2954 Capa Jobs

Raychem RPG Private Limited. is looking for Executive - QA to join our dynamic team and embark on a rewarding career journey Strategic Quality Planning: Developing and executing a strategic quality plan that aligns with the organization's objectives and quality goals Quality Leadership: Providing leadership and direction to the quality assurance and quality control teams, often including Quality Managers and other quality professionals Quality Standards and Policies: Establishing and enforcing quality standards, procedures, and policies to ensure that products or services meet or exceed customer expectations Process Improvement: Identifying opportunities for process improvements, quality enh...

Role & responsibilities 1. To analyse customer related complaints carefully and do appropriate analysis of the same 2. Reply to customer (in consultation with Senior) in appropriate formats like 8D or CAPA 3. Timely reply to customer queries related to open issues or unclised complaints 4. Coordination with required depts or functions to close a customer concern or complaint 5. Conducting pre-audits as per customer requirements (individually or in a contributor role) 6. Acting as a single point of contact between company and customer. 7. Escalating unresolved issues or complaints to Seniors 8. Be a part of CFT as and when required 9. Be a team member of CQA reviews 10. CQA monthly performanc...

Role & responsibilities Conduct incoming, in-process, and final inspection of components as per defined standards and inspection plans. Perform Goods Receipt Note (GRN) clearance through ERP-based systems. Interpret engineering drawings and quality plans to execute effective inspection and quality control measures. Utilize precision measuring instruments (e.g., Vernier, Micrometer, Height Gauge, CMM) for dimensional and functional inspections. Conduct supplier end inspections and audits to ensure adherence to quality specifications and standards. Handle and analyze non-conformance issues , and implement effective Corrective and Preventive Actions (CAPA) both internally and at the supplier en...

Tata Elxsi is among the worlds leading providers of design and technology services across industries, including automotive, broadcast, communications, healthcare, and transportation. Tata Elxsi works with leading OEMs and suppliers in the automotive and transportation industries for R&D, design, and product engineering services from architecture to launch and beyond. Roles and Responsibilities: Implement, maintain, and improve the Medical Device Quality Management System in compliance with ISO 13485, FDA 21 CFR 820, MDSAP, EU MDR and applicable regulatory requirements. Ensure implementation and maintenance of software life-cycle processes as per IEC 62304. Responsible for design and developm...

Quality Management: Oversee quality control (QC) systems and operations within the plant to ensure products meet customer specifications. Ensure all manufacturing processes adhere to regulatory requirements (e.g., ISO, GMP) and quality standards.

We are seeking a highly motivated and experienced Management Representative to oversee the implementation of the American Petroleum Institute (API) Q1 specification in our organization. The Management Representative will be responsible for ensuring that all aspects of the API Q1 standard are fully implemented and integrated into our quality management system. The ideal candidate should possess strong leadership and communication skills, a thorough understanding of the API Q1 specification, and the ability to work effectively with cross-functional teams. Job Responsibilities: Develop and implement a comprehensive plan for the implementation of the API Q1 specification Coordinate and lead cros...

Role & responsibilities Implement and maintain the Quality Management System (QMS) as per relevant standards Ensure timely resolution of non-conformities and implement corrective actions Plan and conduct internal and external audits (ISO, IATF, customer audits, etc.). Lead root cause analysis (RCA) and problem-solving for internal non-conformance and customer complaints Implement Corrective and Preventive Actions (CAPA) to prevent recurrence of issues. Conduct supplier audits and assessments to ensure that incoming materials meet quality standards Preferred candidate profile Experience in quality assurance, preferably in manufacturing, pharmaceuticals, lubricating oils, etc. Familiarity with...

Conduct root cause analysis and implement (CAPA) 8D methodology. (Cpk/Ppk) (APQP) and Production Part Approval Process (PPAP) activities. For complete JD WhatsApp QMR to 7483236645 P.S: Shortlisted candidates will have to attend F2F Interview Required Candidate profile Candidate with min 7-8 years experience & 4 years as MR. Bangalore candidates only apply since the interview mode is Face to Face

Quality Assurance management in precision machining: Ensure compliance with aerospace-grade quality standards & customer requirements by monitoring machining processes, inspecting critical components & driving continuous improvement initiatives Required Candidate profile Mechanical/ Production/ Industrial Engineer 10-15 year experience in Quality with deep knowledge of machining & mfg processes Expertise in AS9100/ ISO 9001 systems Ability to lead & develop a team

Meeting management QA Targets Skilled in QC tools Responsible for Customer complaint/query QA Improve plan as per last yr defects Controlling internal/external PPM RedBin/RCA/WHY-WHY Analysis Enhance QA Strategy CFT Wiring Harness knowledge is a must

1.Strong experience in heavy fabrication and machining processes. 2.Experience with PPAP, FMEA, SPC, MSA, and CAPA. 3. NDT LEVEL -II certification in VT,RT, UT, PT, MPT will be prefer. 4. Knowledge fabrication / machining Drawing Reading. Required Candidate profile 5. Control & monitoring on the quality of every Stage Inspection As per QAP. 6.knowledge of Fabrication Processes & machining processes (turning, milling, grinding, drilling, CNC operations).

Role & responsibilities QMS Related Activity: - 1. Handling of market complaint investigation, documentation and follow-up and reports closure 2. Handling of CAPA & change control activity. 3. Issuance, control and retrieval or batch records, SOPs, Logbook, and other documents. 4. Prepare and review Annual product quality review. 5. Management of control sample room. 6. Preparation and review of SOP. IPQA Related Activity: - 7. To take shop floor round and do gap analysis between practices followed vs GMP practices. 8.. To review all executed BMR, BPR and Final Batch Release of Finished Product in SAP for Sale or Distribution. 9.To perform line clearance and In-process checks in manufacturin...

Right-first-time assembly&testing Early detection of defects Root cause elimination Continuous improvement of product&process quality Act as a bridge between Assembly,Testing,Engineering&Management Performs process audit Follows up on countermeasures

Job Title: Quality Control Manager Pharma Industry: Pharmaceuticals Functional Area: Quality Control Role Category: Quality Control Manager Job Location: Sterling Healthcare Ltd., Talegaon, Pune Employment Type: Full-Time Experience Required: 5– 10 Years Job Description Sterling Healthcare Ltd. is seeking an experienced Quality Control Manager to lead and manage Quality Control laboratory operations in a pharmaceutical manufacturing environment. The role is responsible for ensuring product quality, regulatory compliance, and adherence to GMP and global quality standards . Key Responsibilities Manage and oversee day-to-day operations of the Quality Control laboratory Ensure testing of raw mat...

USV (Pharma) is Hiring Senior Manager - QA (Sterile) for USFDA Formulation Manufacturing Plant based at Daman near Vapi. We are looking for dynamic professionals having more than 15 years of experience in hard core injectables (Liquid Vials, Ophthalmic and Pre-filled syringes). The incumbent must be having the thorough knowledge of IPQA, Qualification and Validation, QMS Aseptic techniques and practices. Should have faced the Regulatory Audit (USFDA, MHRA, EU GMP, TGA) and should be able to explain the auditors during inspections. Excellent verbal and written communication are expected. Oversee and manage QMS processes including Deviation Management, CAPA, Change Control, Risk Management, an...

Developing, implementing, maintaining quality systems to ensure products and processes meet company standards, customer requirements, and applicable regulatory norms. The role focuses on continuous improvement, compliance, and customer satisfaction

Roles and Responsibilities Ensure smooth operation of production activities by monitoring and coordinating with various departments. Implement lean manufacturing principles to improve productivity, quality, and efficiency. Conduct CAPA investigations and implement corrective actions to prevent recurrence of defects or issues. Maintain a clean and organized work environment using the 5S system. Collaborate with cross-functional teams to resolve problems and optimize processes. Desired Candidate Profile 12-15 years of experience in Production Management or related field (Pharmaceutical industry preferred). B.Sc (Chemistry), MS/M.Sc(Science) degree from a recognized university. Strong understan...

Job Title: Final Quality Checker / Quality Engineer Location: Naigaon Department: Quality Key Responsibilities Develop, implement, and maintain quality standards and quality control systems . Monitor and analyze quality performance and identify areas for improvement. Perform final inspection and testing of materials, equipment, processes, and finished products to ensure specifications are met. Conduct in-process and final QC checks and ensure compliance with quality requirements. Train production personnel to improve product quality and reduce rejections . Collaborate with Production and R&D teams to address and resolve quality issues. Handle customer complaints , perform CCR / root cause an...

Position :- Quality Mechanical Engineer Qualification :- B.E / B.Tech Mechanical Engineer Experience :- 2 to 5 Years Industry :- Oil & Gas / Oil Field Equipment Manufacturing Location :- Makarpura (Vadodara)

Position: Executive- Product Development Key Responsibilities Collaborating with cross functional teams (RED, Quality, Procurement) to translate market research insights into technical product requirements and initial development roadmaps. Conducted pricing intelligence and sales forecasting by leveraging competitor benchmarking, market data, and third-party analytics platforms. Supported creation of product feasibility studies, cost analysis reports, and vendor capability evaluations for management decision making. Performed technical feature tracking and failure analysis of competitor SKUs to guide product differentiation and design optimization. Participated in vendor interactions for raw...

Role Overview: Join EY as a Regulatory Compliance Senior in the Enterprise Risk team where you will assist clients by understanding their business needs and delivering solutions in line with EY guidelines. Your role involves establishing and maintaining relationships, driving projects to completion with high-quality deliverables, and leading internal initiatives to achieve operational efficiency. Key Responsibilities: - Configure, customize, and deploy Veeva Vault QMS modules (QRM, CAPA, Change Control, Complaints) to align with client-specific quality processes and regulatory requirements. - Design workflows, object lifecycles, security roles, and page layouts to support scalable and compli...

Knowledge of HPDC Process, SPC MSA, 7QC Tools, 5`S, Drawing, inspection instruments, Problem solving, component & Tools inspection, Pooka Yoka, Why why analysis, KAIZEN, PPM, Rejection Monitoring, MIS Data, Machine process Knowledge, Aluminum Casting

We are looking for an experienced IPDRG Specialty Auditor to perform pre-bill and post-bill inpatient DRG audits , ensuring accurate DRG assignment, CC/MCC integrity, ICD-10-PCS correctness, and compliance with CMS and official coding guidelines . This is a specialty audit role , not a production coding position. Key Responsibilities Perform pre-bill and post-bill IPDRG audits Validate: Principal Diagnosis (UHDDS) CC/MCC clinical support ICD-10-PCS procedures and root operation selection DRG accuracy and variance impact Review inpatient documentation: H&P, Progress Notes, Operative Notes, Discharge Summary Ensure compliance with: ICD-10-CM / ICD-10-PCS guidelines Coding Clinic CMS IPPS rules...

Proziod Analytics is looking for Data Analyst -2 to join our team Roles and Responsibility Design, develop, and implement automated tests for complex software applications. Collaborate with cross-functional teams to identify and prioritize testing requirements. Develop and maintain test automation frameworks and tools. Analyze and report defects found during testing. Participate in agile development methodologies and collaborate with developers to resolve issues. Continuously improve testing processes and procedures. Job Requirements Strong knowledge of automation testing principles and methodologies. Experience with test automation frameworks and tools such as Selenium or Appium. Excellent ...

Job Responsibilities : Inspection of received samples and identifies the in-coming samples and segregates to different groups as per the testing requirementmunicate to shift in charge for abnormal samples or non-receipt of samples Inspection of received finished product samples, distribution of finished product sample to the different sections of the laboratory Analysis of finished product and carry out the complete analysis as per contractual methods and specifications and ensure effective sample management Carry out required tests as per provided standard test methods Detect exceptions or deviations in test results and report to Shift In charge immediately Actions/ communication on re samp...