2277 Capa Jobs - Page 45

Perform NDT inspections using certified methods (e.g., UT, RT, MT, PT, VT) according to approved procedures. Evaluate, interpret, and report test results with accuracy and technical clarity. Ensure that NDT activities comply with relevant standards such as ASNT, ISO, ASME, API, or customer-specific requirements. Prepare and maintain NDT reports, records, and documentation in a timely manner. Assist in the development and review of NDT procedures and techniques. Ensure NDT equipment is properly maintained, calibrated, and used correctly. Report any non-conformances or defects and participate in root cause analysis as required. Collaborate with engineering, production, and quality teams to res...

•Ensure timely completion of Product/Raw Materials analysis and timely release of RM/PM/ Finished Goods in SAP. •Ensuring achievement of production targets as per the HACCP, FSSC 22000 - product quality, hygiene, GMP, PRP and food safety etc.

Designation - Sr. Executive / Asst. Manager - Quality Assurance Company - Leading Pharma Raw Material Mfg. Company Job Location - Ahmedabad Qualification - B.Sc. / M.Sc. / B.E.- Chemical / B.Pharm Experience - Min. 6+yrs. and above Required Candidate profile Company coming up with Greenfield Project Responsible for handling QA / GMP Related documentation QMS, Audit Preparation, Vendor Questionnaire, Market Compliant & Customer Compliance

About the Role: We are looking for a proactive and technically skilled Quality Assurance Engineer to join our manufacturing team focused on industrial machinery and machine tools . The ideal candidate should have hands-on experience in mechanical inspection, quality systems, and problem-solving within a precision engineering or heavy equipment environment. Key Responsibilities: Perform incoming, in-process, and final quality inspections of mechanical parts, subassemblies, and finished equipment. Utilize measuring instruments such as vernier calipers, micrometers, height gauges, bore gauges, and CMMs . Interpret engineering drawings and GD&T standards to validate part accuracy. Document and m...

Job Summary: As a Senior Electrical Engineer with a valid license, you will be responsible for designing, developing, testing, and managing the installation and maintenance of electrical systems, equipment, and devices. Your primary focus will be to ensure compliance with safety standards, enhance energy efficiency, and troubleshoot electrical issues to ensure seamless operational continuity. You will play a crucial role in planning, scheduling repairs and maintenance, and guaranteeing continuous production operations. Collaborating with maintenance and production staff, you will develop preventive maintenance plans and execute them effectively. Your expertise should include working experien...

As a Document Management Specialist in the sterile manufacturing department, you will be responsible for various crucial tasks. Your primary duties will include managing documents such as BMRs, BPRs, and master SOPs. You will be in charge of preparing and reviewing master production documents and ensuring the Unit Area File (UAF) is functioning correctly in the designated area. Additionally, you will handle change control processes, deviations, investigations, and CAPA activities. Providing training to subordinates, technicians, and operators within the department will also be a key aspect of your role. It is essential to perform any activities assigned by the Head of Department (HOD) beyond...

As a Clinical Nurse 2 in the EC Other Surgery Services department at UC San Diego Health, you will be part of a Magnet designated organization, recognized for nursing excellence. Your autonomous nursing care skills will be crucial in assessing and providing appropriate nursing actions for patient care populations. You are expected to practice autonomously in alignment with ANA Standards of Practice and Professional Performance, exercising independent judgment within interdisciplinary and multidisciplinary patient care approaches. You will need to be a graduate from an accredited school of nursing with a Registered Nurse (RN) license issued by the State of California. ACLS certification is re...

The role involves ensuring CGMP compliance and supervising overall production activities of the manufacturing area of multiple assigned manufacturing lines. Additionally, the position requires reviewing and maintaining online documents. You will be responsible for the preparation, review, revision, control, and implementation of standard operating procedures. You will also handle the preparation and review of master production documents, protocols, reports, and various document management tasks such as BMRs and BPRs. Your duties will include managing Change Control, Deviations, CAPA, Investigations, and ensuring line clearance activities are conducted before operations like manufacturing, fi...

We are seeking a motivated and detail-oriented Injectable Plant Compliance Manager to join our team. The ideal candidate will be responsible for ensuring compliance with all regulatory requirements and industry standards specific to the production of injectable pharmaceutical products. This role will serve as a key leader in maintaining quality assurance, overseeing audits, and implementing compliance systems to ensure the safety and efficacy of our products.

supplier quality, Overall quality & quality control, ISO, CAPA, PPAP, APQP, FMEA, MSA, SPC, Six sigma methodologies, NPD, Immediate join, Auto preferred, auto components manufacturing company experience, TS, Supplier comply

Role & responsibilities Preferred candidate profile

Roles and Responsibilities Conduct quality audits, inspections, and testing of electrical panels, control panels, switchgear products to ensure compliance with IEC standards and ISO 9001:2015. Develop and implement quality plans, procedures, and SOPs for incoming quality control (IQC), internal process quality control (IPQC), final product inspection (FQI), and supplier quality assurance. Perform root cause analysis (RCA) investigations on defective products or non-conformities using tools like 7 QC Tools. Collaborate with cross-functional teams to identify areas for improvement through kaizen events and implement corrective actions through CAPAs. Ensure timely completion of NCR reports and ...

Job Description Manager Quality (QA & QC) Position: Manager Quality (QA & QC) Location: Taloja Manufacturing Site Reports To: Senior Management / Plant Head / Director Quality Department: Quality Assurance & Quality Control About KCIL Specialty Chemicals KCIL Specialty Chemicals is one of Indias leading chemical manufacturing companies with a strong legacy of innovation, quality, and sustainability . With a robust turnover of 350 crores and ambitious plans to reach 500 crores in the next 4 years, KCIL is rapidly expanding its footprint in the specialty chemicals sector. We operate from 5 strategic manufacturing locations in Taloja , supported by state-of-the-art infrastructure that ensures h...

The role involves handling document issuance, distribution, and retrieval, including verification of various documents such as Batch Manufacturing records, Protocols, layouts, specifications, etc. Issuing approved Standard Formats and Logbooks to User Departments, as well as managing line-clearance checklists, interventions checklist, and BMR/BPR pages. Additionally, handling proposed changes per the change control procedure, assessing associated risks/impacts, and ensuring the implementation of action plans. Conducting investigations using root cause analysis tools, performing additional studies, and deriving appropriate CAPA. Managing recommended CAPA and evaluating the implementation of r...

As a Quality Assurance Specialist, your responsibilities will include reviewing all Master Production and Control Record (MPCR) and Batch Packing Records (BPR), as well as Standard Operating Procedures (SOPs). You will need to meticulously review specifications and testing procedures for starting materials, packaging materials, in-process products, finished products, working standards, and stability (Shelf life). Additionally, you will be tasked with reviewing Out-of-Specification (OOS) investigation reports and participating in investigations related to complaints, vendor audits, external testing laboratories audits, and the subsequent Corrective and Preventive Actions (CAPA). You will also...

As a Senior Manager in the Engineering and Projects department at Sun Pharmaceutical Industries Ltd, located in Dewas SGO - Engineering Block P, your role as the Engineering Penem Head involves overseeing various engineering and maintenance activities. With over 15 years of experience and a B.E. in Electronics, you will be responsible for managing activities related to Block P (Sterile), Block F (OSD), Supporting Facilities (Micro/Stability, QC, Warehouse, and Export Warehouse), as well as the external area. Your responsibilities include maintaining and managing the expenses within the budget, reviewing and implementing preventive maintenance, facility maintenance, and calibration systems ef...

The Full Stack Developer position at ClinRT Global Services in Pune requires a minimum of 2 years of experience in Angular and .NET core. ClinRT is committed to revolutionizing clinical trials through its Interactive Response Technology (IRT) platform, aimed at enhancing efficiency, accuracy, and compliance in drug development. As a trusted partner to pharmaceutical companies, researchers, and healthcare professionals, ClinRT streamlines patient interaction, randomization, drug supply management, and data management for a seamless clinical trial process. The Clinical QA Manager role involves overseeing the quality of activities related to the IRT platform used in clinical trials developed by...

As a Senior Manager in R&D Quality (Pharmacovigilance Quality Assurance) at Sun Pharmaceutical Industries Ltd in Gurgaon, your primary responsibility will be to implement a well-defined Quality Assurance program in compliance with regional and global regulatory requirements, SOPs, and company policies. You will play a key role in developing and executing global Pharmacovigilance auditing programs, ensuring adherence to established Quality Systems. Your duties will include conducting audits at Sun Pharma sites associated with Pharmacovigilance activities, as well as auditing outsourced parties, affiliates, and partners involved in Pharmacovigilance operations. You will manage the Internal Aud...

1. QA Executive Junior Level Experience Required: 24 years Salary Offered: 20,000 per month Job Summary: We are seeking motivated QA Executives with 24 years of experience to support daily quality assurance activities in a GMP-regulated pharmaceutical facility. The role will focus on documentation review, QA activities, and ensuring compliance with regulatory standards. Key Responsibilities: Review batch manufacturing and packing records Line clearance for production and packaging activities Support in handling deviations, change controls, CAPA, and incident reports Ensure compliance with cGMP and Revised Schedule M requirements Participate in in-process checks and quality monitoring Assist ...

You will be responsible for leading the deployment and optimization of Quality Management System (QMS) processes as a Subject Matter Expert (SME) for Veeva Vault QMS. Your main focus will be on ensuring compliance, efficiency, and user adoption by utilizing your deep domain expertise in QMS processes within the life sciences or pharmaceutical industry. Your key responsibilities will include serving as the SME for Veeva Vault QMS, leading deployment, configuration, and optimization efforts. You will need to understand existing QMS processes and workflows, identify areas for improvement, and work closely with stakeholders to gather requirements. Additionally, you will design, implement, and re...

IMEA (India, Middle East, Africa) India LIXIL INDIA PVT LTD Employee Assignment Not remote Full Time 1 August 2025 Dealer network sales-managing & appointing new sub-dealers in a given territory by completing all formalities, Regularly meeting and developing relationships with Architects, Builders, interior designers, etc to generate inquiries and close sales, Achievement of targeted sales volumes through Retail & Distribution Sales Procurement of orders from dealers and timely supply thereon, Work in coordination with the marketing team for proper and timely display, Conducting Architect & plumber meetings to promote the products, Informing management about the competitors strategy and pric...

We are Hiring for Automation/ Machine Maintenance Experience and Education: Diploma with Electrical & Electronics/ Electronics & Communication/Mechanical/ Mechatronics with 2~6 years of Experience Engineering with Electrical & Electronics/ Electronics & Communication/Mechanical/ Mechatronics with 1~3 years of Experience Preferred with Electronics Manufacturing Industries, Automation Service Support team & Auto Electric Manufactures Work Experience in Automations, Continuous Process Equipment, Robotic interface Machines. Knowledge and Skills: Capable to Understand the Machine Process and Application Capable to Understand the Electrical, Pneumatic Devices & Circuits Knowledge in 5S and Kaizen ...

Treasury Treasury at Deutsche Bank is responsible for sourcing, managing, and optimizing Deutsche Bank's financial resources and providing high-quality steering to the Bank on financial resource deployment. Treasury's fiduciary mandate encompasses the Bank's funding pools, asset and liability management (ALM), liquidity reserves management, and supporting businesses in delivering their strategic targets at the global and local levels. Further, Treasury manages all financial resource optimization to implement the group's strategic objective and maximize long-term return on average tangible shareholders' equity (RoTE). The current role is part of the Treasury Office in Mumbai. The position req...

To ensure the 5S & Safety in the respective area To assure the quality during production as per Product Specification on drawings SOP through first piece inspections & inprocess inspection To handle the internal customer complaints & submit the CAPA Required Candidate profile •To handle the internal customer complaints & submit the CAPA accordingly. •To implement & maintain the documentation as per the requirements. •Calibration plan of IMTE & Standard Operating Procedure

Key Responsibilities: Lead the implementation, maintenance, and enhancement of the Quality Management System as per ISO 13485:2016 and relevant international standards. Manage and oversee the Corrective and Preventive Action (CAPA) system, ensuring timely investigation, root cause analysis, and closure. Plan, schedule, and conduct internal audits across departments; coordinate and support external audits by customers, certification bodies, or regulatory authorities. Evaluate and resolve non-conformances (NCs), manage deviation records, and ensure corrective measures are implemented effectively. Collaborate with cross-functional teams to drive quality improvements and process compliance acros...