2277 Capa Jobs - Page 34

A QC Officer performs visual inspections, tests, and measurements on raw materials, in-process products, and finished goods. This is done to identify any defects or deviations from the quality standards and specifications. Required Candidate profile Previous experience in a quality control, quality assurance, or manufacturing environment is highly valued. A strong understanding of quality control principles, testing methods

LTIMindtree Hiring for Trackwise Consultant with CAPA Investigation workflows. Notice period-immediate to 30 days only. Exp-5 to 8 yrs. Location- Pan india(Any Ltimindtree location) Skill :Track wise if interested Share me these details along with CV-Richa.Srivastava@ltimindtree.com Total Experience in Track wise - Relevant exp.in CAPA Investigation and Labware - Current CTC- Expected CTC- Holding offers if any- Current Location- Preferred Location- Notice period- Skills- Date of Birth- PAN No- Passport size photo- Pan no- Availability for interview- Job description- Trackwise Strong understanding of CAPA Investigation workflows LIMS Expertise in Labware modules Product LOT EM Stability Inve...

Position: Engineer - Quality Assurance Job Description :- Perform in-process quality inspections (First-off, Middle-off, Last-off). Prepare part dimension reports using VMS (Video Measuring System). Create and maintain PPAP, MSA, SPC, and layout inspection reports. Coordinate with customers for system and PPAP audits, and ensure timely closure of audit points. Conduct joint inspections with customers for new parts and obtain approvals. Collaborate with suppliers for new product layout inspections. Monitor and complete daily plan vs. actual parts for dispatches in PDI inspection. Prepare and maintain QMS and IATF-related documents and reports. Handle in-house and customer complaints using 8D ...

• Assigning batch details • Preparing the batch CoAs • Keeping the entry of Inward and Outward details • Regulatory market review or our products and verify guidelines Required Candidate profile Candidates with excellent knowledge in COA, Batch Details, Batch Record, Vendor qualification, CAPA, Customer Query resolution.

Role & responsibilities Infosys BPM focuses on integrated end-to-end outsourcing and delivers transformational benefits to its clients through reduced costs, ongoing productivity improvements, and process reengineering. Todays operational landscape is quite complex and business processes are critical in achieving the company’s goals and any inefficiencies in processes will lead to lesser agility and make companies lose their competitive edge in the market. We at Infosys BPM Quality team work closely with delivery and client stakeholders and use various continuous improvement levers to build a strong process improvement culture in client engagement which helps processes to achieve higher effi...

The candidate will be responsible for Environment, Health & Safety activities Conducting the Risk Assessment in work place and update periodically, documentation Internal Safety audit. Reviews Compliance Audits. Preferred-Candidate from Mfg Industry

Role Overview: You will be joining our Brand SIA (Steel Infra Agro) as a Quality Manager, where your primary responsibility will be ensuring the highest quality standards through process-oriented approaches. Your expertise in PPAP, QC Tools, CAPA, Defect Analysis, and Control Plans will be crucial in maintaining and enhancing our products and processes. Collaborating with cross-functional teams and fostering a culture of excellence will be key aspects of your role. Key Responsibilities: - Implement process-oriented approaches to ensure adherence to quality standards and specifications. - Conduct defect analysis and drive Corrective and Preventive Actions (CAPA) to resolve and prevent issues....

Role Overview: As a Raw Material Quality Control Analyst, your main responsibility will be to ensure that all raw materials (API & excipients) used in manufacturing are sampled, tested, and released according to pharmacopeial/in-house specifications and regulatory standards before they are utilized in production. You will play a crucial role in maintaining the quality and integrity of raw materials used in pharmaceutical manufacturing processes. Key Responsibilities: - Receive and verify raw material intimation from the warehouse. - Conduct GMP-compliant sampling using appropriate tools and in classified environments (if applicable). - Properly label samples and maintain sampling logbooks. -...

Role Overview: You will be joining Syngene International Ltd. as a Senior Executive 9-II in the Quality Assurance department at the Mangaluru location. Your main responsibility will be to provide in-process Quality Assurance support for executing GMP manufacturing activities at the Mangalore manufacturing facilities. You will ensure that the Site Quality system is always in compliance and ready for Regulatory & Client inspections by following all necessary quality procedures. Additionally, you will handle change controls, deviations, CAPAs, and assure online documentation integrity. Key Responsibilities: - Provide In-process Quality Assurance support for GMP manufacturing activities - Ensure...

Skill required: Regulatory Services - Life Sciences Regulatory Affairs Designation: LifeScience Regulatory Svs Associate Qualifications: Bachelor of Pharmacy/Master of Pharmacy Years of Experience: 1 to 3 years About Accenture Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. Visit us at www.accenture.com What would you do You will be aligne...

Key Responsibilties: Quality Assurance & Control Supervise daily quality inspection activities in the press shop. Conduct in-process, patrol, and final inspections of sheet metal components. Verify compliance with customer drawings, specifications, and GD&T requirements. Ensure adherence to SPC, MSA, and quality documentation as per IATF 16949 / ISO 9001 standards. Monitor critical quality parameters including burrs, cracks, dimensional accuracy, flatness, thickness, and surface finish. Process Monitoring Implement and maintain quality checkpoints for blanking, piercing, bending, and forming operations. Verify First Piece Inspection (FPI) and approve production startup. Collaborate with pres...

Designation- QA Executive Looking for QA Executives/Sr. Executives from Injectables and formulations background only. Roles and Responsibilities: 1.Responsible for all Quality Management System (QMS) and documentation activities in the plant. 2. Responsible for logging, review, follow-up and closure of Change controls, Deviations, Corrective and Preventive actions, OOS, OOT, Market complaints and Product recalls. 3. Responsible for investigations of different deviations, OOS, OOT, market complaints, product recalls and Risk assessments. 4. Responsible for preparation of internal audit schedules and coordination and organization of audit meetings and participation as Auditee / Auditor. 5. Res...

Customer handeling, quality documents maintaining, 8d capa, Monthly audit, monthly reports submission

We are seeking a highly skilled and experienced professional in Quality Assurance (QA) and Quality Control (QC) for our insulator manufacturing unit based out at Sitharampur Shabad Telangana. The ideal candidate will have a comprehensive understanding of industrial operations, incoming raw material testing industry standards, and quality testing procedures, with specialized expertise in composite insulator production. Key Responsibilities Oversee QA & QC operations throughout the insulator manufacturing lifecycle Implement and monitor testing procedures for various insulator types. Ensure adherence to Indian and International Standards for insulator production Conduct technical calculations,...

We are seeking a highly skilled and experienced professional in Quality Assurance (QA) and Quality Control (QC) for our insulator manufacturing unit based out at Sitharampur Shabad Telangana. The ideal candidate will have a comprehensive understanding of industrial operations, incoming raw material testing industry standards, and quality testing procedures, with specialized expertise in composite insulator production. Key Responsibilities Oversee QA & QC operations throughout the insulator manufacturing lifecycle Implement and monitor testing procedures for various insulator types. Ensure adherence to Indian and International Standards for insulator production Conduct technical calculations,...

Interested candidates can share their CV on pooja.singh@hamiltonindia.in with subject line- " Applying for Quality Manager | Injection Moulding | Manufacturing Industry" Role & responsibilities Quality Assurance of Procured Items:- Assure quality of bought-out and sub-contracted items and raw materials. Stabilize the incoming process for outsourced parts, set SOPs, and standards for in-house and vendor processes. Conduct vendor audits and implement improvement plans through systematic Corrective and Preventive Actions (CAPA). Customer Complaint Analysis: Analyze customer complaints and implement improvement plans at plant manufacturing and design levels. Promptly address marketing queries re...

Perform preventative maintenance and calibration of Instruments(PT,TT,LT,FT,CV,XV) and DCS/PLC systems. Addressing the Complaint & Trouble Shooting problems regarding instruments and Control system. Read the reports on incomplete/pending jobs from the previous shift on issues such as major/minor breakdowns, emergencies on calibration/repair/troubleshooting from Production, QC, R&D &/or Maintenance departments and attend to them on a priority Basis Understanding and maintaining of calibration records and compliance documents Make rounds of the plant and conduct routine/preventive maintenance of all the instruments Installation and commissioning of field instruments for new project(s) as per t...

Reporting of Unsafe Act & Unsafe conditions on daily basis. Follow the Work Permit System procedure and issue the work permit on daily requirement. To conduct and monitor the safety talk records along with HSE representative. Emergency communications as per On Site Emergency Plan Engage actively in accident and incident investigations, ensuring that corrective and preventive actions (CAPA) are promptly implement. To conduct the internal safety audits and various facility inspections and tracking the recommendation compliance To conduct and participate in mock drills. Conduct on the job training, classroom training on Safety & Health topics HIRA & JSA of critical activities to be conducted Sh...

Level: L2+L3 L2 (Experience 3-5 Years, Incase not explicitly mentioned) Log and manage Problem Management (PM) tickets with end-to-end ownership in SNOW. Coordinate initial problem records with relevant SMEs and CUSTOMER SPOCs. Automate PM workflows and dashboards in SNOW. Lead weekly and monthly governance meetings to analyze trends and recurring issues. Identify potential problems through trend analysis, incident patterns, and RCA. Drive RCA and CAPA submissions within defined timelines. Coordinate change management for deploying permanent fixes. Continuously improve PM processes based on lessons learned. Publish monthly PM reports and dashboards, and weekly reports to resolver groups. Mai...

Level: L2+L3 L2 (Experience 3-5 Years, Incase not explicitly mentioned) Log and manage Problem Management (PM) tickets with end-to-end ownership in SNOW. Coordinate initial problem records with relevant SMEs and CUSTOMER SPOCs. Automate PM workflows and dashboards in SNOW. Lead weekly and monthly governance meetings to analyze trends and recurring issues. Identify potential problems through trend analysis, incident patterns, and RCA. Drive RCA and CAPA submissions within defined timelines. Coordinate change management for deploying permanent fixes. Continuously improve PM processes based on lessons learned. Publish monthly PM reports and dashboards, and weekly reports to resolver groups. Mai...

As a Material Management Specialist, your role involves planning and controlling inventories of raw materials and packaging materials to meet production requirements. You will coordinate with Purchase and Quality Control teams to ensure timely availability and release of materials. Additionally, you will oversee the receipt, storage, and dispensing of materials in compliance with SOPs, MSDS, and safety requirements. It will be your responsibility to manage the return, rejection, and destruction of non-conforming materials following established procedures. Your key responsibilities include: - Planning and controlling inventories of raw materials and packaging materials - Coordinating with Pur...

As the Site QA Head at Sun Pharmaceutical Industries Ltd, your role will involve managing overall quality assurance oversight and site activities related to quality systems. This includes documentation review, SOP updates, in-process quality assurance, sampling and batch release, preventive maintenance, calibration, qualification, validation, internal audits, compliance, quality oversight of electronic systems, budget management, continuous improvement of quality systems, RA support, monitoring of pest control, and retention sample management as per Good Manufacturing Practices requirements. Your key responsibilities will include: - Defining operational strategy and road map for quality assu...

Quality assessments on all incoming materials from vendors and outgoing products shipping. Reject all product materials that fail meet quality expectations. Read blueprints, plans, and specifications to understand requirements products and services.

Job Track Description: Performs business support or technical work, using data organizing and coordination skills. Performs tasks based on established procedures. In some areas, requires vocational training, certifications, licensures, or equivalent experience. General Profile Expands skills within an analytical or operational process. Maintains appropriate licenses, training, and certifications. Applies experience and skills to complete assigned work. Works within established procedures and practices. Establishes the appropriate approach for new assignments. Works with a limited degree of supervision. Functional Knowledge Has developed skillset in a range of processes, procedures, and syste...

Long Description IMS Development & Implementation: Collaborate with cross-functional teams to design and implement the IMS, ensuring alignment with industry standards (e.g., ISO 9001, ISO 45001 & ISO 14001), relevant regulatory and customer requirements. Develop IMS documentation, including policies, procedures, work instructions, forms, and templates, to establish a clear framework for processes and practices. Compliance & Auditing: Conduct regular internal audits to assess the effectiveness and compliance of the IMS processes and procedures. Identify risks and areas for improvement, work with stakeholders to implement corrective actions and preventive measures. Training & Awareness: Develo...