1365 Quality Systems Jobs - Page 27

Participate in software development: - Analyse and review customer requirements - Write and review detailed software technical specifications - Participate in architecture definition, documentation, and review - Prepare estimates for the complete design, implementation, and testing of new features to support project planning - Create and update design documentation throughout lifecycle and review designs of others - Implement required software functionality meeting established requirements, specifications and quality. - Create and execute unit and system test plans and review the plans of others - Aid in the investigation and resolution of customer support issues - Lead a small team of softw...

Job Description : Job Title: Executive - Quality About the Function: Our Supply Chain and Manufacturing team are problem-solvers, sourcing, producing, and delivering our much-loved brands to delight customers around the globe. Over half of Diageo's 30,000+ people work in Supply Chain and Manufacturing. It's an intricate and sophisticated operation that's the product of logistical, manufacturing, and technical collaborations. Our teams in 100 sites in over 30 countries cover production facilities, supplier relationships, customer collaborations and third-party agreements. We're committed to realising our Society 2030: Spirit of Progress goals, to protect the environment and support our farmer...

Position : IMS Lead Auditor Location : Belgaum, Karnataka, India Key Responsibilities: We are looking for an experienced auditor with a pragmatic approach to ISO 9001, 14001 and 45001 Management System Audits. The successful candidate will have carried out audits across all levels of organization. Engineering graduates with Quality, Environmental, Health and Safety management system as area of specialization in 10 years full time work experience in manufacturing industry out of which at least 5 years in Quality, Environmental, Health and Safety management system. Lead Auditor Certifications such as ISO 9001, 14001 and 45001Proficient with MS Office (word, excel, power point). Good communicat...

The ideal candidate for this role is a critical thinker who will proactively enhance the quality systems of the company. You will achieve this by conducting internal audits, actively participating in process improvement programs, and engaging with key partners to gather constructive feedback. Your responsibilities will include developing standardized production, quality, and customer-service standards. You will also be tasked with identifying potential risks before they escalate into issues, with a focus on root cause analysis and preventive action. Additionally, you will conduct internal and external quality audits and create detailed reports based on your findings. Building a cohesive team...

You will be responsible for programming and operating ZEISS Coordinate Measuring Machines at CX Precision, located in Sricity, Tada, Andhra Pradesh. Your main duties will include conducting dimensional inspections of precision components, applying GD&T principles to verify profiles and tolerances, and generating detailed inspection reports for various purposes such as PPAP and customer approval. Additionally, you will be required to train operators and junior inspectors on CMM operation and measurement techniques. You must have the ability to develop, edit, and validate CMM programs using CAD models and engineering drawings. Conducting First Article Inspections (FAI), in-process checks, and ...

At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world. Job Overview TE Connectivitys R&D/Product Development Engineering Teams conceive original ideas for new products, introduce them into practice. They are responsible for product development, and qualification from market definition through production and release; assist in the qualification of suppliers for new products to ensure suppliers deliver quality parts, materials, and services for new or improved manufacturing processes; conduct feasibility studies, testing on new and modified designs; direct and support detailed design, testing, ...

Responsibilities & Key Deliverables Knowledge of Transmission / Transaxle Assembly /Gear Box Process. In depth knowledge about PFMEA / Control Plan / PFC . (Machining & Assembly) Knowledge of Performance test parameters of Gear Box like NVH Analysis & Gear Geometry. Knowledge of Basic Machining Process of Gears & Housings. Knowledge of New Product Development Process. Knowledge of Quality Systems in general and TS- 16949, APQP, PPAP. Responsible for continuous process improvement on shop floor through various improvement tools like Kaizen, QC story, DOE etc. Ensure adherence to & continuous support in productivity, quality, Cost & delivery improvement initiatives Tooling Design, 2D drawing &...

ORGANISATIONAL OVERVIEW Lambda Therapeutic Research is a Global full-service Clinical Research Organization (CRO) with its headquarters in Ahmedabad, India. With facilities and operations strategically located in Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK) and Warsaw (Poland), we offer comprehensive end-to-end clinical research services to the global innovator, biotech, and generic pharmaceutical industries. JOB DETAILS To determine whether all trial related activities were conducted, data recorded, analyzed and reported accurately & in compliance to all applicable Regulatory requirements, Organizational requirements (Policy, Procedures and processes) a...

Position Summary: The Global Clinical Supply Chain (GCSC) Compliance Manager ensures GxP compliance within GCSC by providing QMS operational support and partnering in business activities, while identifying and supporting process improvements. The role involves managing Global Clinical Supply Chain compliance, monitoring process performance, performing trend analysis and supporting audit/inspection readiness. The incumbent will proactively identify and report to management any operational and systemic compliance issues and/or risks related to clinical supply chain end-to-end processes. Key Responsibilities: Collaborate with GCSC functions to maintain GxP compliance and to support business act...

Greetings from Synergy Resource Solutions, a leading recruitment consultancy firm. Our Client is a leading MNC Manufacturing company in field of screening & auxiliary solutions for Petrochemicals, Food, beverages & Chemicals companies. Company has more than 200 employees & having their plant at Sanand GIDC, Ahmedabad. They are looking for staff for below mentioned position:- About the Role: Position: Global Supply Engineer Experience required: 7-10 years CTC: 8 - 9.50 LPA Location: Sanand (Ahmedabad) Position Overview The Global Supply Engineer is responsible for ensuring reliable, cost-effective, and high-quality supply of parts, materials, or equipment from a global supplier base. This rol...

Position Title Assistant Vice President - Quality Position Summary The Quality Head will be responsible for establishing, implementing, and maintaining robust quality systems to ensure the highest standards in conductor manufacturing. This role involves overseeing quality control, assurance, and continuous improvement processes, ensuring compliance with customer specifications, industry standards, and regulatory requirements. Key Accountabilities / Responsibilities Quality Management System (QMS): Develop, implement, and maintain the Quality Management System (QMS) in line with ISO and other relevant standards. Conduct regular audits to ensure compliance with QMS and drive improvements where...

Job Summary: We are seeking a meticulous and experienced R&D/Quality Control Manager to oversee our quality control department and ensure that all operations and products meet established quality standards. The ideal candidate will have a strong background in geosynthetics, with hands-on experience in testing, report making, MTC preparation, quality control documentation, and lab accreditation processes.

Purpose: Senior Quality Analyst will be the owner of the nonconformance and Corrective and Preventive Actions (CAPA) processes, initiate, manage all company CAPA, lead cross-functional teams to drive for root cause analysis, host appropriate and efficient meetings, establish and manage timelines for timely closure and completion of nonconformances and CAPA, manage continuous improvement initiatives across the company. They will provide guidance for the improvement of the Clinisys Quality Management System including business processes, products, software systems, training and reporting of metrics and trends in accordance with internal and external regulations, policies, and procedures. The Se...

This position is accountable for performing activities in support of the validation and compliance of a computerized system to ensure the system meets its intended use. This position will work with IT team(s) to ensure a computerized system is compliant with applicable regulations (21 CFR Part 11, GxP Regulations) and Baxter Quality Management System requirements. Support the Validation activities during the deployment of any new GxP Application. What you ll be doing Review project teams work to ensure quality (design walk-through, code review, test results, etc.) and alignment to the processes, standards, and regulatory requirements. Responsible for the conduct of Verification and Validatio...

As our ME Associate (Manufacturing Engineer), you ll play a key role in designing, improving, and standardizing manufacturing processes to maximize efficiency and deliver high-quality outcomes for our customers. Your impact? You ll enable smoother production operations, stronger alignment with the Danfoss Business System, and measurable improvements in cost, quality, and delivery directly benefiting both customers and the organization. You ll collaborate with operations, process engineering, and cross-functional global teams, taking ownership of manufacturing engineering activities (including advanced manufacturing and process engineering support), helping us move toward a more efficient and...

Oracle Fusion Analytics Warehouse (FAW) / Fusion Data Intelligence (FDI) Consultant Minimum 4 years experience from FAW (Fusion Analytics Warehouse) /FDI (Fusion Data Intelligence) as admin and developer and overall 6+ Year experience is preferred Development and maintenance of Oracle Fusion Analytics Warehouse- building data models, reports and dashboards, end user training and support, manage data model, data pipelines, security and perform any customizations Lead and own all technical aspects of FAW/FDI - ERP/HCM implementations and/or customizations including data migrations, data quality, systems integrations, 3rd-party applications, and custom development Having Oracle fusion HCM techn...

Maintain and update quality documentation, COAs (Certificate of Analysis), MSDS, batch records, data records Coordinate with vendors and internal teams for quality-related queries and pending documents Coordinate with Sales Team for Specifications / Query Support internal and external audits and implement corrective actions Assist in customer complaint investigations and root cause analysis QC & QA Documentation Handling claims for all activities Knowledge of KOSHER, HALAL, MSDS, FSSAI Check verifies and update parameters of the products like Haz class, FEMA Nos Ensuring that products comply with relevant supporting quality standards, regulatory compliance (egFSSAI) Ensure compliance with ap...

Bachelors degree in Life Sciences, Engineering, or a related field. 3-5 years of experience in QA roles with strong focus ondocumentation and compliance in the medical device industry. In-depth knowledge of ISO 13485, FDA QSR, EU MDR, and risk management (ISO 14971). Proven experience with QMS documentation management and inspection/audit readiness. Familiarity with risk management tools (e.g., FMEA, Hazard Analysis). Strong attention to detail and high standards for documentation accuracy. Experience in a startup or fast-paced, resource constrained environment preferred. Excellent written and verbal communication skills. Preferred Qualifications: Certified Quality Auditor (CQA), Six Sigma, ...

About the Role We are seeking a highly skilled and motivated Management Representative (MR) to oversee the implementation, maintenance, and continual improvement of our Quality Management System (QMS) in alignment with IATF 16949 and ISO standards. The MR will be responsible for ensuring compliance, conducting audits, driving quality initiatives, and acting as the primary liaison between top management and external certification bodies. Key Responsibilities Act as the primary representative of top management for QMS matters. Ensure that the Quality Management System (QMS) is established, implemented, and maintained effectively across all departments. Plan, conduct, and monitor internal quali...

Job Summary : We are seeking a proactive and experienced Quality Head to lead the quality assurance and quality control functions at our manufacturing plant in Miraj MIDC. The ideal candidate will bring a strong understanding of quality systems, regulatory requirements, and manufacturing processes, with a focus on continuous improvement and operational excellence. Key Responsibilities : Lead the plant quality function and ensure adherence to quality standards and systems (IATF, ISO). Develop, implement, and maintain Quality Management Systems (QMS). Supervise in-process, incoming, and final inspections to ensure defect-free products. Drive implementation and monitoring of APQP, PPAP, FMEA, S...

Role & responsibilities GOOD KNOWLEDGE OF IATF AND QMS AUDIT BOTH CUSTOMER AND INTERNAL Preferred candidate profile QUALITY KNOWLEDGE OF CASTING AND MACHINING

The Impact You'll Make As our ME Associate (Manufacturing Engineer), you'll play a key role in designing, improving, and standardizing manufacturing processes to maximize efficiency and deliver high-quality outcomes for our customers. Your impact You'll enable smoother production operations, stronger alignment with the Danfoss Business System, and measurable improvements in cost, quality, and delivery-directly benefiting both customers and the organization. You'll collaborate with operations, process engineering, and cross-functional global teams, taking ownership of manufacturing engineering activities (including advanced manufacturing and process engineering support), helping us move towar...

The opportunity Finished product testing and analytical method development by HPLC, GC, IC, UV etc. Analytical method validation and transfers, analysis of API, Finished product R&D samples How you ll spend your day Analysis of Solid oral dosage i. e. Dissolution, Assay, CU, BU and Related substances etc. Analysis of samples received from Formulation department (samples include in-process, finished product, pre-formulation study samples and stability samples etc. ). To carry out analytical method development and method validation, in-process samples and finished products. To carry out analytical method transfer activity to QC, Goa. Handling and testing of hi-potent compounds/molecules Troubl...

Quality manager required from a mobile accessories company Qualification - any electronics Exp- min 10 yrs salary- max 70000 Location - kundli, sonipat. Wtsapp me resume at 8295842337- Mr. Bansal

BACKGROUND . GENERAL Location of Job: Jaisalmer, Rajasthan. No. of Positions: 5 Job type : Contractual for 1-year, renewable basis project requirements. Reporting to : Project Manager. JOB PURPOSE The Medical Officer will be responsible for medical check-ups of the serving community through Camp duties at MMU following the visit roster, treating and providing consultation to the patients and maintaining. The Medical Officer will analyze medical check-up data and conduct regular inspection of equipments, maintaining the inventory of medicine required at MMU. S/he ensure compliance of the requirements and protocols as per Govt Rules. S/he will present the data to management and make suitable a...