary Medicine Biomedical science - e.g. haematology, virology, molecular diagnostics Nursing Pharmacy, Pharmacology, Toxicology Physiology Education In addition to a relevant educational degree, candidates must have a minimum 4 years’ work experience (full time) in an In-Vitro diagnostic medical device related industry, academia or hospital environment, with at least 2 of these years in the design, manufacturing, testing or use of the device in which they are qualified to Audit or Assessment, and/or experience as an assessor or auditor in a notified body. Specifically: Auditor - Practical experience in the quality management system and specific production process/technologies for the IVD medical devices. Assessor - Practical experience in conducting and/or assessing performance evaluation data or related scientific aspects with in-vitro diagnostic medical devices in one or more of the following areas Microbiology, Immunology, Genetic testing/Cancer Biology and Molecular Biology. A PhD in a relevant area for in-vitro diagnostic medical devices can substitute 3 years of work experience provided it includes 2 years’ experience in design, manufacture or testing. In addition to the above, knowledge of the following would be preferred: An excellent working knowledge of medical device management systems, standards and medical device compliance/auditing techniques. Work experience in positions with significant QA Regulatory or management systems responsibility. Experience with Harmonized medical device standards for In-Vitro diagnostic medical devices. Experience with Risk Management EN ISO 14971. Medical device experience from auditing/work. Experience auditing against recognized standards. Experience of working under own initiative and in planning and prioritizing workloads. Should have a flair for technical writing, essential for exhaustive report writing.

Job description Title : Rebar Detailer Experience : 3+years Location : Chennai Software's Known : CADSRC/Rebar CAD Roles and responsibility Prepare Shop detailed drawings of reinforced concrete elements like Foundation, columns, beams, walls/core wall/shear walls, slab, Elevator structure, stair etc. To generate Bar Bending Schedule manually as well with industrial software's Ability to manage Structural steel, Architectural & MEP functional drawings will be added an advantages Review and analyze the project documents identifying the drawing and specification conflicts, insufficient information, and missing dimensions. Coordinate and communicate with clients & team members. Working as part of a project team to provide deliverables and meet deadlines while providing quality control quality assurance to ensure these deliverables are on - time and of a high quality. Material take off Inter disciplinary interaction To perform quality checks Preparation of Roof framing and arrangement drawings Preparation of Foundation arrangement with detailed drawings Detailed structural fabrication drawings showing details for fabrication (Joint welding details, Riveting details etc.) Candidate Profile Degree in Civil Diploma/B. Tech with 3+ years' experience in Building services industry as a Draftsman Good Communication knowledges Experience in using various internationals codes and standards like BS & EN codes Experience in working for an international client / projects a plus If Interested share me your resume Phone Number : +91 8925278194 Email Id : swathi@conservesolution.com Address: No 15 and 16, 1st Link Road, Nehru Nagar, Kottivakkam (OMR),Chennai, Tamil Nadu 600096

About Us We are the independent expert in assurance and risk management. Driven by our purpose, to safeguard life, property, and the environment, we empower our customers and their stakeholders with facts and reliable insights so that critical decisions can be made with confidence. As a trusted voice for many of the world’s most successful organizations, we use our knowledge to advance safety and performance, set industry benchmarks, and inspire and invent solutions to tackle global transformations. About SCPA We help our customers respond to the increased demand for trust and transparency around products, assets, supply chains, and ecosystems, driving the transformation of the assurance industry. Whether certifying products, sharing claims or optimizing and decarbonizing supply chains, DNV helps companies manage risks and realize their long-term strategic goals, improving ESG performance and generating lasting, sustainable results. Drawing on our wide technical and industry expertise, we work with companies worldwide to bridge trust gaps among consumers, producers and suppliers. About The Role As part of our continued growth, we are looking to recruit technical and experienced In-Vitro Diagnostic Medical Device Assessors and Lead Auditors. The successful candidates will be responsible for planning and conducting audits / assessments against the manufacturing of medical devices, in accordance with ISO 13485, IVDR 2017/746 and MDSAP standards, enabling the delivery of assessment and certification services that meet customer requirements and appropriate accreditation standards. Key Accountabilities: Assessor Conduct assessments (either desk-based or on client’s sites) in accordance with established procedures, maintaining a high standard of service delivery that ensures effective customer communication. Conduct Technical File reviews specific for products being authorized. Complete all chargeable work within the required timeframes to ensure customer satisfaction and efficiency of the business. Complete specific projects in relation to IVDR procedures, processes, systems and documentation as requested by the Operations Manager. If required, undertake reviews of files and make certification decisions within target timescales and in line with DNV policies and accreditation/approval requirements. Key Accountabilities: Auditor Responsible to carry out audits of the manufacturer's quality management system (QMS) and of its suppliers and/or subcontractors when appropriate and to draw up records and reports on the corresponding audits. Conduct surveillance audits including follow-up activities in accordance with established procedures, maintaining a high standard of service delivery that ensures effective customer relationships. Complete all chargeable work within the required timeframes to ensure customer satisfaction and efficiency of the business. Complete projects in relation to IVDR procedures, processes, systems and documentation as requested by the Operations Manager. If required, undertake reviews of files and make certification recommendations within target timescales and in line with DNV policies and accreditation/approval requirements. Project manage auditing teams, as appropriate, to maximize efficiencies, enhance client satisfaction and ensure compliance with standards. What we offer Flexible work arrangements for better work-life balance Generous Paid Leaves (Annual, Sick, Compassionate, Local Public, Marriage, Maternity, Paternity, Medical leave) Medical benefits ( Insurance and Annual Health Check-up) Pension and Insurance Policies (Group Term Life Insurance, Group Personal Accident Insurance, Travel Insurance) Training and Development Assistance (Training Sponsorship, On-The-Job Training, Training Programme) Additional Benefits (Long Service Awards, Mobile Phone Reimbursement) Company bonus/Profit share. *Benefits may vary based on position, tenure/contract/grade level* DNV is an Equal Opportunity Employer and gives consideration for employment to qualified applicants without regard to gender, religion, race, national or ethnic origin, cultural background, social group, disability, sexual orientation, gender identity, marital status, age or political opinion. Diversity is fundamental to our culture and we invite you to be part of this diversity. About You Assessors and Auditors shall have a technical college degree in a relevant product or medical area, as described below. In-Vitro Diagnostic devices: Biology or Microbiology Chemistry or Biochemistry Human Physiology Medical Technology or Biotechnology Medicine, Veterinary Medicine Biomedical science - e.g. haematology, virology, molecular diagnostics Nursing Pharmacy, Pharmacology, Toxicology Physiology Education In addition to a relevant educational degree, candidates must have a minimum 4 years’ work experience (full time) in an In-Vitro diagnostic medical device related industry, academia or hospital environment, with at least 2 of these years in the design, manufacturing, testing or use of the device in which they are qualified to Audit or Assessment, and/or experience as an assessor or auditor in a notified body. Specifically: Auditor - Practical experience in the quality management system and specific production process/technologies for the IVD medical devices. Assessor - Practical experience in conducting and/or assessing performance evaluation data or related scientific aspects with in-vitro diagnostic medical devices in one or more of the following areas Microbiology, Immunology, Genetic testing/Cancer Biology and Molecular Biology. A PhD in a relevant area for in-vitro diagnostic medical devices can substitute 3 years of work experience provided it includes 2 years’ experience in design, manufacture or testing. In addition to the above, knowledge of the following would be preferred: An excellent working knowledge of medical device management systems, standards and medical device compliance/auditing techniques. Work experience in positions with significant QA Regulatory or management systems responsibility. Experience with Harmonized medical device standards for In-Vitro diagnostic medical devices. Experience with Risk Management EN ISO 14971. Medical device experience from auditing/work. Experience auditing against recognized standards. Experience of working under own initiative and in planning and prioritizing workloads. Should have a flair for technical writing, essential for exhaustive report writing.

Job Responsibilities We are seeking a skilled and detail-oriented Auto Cad Designer with 2–3 years of hands-on experience in drafting and design. The ideal candidate will be responsible for creating technical drawings, layouts, and plans using Auto Cad software in support of engineering, architectural, or manufacturing projects. Prepare & Revise all HVAC shop drawings. Scope of Work Provide equipment as shown and specified including heating, ventilating and air conditioning (HVAC). This work shall include the following building and drawings complete with specifications. Key Responsibilities: Create 2D and/or 3D technical drawings, schematics, and layouts using Auto Cad. Work from sketches, specifications, and other design data to develop accurate drawings. Coordinate with engineers,or senior designers to ensure designs meet project requirements. Revise drawings as changes occur and maintain drawing files and documentation. Ensure accuracy, quality, and compliance with company and industry standards. Assist in design calculations and prepare bill of materials (BOM) when needed. Support the project team during various phases of design and construction. Required Skills & Qualifications: Diploma or Bachelor's degree in Engineering, Drafting, or a related field. 2–3 years of experience using Auto Cad in a professional environment. Solid understanding of drafting standards, engineering terminology, and design practices. Job Types: Full-time, Permanent, Fresher Pay: ₹15,000.00 - ₹25,000.00 per month Benefits: Health insurance Provident Fund Ability to commute/relocate: Surat, Surat, Gujarat: Reliably commute or planning to relocate before starting work (Required) Work Location: In person Application Deadline: 30/05/2025

Position: Trainee Architect to Senior Architect Overview We are seeking a qualified and detail-oriented architect who can produce accurate and clear architectural drawings using AutoCAD. The ideal candidate will have a solid understanding of the complete project lifecycle, the ability to coordinate effectively with stakeholders, and a commitment to delivering high-quality work on time. Adherence to quality standards and regulatory requirements is essential for this role. Responsibilities Prepare detailed architectural drawings including plans, elevations, sections, and details. Apply engineering principles, mathematics, material science, and construction methods to achieve optimal design outcomes. Develop complete construction drawing sets and ensure accuracy and clarity. Conduct site visits to evaluate work quality and ensure compliance with safety standards. Monitor construction processes and provide technical recommendations as needed. Collaborate with cross-functional teams to define project goals, schedules, and budgets. Continuously improve design processes while maintaining high quality standards. Education and Background Bachelor’s degree in Architecture or Diploma in Architecture (site experience not mandatory; internships or relevant project work preferred). Any graduate with relevant architectural drafting experience will also be considered. Skills and Proficiencies Proficiency in AutoCAD , SketchUp , and Lumion (knowledge of other 3D visualization tools is a plus). Strong architectural knowledge and drafting skills. Fair understanding of structural drawings. Experience producing construction documents. Excellent communication, interpersonal, and time management skills. Ability to work independently with minimal supervision. Proficiency in Microsoft Office Suite. Good command of English (listening, reading, and writing). Flexible, ambitious, and adaptable to work on various project types and stages. Experience Fresher to 4+ years in architecture or construction.

We are seeking a talented 2D & 3D Draughtsman with strong proficiency in AutoCAD , specifically for the events and exhibitions industry . The ideal candidate will be responsible for translating creative concepts, design sketches, and client briefs into accurate and detailed 2D technical drawings for event setups, stage designs, exhibition booths, and temporary structures. Company Description MCI is an independent global marketing communications group that focuses on a human-first approach. We specialize in events, congress organization, community solutions, and digital communications, offering a comprehensive portfolio that includes social and content marketing, research, and insights. With headquarters in Geneva, MCI has a global presence across 60 offices in 31 countries. We have been driving positive change for the world’s leading brands, associations, and not-for-profit organizations for over three decades. In India, we have been delivering successful events through our Offices in New Delhi & Mumbai and operating through satellite offices in Bengaluru and Hyderabad. MCI India has proudly earned the prestigious Great Place to Work certification , a testament to our exceptional workplace culture and commitment to our people! Corporates from the Technology, Consulting, Automotive, and Energy sectors amongst others dominate our client portfolio. Being a part of MCI Group, our key strength lies in being 'GLOCAL' - offering global standards with local expertise. Key Responsibilities: Create detailed 2D,3D working drawings (layouts, elevations, sections) using AutoCAD Coordinate with the design team and project managers to translate conceptual designs into technical drawings Ensure that drawings adhere to industry and company standards, including measurements, annotations, and scale Revise and update drawings as per the venue, stage design, halls, conference venue and as per client feedback Maintain and organize drawing archives and documentation for each project Collaborate with internal operations & client servicing teams for technical accuracy and feasibility Requirements: Proficiency in AutoCAD (2D & 3D drafting is mandatory) 1–3 years of experience as a 2D & 3D Draughtsman in experiential events, conferences, exhibition industries are preferred. Strong understanding of event space planning, structural detailing, and material usage. Ability to read and interpret architectural drawings, detailed floor plans, elevations, and sectional views for client presentations Good communication and team coordination skills Attention to detail and ability to work under timelines. Job Type: Full-time Pay: ₹20,000.00 - ₹25,000.00 per month Ability to commute/relocate: Sultanpur, Delhi, Delhi: Reliably commute or planning to relocate before starting work (Preferred) Application Question(s): Do have any experience with event, exhibitions or conferences industry? What's your notice periods? Work Location: In person

About Us We are the independent expert in assurance and risk management. Driven by our purpose, to safeguard life, property, and the environment, we empower our customers and their stakeholders with facts and reliable insights so that critical decisions can be made with confidence. As a trusted voice for many of the world’s most successful organizations, we use our knowledge to advance safety and performance, set industry benchmarks, and inspire and invent solutions to tackle global transformations. About SCPA We help our customers respond to the increased demand for trust and transparency around products, assets, supply chains, and ecosystems, driving the transformation of the assurance industry. Whether certifying products, sharing claims or optimizing and decarbonizing supply chains, DNV helps companies manage risks and realize their long-term strategic goals, improving ESG performance and generating lasting, sustainable results. Drawing on our wide technical and industry expertise, we work with companies worldwide to bridge trust gaps among consumers, producers and suppliers. About The Role As part of our continued growth, we are looking to recruit technical and experienced In-Vitro Diagnostic Medical Device Assessors and Lead Auditors. The successful candidates will be responsible for planning and conducting audits / assessments against the manufacturing of medical devices, in accordance with ISO 13485, IVDR 2017/746 and MDSAP standards, enabling the delivery of assessment and certification services that meet customer requirements and appropriate accreditation standards. Key Accountabilities: Assessor Conduct assessments (either desk-based or on client’s sites) in accordance with established procedures, maintaining a high standard of service delivery that ensures effective customer communication. Conduct Technical File reviews specific for products being authorized. Complete all chargeable work within the required timeframes to ensure customer satisfaction and efficiency of the business. Complete specific projects in relation to IVDR procedures, processes, systems and documentation as requested by the Operations Manager. If required, undertake reviews of files and make certification decisions within target timescales and in line with DNV policies and accreditation/approval requirements. Key Accountabilities: Auditor Responsible to carry out audits of the manufacturer's quality management system (QMS) and of its suppliers and/or subcontractors when appropriate and to draw up records and reports on the corresponding audits. Conduct surveillance audits including follow-up activities in accordance with established procedures, maintaining a high standard of service delivery that ensures effective customer relationships. Complete all chargeable work within the required timeframes to ensure customer satisfaction and efficiency of the business. Complete projects in relation to IVDR procedures, processes, systems and documentation as requested by the Operations Manager. If required, undertake reviews of files and make certification recommendations within target timescales and in line with DNV policies and accreditation/approval requirements. Project manage auditing teams, as appropriate, to maximize efficiencies, enhance client satisfaction and ensure compliance with standards. What we offer Flexible work arrangements for better work-life balance Generous Paid Leaves (Annual, Sick, Compassionate, Local Public, Marriage, Maternity, Paternity, Medical leave) Medical benefits ( Insurance and Annual Health Check-up) Pension and Insurance Policies (Group Term Life Insurance, Group Personal Accident Insurance, Travel Insurance) Training and Development Assistance (Training Sponsorship, On-The-Job Training, Training Programme) Additional Benefits (Long Service Awards, Mobile Phone Reimbursement) Company bonus/Profit share. *Benefits may vary based on position, tenure/contract/grade level* DNV is an Equal Opportunity Employer and gives consideration for employment to qualified applicants without regard to gender, religion, race, national or ethnic origin, cultural background, social group, disability, sexual orientation, gender identity, marital status, age or political opinion. Diversity is fundamental to our culture and we invite you to be part of this diversity. About You Assessors and Auditors shall have a technical college degree in a relevant product or medical area, as described below. In-Vitro Diagnostic devices: Biology or Microbiology Chemistry or Biochemistry Human Physiology Medical Technology or Biotechnology Medicine, Veterinary Medicine Biomedical science - e.g. haematology, virology, molecular diagnostics Nursing Pharmacy, Pharmacology, Toxicology Physiology Education In addition to a relevant educational degree, candidates must have a minimum 4 years’ work experience (full time) in an In-Vitro diagnostic medical device related industry, academia or hospital environment, with at least 2 of these years in the design, manufacturing, testing or use of the device in which they are qualified to Audit or Assessment, and/or experience as an assessor or auditor in a notified body. Specifically: Auditor - Practical experience in the quality management system and specific production process/technologies for the IVD medical devices. Assessor - Practical experience in conducting and/or assessing performance evaluation data or related scientific aspects with in-vitro diagnostic medical devices in one or more of the following areas Microbiology, Immunology, Genetic testing/Cancer Biology and Molecular Biology. A PhD in a relevant area for in-vitro diagnostic medical devices can substitute 3 years of work experience provided it includes 2 years’ experience in design, manufacture or testing. In addition to the above, knowledge of the following would be preferred: An excellent working knowledge of medical device management systems, standards and medical device compliance/auditing techniques. Work experience in positions with significant QA Regulatory or management systems responsibility. Experience with Harmonized medical device standards for In-Vitro diagnostic medical devices. Experience with Risk Management EN ISO 14971. Medical device experience from auditing/work. Experience auditing against recognized standards. Experience of working under own initiative and in planning and prioritizing workloads. Should have a flair for technical writing, essential for exhaustive report writing.

SunStripe is looking for an experienced Senior Engineer BESS to join our Design & Engineering team for Utility-Scale Solar PV & Battery Energy Storage Systems (BESS) projects. The ideal candidate will have hands-on drafting experience, strong expertise in electrical layouts, schematics, and optimization, and exposure to the US, India or other overseas markets. This role requires proficiency in CAD-based tools, an understanding of electrical system layouts, and the ability to optimize designs for efficiency and cost-effectiveness. Candidates must have detailed experience on Large ground mount projects. The candidate will be reporting to the Manager- Design & Engineering (Electrical). Key Responsibilities: 1. Electrical Drafting & Design Development Prepare detailed electrical drawings, including single-line diagrams (SLDs),three-line diagrams, grounding layouts, and AC/DC wiring diagrams for solar PV and BESS projects for Utility Scale ground Mount Solar Project. Develop plant layouts, conduit/cable routing, substation layouts, and equipment arrangements. Good understanding of regulations, zoning and compliance requirements. Create as-built drawings, shop drawings, and IFC (Issued for Construction) drawings for solar + storage projects. Work closely with design engineers and project managers to ensure accuracy and compliance with specifications. 2. Solar PV & BESS System Optimization Optimize array layouts, inverter placement, electrical BOS (Balance of System) design, and cable schedules to reduce costs and improve efficiency. Use AI-driven tools and automation software to enhance design workflows and reduce manual drafting efforts. Ensure optimal land utilization and power evacuation strategies in collaboration with the engineering team. 3. CAD & Design Tools Proficiency Utilize AutoCAD, AutoCAD Electrical and other CAD tools for high-quality drawings. Work on GIS-based tools and electrical modelling software to enhance system design precision. Maintain drawing databases, version control, and documentation for all design files. 4. Collaboration & Cross-Functional Coordination Coordinate with structural, mechanical, and civil design teams to integrate electrical layouts with site plans. Work with procurement teams to ensure drawings align with vendor specifications and equipment compatibility. Provide technical drafting support for engineering teams working on interconnection, relay coordination, and power system studies. Requirements Required Qualifications & Experience: 4-7 years of hands-on experience in electrical drafting for Utility-Scale Solar PV and BESS projects. Strong expertise in AutoCAD, AutoCAD Electrical, PVsyst, and similar CAD tools. Experience working with US utilities, developers, or other overseas solar markets is highly preferred. Familiarity with electrical BOS (Balance of System), high-voltage equipment layouts, and Single Line Diagram Good understanding of NEC, NFPA, IEEE, IEC, and UL standards for solar + storage systems. Ability to optimize electrical layouts for efficiency, cost reduction, and improved energy yield. Strong organizational skills with experience managing multiple projects and drawing versions. Preferred Skills & Certifications: Professional CAD Certification in AutoCAD or AutoCAD Electrical. Knowledge of GIS-based tools, SCADA system layouts, and power system simulation tools is a plus.

About Us We are the independent expert in assurance and risk management. Driven by our purpose, to safeguard life, property, and the environment, we empower our customers and their stakeholders with facts and reliable insights so that critical decisions can be made with confidence. As a trusted voice for many of the world’s most successful organizations, we use our knowledge to advance safety and performance, set industry benchmarks, and inspire and invent solutions to tackle global transformations. About SCPA We help our customers respond to the increased demand for trust and transparency around products, assets, supply chains, and ecosystems, driving the transformation of the assurance industry. Whether certifying products, sharing claims or optimizing and decarbonizing supply chains, DNV helps companies manage risks and realize their long-term strategic goals, improving ESG performance and generating lasting, sustainable results. Drawing on our wide technical and industry expertise, we work with companies worldwide to bridge trust gaps among consumers, producers and suppliers. About The Role As part of our continued growth, we are looking to recruit technical and experienced In-Vitro Diagnostic Medical Device Assessors and Lead Auditors. The successful candidates will be responsible for planning and conducting audits / assessments against the manufacturing of medical devices, in accordance with ISO 13485, IVDR 2017/746 and MDSAP standards, enabling the delivery of assessment and certification services that meet customer requirements and appropriate accreditation standards. Key Accountabilities: Assessor Conduct assessments (either desk-based or on client’s sites) in accordance with established procedures, maintaining a high standard of service delivery that ensures effective customer communication. Conduct Technical File reviews specific for products being authorized. Complete all chargeable work within the required timeframes to ensure customer satisfaction and efficiency of the business. Complete specific projects in relation to IVDR procedures, processes, systems and documentation as requested by the Operations Manager. If required, undertake reviews of files and make certification decisions within target timescales and in line with DNV policies and accreditation/approval requirements. Key Accountabilities: Auditor Responsible to carry out audits of the manufacturer's quality management system (QMS) and of its suppliers and/or subcontractors when appropriate and to draw up records and reports on the corresponding audits. Conduct surveillance audits including follow-up activities in accordance with established procedures, maintaining a high standard of service delivery that ensures effective customer relationships. Complete all chargeable work within the required timeframes to ensure customer satisfaction and efficiency of the business. Complete projects in relation to IVDR procedures, processes, systems and documentation as requested by the Operations Manager. If required, undertake reviews of files and make certification recommendations within target timescales and in line with DNV policies and accreditation/approval requirements. Project manage auditing teams, as appropriate, to maximize efficiencies, enhance client satisfaction and ensure compliance with standards. What we offer Flexible work arrangements for better work-life balance Generous Paid Leaves (Annual, Sick, Compassionate, Local Public, Marriage, Maternity, Paternity, Medical leave) Medical benefits ( Insurance and Annual Health Check-up) Pension and Insurance Policies (Group Term Life Insurance, Group Personal Accident Insurance, Travel Insurance) Training and Development Assistance (Training Sponsorship, On-The-Job Training, Training Programme) Additional Benefits (Long Service Awards, Mobile Phone Reimbursement) Company bonus/Profit share. *Benefits may vary based on position, tenure/contract/grade level* DNV is an Equal Opportunity Employer and gives consideration for employment to qualified applicants without regard to gender, religion, race, national or ethnic origin, cultural background, social group, disability, sexual orientation, gender identity, marital status, age or political opinion. Diversity is fundamental to our culture and we invite you to be part of this diversity. About You Assessors and Auditors shall have a technical college degree in a relevant product or medical area, as described below. In-Vitro Diagnostic devices: Biology or Microbiology Chemistry or Biochemistry Human Physiology Medical Technology or Biotechnology Medicine, Veterinary Medicine Biomedical science - e.g. haematology, virology, molecular diagnostics Nursing Pharmacy, Pharmacology, Toxicology Physiology Education In addition to a relevant educational degree, candidates must have a minimum 4 years’ work experience (full time) in an In-Vitro diagnostic medical device related industry, academia or hospital environment, with at least 2 of these years in the design, manufacturing, testing or use of the device in which they are qualified to Audit or Assessment, and/or experience as an assessor or auditor in a notified body. Specifically: Auditor - Practical experience in the quality management system and specific production process/technologies for the IVD medical devices. Assessor - Practical experience in conducting and/or assessing performance evaluation data or related scientific aspects with in-vitro diagnostic medical devices in one or more of the following areas Microbiology, Immunology, Genetic testing/Cancer Biology and Molecular Biology. A PhD in a relevant area for in-vitro diagnostic medical devices can substitute 3 years of work experience provided it includes 2 years’ experience in design, manufacture or testing. In addition to the above, knowledge of the following would be preferred: An excellent working knowledge of medical device management systems, standards and medical device compliance/auditing techniques. Work experience in positions with significant QA Regulatory or management systems responsibility. Experience with Harmonized medical device standards for In-Vitro diagnostic medical devices. Experience with Risk Management EN ISO 14971. Medical device experience from auditing/work. Experience auditing against recognized standards. Experience of working under own initiative and in planning and prioritizing workloads. Should have a flair for technical writing, essential for exhaustive report writing.

Job Summary: As a QAQC Engineer (Fresher), you will be trained to ensure the quality and compliance of our company's products, services, and projects. Your primary responsibility will be to learn, assist, and gradually implement quality control procedures and processes to meet industry standards and regulatory requirements. You will work under the guidance of senior engineers, collaborating with various departments to identify potential quality issues, assist in implementing corrective actions, and maintain a high level of quality across all aspects of our organization's operations. Additionally, you will receive hands-on training in non-destructive tests on weld joints, conducting dimensional control inspections of major structures after installation, and reading complex production drawings for quality checks. Responsibilities: Quality Control and Assurance: Learn and assist in developing and maintaining QAQC procedures, standards, and protocols to ensure compliance with industry regulations and company policies. Inspection and Testing: Support senior engineers in conducting inspections, audits, and tests on materials, processes, and products. Assist production teams in maintaining compliance and resolving issues. Non-Destructive Testing (NDT): Receive training to perform non-destructive tests on weld joints to ensure weld quality and integrity according to industry standards and specifications. Dimensional Control Inspections: Assist in dimensional control inspections of major structures after installation, using design drawings to verify dimensions and alignment. Complex Production Drawing Interpretation: Learn to read and interpret complex production drawings to carry out quality checks and ensure compliance with design specifications. Quality Checking: Support quality checks at every stage of production to maintain consistent standards. Production Standard Monitoring: Assist in monitoring production operations to ensure adherence to quality requirements. Collaboration with Draughtsman: Work with draughtsman during class inspections to verify project dimensions and accuracy. Issue Reporting: Assist in documenting and reporting quality-related issues to site managers during construction for timely resolution. Construction Methodology Improvement: Contribute ideas and support initiatives to improve project efficiency and quality. Quality Control Tests for Moulders: Learn and help conduct quality control tests for moulders to verify the quality of their products and materials. Material Inspection at Goods Receipt: Support material inspections during goods receipt at the store to ensure they meet the required quality standards. Project Coordination: Work with supervisors and site teams to support project coordination efforts. lssue Tracking and Resolution: Assist in recording and addressing quality-related issues during the project. Planning Responsibilities: Daily Constraints Study and Reporting: Assist in analyzing and reporting on daily constraints faced during project execution. Weekly Summary of Constraints: Support the preparation of weekly summaries of identified constraints. Daily Project Tracking: Learn to track project progress using Primavera or other planning tools. Support for Quarterly Plans: Assist in preparing and supporting quarterly project plans. Support for Monthly Plans: Collaborate with the planning team to develop and support monthly plans. Help with Bi-Weekly Plans: Assist the site team in preparing bi-weekly plans. Weekly Plan Review: Help review weekly plans submitted by departments. Project Schedule Preparation: Learn to assist in preparing project schedules with key activities, resources, and timelines. Requirements: Mandatory: B.Tech in Mechanical Engineering. Strong interest in quality control and assurance processes. Eager to learn and adapt to industry standards, tools, and methodologies. Analytical mindset with a keen eye for detail. Good communication skills and ability to work in a team environment. Ability to manage time effectively and work on multiple tasks. Basic knowledge of engineering drawings and measurements (training will be provided). Salary Range: ₹18,000 per month. Job Types: Full-time, Permanent, Fresher Pay: From ₹18,000.00 per month Benefits: Leave encashment Paid sick time Paid time off Ability to commute/relocate: Cherthala, Kerala: Reliably commute or planning to relocate before starting work (Required) Application Question(s): What is your expected salary?

Hardware Engineer Are you a Hardware Engineer who wants to contribute to the development of high-quality machines and technical solutions? Then we are looking for you! As a Hardware Engineer, you are responsible for designing, drawing and developing electrical installations for our machines. You will work together in a dynamic team of technical specialists and play a key role in realizing high-quality products that meet the highest quality standards. Ready for a role in which you can use your expertise? Then grab this opportunity to work with us as a Hardware Engineer! What will you do? ·You are responsible for the design and functional drawing of electrical schematics in E-Plan. ·You ensure a correct translation of technical specifications into a detailed design. ·You actively contribute ideas and suggest improvements to optimise the efficiency, quality and reliability of installations. ·You will regularly communicate with colleagues and suppliers, in consultation with the purchasing department, to coordinate designs and solve technical issues. Your profile ·You have completed a technical university education in electrical engineering or industrial automation. ·You have in-depth knowledge of mechatronics, control technology, machine directives and relevant industrial standards. ·You have extensive experience with functional drawing in software (preferably E-Plan) and the independent design and elaboration of electrical diagrams. ·You have a fluent command of the English language. What we are looking for! ·You have strong communication skills and the ability to work effectively in a team. ·You have a hands-on mentality with a practical and solution-oriented approach. ·You work independently and tackle technical issues proactively. ·You are accurate and have an eye for detail in design and execution. What do we offer you? ·A challenging, full-time position in an international and growing organization. ·A competitive salary. ·Excellent fringe benefits. ·Training and education to further develop your personal skills. ·A pleasant working atmosphere in a dynamic team. ·Traveling to Netherlands on a regular

As an Electrical Technician, the candidate will work with Electrical Engineers in designing, wiring and diagnosing electrical circuits. Creation of Electrical Wiring Drawing will also be the responsibility of the candidate. Regular maintenance of shopfloor machines and record-keeping will be part of the job. Responsibilities: Read and interpret technical diagrams, blueprints, and schematics Wiring of electrical panels according to the wiring diagram Regular machine maintenance Requirements: ITI in Electrical Engineering Strong understanding of electrical systems, circuits, and wiring. Proficiency in using electrical tools, testing devices, and diagnostic equipment. Basic knowledge of MS Office Good communication skills and the ability to follow technical instructions. Job Types: Full-time, Permanent, Fresher Pay: ₹14,000.00 - ₹16,000.00 per month Benefits: Food provided Health insurance Leave encashment Paid time off Provident Fund Ability to commute/relocate: Magadi Road, Bengaluru, Karnataka: Reliably commute or planning to relocate before starting work (Required) Education: Higher Secondary(12th Pass) (Required) Experience: Electrical: 1 year (Preferred) Language: Kannada (Preferred) Work Location: In person Application Deadline: 30/03/2025 Expected Start Date: 01/09/2025

About Us We are the independent expert in assurance and risk management. Driven by our purpose, to safeguard life, property, and the environment, we empower our customers and their stakeholders with facts and reliable insights so that critical decisions can be made with confidence. As a trusted voice for many of the world’s most successful organizations, we use our knowledge to advance safety and performance, set industry benchmarks, and inspire and invent solutions to tackle global transformations. About SCPA We help our customers respond to the increased demand for trust and transparency around products, assets, supply chains, and ecosystems, driving the transformation of the assurance industry. Whether certifying products, sharing claims or optimizing and decarbonizing supply chains, DNV helps companies manage risks and realize their long-term strategic goals, improving ESG performance and generating lasting, sustainable results. Drawing on our wide technical and industry expertise, we work with companies worldwide to bridge trust gaps among consumers, producers and suppliers. About The Role As part of our continued growth, we are looking to recruit technical and experienced In-Vitro Diagnostic Medical Device Assessors and Lead Auditors. The successful candidates will be responsible for planning and conducting audits / assessments against the manufacturing of medical devices, in accordance with ISO 13485, IVDR 2017/746 and MDSAP standards, enabling the delivery of assessment and certification services that meet customer requirements and appropriate accreditation standards. Key Accountabilities: Assessor Conduct assessments (either desk-based or on client’s sites) in accordance with established procedures, maintaining a high standard of service delivery that ensures effective customer communication. Conduct Technical File reviews specific for products being authorized. Complete all chargeable work within the required timeframes to ensure customer satisfaction and efficiency of the business. Complete specific projects in relation to IVDR procedures, processes, systems and documentation as requested by the Operations Manager. If required, undertake reviews of files and make certification decisions within target timescales and in line with DNV policies and accreditation/approval requirements. Key Accountabilities: Auditor Responsible to carry out audits of the manufacturer's quality management system (QMS) and of its suppliers and/or subcontractors when appropriate and to draw up records and reports on the corresponding audits. Conduct surveillance audits including follow-up activities in accordance with established procedures, maintaining a high standard of service delivery that ensures effective customer relationships. Complete all chargeable work within the required timeframes to ensure customer satisfaction and efficiency of the business. Complete projects in relation to IVDR procedures, processes, systems and documentation as requested by the Operations Manager. If required, undertake reviews of files and make certification recommendations within target timescales and in line with DNV policies and accreditation/approval requirements. Project manage auditing teams, as appropriate, to maximize efficiencies, enhance client satisfaction and ensure compliance with standards. What we offer Flexible work arrangements for better work-life balance Generous Paid Leaves (Annual, Sick, Compassionate, Local Public, Marriage, Maternity, Paternity, Medical leave) Medical benefits ( Insurance and Annual Health Check-up) Pension and Insurance Policies (Group Term Life Insurance, Group Personal Accident Insurance, Travel Insurance) Training and Development Assistance (Training Sponsorship, On-The-Job Training, Training Programme) Additional Benefits (Long Service Awards, Mobile Phone Reimbursement) Company bonus/Profit share. *Benefits may vary based on position, tenure/contract/grade level* DNV is an Equal Opportunity Employer and gives consideration for employment to qualified applicants without regard to gender, religion, race, national or ethnic origin, cultural background, social group, disability, sexual orientation, gender identity, marital status, age or political opinion. Diversity is fundamental to our culture and we invite you to be part of this diversity. About You Assessors and Auditors shall have a technical college degree in a relevant product or medical area, as described below. In-Vitro Diagnostic devices: Biology or Microbiology Chemistry or Biochemistry Human Physiology Medical Technology or Biotechnology Medicine, Veterinary Medicine Biomedical science - e.g. haematology, virology, molecular diagnostics Nursing Pharmacy, Pharmacology, Toxicology Physiology Education In addition to a relevant educational degree, candidates must have a minimum 4 years’ work experience (full time) in an In-Vitro diagnostic medical device related industry, academia or hospital environment, with at least 2 of these years in the design, manufacturing, testing or use of the device in which they are qualified to Audit or Assessment, and/or experience as an assessor or auditor in a notified body. Specifically: Auditor - Practical experience in the quality management system and specific production process/technologies for the IVD medical devices. Assessor - Practical experience in conducting and/or assessing performance evaluation data or related scientific aspects with in-vitro diagnostic medical devices in one or more of the following areas Microbiology, Immunology, Genetic testing/Cancer Biology and Molecular Biology. A PhD in a relevant area for in-vitro diagnostic medical devices can substitute 3 years of work experience provided it includes 2 years’ experience in design, manufacture or testing. In addition to the above, knowledge of the following would be preferred: An excellent working knowledge of medical device management systems, standards and medical device compliance/auditing techniques. Work experience in positions with significant QA Regulatory or management systems responsibility. Experience with Harmonized medical device standards for In-Vitro diagnostic medical devices. Experience with Risk Management EN ISO 14971. Medical device experience from auditing/work. Experience auditing against recognized standards. Experience of working under own initiative and in planning and prioritizing workloads. Should have a flair for technical writing, essential for exhaustive report writing.

Design Cafe is hiring Senior Interior Designer for Andheri & Thane (Oshiwara Store) Address : Ground Floor, Vicino Mall, Shop no 18, 18A, Off New Link Rd, Oshiwara, Andheri West, Mumbai, Maharashtra 400102 Address: Shop No-11, Dosti Imperia, Ghodbunder Rd, opposite R-Mall, Manpada, Thane West, Thane, Maharashtra 400607 Experience : 3 to 5 year of experience Modular Residential Interior Experience is a must . Job Description / Responsibilities: Assesses and meets client requirements and desires through regular meetings and conferences Produces sketches, drawings, and floor plans to illustrate concepts and finished projects using computer-aided design programs (CAD) and hand-drawing skills Creates idea boards to communicate design concepts to clients Strong understanding and demonstrated aptitude of design principles Excellent portfolio of previous works Creative talent, imagination, and eye for design. Requirements : You must have min 3 plus years of experience in residential projects Modular interior Experience is a must Registered Diploma or Degree in Interior Design or Architecture Experience in handling clients and handling projects independently Excellent knowledge of AutoCAD, Google Sketch-up Strong verbal and written English communication skills, ability to convey complex ideas effectively and efficiently . Qualification: Academic: Diploma in Interior Designing (2/3 years), B.Arch Technical / Professional: Interior Designer Google Sketch-up AutoCAD Microsoft office Interested: Drop in your profile at - rajshree.dayal@designcafe.com

About Us We are the independent expert in assurance and risk management. Driven by our purpose, to safeguard life, property, and the environment, we empower our customers and their stakeholders with facts and reliable insights so that critical decisions can be made with confidence. As a trusted voice for many of the world’s most successful organizations, we use our knowledge to advance safety and performance, set industry benchmarks, and inspire and invent solutions to tackle global transformations. About SCPA We help our customers respond to the increased demand for trust and transparency around products, assets, supply chains, and ecosystems, driving the transformation of the assurance industry. Whether certifying products, sharing claims or optimizing and decarbonizing supply chains, DNV helps companies manage risks and realize their long-term strategic goals, improving ESG performance and generating lasting, sustainable results. Drawing on our wide technical and industry expertise, we work with companies worldwide to bridge trust gaps among consumers, producers and suppliers. About The Role As part of our continued growth, we are looking to recruit technical and experienced In-Vitro Diagnostic Medical Device Assessors and Lead Auditors. The successful candidates will be responsible for planning and conducting audits / assessments against the manufacturing of medical devices, in accordance with ISO 13485, IVDR 2017/746 and MDSAP standards, enabling the delivery of assessment and certification services that meet customer requirements and appropriate accreditation standards. Key Accountabilities: Assessor Conduct assessments (either desk-based or on client’s sites) in accordance with established procedures, maintaining a high standard of service delivery that ensures effective customer communication. Conduct Technical File reviews specific for products being authorized. Complete all chargeable work within the required timeframes to ensure customer satisfaction and efficiency of the business. Complete specific projects in relation to IVDR procedures, processes, systems and documentation as requested by the Operations Manager. If required, undertake reviews of files and make certification decisions within target timescales and in line with DNV policies and accreditation/approval requirements. Key Accountabilities: Auditor Responsible to carry out audits of the manufacturer's quality management system (QMS) and of its suppliers and/or subcontractors when appropriate and to draw up records and reports on the corresponding audits. Conduct surveillance audits including follow-up activities in accordance with established procedures, maintaining a high standard of service delivery that ensures effective customer relationships. Complete all chargeable work within the required timeframes to ensure customer satisfaction and efficiency of the business. Complete projects in relation to IVDR procedures, processes, systems and documentation as requested by the Operations Manager. If required, undertake reviews of files and make certification recommendations within target timescales and in line with DNV policies and accreditation/approval requirements. Project manage auditing teams, as appropriate, to maximize efficiencies, enhance client satisfaction and ensure compliance with standards. What we offer Flexible work arrangements for better work-life balance Generous Paid Leaves (Annual, Sick, Compassionate, Local Public, Marriage, Maternity, Paternity, Medical leave) Medical benefits ( Insurance and Annual Health Check-up) Pension and Insurance Policies (Group Term Life Insurance, Group Personal Accident Insurance, Travel Insurance) Training and Development Assistance (Training Sponsorship, On-The-Job Training, Training Programme) Additional Benefits (Long Service Awards, Mobile Phone Reimbursement) Company bonus/Profit share. *Benefits may vary based on position, tenure/contract/grade level* DNV is an Equal Opportunity Employer and gives consideration for employment to qualified applicants without regard to gender, religion, race, national or ethnic origin, cultural background, social group, disability, sexual orientation, gender identity, marital status, age or political opinion. Diversity is fundamental to our culture and we invite you to be part of this diversity. About You Assessors and Auditors shall have a technical college degree in a relevant product or medical area, as described below. In-Vitro Diagnostic devices: Biology or Microbiology Chemistry or Biochemistry Human Physiology Medical Technology or Biotechnology Medicine, Veterinary Medicine Biomedical science - e.g. haematology, virology, molecular diagnostics Nursing Pharmacy, Pharmacology, Toxicology Physiology Education In addition to a relevant educational degree, candidates must have a minimum 4 years’ work experience (full time) in an In-Vitro diagnostic medical device related industry, academia or hospital environment, with at least 2 of these years in the design, manufacturing, testing or use of the device in which they are qualified to Audit or Assessment, and/or experience as an assessor or auditor in a notified body. Specifically: Auditor - Practical experience in the quality management system and specific production process/technologies for the IVD medical devices. Assessor - Practical experience in conducting and/or assessing performance evaluation data or related scientific aspects with in-vitro diagnostic medical devices in one or more of the following areas Microbiology, Immunology, Genetic testing/Cancer Biology and Molecular Biology. A PhD in a relevant area for in-vitro diagnostic medical devices can substitute 3 years of work experience provided it includes 2 years’ experience in design, manufacture or testing. In addition to the above, knowledge of the following would be preferred: An excellent working knowledge of medical device management systems, standards and medical device compliance/auditing techniques. Work experience in positions with significant QA Regulatory or management systems responsibility. Experience with Harmonized medical device standards for In-Vitro diagnostic medical devices. Experience with Risk Management EN ISO 14971. Medical device experience from auditing/work. Experience auditing against recognized standards. Experience of working under own initiative and in planning and prioritizing workloads. Should have a flair for technical writing, essential for exhaustive report writing.

Job Title: Draftsman – Interior & Architecture Location: 389P-390, 1st floor, Sector 29, Gurugram Haryana, 122022 Department: Design / Projects Reporting To: Senior Architect / Interior Designer Job Summary: We are seeking a skilled Draftsman with expertise in interior and architectural drawings to support our design and project teams. The role involves creating accurate, detailed, and timely drawings for residential, commercial, and hospitality projects, ensuring they meet client requirements and industry standards. Key Responsibilities: Prepare detailed 2D drawings, working drawings, and layouts for interior and architectural projects. Convert conceptual designs and sketches into precise technical drawings. Prepare plans, elevations, sections, and detailed joinery drawings . Coordinate with design teams to incorporate client feedback into updated drawings. Ensure all drawings comply with applicable building codes, standards, and specifications. Work closely with site teams for measurement taking and on-site verification. Maintain and organize drawing files and project documentation. Assist in material specification documentation where required. Qualifications & Skills: Diploma / Degree in Architecture, Interior Design, or related field. Proficiency in AutoCAD (knowledge of SketchUp, Revit, or 3D Max will be an added advantage). Minimum 2–4 years of experience as a Draftsman in interiors and architecture. Strong understanding of interior detailing, joinery, and materials. Ability to read and interpret architectural and interior drawings. Good communication and coordination skills. Attention to detail and ability to work under deadlines. Employment Type: Full-time Salary: As per industry standards Job Type: Full-time Pay: ₹15,000.00 - ₹25,000.00 per month Work Location: In person

About Us We are the independent expert in assurance and risk management. Driven by our purpose, to safeguard life, property, and the environment, we empower our customers and their stakeholders with facts and reliable insights so that critical decisions can be made with confidence. As a trusted voice for many of the world’s most successful organizations, we use our knowledge to advance safety and performance, set industry benchmarks, and inspire and invent solutions to tackle global transformations. About SCPA We help our customers respond to the increased demand for trust and transparency around products, assets, supply chains, and ecosystems, driving the transformation of the assurance industry. Whether certifying products, sharing claims or optimizing and decarbonizing supply chains, DNV helps companies manage risks and realize their long-term strategic goals, improving ESG performance and generating lasting, sustainable results. Drawing on our wide technical and industry expertise, we work with companies worldwide to bridge trust gaps among consumers, producers and suppliers. About The Role As part of our continued growth, we are looking to recruit technical and experienced In-Vitro Diagnostic Medical Device Assessors and Lead Auditors. The successful candidates will be responsible for planning and conducting audits / assessments against the manufacturing of medical devices, in accordance with ISO 13485, IVDR 2017/746 and MDSAP standards, enabling the delivery of assessment and certification services that meet customer requirements and appropriate accreditation standards. Key Accountabilities: Assessor Conduct assessments (either desk-based or on client’s sites) in accordance with established procedures, maintaining a high standard of service delivery that ensures effective customer communication. Conduct Technical File reviews specific for products being authorized. Complete all chargeable work within the required timeframes to ensure customer satisfaction and efficiency of the business. Complete specific projects in relation to IVDR procedures, processes, systems and documentation as requested by the Operations Manager. If required, undertake reviews of files and make certification decisions within target timescales and in line with DNV policies and accreditation/approval requirements. Key Accountabilities: Auditor Responsible to carry out audits of the manufacturer's quality management system (QMS) and of its suppliers and/or subcontractors when appropriate and to draw up records and reports on the corresponding audits. Conduct surveillance audits including follow-up activities in accordance with established procedures, maintaining a high standard of service delivery that ensures effective customer relationships. Complete all chargeable work within the required timeframes to ensure customer satisfaction and efficiency of the business. Complete projects in relation to IVDR procedures, processes, systems and documentation as requested by the Operations Manager. If required, undertake reviews of files and make certification recommendations within target timescales and in line with DNV policies and accreditation/approval requirements. Project manage auditing teams, as appropriate, to maximize efficiencies, enhance client satisfaction and ensure compliance with standards. What we offer Flexible work arrangements for better work-life balance Generous Paid Leaves (Annual, Sick, Compassionate, Local Public, Marriage, Maternity, Paternity, Medical leave) Medical benefits ( Insurance and Annual Health Check-up) Pension and Insurance Policies (Group Term Life Insurance, Group Personal Accident Insurance, Travel Insurance) Training and Development Assistance (Training Sponsorship, On-The-Job Training, Training Programme) Additional Benefits (Long Service Awards, Mobile Phone Reimbursement) Company bonus/Profit share. *Benefits may vary based on position, tenure/contract/grade level* DNV is an Equal Opportunity Employer and gives consideration for employment to qualified applicants without regard to gender, religion, race, national or ethnic origin, cultural background, social group, disability, sexual orientation, gender identity, marital status, age or political opinion. Diversity is fundamental to our culture and we invite you to be part of this diversity. About You Assessors and Auditors shall have a technical college degree in a relevant product or medical area, as described below. In-Vitro Diagnostic devices: Biology or Microbiology Chemistry or Biochemistry Human Physiology Medical Technology or Biotechnology Medicine, Veterinary Medicine Biomedical science - e.g. haematology, virology, molecular diagnostics Nursing Pharmacy, Pharmacology, Toxicology Physiology Education In addition to a relevant educational degree, candidates must have a minimum 4 years’ work experience (full time) in an In-Vitro diagnostic medical device related industry, academia or hospital environment, with at least 2 of these years in the design, manufacturing, testing or use of the device in which they are qualified to Audit or Assessment, and/or experience as an assessor or auditor in a notified body. Specifically: Auditor - Practical experience in the quality management system and specific production process/technologies for the IVD medical devices. Assessor - Practical experience in conducting and/or assessing performance evaluation data or related scientific aspects with in-vitro diagnostic medical devices in one or more of the following areas Microbiology, Immunology, Genetic testing/Cancer Biology and Molecular Biology. A PhD in a relevant area for in-vitro diagnostic medical devices can substitute 3 years of work experience provided it includes 2 years’ experience in design, manufacture or testing. In addition to the above, knowledge of the following would be preferred: An excellent working knowledge of medical device management systems, standards and medical device compliance/auditing techniques. Work experience in positions with significant QA Regulatory or management systems responsibility. Experience with Harmonized medical device standards for In-Vitro diagnostic medical devices. Experience with Risk Management EN ISO 14971. Medical device experience from auditing/work. Experience auditing against recognized standards. Experience of working under own initiative and in planning and prioritizing workloads. Should have a flair for technical writing, essential for exhaustive report writing.

Position: Faculty – Design Foundation Year School: School of Architecture and Design Program: Bachelor of Design (B.Des) Job Description: We are seeking dynamic and passionate design educators to join our team as Foundation Year Faculty for the Bachelor of Design program. The ideal candidate will have expertise in one or more of the following areas: Design Thinking, Drawing and Visualization, Material Exploration, Visual Communication, or Contextual Studies. The role involves teaching first-year undergraduate students, mentoring them through the fundamentals of design, and laying a strong interdisciplinary foundation. Key Responsibilities: Deliver engaging studio and theory-based sessions Develop and assess assignments aligned with the program's pedagogical vision Encourage critical thinking, observation, and hands-on learning Collaborate with peers on curriculum development and project-based learning modules Qualifications: Bachelor’s or Master’s degree in Design or related discipline Prior teaching experience or professional practice in design preferred Strong communication, mentorship, and collaboration skills

Shadow design discussions the Senior Designer does with clients; prepare Minutes of Meetings and keep track of project milestones to ensure a timely and high-quality delivery Assist the Senior Designer in 3D designs using SpaceCraft (HomeLane Software) and Sketchup; recommend enhancements and be a sounding board for the Senior Designer Be available for Site Visits, Masking along with the Senior Designer; take on the responsibility of file management across HomeLane tech systems Assist the Senior Designer in creating commercial proposals using SpaceCraft and other quoting tools; validate quotes to ensure customers get a transparent and fair estimate. Coordinate with various stakeholders to ensure a great design outcome; build relationships with teams like sales, drawing QC, project management teams and planners. Mandatory Qualifications: Design education background - B.Arch, B.Des, M.Des, Diploma in Design 0-1yr of experience in Interior Design / Architecture Good communication & presentation skills Basic knowledge of Modular furniture Practical knowledge of SketchUp A great attitude.

Urgent Hiring Design Engineer | 20 Positions Location: Rajkot Shapar, Ravki, Metoda, Bhunava, Hadamtala Industry: Auto Parts | Machine Manufacturing | Casting | Engineering Role Overview Design mechanical components and assemblies using Creo, AutoCAD, Solid Edge, Solid Works NC tools, ensuring manufacturability and alignment with customer requirements. Qualification Experience Diploma / BE / B.Tech in Mechanical, Mechatronics, or related discipline Experience: 1 to 10 years Certification in Creo (3D) and AutoCAD (2D) Basic knowledge of NC (Numerical Control) systems preferred Strong understanding of Engineering Drawing, Machine Design, GDT, ISO/ASME Standards Technical Skills Required CAD Software: Creo, AutoCAD, Solid Edge CAM/NC Tools: Basic understanding of NC software/applications Drawing Standards: Familiar with ISO/ASME standards Other: GDT, BOM preparation, ECN handling, DFM/DFA principles Key Responsibilities Create 3D part assembly models (Creo/Solid Edge) Draft 2D manufacturing drawings (AutoCAD) with GDT Modify existing designs based on ECN or customer input Conduct tolerance analysis, stack-up, and interference checks Prepare BOM and coordinate with cross-functional teams Vendor interaction for tool development prototyping Maintain drawing control and participate in design validation Salary Benefits CTC: Up to 6.00 LPA Facilities: Transportation Canteen Working Hours: 9:00 AM 7:00 PM Weekly Off: Wednesday Notice Period: Immediate Joiners Preferred Apply Now Email your resume to: hr@steerway.in Call / WhatsApp: 76240 13188 | 70463 70463 Note: We do NOT charge any fees from candidates. Get Instant Job Alerts on WhatsApp Join Our Channel: https://whatsapp.com/channel/0029VaJ5TI86mYPV6BnJMv3x Team Steerway Business Consultants Empowering Talent | Enabling Growth www.steerway.in This job is provided by Shine.com