561 Iso Standards Jobs - Page 9

Role & responsibilities Job Description -Software Quality Engineer (QA/RA) Design, develop, and optimize high-performance SAMD applications using SIMD for real-time. Ensure all software development complies with regulatory standards such as IEC 62304, ISO 13485, FDA 21 CFR Part 820, and EU MDR. Collaborate with cross-functional teams (RA/QA, Software/firmware development, and R&D teams) to ensure the software meets safety and performance requirements. Create and maintain documentation such as SDLC deliverables, Risk management files, Verification and Validation protocols, Usability, and Cybersecurity deliverables. Participate in internal audits, regulatory submissions, and post-market survei...

Design engg of Material handling system such as Ash Handling System, Soot Blowers etc. NPD activities Know materials & other engg standards eg. IS, ASME, DIN General arrangement drawings, data sheets, mfg drawing & BoMs knows environmental standards Required Candidate profile Technical clarification of design with dept, client, agencies -coordinate with foreign office -Supervise team -Inventor 3D CAD Preference to Early Joiner share cv; info.dronehr@gmail.com 9990013340-WA

Role & responsibilities Maintains familiarity with FDA, EU, and other relevant guidelines and industry standards to ensure that documents meet or exceed sponsor and regulatory requirements and guidance. Represents the editorial group in Medical Writing, on study teams, and in cross-departmental project teams as needed. Monitors timelines and budgets for assigned projects and updates the Lead Medical Writer, Project Manager, and/or direct supervisor (as appropriate) if deliverables are at risk. Provides technical support and expertise as appropriate. Conducts training of medical editing staff and functions as a mentor. Advises medical writers, medical editors, and study teams on data integrit...

Role & responsibilities Maintains familiarity with FDA, EU, and other relevant guidelines and industry standards to ensure that documents meet or exceed sponsor and regulatory requirements and guidance. Represents the editorial group in Medical Writing, on study teams, and in cross-departmental project teams as needed. Monitors timelines and budgets for assigned projects and updates the Lead Medical Writer, Project Manager, and/or direct supervisor (as appropriate) if deliverables are at risk. Provides technical support and expertise as appropriate. Conducts training of medical editing staff and functions as a mentor. Advises medical writers, medical editors, and study teams on data integrit...

Role & responsibilities : Minimum 5 years of experience in Project Management. Must possess excellent communication skills and should be proficient in Microsoft Office. Should have prior experience in team handling. Mentors and leads less experienced medical writers on complex projects, as necessary. Acts as lead for assigned writing projects. Manages medical writing activities associated with individual studies, coordinating medical writing activities within and across departments with minimal supervision. Compiles, writes, and edits medical writing deliverables including operating guidance documents, SOPs, training guides, etc., and serves as a medical writer within and across departments ...

Compiles, writes, edits, and coordinates medical writing deliverables that present scientific information clearly and accurately, and works as a medical writer within and across departments with minimal or moderate supervision. Completes a variety of documents that may include clinical study protocols and clinical study protocol amendments; clinical study reports; patient narratives; annual reports; investigator brochures; informed consents; annual reports; plain language summaries; periodic safety update reports; journal manuscripts; and abstracts, posters, and presentations for scientific meetings. Adheres to established regulatory standards, including, but not limited to, ICH E3 guideline...

Compiles, writes, edits, and coordinates medical writing deliverables that present scientific information clearly and accurately, and works as a medical writer within and across departments with minimal or moderate supervision. Completes a variety of documents that may include clinical study protocols and clinical study protocol amendments; clinical study reports; patient narratives; annual reports; investigator brochures; informed consents; annual reports; plain language summaries; periodic safety update reports; journal manuscripts; and abstracts, posters, and presentations for scientific meetings. Adheres to established regulatory standards, including, but not limited to, ICH E3 guideline...

Manual Testing Proven prior hands-on experience (5+ years) in testing medical device software Prior experience in Integration, Regression and System testing. Prior experience in tools like HP ALM Experience in FDA compliant test documentation. Experience in Agile development processes and methodologies. Possess sound knowledge of test methodologies. Experience is defect management tool Strong knowledge of STLC System requirement analysis Author detailed Test plan, test protocols, trace matrices and test reports Good documentation practice.

Senior Security and Compliance Engineer Experience: 5 - 8 Years Exp Salary : competitive Preferred Notice Period : Within 30 Days Opportunity Type: Hybrid (Bengaluru) Placement Type: Permanent (*Note: This is a requirement for one of Uplers' Clients) Must have skills required : Information Security OR Statutory Compliance, Cloud Security Hiver (One of Uplers' Clients) is Looking for: Senior Security and Compliance Engineer who is passionate about their work, eager to learn and grow, and who is committed to delivering exceptional results. If you are a team player, with a positive attitude and a desire to make a difference, then we want to hear from you. Role Overview Description Opportunity: ...

Job description Responsibilities: Qualify suppliers according to company standards & management of approved supplier list per purchasing control compliance. Initiate and drives SCAPAs/NCRs to suppliers not performing/or adhering to company standards. Manage supplier change requests . Assess supplier performance on periodic basis & drive necessary action for continous improvement. Establish a process & ensures that suppliers deliver quality parts, materials, and services. Lead PPAP execution with supplier and ensure robust supplier process qualification/validation through IQ, OQ & PQ methodology. Monitors parts from acquisition through the manufacturing cycle and communicates and resolves sup...

As the Design Head of Packaging Machinery, you will be responsible for leading mechanical design and research & development activities for high-speed packaging and bottling machinery to ensure continuous innovation, superior quality, and optimal performance. Your key role will involve overseeing the design of various components such as moulds, conveyors, filling lines, and packaging machinery. You will be tasked with managing the entire product development lifecycle from conceptualization to commissioning. It will be your responsibility to ensure compliance with CE, ISO, GMP standards, and customer specifications. Additionally, you will be expected to implement design automation, CAD best pr...

As the BIM Manager at our company, you will be responsible for managing and implementing Building Information Modelling (BIM) strategies across projects. Your role will involve ensuring compliance with BIM standards, promoting digital ways of working, and engaging in high-level communication with stakeholders and global teams to align digital workflows with business objectives. Your strong project management skills will be essential in bringing in business opportunities from global teams and optimizing project execution. Additionally, staying updated on the latest digital technologies and practices will be crucial to enhancing BIM processes. Your key responsibilities will include developing ...

Maintain and update ISO standards documents and records. Assist in the development, implementation, and review of policies and procedures for standardization and compliance to Management standards. Ensure that the Quality Management System (QMS), GMP, and Food Safety Management System (FSMS) meet business and certification needs by establishing a review mechanism to highlight critical concerns to the management team. Ensure proper documentation control, distribution, system compliance, and preparation for Management Review. Stay informed about internal and external audits. Prepare all sectors for both 3rd party certification body and customer audits. Manage internal and external Corrective A...

You are an accomplished leader responsible for heading the Gujarat operations, with a primary focus on driving sales growth, client acquisition, and P&L management. Your role is crucial in ensuring revenue generation, profitability, and regional market expansion while maintaining operational excellence. By playing a pivotal role in the company's growth and achieving sustainable business results, you contribute significantly to enhancing market value. With 15 to 20 years of experience in overseeing and managing facility management services across multiple sites, you excel in strategic planning, service delivery, budgeting, team leadership, client relationship management, compliance, and opera...

Location: Pune, India Experience: 3-5 years in quality assurance for industrial equipment / fabricated assemblies Education: Bachelors degree in Engineering from a premium institute (Mechanical / Production / Metallurgy preferred) About the Company Enabling.Win Pvt. Ltd. is a conveyor manufacturing company with deep expertise in the Food Processing Industry, expanding into global markets. We are committed to worldclass manufacturing standards and long lasting equipment performance, and we need a QA Engineer who thrives on precision, structure, and accountability. Role Purpose This role is for a hands on quality professional with solid experience in stainless steel fabrication who can build, ...

At EY, you'll have the chance to build a career as unique as you are, with the global scale, support, inclusive culture, and technology to become the best version of you. And we're counting on your unique voice and perspective to help EY become even better, too. Join us and build an exceptional experience for yourself, and a better working world for all. As part of our EY-NFS TPRM team, you will help clients enhance their business performance by translating their strategies into realities. Working with EY-high performing teams, you will help clients to grow, innovate, protect, and optimize their business performance. We're looking for Seniors with expertise in Third-Party Risk Management to ...

The role of Transformer Bushing Quality Control and Service Professional at Hitachi Energy in Vadodara involves leading a team of young and diverse technical experts to ensure consistent quality through rigorous quality control processes for Bushings. The position focuses on addressing non-conformities and supporting continuous improvement initiatives in Testing & Services, contributing to Hitachi Energy's vision of delivering smarter and more sustainable energy solutions. As the Quality Control Engineering lead, your responsibilities include designing, developing, and implementing testing methods and equipment to ensure conformity to established quality protocols and standards. You will pla...

You will be responsible for PCB design engineering tasks within the Engineering Department at Systel, Inc. Your primary duty will be to utilize Altium Designer for PCB layout and schematic capture, with at least 7 years of experience handling PCBs up to 10 layers. Proficiency in Altium Designer version 19 or higher is required, along with expertise in managing components and supplier issues including updating component libraries. Knowledge of standard PCB layout guidelines such as trace-to-trace voltage ratings, layer stack ups, and signal integrity is essential. Effective communication with various departments in the organization is crucial, both verbally and in writing using tools like Mic...

The Quality and Inspection Engineer/Senior Engineer at Rotomag Enertec Limited, located in Napa-Borsad, is responsible for ensuring that products meet established quality standards and specifications. This pivotal role involves inspecting materials, components, and finished goods, identifying defects, and implementing corrective actions to maintain consistent product quality throughout the manufacturing process. Key responsibilities of this role include conducting receiving, in-process, and final inspections, coordinating with suppliers for corrective actions and improvements, reviewing and interpreting technical drawings, specifications, and quality standards, developing and implementing in...

Are you ready to make an impact At ZF, we are searching for talented individuals to join our team. As a FutureStarter, you will have the exciting opportunity to shape the future of mobility and be part of something extraordinary. The Global Sustainability/HSE team at ZF Wind Power is dedicated to leading the organization towards a more sustainable future. As the Global Head of Sustainability & HSE, you will play a crucial role in developing and implementing the company's Sustainability/HSE strategy in coordination with internal and external stakeholders. Working closely with various departments worldwide, including HR, Legal, R&D, Finance, Purchasing/Supplier Quality, Logistics, and producti...

As a Senior Managerial position of QAQC & Operational Excellence at our Pune head office, you will be responsible for establishing, leading, and continuously enhancing the Quality function across system quality, supply quality, and field quality for utility-scale renewable energy projects. Your primary focus will be on architecting and institutionalizing a world-class QA & QC department, defining policies, processes, and metrics to ensure defect-free, compliant, and high-performance assets are delivered by EPC partners. Your role will involve setting up the QA & QC department structure, roles & responsibilities, and resourcing plan aligned with project pipelines. You will develop and deploy ...

As a Textile Quality Control Technician, you will be responsible for conducting physical, chemical, and mechanical tests on fabrics, yarns, and garments in accordance with ISO, ASTM, and AATCC standards. Your main duties will include measuring key textile properties such as GSM, tensile strength, tear resistance, shrinkage, pilling, and colorfastness. You will be in charge of operating, calibrating, and maintaining lab equipment such as GSM cutters, tensile testers, spectrophotometers, and crock meters. In this role, it will be crucial to accurately record test data and prepare detailed reports for internal review and client submission. You will also be tasked with inspecting incoming raw ma...

You will be responsible for monitoring and calibrating inspections to test the quality of milk and milk products according to ISO standards. Your role will involve implementing cleanliness, hygiene, and food safety management practices. As the Incharge of Quality, your primary duties will include ensuring the quality of raw milk, processing, and finished dairy products. You will be required to implement and monitor quality control procedures and food safety standards. Regular lab tests, inspections, and audits will need to be conducted to maintain compliance with regulatory and industry standards such as FSSAI and HACCP. Additionally, you will be responsible for training and supervising qual...

Date: 8 Aug 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Essential Functions Designation: Sr. Executive Job Location: Bangalore Department: Engineering and maintenance About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scie...

As a Quality Assurance Specialist at Roquette, you will play a crucial role in managing, developing, and optimizing customer satisfaction through stringent monitoring of quality parameters. Your responsibilities will include upskilling the process team, enabling HACCP study, and involving in RCA to address any process deviations. Reporting to the Site QA Manager and working as part of the QA team, you will support overall site QA activities. Your key accountabilities will involve guaranteeing customer satisfaction and ensuring food safety performance by actively contributing to the site Quality strategy, policy, and standards. You will lead external and internal Quality audits, follow-up on ...