12 Test Protocols Jobs

As a Quality Control In-charge at our company, your primary role will be to maintain and ensure product quality across all stages - from raw material inspection to manufacturing, packaging, shipping, and inventory management. You will be responsible for developing, implementing, and monitoring robust Quality Control procedures to uphold certification standards such as ISO, UL, SASO, and CL, ensuring compliance with relevant regulations. **Key Responsibilities:** - Develop, implement, and maintain Quality Control procedures and standards across all processes, including raw material inspection, production, packaging, storage, shipping, and inventory management. - Oversee and manage the QC team...

As a Clinical Validation Specialist at Philips Enterprise Informatics (EI), you will be at the forefront of AI innovation in medical software, collaborating with various departments and Business Innovation Units to ensure regulatory compliance and optimal customer satisfaction. Your role is crucial in shaping the clinical validation of products and applications across various domains like PACS, Digital Pathology, Cardiovascular, and more. **Key Responsibilities:** - Support the validation of innovative (AI) solutions and technologies to address identified needs and challenges. - Contribute to advancing healthcare technology by ensuring innovations are safe, effective, and compliant with regu...

In this role, you will be responsible for ensuring product performance assurance by designing and implementing validation processes and test protocols. Your key accountability will include ensuring alignment with customer requirements and regulatory standards during validation, as well as ensuring that products comply with applicable regulatory departments. Key responsibilities you will undertake include: - Preparing Testing Plans, DVP, and Control Plans in accordance with Test Standards. - Executing Product Validations based on the Design Validation Plan (DVP) and Automotive Standards within the Customer's timeframe. - Handling end-to-end Parts Homologation at ARAI. - Reviewing Test Reports...

Role Overview: As an intern in the R&D team at MGT, you will have the exciting opportunity to work on cutting-edge technologies and make a valuable contribution to the manufacturing sector in India. Your role will involve being a student pursuing a Bachelor's or Master's degree from a reputable institution with a strong academic background. You will be expected to demonstrate a keen interest in core technologies, be eager to learn on the job, and have your projects and tasks tailored to your availability and interests. The preferred duration of the internship is six months, although accommodations can be made for a minimum availability of 3 months. Key Responsibilities: - Pursuing a Bachelor...

As a Sr. Validation Engineer at CMIC CMO USA Corporation in Cranbury, NJ, your role involves utilizing pharmaceutical science analytics to author validation protocols in compliance with cGMP/FDA standards. You will be responsible for planning, managing, and executing start-up, commissioning, and validation of new pharmaceutical equipment. Additionally, you will draft and implement qualification protocols, resolve deviations and CAPA, prepare validation reports, develop SOPs for manufacturing and packaging equipment, as well as write test protocols. **Key Responsibilities:** - Author validation protocols in compliance with cGMP/FDA standards - Plan, manage, and execute start-up, commissioning...

Thorough Knowledge of Medical Device Testing Experience: Minimum 2 years Qualification: M.Sc. in Chemistry Job Description: We are seeking a Chemical Analyst with thorough knowledge of medical device testing. The candidate will be responsible for conducting chemical analyses and ensuring compliance with industry standards and quality requirements in medical device testing. Key Responsibilities: Perform chemical testing and analysis of medical devices as per protocols. Ensure accuracy and reliability of test results. Maintain and calibrate laboratory instruments and equipment. Document test procedures, observations, and results accurately. Collaborate with cross-functional teams to support pr...

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...

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 assuranc...

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 quali...

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. H...

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...

Test Lead - Embedded Software Domain: Medical (must have) Location: Bangalore 5 days WFO white field Skill: Experience in qualification of System(computer systems or Analytical instruments). Extensive validation experience in 21 CFR Part 11. Good understanding of GxP standards. Good Knowledge in Data Integrity Well acquainted with all the phases of Validation Life Cycle (VLC). Expertise in planning and execution of Validation Master Plan, requirements gathering (User Requirement Specifications), QRA. Extensive experience in creating, reviewing and executing test protocols (Installation Qualification (IQ), Operational Qualification (OQ) and Performance Qualification (PQ)), Traceability Matrix...