10 Qms Standards Jobs

As an MBBS-qualified professional, you will be leading healthcare BPO projects focusing on EHR, medical coding, and health insurance processes. Your role will involve client management, operational leadership, and ensuring process excellence. - Manage end-to-end delivery of healthcare BPO projects with a strong emphasis on quality and efficiency. - Drive client communication, stakeholder management, and build strong relationships. - Oversee project accounting, budgeting, and maintain financial performance. - Lead, coach, and develop high-performing teams. - Implement process improvements, automation initiatives, and develop reporting dashboards. - Ensure compliance with healthcare regulation...

SFO TECHNOLOGIES PVT LTD JOB TITLE Engineer Quality BUSINESS/MODALITY Aerospace/Defense/Industrial/Medical Products Electronics + Box build assemblies DIVISION SFO-Electronics, Kochi REPORTS TO BU – Quality head JOB DETAIL Responsible for understanding Customer requirements and ensuring compliance to them in manufacturing Process & Finished Product. Interfacing with Customer on all matters related to Quality. DUTIES & RESPONSIBILITIES Engage with Engineering and Cross Functional teams from the initial stages of Project discussions in order to understand customer requirements. Participate in NPI build process and FAI Qualifications for Medical and Industrial projects. Co ordinate Customer eva...

You are required to lead healthcare BPO projects focusing on EHR, medical coding, and health insurance processes. Your role involves managing client relationships, ensuring operational excellence, and leading high-performing teams. - Manage end-to-end delivery of healthcare BPO projects with a focus on quality and efficiency. - Drive client communication, stakeholder management, and relationship building. - Oversee project accounting, budgeting, and financial performance. - Lead, coach, and develop high-performing teams. - Implement process improvements, automation initiatives, and reporting dashboards. - Ensure compliance with healthcare regulations and maintain QMS standards. - Analyze met...

As a Quality Control Supervisor at Varel Energy Solutions in Faridabad, India, your role will involve supervising, planning, coordinating, mentoring, and directing quality control inspectors in the Machine Shop. Your main responsibilities will include: - Developing, implementing, and maintaining quality control processes and procedures for Final Inspection - Monitoring verification of various instruments as per the requirements - Reporting and verifying Non-conformances and their root cause analysis - Monitoring NPD Parts & their standard requirements - Ensuring final inspection of all types of products according to work authorization, drawing & client PO requirements - Releasing products ac...

You will be responsible for Vaccine Manufacturing (Cell Culture) which includes: - Reviving and subculturing MRC-5 cells - Counting cells and preparing MCB/WCB - Handling Roller bottles, Cell stacks, and TCFs - Preparing media and in-process buffers in media mixing vessels - Virus infection and harvesting procedures - Working with Chicken embryo fibroblast cells, pooling embryos, and seeding RBs In the Quality Control department, your tasks will involve: - Performing biochemical, chromatography, electrophoresis, and immunoassay techniques - Utilizing cell culture and molecular techniques - Conducting Analytical Method Validation (AMV) and Development and Transfer Quality Control - Adhering t...

Role Overview: You will be responsible for utilizing your expertise in Medical Electronics Design & Consulting to contribute to the introduction of Medical Technology. With over 10 years of experience in the field, you will play a crucial role in the complete Medical electronic devices/equipment/product Design Lifecycle, covering aspects such as Value Discovery, architecting, Design, and Testing. Your exposure will extend to current architectures like Internet of Medical Things (IoMT), Microservices/SoA, AI enabled therapeutics/diagnostics/medical imaging/personalized medicine/prognostics/telemedicine, SaMD, Digital healthcare/surgical platforms, etc. Furthermore, your knowledge of Robotics ...

As a Quality Control Supervisor at VES in Faridabad, India, your primary responsibility will be to supervise, plan, coordinate, mentor, and direct quality control inspectors in the Machine Shop. Your role will involve ensuring the continuous production of products that meet established standards by personally performing the following duties. You will be tasked with developing, implementing, and maintaining quality control processes and procedures for Final Inspection. Monitoring the verification of various instruments as per requirements, reporting and verifying non-conformances along with their root cause analysis, and overseeing NPD Parts & their standard requirements will be part of your ...

As the Deputy General Manager - ETS at Lauritz Knudsen Electrical and Automation, your primary responsibility will be to ensure the quality assurance of tooling components and assemblies. You will oversee all inspection activities to guarantee the highest standards of quality. In addition, you will be expected to utilize your expertise in metrology to effectively use equipment such as callipers, CMM, and optical measurement tools for precise measurements. Managing the calibration process for all measuring instruments will be a crucial part of your role. This includes identifying calibration requirements, determining calibration frequencies, and maintaining accurate records to ensure accuracy...

About ValGenesis: ValGenesis is a leading digital validation platform provider for life sciences companies. The ValGenesis suite of products is utilized by 30 of the top 50 global pharmaceutical and biotech companies to achieve digital transformation, total compliance, and manufacturing excellence across their product lifecycle. About the Role: As a Junior Validation Engineer at ValGenesis, you will work as a team member in the Validation department. Your primary responsibility will be to validate all product releases. Requirements: - A BE/BS degree in Biomedical, Pharmaceutics, or a related field. - Knowledgeable about the product development life cycle. - Familiar with drug development and...

Maintain and improve the QMS in accordance with IATF 16949 and ISO 9001 standard Prepare and facilitate internal and external audits, including MAIS and IATF 16949 audits. Develop and update quality procedures, work instructions, and documentation Required Candidate profile Maintain document control and ensure effective change management in quality documentation. Support PPAP, FMEA, APQP, and MSA activities in alignment with automotive quality standards