Mechanical Designer - Stet jobs at Philips in India, Pune

Your role:

• In this role, you have the opportunity toKey Requirement:
  ▪▪
  End to End engineering support for supplier-initiated change requests includes part design, tooling, and manufacturing location changes·
  ▪
  Follow design controls governed by FDA· Should have hands on experience of Design verification, Validation, protocol documentation.
  ▪▪
  Conduct DFM, DFA reviews with suppliers.
  ▪
  Should have hands on experience on Windchill

You're the right fit if you have:

• To succeed in this role, you should have the following skills and experience
• •B.S. in Mechanical Engineering with 8-12 years of proven design engineering and product development experience
  Experience supporting supplier transfer & sustaining projects
• •Demonstrated strong analytical and problem-solving skills
  •Knowledge of manufacturing quality systems and working in a regulated industry
  •Experience with geometric dimensioning and tolerance
  •Strong English written and verbal communication skills required
  •Creates 3D models, assembly and detailing including drawing conversions
  •Apply GD&T and perform Tolerance stack-up analysis for components/Sub-system.
  •Review and ensure adequacy of supplier part qualification activities
  •Performing hand calculations for design feasibility
  •Shall have hands-on expertise in Engineering change Management
  •Provide technical support to suppliers & other departments to fulfil project/productions

We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.
• Learn more about .
• Discover .
• Learn more about .
If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our culture of impact with care .

• Analyzes and troubleshoots testing failures, documenting them in the anomaly database, initiating corrective actions as necessary and ensuring respect for established protocols, working under general supervision.
• Executes targeted development assignments within the defined scope, complies with working agreements with teams, making timely and effective decisions to achieve closure on work items.
• Synthesizes proven approaches and integrates multiple strategies to solve complex problems or optimize solutions in product designs and manufacturing processes.
• Develops and implements new product designs and design improvements for instrumentation in the medical device field, ensuring alignment with customer requirements.
• Participates in the technical development of a Continuous Integration and Continuous Deployment framework for multiple initiatives, ensuring process optimization and efficiency.
• Conducts preliminary studies and modifies subsystem designs to address complex problems, deriving specifications from customer requirements and ensuring adherence to regulatory standards and company quality systems..
• Collaborates with engineers to devise integration phases, criteria, and tests, assists in the designing of features for digitally-assisted medical solutions and supports installation, integration, and monitoring of external clinical sites.
• Keeps abreast of developments within the field, exchanges information effectively to promote cross-functional collaboration, interacts with stakeholders to ensure alignment on project goals and timelines.
• Conducts experimental activities related to test project outcomes, analyzes data, and evaluates results to inform decision-making and implementation of improvements.

• Specify image chain requirements as part of a development project and Test and verify image chain component (Generator, Tube, Collimator, Detector, Monitor etc) against the requirement
• Be responsible for integrating image chain components, adjustment & calibration and verifying the system with respect to meeting the safety, functional, performance and reliability.
• Be responsible for selection of image chain components and subsystems to achieve target cost and image quality.
• Be responsible for detailed technical design for the components including DFMEA, Risk assessment.
• Lifecycle management of image chain components including obsolescence management.
• Collaborate with cross-functional/cross regional teams to release design changes and customer support
• Align with supplier on the requirements and design aspect to ensure products quality.
• Evaluate New and competitive technology for image chain subcomponents.
• Good team player with ability to work independently and act pro-actively.

Minimum required Education:

• Electrical/ Electronic/Biomedical background (B.Tech/M.tech) with 8+ years’ experience
• Solid experience with Power electronics and electronics product design and development
• Analog and Digital circuit design. familiar with Operational amplifiers, Inverter design ( SiC technology) , H- bridge design , Power transformers design
• Understanding X-ray Physics, having Generator, Tube, Collimator, Detector or Monitor knowledge is plus
• Strong understanding of Medical QMS and lifecycle management processes.
• Strong Communication skills: Ability to present technical data/concepts concisely and effectively to various audiences/stakeholders
• Understanding medical standards like IEC 60601-1, IEC 60601-1-3, IEC 60601-2-54
• Detailed/ Structured documentation practices and decision making
• Analytical/Fact Based/Logical problem solver

We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.
• Learn more about .
• Discover .
• Learn more about .
If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our culture of impact with care .

Mechanical Engineer

Job Description-

You are responsible for executing engineering requirements analysis, developing, and validating test plans, and ensuring compliance with regulatory standards, working under general supervision. The role documents design specifications and results, implementing design improvements, and troubleshooting technical issues, while mentoring junior team members. The role participates in design reviews, provides insights for continuous improvement, and adheres to company policies and quality standards. The role evaluates external vendors and technologies for integration, maintains component performance and reliability, and fosters strategic partnerships to enhance product innovation

Your role:

• Design and detail components and systems
• Obtain parts and create prototypes.
• Successfully interact with associates in other departments, such as Manufacturing Operations, Procurement, and engineering staff, to achieve project and product objectives.
• Be a highly motivated, self-disciplined, open-minded individual possessing hands-on skills.

• Requirements detailing, design specification preparation, implementation, test, and integration of Unit per the higher-level Requirement and - Design specifications/architectures.
• Ensures the mutual consistency and efficient integration of the separate modules in modular, easy-to-maintain units that meet the product specification.
• Understands and communicates the consequences of their design on the architecture.
• Determines the Unit interfaces (HW/SW) in close consultation with relevant disciplines.
• Ensures that there is proper documentation for his/her design.
• Keeps abreast of technical developments in own field through study of the literature and technical contacts and propagates it.
• Define, execute, and take the lead in concept and feasibility studies with a limited scope to investigate the usability of new technologies.
• Contributes to technology roadmaps and other strategic-related activities.
• Takes technological or process-related improvements initiatives within the scope of at least the mechanical development group.
• Contributes to the Work Breakdown Structure/ the planning process of his/her area.
• Draws up personal schedule and reports on progress.
• Inspires team members to get the job done.
• Performs work in line with the processes that have been agreed in the department.

You're the right fit if:

• Bachelor's Degree/ Vocational Education in Engineering, (8 to 10 years exp)
• 8-10 years of relevant experience in design & development of electro-mechanical sub-systems & systems.
• Strong communication and collaborative abilities proactively seek out expertise and advice and input from others in a collaborative team-environment, Project Management skills (Dealing with suppliers)
• In-depth knowledge and 8+ years of experience in the development of mechanical design
• Experience in creating design concepts and mechanical designs of complex parts or assemblies.
• Strong knowledge and experience in CAD/CAE. such Creo, NX,, LCM- Life cycle management.
• Experience in metal or plastic crafts would be appreciated
• Experience in PDM/ PLM (Windchill)
• Good knowledge of Development methodology
• Six Sigma green belt is a plus

We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.
• Learn more about .
• Discover .
• Learn more about .

Job Title

Job Description

The primary function within this role is to execute Manufacturing Engineering activities through the course of high-quality process Verification & Validation activities.

In this role you are responsible to sustain and improve processes, tools and equipment of the Manufacturing systems, to ensure predictable, reliable, stable and efficient production processes. Supporting troubleshooting activities. Catcher of new product industrialization projects and manufacturing transfers for the site.

You will be responsible for driving meaningful and innovative Process Validation and suggesting in improving the process and support in Process Verification , Validation , IQ,OQ,PQ to improve quality and reduce cost, as well as performing the role of a technical lead in taking the product development through manufacturing release while transferring products from Engineering to Manufacturing and manage sustaining of different devices by following PDLM-MLD process.

In this role, you will be responsible for supporting Philips business like MRI, RF, IGT, SR&C DXR etc, you will ensure that all processes are capable to deliver consistent output as per-defined specification & consistent with the higher-level requirements

You are responsible for

• Is catcher of PDLM subprojects from Product Industrialization Engineer for a specific technology
• To follow the good manufacturing practices (GMP) .
• comprehension of DMR translation to production processes.
• Provides input for Manufacturing requirements in PDLM.
• To guide and perform PV related tests (e.g TMV, IQ, OQ & PQ) on the shop floor.
• Creates Quality Control Plan and Work Instructions
• Oversees equipment installation and supports ramp up of specific processes at the site
• May execute equipment installation and supports ramp-up of specific processes at the site
• Supports implementation of design changes
• Execute improvements in manufacturing processes, tools and equipment. This is for quality and efficiency improvements.
• Applies lean manufacturing principles
• Employs equipment, practices, and procedures which promote a healthy, safe, and secure work environment
• Executes the processes and standards with embedded quality into the way of working including adherence to compliance with safety, Cost regulatory- and environmental requirements as well as local laws, Philips General Business principles and other policies.
• Initiates and oversees process technology development activities in the context of New Product Generation as well as product and solution technology roadmap.
• Ensures adherence to the applicable process for product introductions, qualifications and release
• Responsible for Manufacturing input in PDLM process focusing on DfMAT
• Can lead & support quality-related problem-solving and root cause analysis during design and manufacturing
• Uses post-market analytics and statistics to report on product quality performance in the field (provide feedback to manufacturing, suppliers, or design teams) and initiates field actions when required
• Oversees equipment installation and supports ramp up of specific processes at the site
• Gives input from factory side to the sign-off at SR milestone & project close Implements
• Lead, prepare, and participate/be the main escort in internal and external audits
• Frequently interacts with supervisors and functional peer groups. Interaction normally requires the ability to gain the cooperation of others, conducting presentations of technical information concerning specific projects or schedules.
• Review/leadership for control of nonconforming products (QNs/MRB), including risk assessments.
• Review/leadership for product nonconformance investigation activities.
• Review/leadership for DEFOAs.
• Review/leadership for receiving inspection plans (RIPS)
• Review/leadership for Process Validation protocols and reports.
• Review/leadership for CAPA investigation activities
• Review/leadership for design/process changes (ECO/CRB)
• Assists, produces and completes STET Quality & Process Engineering related activities and documentation under direct supervision.
• Assists in ensuring that STET project supplier components / products (including spare parts and services) are released according to agreed specifications and APQP – PSW quality requirements.
• Assists in the support of CoNQ projects, and project management in the effective and timely risk
• Support of Regulatory agency audits and inspections in areas of responsibility.
• Review/leadership relating to accurate recordkeeping (GDPs) • Interface with cross-functional teams to ensure compliance and timely product releases
• Applies lean manufacturing principles

You are a part of

We work directly with our cross-functional and cross-discipline partners, including marketing, clinical specialists, service personnel and R&D, to deliver solutions through the execution of PDLM, Lifecycle, and Solutions Processes, with deliveries that exceed our customers' expectations.

• To succeed in this role, you should have the following skills and experience.
• Bachelor’s or master’s degree in production, mechanical, Electrical, Electronics engineering with 4-7 years’ experience.
• Strong quality assurance management experience, minimum 5 years in quality assurance
• Strong design control and new product development experience
• Strong analytical abilities
• Experience in CAD and PLM software’s
• Professional knowledge in ISO 13485, FDA 820, ISO14971, FDA/MDR/MDSAP
• Knowledge of FDA and IEC Standards is a plus.
• Disciplined team worker, ability to work independently.
• Ability to present ideas and to convince project team members.
• Be structured and self-organized.
• Positive ‘can do’ attitude.
• Quality mindset in analysis and documentation
• Excellent communication, both verbal and written
• Preferably already verification or validation background/ experience
• Design for 6 sigma / DMAIC is preferred
• Design for manufacturing, assembly and testability.
• Understanding special Process like Brazing, Soldering, Cleaning will be added advantage
• Basic regulatory understanding about ISO 13485, ISO 14971 will be added advantages
• Supportive in CAPA analysis
• A background in Data Analytics will be preferred.
• Integrated Supply Chain Management
• Capable to solve complex mfg. process Problem.
• Master data management (system) change Management
• He/ She should be good at Logistics Fundamentals, Manufacturing Fundamentals, Master data management (system), Operational Excellence, Operational Risk
• PMI Competencies (Project Management) or Certification will be added advantage
• Good Knowledge about Procurement & Sourcing Fundamentals
• Product Innovation & Lifecycle
• Capable of working independently in software tools Windchill, Minitab & SAP.
• Hands-on experience on performing Process Validations, Test Method Validations and MSA Studies (Process capability studies).

In return, we offer you.

• A rewarding career in Philips with an attractive package.
• An extensive set of tools to drive your career, such as a personal development budget, training, and coaching.
• Attractive collective health insurance package
• Opportunity to buy Philips shares and products with discount.

You will be responsible for driving meaningful and innovative product development, generating ideas/concepts in feature development to improve quality and reduce cost, as well as performing the role of a technical lead in taking the product development through manufacturing release while transferring products between suppliers and manage sustaining of different devices by following PDLM/MLD process.

To be part of an exciting team and contribute to the design, development and maintenance of Diagnostic Imaging (MRI, CT/AMI, DXR etc.) components and products. In this role of Mechanical System Designer, you are responsible for the development and maintenance of Image Acquisition Platform (IAP) - Hardware Systems/Subsystems and will gain substantial knowledge of complex systems in medical imaging environment. Together with a multidisciplinary team of engineers, you play a crucial role in getting these systems/sub-systems to the required performance, by understanding the electrical, electronics and controls and looking for the best solutions within those boundaries. This requires broad orientation, conceptual skills and a “can do” mentality, keeping abreast with all trends

Your role:

• Leading the development and release of system/ electro-mechanical modules or reverse engineer existing products to improve overall long-term system quality, reliability, yield rates, and cost effectiveness.
• Working with a cross-functional team to ensure the design and development of electromechanical components to meet the needs of the internal and external customers.
• Working with design partners/suppliers and lead product development activities from design concept to manufacturing release.
• Using modelling and simulation tools to create and modify architectures, 3D designs, and 2D drawings.
• Drive continuous improvement projects related to design implementation, manufacturing process, product quality and reliability.
• Requirements, design, implementation, test and integration of module/sub-system in accordance with the higher-level architectural requirements and design specifications
• Ensuring that the design is consistent with the higher-level architecture and requirements
• Ensuring that the proposed design would have the safety, reliability and quality features built-in
• Responsible for ensuring that the design meets the performance, quality and cost criteria
• Conduct concept and feasibility studies. Leads the introduction of new technologies
• Ensuring that there is proper documentation per standards for the developed design
• Ensuring the mutual consistency and efficient integration of the separate components in modular design that meets the product specification
• Ensuring that his design modules meet the product certification requirements
• Drawing up personal schedule and reports on progress
• Defining and assessing the Work Breakdown Structure/planning/costs of his/her area
• Being abreast of technical developments in own field through study of literature and technical contacts
• Maintaining product and company reputation by complying with country specific regulations
• Supplier evaluation and communication

You're the right fit if you have :

• M.Tech / B.E/ B.Tech in Mechanical/ Electrical/ Electronics or Equivalent Engineering
• 10+ years of relevant experience in design & development of electro-mechanical subsystems & systems.
• Strong communication and collaborative abilities proactively seeks out expertise and advice and input from others in a collaborative team-environment.
• Experience in developing the requirements for electro-mechanical assemblies.
• Knowledge in part qualification and statistical process studies such as CP and CPK and be able to work with suppliers to improve part process capability.
• Experience in lifecycle testing and verification activities of cables to meet functional and lifecycle requirements.
• Experience working with suppliers and design partners, including part/module development and resolving technical issues.
• Strong technical writing/ documentation skills for regulated medical device design environment, including requirements definition.
• Knowledge of good design practices and experienced with DFMEA.
• Knowledge of EMI/EMC standards and testing for conformance • Knowledge of mechanical design compatibility aspects
• Knowledge of IEC 60601 standards will be an added advantage
• Knowledge of Embedded Software Programming will be an added advantage
• Ability to understand and debug problems across hardware/software boundaries
• Knowledge of Global Medical Quality and Regulatory Standards e.g. IEC, FDA, UL, CE, CSA etc.
• Demonstrated ability to effectively work with cross-functional stakeholders to ensure the design meets their expectations and needs, and that the needs/requirements are properly documented.
• Experience with document control systems (E-Matrix, Agile) and FDA/ISO regulated medical device design environment.

Onsite roles require full-time presence in the company’s facilities.
This is an office - Based role.• Learn more about .
• Discover .
• Learn more about .

You are responsible for

• Support global cross functional teams for assigned supplier transfer & sustaining projects
• Understands Products packaging requirements & specifications
• Creates engineering drawings & specifications of product packaging
• Creates 3D models, assembly and detailing including drawing conversions
• Apply GD&T and perform Tolerance stack-up analysis for components/Sub-system.
• Update designs of components and subsystems to improve manufacturability, performance, quality, and cost
• Review and ensure adequacy of supplier part qualification activities
• Work closely with the engineering to optimize packaging supply base for cost, lead time,

Quality, regionalization, standardization, supply assurance and compliance with regulatory & internal requirements

• Mechanical design and design changes of a module/sub system/ system
• Conduct DFM, DFA reviews with suppliers for Packaging solutions
• Identifying the suitable Packaging materials for designs and creating and releasing BOM
• Performing hand calculations for the design feasibility
• Must be very good and hands on with 2D & 3D (prefer - Creo, Solid works.)
• Hands on Windchill/ Agile / PLM software ‘s
• Work with manufacturing departement & ensure packaging designs are optimized
• Shall have hands-on expertise in Engineering change Management
• Develop test plans to ensure that the packaging meets specification.

To succeed in this role, you should have the following skills and experience

• BE/B.Tech. in Mechanical Engineering/Automobile /Industrial
• MS in engineering preferred
• 4-7 years of proven design engineering and product development experience
• Experience supporting global projects
• Experience with CAD software(s)
• Experience In working with ISTA standards & other Packaging standards
• Demonstrated strong analytical and problem-solving skills
• Knowledge of manufacturing quality systems and working in a regulated industry
• Experience with geometric dimensioning and tolerance
• Working knowledge of Microsoft Project, Excel, Power Point, and Word required
• Strong English written and verbal communication skills required

In return, we offer you

• A rewarding career in Philips with attractive package.
• Extensive set of tools to drive your career, such as a personal development budget, free training and coaching
• Attractive collective health insurance package
• Opportunity to buy Philips shares and products with discount

You will be responsible for driving meaningful and innovative product development, generating ideas/concepts in feature development to improve quality and reduce cost, as well as performing the role of a technical lead in taking the product development through manufacturing release while transferring products between suppliers and manage sustaining of different devices by following PDLM/MLD process.

To be part of an exciting team and contribute to the design, development and maintenance of Diagnostic Imaging (MRI, CT/AMI, DXR etc.) components and products. In this role of Mechanical System Designer, you are responsible for the development and maintenance of Image Acquisition Platform (IAP) - Hardware Systems/Subsystems and will gain substantial knowledge of complex systems in medical imaging environment. Together with a multidisciplinary team of engineers, you play a crucial role in getting these systems/sub-systems to the required performance, by understanding the electrical, electronics and controls and looking for the best solutions within those boundaries. This requires broad orientation, conceptual skills and a “can do” mentality, keeping abreast with all trends

Your role:

• Leading the development and release of system/ electro-mechanical modules or reverse engineer existing products to improve overall long-term system quality, reliability, yield rates, and cost effectiveness.
• Working with a cross-functional team to ensure the design and development of electromechanical components to meet the needs of the internal and external customers.
• Working with design partners/suppliers and lead product development activities from design concept to manufacturing release.
• Using modelling and simulation tools to create and modify architectures, 3D designs, and 2D drawings.
• Drive continuous improvement projects related to design implementation, manufacturing process, product quality and reliability.
• Requirements, design, implementation, test and integration of module/sub-system in accordance with the higher-level architectural requirements and design specifications
• Ensuring that the design is consistent with the higher-level architecture and requirements
• Ensuring that the proposed design would have the safety, reliability and quality features built-in
• Responsible for ensuring that the design meets the performance, quality and cost criteria
• Conduct concept and feasibility studies. Leads the introduction of new technologies
• Ensuring that there is proper documentation per standards for the developed design
• Ensuring the mutual consistency and efficient integration of the separate components in modular design that meets the product specification
• Ensuring that his design modules meet the product certification requirements
• Drawing up personal schedule and reports on progress
• Defining and assessing the Work Breakdown Structure/planning/costs of his/her area
• Being abreast of technical developments in own field through study of literature and technical contacts
• Maintaining product and company reputation by complying with country specific regulations
• Supplier evaluation and communication

You're the right fit if you have :

• M.Tech / B.E/ B.Tech in Mechanical/ Electrical/ Electronics or Equivalent Engineering
• 10+ years of relevant experience in design & development of electro-mechanical subsystems & systems.
• Strong communication and collaborative abilities proactively seeks out expertise and advice and input from others in a collaborative team-environment.
• Experience in developing the requirements for electro-mechanical assemblies.
• Knowledge in part qualification and statistical process studies such as CP and CPK and be able to work with suppliers to improve part process capability.
• Experience in lifecycle testing and verification activities of cables to meet functional and lifecycle requirements.
• Experience working with suppliers and design partners, including part/module development and resolving technical issues.
• Strong technical writing/ documentation skills for regulated medical device design environment, including requirements definition.
• Knowledge of good design practices and experienced with DFMEA.
• Knowledge of EMI/EMC standards and testing for conformance • Knowledge of mechanical design compatibility aspects
• Knowledge of IEC 60601 standards will be an added advantage
• Knowledge of Embedded Software Programming will be an added advantage
• Ability to understand and debug problems across hardware/software boundaries
• Knowledge of Global Medical Quality and Regulatory Standards e.g. IEC, FDA, UL, CE, CSA etc.
• Demonstrated ability to effectively work with cross-functional stakeholders to ensure the design meets their expectations and needs, and that the needs/requirements are properly documented.
• Experience with document control systems (E-Matrix, Agile) and FDA/ISO regulated medical device design environment.

Onsite roles require full-time presence in the company’s facilities.
This is an office - Based role.• Learn more about .
• Discover .
• Learn more about .