5 Test Protocols Jobs

At Medtronic, you can embark on a life-long journey of exploration and innovation, all while advocating for healthcare access and equity for all. Your leadership will be purpose-driven, aimed at removing barriers to innovation in a more interconnected and compassionate world. You will be responsible for both manual and test automation tasks, engaging in Sprint planning, understanding project scope and timelines, and developing automation scripts based on feature requirements. Collaboration with system and software teams is crucial, ensuring adherence to testing protocols and conducting traceability analysis to ensure all requirements are met. Proactively identifying technical limitations and proposing solutions will be part of your role, along with understanding technological and V&V challenges in detail. Reporting to the Engineering Manager, you will interface with the V&V Lead and collaborate frequently with team members from various disciplines, including hardware engineers. Your role may involve interactions with clinicians, third-party vendors, manufacturers, subcontractors, and other users to develop project requirements and schedules. The ideal candidate will have 5-7 years of software testing experience, preferably in the medical device industry, and at least one year of test automation experience. A degree in Computer Sciences, Electronics, or Electrical Engineering is required, with additional preference given to candidates with advanced degrees in the same fields. Key skills include experience in manual testing, analyzing requirements, deriving test cases, identifying gaps or ambiguities in requirements, working on Ubuntu/Linux and/or Windows Applications, and using Requirements Management and configuration management tools. Proficiency in modern software testing tools, object-oriented programming, scripting/programming languages like Python and JavaScript, and knowledge of regulatory industry practices are advantageous. Medtronic offers competitive salaries and a flexible benefits package, reflecting a commitment to employee well-being and success. As a global healthcare technology leader, Medtronic focuses on addressing complex health challenges and improving lives worldwide through innovative solutions. The mission to alleviate pain, restore health, and extend life unites a diverse team of passionate individuals dedicated to engineering extraordinary solutions for real people.,

Job Summary: We are seeking a meticulous and detail-oriented NPD (New Product Development) Documentation Specialist to join our dynamic team. The ideal candidate will be responsible for managing and maintaining all documentation related to our NPD process, ensuring accuracy, compliance, and accessibility. This role requires strong organizational skills, a keen eye for detail, and the ability to work collaboratively with cross-functional teams. Responsibilities: Develop and maintain comprehensive documentation for the entire NPD lifecycle, including project plans, design specifications, test protocols, and validation reports. Collaborate with product development, engineering, quality assurance, and regulatory affairs teams to gather necessary information and ensure documentation completeness and accuracy. Ensure all NPD documentation adheres to regulatory requirements and industry standards. Organize and manage documentation in a systematic and accessible manner, utilizing document management systems where applicable. Review and revise documentation as necessary to reflect changes in project scope, schedule, or requirements. Provide training and guidance to team members on documentation standards and best practices. Support audits and inspections by regulatory authorities or external auditors by providing accurate and timely access to documentation. Qualifications: Bachelors degree in a relevant field such as Engineering, Mechanical ,Technical Writing, or a related discipline. Proven experience (5 years) in documentation management within a regulated industry, preferably in new product development or a similar technical environment. Strong understanding of document control practices, quality systems, and regulatory requirements (e.g., FDA, ISO standards). Excellent written and verbal communication skills, with the ability to translate technical information into clear and concise documentation. Proficiency in document management software and tools (e.g., Microsoft Office Suite, SharePoint, Documentum). Highly organized with the ability to manage multiple priorities and deadlines effectively. Attention to detail and a commitment to accuracy in all documentation tasks. Job Type: Full-time Benefits: Flexible schedule Leave encashment Experience: NPD Documentation: 5 years (Preferred) Work Location: In person,

What you will do In this vital role you will lead the execution of complex or novel assignments requiring strategic planning and development of new and/or improved validation techniques, deviations, and procedures. In this position you will supervise validation activities through internal audits and conduct risk assessments to identify the need for requalification and establish policies for computer system re-validation. This individual will actively participate during all phases of qualification/validation of computerized systems: evaluate projects; provide guidance and technical information to others (lead qualification/validation activities); determine and establish requirements for qualification/validation of each individual system/equipment; formulate independent decisions related to qualification/verification activities. Responsibilities Review validation/qualification packages of computerized systems for completeness and accuracy, sound rationale, Regulatory expectations, compliance with validation policies and procedures, and accurate data analysis. Serve as Owner or QA Contact for handling the Deviations. Compare results against acceptance criteria and work with appropriate departments to resolve exceptions and deviations. Bring critical exceptions or deviations to managements attention and initiate and enforce necessary improvements and corrections to established systems and processes. Initiate, implement, and track completion of Change Control and deviation requests related to computer systems. Participation and support of regulatory inspections. The individual will be required to work from our office located in Hyderabad India (Amgen India-AIN). The candidate will be required to go into the office as dictated by the site policy. Validation Validation Documentation: Review and approve all validation documentation, ensuring compliance with regulatory requirements and internal quality standards. Requirement Specifications & Test Protocols: Review and approve Requirement Specifications, Design Specifications, Test Protocols, Validation Plans, Summary Reports, and Requirement Traceability Matrices. System Life Cycle Documents: Review and approve System Life Cycle Documents (e.g., test protocols) prior to their use in production. Data Integrity Assessments: Review and approve Data Integrity Assessments to ensure data is accurate and complies with regulatory standards. Change Control Management: Initiate, review, and approve Change Control requests, acting as the QA contact for changes in systems (e.g Trackwise/Veeva , ServiceNow) Periodic Review/Audit Trail System Periodic Reviews & Audit Trails: Review and approve periodic system reviews and audit trail reports to ensure system integrity and compliance. Supplier Management Supplier Evaluations : Provide support for supplier evaluations as needed, ensuring suppliers meet quality, compliance, and performance standards. Deviation & CAPA Management: Initiate and manage deviations (major and minor) as required. Serve as the primary QA contact for deviations, ensuring proper investigation and resolution. Act as the quality reviewer and approve for problem records in ServiceNow, ensuring that all records meet internal quality standards. CAPA & Effectiveness Verification (EV): Serve as the QA contact or owner for Corrective and Preventive Actions (CAPA) and Effectiveness Verification (EV) records, ensuring timely and effective resolution. Responsible as a Business Owner for overseeing and managing specific GxP Computerized Systems programs and projects, ensuring compliance with regulatory standards and alignment with business objectives. Independently develop solutions that are thorough, practical and consistent with functional objectives. Review and approve operational and administrative Standard Operating Procedures (SOPs) and Work Instructions, ensuring alignment with regulatory and quality standards. Apply analytical skills to evaluate complex problems, utilizing both qualitative and quantitative data, including trend analysis, to develop effective solutions. Contributes to continuous improvement efforts and initiatives. Assists with training initiatives and strategy as required. Provides support for the Management Review Process when needed. Supports the Integrated Systems Assessment (ISA) Process as necessary. Participates in and aids with regulatory inspections as required. What we expect from you We are all different, yet we all use our unique contributions to serve patients. Basic Qualifications: Masters degree with a minimum of 7 years experience in Software and Systems Quality assurance OR Bachelors degree with a minimum of 10 years of Software and Systems Quality assurance experience Preferred Qualifications: Strong understanding of the regulations outlined in 21 CFR Part 11, EU Annex 11, GAMP standards. Proven experience in the validation of computerized systems and strong understanding and application of GxP regulations (GMP, GLP, GCP, GPvP, GDP). Experience managing quality assurance processes, including Change controls, Deviations, CAPAs and effectiveness checks. Demonstrated ability to handle and resolve complex quality issues using analytical and problem-solving skills. Strong decision-making abilities with the capacity to drive tasks to completion. Ability to work independently with minimal supervision. Leadership skills with experience leading projects, teams, or tasks. Experience with tools and systems such as HP ALM, Jira, Confluence, Track Wise , Documentation Management Systems, LIMS, SAP and Maximo. Broad technical expertise within specialty area and familiarity with industry standards. Ability to provide training, guidance, and contribute to team quality. Works closely with leadership / senior staff and external experts to extend capabilities and enhance performance.

Job Brief Acufore is seeking a Design Engineer, to work in a balanced environment of fast-growing company with established clienteles. Job Description -Participate within a Team culture, from generating ideas, generating system requirement document, concept sketches, initial design with list of product requirement, detailed design with proper placement and wire harnessing, prototyping and testing, working with Sales, manufacturing, and testing team by providing unique out-of-the-box designs utilizing specific scopes of work. -Primary Designs are for custom engineered products such as electro-mechanical, medical and industrial systems or sub-system using SolidWorks, Inventor and Solid Edge. Having good knowledge on manufacturing processes such as machining, Sheetmetal, welding, injection moulding, PDC, etc. - Well experience in developing product requirement document, design concepts, DFMEA, Design Risk analysis, engineering calculations, 3D models generation, design tolerance analysis, good knowledge of elementary analysis and detailed manufacturing and inspection drawings, while working closely with international customers and their fabrications. - Execute design reviews with stake holders and balance requirements such as quality, cost, manufacturability and serviceability. -Communicating with customers and validating/signing-off approval drawings, creating as-built updates, maintaining project records including change-orders/ adders and participating in Lessons-Learned/Best Practices Post Project Analysis. -Attending customer pre-design discussions, project kick-offs call and providing development engineering support. Academic & trades qualifications (UG- B.Tech/B.E./Diploma-Mechanical, Production/Industrial) Work experience & skills 4-6 years of Experience in (Electro-Mechanical Equipment, Sheet metal / plastic / casting design, Basic understanding about GD &T and Manufacturing processes)

1. Education background Electronics communication or Electrical and Electronics Engineer 2. Electronics components understanding and selection, example - Analog and Digital 3. Shall have good experience in components obsolescence management and alternative findings 4.Shall have good understanding on schematics understanding 5.Shall have good understanding or experience in documentation like HRS, Test protocols, Test Record. Implementation plan for alternative Introduction 6. Shall have good understanding or experience in equivalent components selection and creating of Impact Analysis documents 7. Shall have good understanding or experience in communication protocols like( PCIe, NIC, ethernet, Serial communication, SPI, RS232, I2C) and analog electronics Opamp and applications 8. Shall have good understanding or experience in embedded hardware architecture understanding 9.Added advantage if work experience in medical products or Imaging(X ray, CT, MR, ) 10. Added advantage if know about computer memory, SSD, HDD, Raid protocols, DVD, PSU, GPU, NIC, BIOS firmware, OS understanding and Installation, 11. Shall have good understanding or experience in medical products certification and compliance ( EMI, EMC, Safety, ROHS, REACH, UL, CE, WEEE, COC) 12 Good experience in supplier communication and interacting with global stakeholders.