2270 Capa Jobs - Page 18

Responsibilities: Develop & implement quality systems using ISO13485, Six Sigma Green Belt, ISO9001. Conduct audits, manage CAPAs, ensure FDA/QSR/MDR compliance. Work closely with R&D for (NPI) to ensure quality planning (DFMEA, PFMEA, Control Plan)

Knowledge of CNC, VMC operating, ,troubleshooting, Programming ,maintenance ,Rejection control & Why Why Why analysis, Handle rejection analysis through 8D method & take appropriate CAPA, Knowledge calculation OOE,Cycle Time Reduce,4M analysis . Required Candidate profile Strong knowledge of CNC machines and hands-on experience with hydraulic and pneumatic systems Perform preventive, predictive, and corrective maintenance on electrical systems and equipment

Develop and monitor quality KPIs, standards, and documentation (QA/QC reports, checklists, audits, etc.). Handle customer complaints, root cause analysis, and ensure corrective/preventive actions (CAPA). Required Candidate profile Ensure compliance with relevant ISO standards and industry regulations. Lead, train, and mentor the quality team to maintain a culture of quality excellence.

About The Role Skill required: Marketing Operations - Quality Management Designation: Quality Auditing Analyst Qualifications: Any Graduation Years of Experience: 3 to 5 years What would you do? Help balance increased marketing complexity and diminishing marketing resources. Drive marketing performance with deep functional and technical expertise, while accelerating time-to-market and operating efficiencies at scale through Data and Technology, Next Generation Content Services, Digital Marketing Services & Customer Engagement and Media Growth Services.Role requires Digital Marketing Ads & Promotion creation/designAct of overseeing all activities and tasks needed to maintain a desired level o...

Walk-in at Matoda We are hiring multiple positions for our manufacturing facility at Matoda as mentioned below. Please find our current job requirements and venue details mentioned. If any of the requirements match your current job profile, kindly walk in with your latest resume. Role & responsibilities Engineering - (Instrumentation / Process Equipment Maintenance) (Senior Executive / Executive / Senior Officer) Experience - 03 to 10 Years Qualification BE / B Tech QUALITY ASSURANCE IPQA (injectable) / IPQA (OSD) / Documentation (Officer / Senior Officer / Executive/Senior Executive) Experience - 02 to 09 Years Qualification - B. Pharmacy/ M Pharmacy / M.Sc. / B.Sc. MICROBIOLOGY (Officer / ...

About The Role Skill required: Marketing Operations - Quality Management Designation: Creative Production Analyst Qualifications: Any Graduation Years of Experience: 3 to 5 years What would you do? Help balance increased marketing complexity and diminishing marketing resources. Drive marketing performance with deep functional and technical expertise, while accelerating time-to-market and operating efficiencies at scale through Data and Technology, Next Generation Content Services, Digital Marketing Services & Customer Engagement and Media Growth Services.Role requires Digital Marketing Ads & Promotion creation/designAct of overseeing all activities and tasks needed to maintain a desired leve...

About the Role We are looking for an experienced and detail-oriented Assistant Manager CNC Maintenance to ensure the optimal performance, uptime, and reliability of CNC machinery. The role involves preventive and corrective maintenance to support seamless production and minimize downtime. Key Responsibilities Maintenance Planning & Execution: Plan and perform preventive, predictive, and breakdown maintenance for CNC machines (VMC, HMC, Turning Centers, Wire-Cut, EDM). Maintain maintenance logs, history cards, and service records. Troubleshooting & Repairs: Diagnose and resolve mechanical, electrical, and PLC-related faults. Coordinate with OEMs/vendors for complex issues and spare part manag...

Initiate and conduct investigations associated with sterile injectable product manufacturing and processing. To identify true root causes through different tool and identify SMART CAPAs. Review of investigations to ensure content of report in compliance to the site procedure requirements for its completeness, accuracy and adequacy. To investigation market complaints, identify the root causes and respond to partner/customer. To monitor overall investigations matrixes and present to management time to time. Responsible for Quality compliance within the investigation process. Actively involved in regulatory audits as a process SME. Provide management timely updates on critical events. To sustai...

Roles & Responsibilities Conduct post-market data analysis (complaints, adverse events, service reports, literature, vigilance data). Prepare and maintain PMS reports, PSURs, and trend analyses. Support risk management updates and product safety evaluations. Collaborate with cross-functional teams for CAPA and field actions. Ensure compliance with EU MDR, ISO 13485, and ISO 14971 requirements. Support audit and regulatory submission activities. Qualifications Bachelor’s degree in Engineering, Medical, Biomedical, or related field. 3–5 years’ experience in PMS, complaint handling, or post-market quality (medical device preferred). Strong knowledge of EU MDR, ISO 13485, and vigilance reporting...

Responsibilities: * Conduct regular audits & inspections * Ensure compliance with quality standards * Monitor KPIs & report findings * Lead capa investigations & implement corrective actions * Manage change controls process

Responsibilities: Reliability test development and planning Conduct reliability testing & failure analysis Implement FMEA, CPk, Failure Mode Analysis Perform root cause & defect analyses Experience in electronic product/module is preferable

Role & responsibilities To support the QA department (Maintenance of QMS documents) & CSV Computer System Validation & Training Records. Manage the auditing process and keep detailed records. To collaborate with the QA team to ensure that the different departments meet the quality standards and collaborate in the audits contracted by suppliers and internal auditors. All this under the established standards in terms of SOPs, Good Clinical Practice, and the needs of the client. Provide advice, interpretation, help and training to other departments, in GCP, SOPs, regulatory issues and internal company policies related to Quality Assurance. Manage in the definition of internal tools and remote a...

Responsibilities: * Conduct audits and inspections. * Collaborate with cross-functional teams on product development. * Ensure compliance with quality standards. * Develop and implement quality plans.

Key Responsibilities : Oversee the implementation and maintenance of quality systems in compliance with WHO GMP guidelines. Develop, review, and enforce Standard Operating Procedures (SOPs) and quality policies. Prepare for and lead regulatory and client audits, ensuring successful outcomes. Conduct internal audits to assess compliance and identify areas for improvement. Collaborate with production, R&D, and supply chain teams to ensure quality throughout the product lifecycle. Monitor and analyze quality data, preparing reports for senior management. Lead and mentor the quality assurance team, ensuring alignment with company objectives. Qualifications : WHO GMP certification is mandatory. P...

Job Summary: A leading manufacturer is seeking a The Paint Shop Quality Engineer (QC Inspector) will be responsible for ensuring all paint processes and products meet defined quality standards and customer specifications. The role involves performing inspections, monitoring paint tests, maintaining documentation, and supporting continuous improvement in the paint shop. Key Responsibilities: 1. Conduct daily inspections as per drawings, specifications, and customer requirements. 2. Participate in daily morning meetings and plan inspection activities as per PPC/ST requirements. 3. Perform before, during, and after-painting spot checks. 4. Conduct customer inspections and prepare daily inspecti...

We are currently looking for Quality Control Engineer - Fabrication for Leading Sheet Metal Manufacturing Industry, Please find below JD for reference. Qualification: Diploma or BE in Mechanical (Exp. in Mechanical Work will be considered). On-Roll Job 6 Days Working Shift Timings: 9 AM to 6:30 PM Job Profile / Responsibility Minimum exp for Nature of Work: 1. Knowledge of sheet metal/Heavy fabrication 2. Knowledge of Welding Processes (i.e. MIG, TIG). 3. Knowledge of Drawing reading 4. Ability to take proficient decision. 5. Knowledge of KAIZEN, POKA YOKE by implementing such jigs, tools for reduction of Inspection time. 6. Knowledge of ISO standard (i.e. ISO13920, ISO2768). 7. Ability to h...

Job Title: Deputy Manager- Formulation Location: Govandi, Mumbai Department: Corporate Quality Assurance Qualification, Experience and Technical Competency: 1. Master’s Degree in Pharmacy or Science or equivalent scientific field. 2. Minimum 10 years experience in Pharmaceutical Industry (Strong background of Formulation industry with 2 to 3 years experience in Quality Control.) 3. Work experience in Regulatory Sites (USFDA, MHRA, EU GMP) 4. Knowledge of current Good Manyfacturing Practices (cGMP), Quality Management Systems (QMS) and regulatory guidelines. Key Requirements: Responsible for Quality Functions across Own Sites and Contract Sites with adherance to cGMP, Regulatory standards and...

Senior Manager 1

Introduction: Jubilant Bhartia Group is a global conglomerate founded by Mr Shyam S Bhartia and Mr Hari S Bhartia with strong presence in diverse sectors like Pharmaceuticals, Life Science Ingredients, Contract Research & Development Services, Therapeutics, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services Group has global presence employing around 42,000 people across the globe with over 2,400 in North America, Jubilant Pharmova Limited Jubilant Pharmova Limited (formerly Jubilant Life Sciences Limited) is a company with global presence that is involved in Radio pharma, Allergy Immunotherapy, CDMO Sterile Injectable, Contract Research Develo...

Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere For 70 years, our team has driven meaningful innovations in kidney care As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients that is what Vantive aspires to deliver We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful...

Responsibilities: * Conduct quality audits and document findings. * Develop and implement quality systems. * Ensure compliance with ISO standards. * Analyze failures using 8D methodology. * Prepare accurate CAPA reports.

As a Corporate Quality professional at Amneal, you will play a crucial role in bridging communication between departments, CMOs, and sites for writing, tracking, and reporting of events. Your primary responsibility will include ensuring timely submission of Field Alerts (FAR/BPDR) and Illegitimate Drug Notifications to FDA. You will act as an author, coordinator, and issuer as required, while also being responsible for identifying potential issues that may require reporting to FDA. Your role will involve assessing emerging trends and issues that could impact Amneal's compliance, customer experience, or reputation. You will provide support and leadership in determining and implementing CAPAs ...

Inspect and test furniture at all production stages to ensure quality standards. Maintain quality records, reports, and documentation for audits. Collaborate with production and design teams to identify process improvements and reduce defects. Ensure compliance with ISO 9001:2015, safety norms, and company quality policies. Conduct supplier quality checks and implement CAPA (Corrective & Preventive Actions) for recurring issues. Support internal and external audits. Identify production bottlenecks and implement improvements for efficiency, cost optimization, and defect reduction. Skills & Requirements: Strong knowledge of furniture materials, machinery, and production processes. Mandatory ex...

• Develop and maintain databases by acquiring TB-related data from primary and secondary sources, ensuring compatibility with the Nikshay portal. • Design and implement data storage solutions that facilitate efficient retrieval and analysis of TB- related data. • Generate regular and ad-hoc reports, dashboards, and visualizations to provide a clear view of TB program performance to stakeholders, with specific focus on data from the Nikshay portal. • Conduct regular audits of TB data entered in the Nikshay portal to ensure accuracy, completeness, and reliability. • Develop and enforce data quality metrics and standards specifically tailored to TB data to improve overall data integrity. • Prov...

Our solutions are a key part of most industries - electronics, medical research, renewable energy, food production, infrastructure and many more. Working with us means working with the latest technologies and groundbreaking, sustainable innovations. Help Us Build Better - One Supplier at a Time! We're seeking a quality-focused SQA Engineer to join our team in Pune . In this role, you'll ensure that our suppliers consistently meet the high standards required to produce reliable pump components for mining and wastewater applications. What you'll do: Conduct on-site supplier quality audits and inspections Investigate and manage Non-Conformance Reports (NCRs) to resolution Implement corrective a...