837 Capa Jobs - Page 8

Hiring for a manufacturing company. Position: QA Engineer Location: Vadodara Qualification: BSc/MSc (Chem)/BE (Chem) Experience: 2-6 years Role & responsibilities: • Ensure regulatory and chemical compliance with applicable international and domestic standards. Experience in QMS Documentation & Compliance. • Coordinate testing activities with third-party laboratories, including test planning, sample submission, and result interpretation. • Monitor, track, and document compliance status across all relevant products and materials. • Participate in and support 2nd party (customer) and 3rd party (certification/regulatory body) audits, including audit readiness and follow-up actions. • Maintain and update compliance documentation, certifications, and technical files. • Collaborate cross-functionally with R&D, Procurement, and Production to ensure compliance is integrated into the development and manufacturing processes. • Identify risks or non-conformities related to compliance and drive timely corrective and preventive actions (CAPA). • Stay updated on regulatory changes and industry best practices to ensure ongoing adherence. • Understanding of PDOC, GONOGO, IKEA Connect. • Candidates from companies who supply to IKEA will be preferred. Interested candidates share resume on zalak.rohit@cielhr.com

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 end. Perform data analysis of quality rejection reports to identify trends and drive improvements. Support in QMS ISO 9001:2015 compliance and contribute to internal audits (preferably an ISO 9001:2015 Internal Auditor certified). Manage and verify Raw Material Test Certificates and coordinate with NABL-accredited labs for material testing. Maintain and execute calibration schedules for measuring and inspection equipment as per the calibration plan. Apply quality tools such as Statistical Quality Control (SQC) , Failure Mode and Effects Analysis (FMEA) , and Control Plans in the QA process. Use MS Office tools (Word, Excel, Outlook, PowerPoint) for documentation and reporting. Preferred candidate profile Skills and Abilities Strong knowledge of quality inspection techniques and tools. Proficiency in interpreting mechanical drawings and specifications. Familiarity with ERP systems for quality documentation. Understanding of ISO 9001:2015 QMS and audit procedures. Good analytical and problem-solving abilities. Basic computer proficiency in MS Office. Attention to detail and commitment to continuous improvement. Effective communication and coordination skills, especially with suppliers and cross-functional teams. Education and Experience Bachelors degree in mechanical engineering or a related field. 2–3 years of experience in quality assurance preferably in a submersible pumps and motors manufacturing industry / precision engineering / components manufacturing

Role & responsibilities Ensure regulatory and chemical compliance with applicable international and domestic standards Coordinate testing activities with third-party laboratories, including test planning, sample submission, and result interpretation. Monitor, track, and document compliance status across all relevant products and materials. Participate in and support 2nd party (customer) and 3rd party (certification/regulatory body) audits, including audit readiness and follow-up actions. Maintain and update compliance documentation, certifications, and technical files. Collaborate cross-functionally with R&D, Procurement, and Production to ensure compliance is integrated into the development and manufacturing processes. Identify risks or non-conformities related to compliance and drive timely corrective and preventive actions (CAPA). Stay updated on regulatory changes and industry best practices to ensure ongoing adherence. Understanding of PDOC, GONOGO, IKEA Connect. Preferred candidate profile Candidates from companies who supply to IKEA will be preferred.

Doing inspection of electric parts.

RoleKMIL - Monitoring Requirement2 Gender- Male/ Female both are preferred Education Background- CA / MBA (preference would be MBA- Finance) Experience level - 3 to 5 years (relevant experience not required) Preferred profile- Risk team of retail or wholesale division of any Bank / NBFC. The Key profile of Monitoring & Policy Risk Analyst is to carry out Risk Assessments for Pan India CRE Lending Portfolio is laid down below for your reference . Key responsibilities include Implement effective risk management processes for the Construction Finance business verticals to identify potential risk in the underwritten portfolio and ensure portfolio health Carry out background research and gain a thorough understanding on the project, the developer and the regional market, highlighting any negative reports so as to ensure the quality of the invested portfolio. Track the progress of the project and monitor disbursement as per the project lifecycle. Ensure that the disbursement milestones are achieved as per the underwritten sanctioned conditions. Recommend policy amendments/ refinements based on regulatory and market changes Undertake automation of existing processes by liaising with the IT department Prepare various dashboards and reports such as Monthly and quarterly portfolio monitoring report Overdue Analysis Early Warning Signals r eview Deviation Analysis Analytical Insights like Limit/ Renewal Management, Covenant/ PDD Management Trends analysis of the regional P ortfolio Perform various monitoring activities such as NOC issuance- Due diligence for the Monitoring and instruct for Escrow SI Threshold Map collections with the Escrow credits on regular intervals.

Role & responsibilities To review that all relevant quality management systems of Hosur manufacturing site are implemented and well maintained. To review, monitor and improve Quality performance of Hosur manufacturing site. To promote quality attitude, awareness, and mindset of the site by all proper means including training to the cross functional team members. Implement, audit, and develop quality management system, in line with Global quality policy/ manual and procedures relevant to area. Ensure the required process controls are in place wherever they are necessary. To review that testing and inspection of all raw materials, packaging materials and finished goods are carried out as per documented testing procedures and specifications. To review that the release of all raw materials, packaging materials, bulk as per approved SOP before they are used for further production activities. To review the release process of all finished goods as per approved SOP and global requirements including GFS before they are released for distribution. To review all RM and PM used in manufacturing process are from approved suppliers and with the required quality before it reaches Hosur manufacturing site including COA verifications against the documented specifications. To review all the internal lab/ External labs are conducting the testing processes as per the documented procedures and specifications. Ensure appropriate investigation are carried out throughout the manufacturing site in case of any quality related issue and ensure the corrective and preventive actions are implemented to mitigate the identified root causes for the quality issue. Ensure the preparation of training calendar and adherence to the same. To support and conduct self-inspection quality audits across all the QMS areas and continuously improve the QMS implemented at site. To ensure that all audit points/recommendations highlighted in the audit reports are followed up and closed effectively as per the agreed timelines. Review the performance of suppliers on a regular basis. To support all key initiative at the site as key member of the site. To support the site in conducting management review meetings as per the schedule. To accept and execute other responsibilities assigned by the management time to time.

( Team Member - Customer Service) Responsible to provide adequate and quick resolution to all the cases assigned Analyze the complaint trend and present to the senior management Preparing RCA ,Monitoring the cases and initiating corrective action Liaise up and coordinate with business stakeholders to close the cases end to end Job Requirement: Banking knowledge is must (Loan division knowledge is preferred) Good Communication skill (Verbal & Written) Microsoft office hands-on knowledge (Excel/Powerpoint/Word etc.) Graduate n above Min. experience of 5 years n plus

( Team Member - Customer Service) Responsible to provide adequate and quick resolution to all the cases assigned Analyze the complaint trend and present to the senior management Preparing RCA ,Monitoring the cases and initiating corrective action Liaise up and coordinate with business stakeholders to close the cases end to end Job Requirement: Banking knowledge is must (Loan division knowledge is preferred) Good Communication skill (Verbal & Written) Microsoft office hands-on knowledge (Excel/Powerpoint/Word etc.) Graduate n above Min. experience of 5 years n plus

Job Title:- KMIL- Wholesale Banking- Risk Monitoring Analyst Grade:- M4/M5 Location:- Mumbai Track financial and project performance covenant: Monitoring financial and project performance against predefined convenants. Identify deviations and promptly communicate findings to relevant stakeholders. Project performance analysis: Conduct through analysis of project performance metrics. Provide insights and recommendations to mitigate risks. Track Compliances to sanctions conditions: Moniotor compliance with sanctions conditions imposed on credit facilities. Take proactive measures to address any non- compliance issue Site Visit: Conduct on site visit to assess the progress and status of projects. Documents observations and report findings to management Compliance with RERA regulations: Ensure adherence to regulatory guidelines and internal policies. Stay updated on regulatory changes and implement necessary adjustments. Early warning signal tracking: Identify early warning signal as per the existing policy indicating potential credit risks. Collaborate with relevant teams to develop strategies for risk mitigation. Coordination with business and credit underwriting team Liaise with business units and credit underwriting teams to gather relevant data and insights. Collaborate on credit risk assessment and monitoring activities. Job Requirement- MBA with 5 to 8 Years of experience is preferred

The Quality Control Engineer will be responsible for developing and implementing quality control processes for metal parts. This includes inspecting products, testing materials, conducting audits.

ISO/IEC 17025-accredited laboratories. e quality assurance support for our U.S. lab, including document review, internal audits, CAPA management. to mentor train a junior QA professional located onsite in our U.S. laboratory.

You will be responsible for performing wet lab testing and maintaining lab compliance in order to ensure the accuracy and integrity of analytical data. Your key responsibilities will include implementing SOPs and STPs accurately, analyzing samples and recording results, preparing and maintaining reagents and standards, storing control samples with proper documentation, and calibrating laboratory instruments as per schedule. You will also be expected to operate and maintain wet lab instruments, assist in the investigation of deviations and complaints, supervise the cleaning and upkeep of glassware, perform product sampling and analysis, and support in the preparation of specifications and STPs under senior guidance. Additionally, you will review QC documents and records for completeness and accuracy, as well as execute any other tasks assigned by seniors or departmental heads. The ideal candidate for this position should have an MSc in Chemistry and 1-4 years of experience in quality control. It is essential to possess skills in GLP, CAPA, and handling laboratory instruments effectively.,

As a Chemical Lab Officer at Sarigram, you will be responsible for conducting various analytical tasks related to organic, inorganic, and analytical chemistry. With 3-5 years of experience and an MSc in Chemistry, your role will involve performing wet analysis, titration of inorganic materials including acid-base and complexometric titrations, as well as balancing chemical equations. You should also possess the ability to calibrate instruments and demonstrate innovative thinking in problem-solving. Your responsibilities will include the preparation of standard solutions, maintenance of Raw and Rough lab registers, and carrying out instrumental methods of analysis such as Flame Photometry, Refractive Index, and Gas Liquid Chromatography (GLC). Additionally, you will be required to create Certificate of Analysis (COA), specifications, Corrective and Preventive Actions (CAPA), Quality Assurance (QA) documents, Standard Operating Procedures (SOP), Batch Manufacturing Records (BMR), and ensure compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). Effective communication skills are essential as you will be handling email correspondence and interacting with various departments. Proficiency in Microsoft tools such as Word, Excel, and PowerPoint is mandatory. A flexible mindset for multitasking will be advantageous in this role to meet the dynamic requirements of the laboratory environment. Overall, as a Chemical Lab Officer, you will play a vital role in maintaining high-quality standards, ensuring accurate analysis, and contributing to the overall success of the laboratory operations.,

Job Summary As a qualified candidate, you will be leading the Quality Assurance, QC Chemistry and Microbiology Laboratories for the site. Your role will involve developing Standard Operating Procedures (SOPs), ensuring compliance with current Good Manufacturing Practices (cGMP) and regulatory guidelines, and monitoring day-to-day department activities. Responsibilities include reviewing and approving documents, executing in-process controls, participating in investigations, vendor qualification, stability management, and ensuring safety practices. Roles & Responsibilities You will be responsible for organizing the recruitment and training of QA (Quality Assurance) and laboratory personnel for chemistry and microbiology laboratories. You will ensure adherence to systems and procedures by all QA and laboratory personnel. You will be responsible for organizing contract laboratory audits and certification. You will formulate systems and procedures for the effective implementation of cGMP, GLP (Good Laboratory Practices), and other industry practices and regulations for the manufacture, storage, and distribution of drug products. You will plan and monitor the daily activities of different sections of the department, ensuring the availability of required facilities and materials for daily functions. You will ensure timely review and approval of all Master documents, such as SOPs, guidelines, production records, specifications, validation protocols, and other necessary reports/documents. You will be responsible for proper sampling of in-process and finished products, management of reserve and stability samples, and collection of finished products. You will oversee the execution of in-process controls and checks during manufacturing and packing. Your role includes reviewing and releasing/rejecting finished drug product batches, evaluating product recalls, monitoring quantity and disposition of recalled/returned material. You will participate in investigations, providing suitable Corrective and Preventive Actions (CAPA) to prevent recurrence. You will review, approve, and implement CAPA for incidents, change controls, Out of Specifications (OOS) and Out of Trends (OOT) observations. You will manage vendor qualification, material management, vendor audits, stability management, and field alerts as required. As a qualified trainer, you will implement training programs, ensure compliance, and provide training on cGMP and SOPs. You will ensure compliance with CAPA for deficiencies noted in self-inspections, internal audits, and external audits. Your responsibilities include preparing and approving Annual Product Quality Reviews, reporting Adverse Drug Reactions, and ensuring departmental adherence to safety practices. You will also be responsible for ensuring the safety, strength, purity, and efficacy of the product, along with any other assignments from higher management. Qualifications Educational qualification: An M. Pharm/M.Sc. with experience in Sterile products. Minimum work experience: 15 to 20 years. Skills & Attributes Technical Skills Experience in recruitment and training of QA and laboratory personnel in Chemistry and Microbiology laboratories. Experience in establishing systems and procedures for cGMP, GLP, and other industry practices. Experience in handling investigations, audits, and implementing resulting CAPAs. Skills in vendor qualification, audits, and material management. Behavioural Skills Effective leadership and organizational skills for managing laboratory personnel and operations. Detail-oriented mindset for thorough review and approval processes. Strong communication and collaboration skills for audits, investigations, and compliance activities. Commitment to safety practices and reporting Adverse Drug Reactions. Additional Information About the Department Global Manufacturing Organisation (GMO) Dr. Reddy's Laboratories is dedicated to making an impact on global healthcare through precision manufacturing and innovation. With 19 state-of-the-art manufacturing plants across multiple locations, we are a leading force in the pharmaceutical industry. Our capability to deliver quality medicines to patients in 66 countries is driven by benchmarking manufacturing processes and operational excellence. Benefits Offered At Dr. Reddy's, we prioritize your career growth and professional development through personalized learning programs. Our benefits are designed to meet industry standards, including joining & relocation support, family benefits, learning opportunities, medical coverage, and life coverage. Our Work Culture At Dr. Reddy's, our employees are guided by the principle of "Good Health Can't Wait." We see healthcare solutions as a means to help patients lead healthier lives. Our work culture fosters empathy, dynamism, and teamwork, empowering individuals to make a meaningful impact on global healthcare. Visit our career website at [Dr. Reddy's Careers](https://careers.drreddys.com/#!/) for more details.,

As a Quality Control Manager in the CRGO steel manufacturing industry, your primary responsibility will be to develop and implement quality control systems to ensure compliance with national and international standards such as IEC 60404, ASTM A876, and ISO 9001. You will be tasked with monitoring and controlling key process parameters to maintain consistent product quality. Additionally, you will oversee raw material, in-process, and final product inspection, as well as supervise mechanical, electrical, and magnetic property testing. Your role will also involve maintaining detailed QC documentation, preparing quality KPIs and reports for management, and leading, training, and mentoring the QC team. You will be required to conduct performance reviews, coordinate with other teams such as production, maintenance, and R&D, and drive continuous improvement initiatives through methodologies like Six Sigma and Lean. To excel in this role, you should possess in-depth knowledge of CRGO manufacturing and testing standards, familiarity with lab instruments like Epstein Frame and Single Sheet Tester (SST), and strong analytical and problem-solving skills. Proficiency in quality tools such as SPC, FMEA, 8D, CAPA, and ISO systems is essential, along with leadership and team management abilities. Excellent communication and reporting skills are also crucial for effectively handling customer quality audits, liaising with certification bodies, and ensuring traceability and lot-wise quality assurance. In terms of qualifications, a Bachelors or Masters degree in Metallurgy, Materials Science, Mechanical, or Electrical Engineering is required, along with a minimum of 8-10 years of experience in Quality Control, preferably with at least 5 years in the CRGO or a similar electrical steel industry. Holding a Certified Lead Auditor certification for ISO 9001 and ISO 14001 would be advantageous for this position.,

You will be responsible for initiating, reviewing, and approving various quality management systems such as Change Controls, Deviations, Investigations, CAPA, OOS, and Complaints. You will also handle Return Goods and ensure the smooth functioning of the quality system by performing risk assessments as required. Conducting regular internal audits and reviewing/approving all documents including SOPs, Spec & STPs, Forms, protocols, and reports will be part of your duties. Additionally, you will review annual product quality review reports, provide training on cGMP topics to employees, and support customer audits/visits as well as regulatory audits. You will assist in providing necessary documents for amendments, annual updates, regulatory filings, and CMC supporting documentation. Other tasks may include filling out questionnaires, declarations, quality agreements, and executing any additional responsibilities assigned by the Head of Department.,

Independently handling All Quality aspects Must handled IATF & ISO Audits Making all required Documents Maintaining Records Provide Training & Development QMS Customer Handling Fire, Safety, Plant, Manpower, etc. Take Internal & External Audits Required Candidate profile Preferring Candidates who had handled entire quality related One from Aluminum Alloys manufacturing and other from HPDC manufacturing.

Job Title: Assistant Manager CNC Maintenance Department: Engineering / Maintenance Location: Mumbai Reports To: Manager & Senior Manager - Maintenance Qualification: B.E./B.Tech Mechanical / Electrical / Mechatronics Experience: 5+ years in CNC maintenance (preferably in manufacturing, precision engineering, or tooling environment) Job Purpose: To ensure optimal performance, uptime, and reliability of CNC machinery through preventive and corrective maintenance, supporting uninterrupted production and minimizing downtime. Key Responsibilities: • Maintenance Planning & Execution: 1. Plan and execute preventive, predictive, and breakdown maintenance for CNC machines (e.g., VMC, HMC, turning centers, wire-cut, EDM). 2. Maintain and update maintenance logs, history cards, and service records. • Troubleshooting & Repairs: 1. Diagnose mechanical, electrical, and PLC faults on CNC machines. 2. Coordinate with OEMs and vendors for complex issues and spare part procurement. • Performance Monitoring: 1. Monitor machine performance using TPM/OEE metrics and take corrective actions. 2. Conduct root cause analysis (RCA) for frequent or major breakdowns and implement CAPA. • Process & System Improvement: 1. Support upgrades or retrofits of CNC equipment. 2. Recommend improvements for energy efficiency, machine life, and tooling compatibility. • Team & Compliance: 1. Guide and train junior technicians. 2. Ensure adherence to safety, 5S, and ISO/TPM/Lean practices in the maintenance area. Key Skills & Competencies: • In-depth knowledge of CNC machine operations, controls (Fanuc, Siemens, Mitsubishi), and mechanics. • Hands-on experience with hydraulic, pneumatic, lubrication, and electrical systems. • Familiar with TPM principles, maintenance KPIs, and continuous improvement methodologies. • Good communication and vendor coordination skills. • Analytical mindset with problem-solving abilities. Desirable Qualifications (Optional): • Certification in CNC programming or maintenance. • Exposure to Industry 4.0 tools or CMMS systems

We are looking for a seasoned and meticulous Quality Manager to oversee and enhance the Quality Management System (QMS) of our Clinical Diagnostic Laboratory in alignment with ISO 15189:2022 standards and NABL accreditation requirements. Required Candidate profile M.Sc/B.Sc. in Medical Laboratory Technology, Biochemistry, Microbiology.Exp 5–10 yrs in a NABL-accredited diagnostic laboratory, 3 yrs in a quality management role. Perks and benefits Competitive Salary and Benefits

To head and manage overall Quality function of the plant.

Role & responsibilities Lead and manage Incoming (IQC), In-Process (PQC), and Final Quality Control (FQC) processes. Interface with customers, vendors, and cross-functional teams for quality audits, inspections, and approvals. Champion Root Cause Analysis (YY analysis) and drive implementation of effective Corrective and Preventive Actions (CAPA). Ensure compliance to Defense and Aerospace quality standards in design, development, and manufacturing stages. Maintain and continuously improve QMS documentation including SOPs, work instructions, inspection reports, and quality plans. Lead internal and external quality audits, certifications, and statutory compliance. Facilitate cross-departmental coordination for issue resolution and process improvements. Present quality metrics, dashboards, and improvement initiatives to the Managing Director and Senior leadership. Contribute to product and process improvement initiatives, particularly in projects related to Telescopic Masts, Positioners, Tripods, and Power Electronics. Key Skills and Competencies: - Strong understanding of Ok-Ok analysis, and critical inspection points. Solid grasp of ISO/AS9100, ISO 9001 , and other relevant Defense/Aerospace Quality Systems. Proficiency in technical documentation, SOP creation , and QMS tools. Excellent communication, presentation , and stakeholder management skills. Hands-on experience with machining, sheet metal, electronic assembly, and system integration is preferred. Familiarity with defense and Aerospace manufacturing protocols, audit processes , and engineering documentation standards . Desired Candidate Profile: 15+ years of progressive experience in Quality Assurance & Control in Aerospace or Defense manufacturing . Demonstrated capability in leading quality functions , including audits, documentation, and compliance. Experience working directly with customers, OEMs, and defense procurement teams . Should be self-driven, detail-oriented, and possess strong problem-solving and analytical skills.

Q Team Member Job Type: Contractual Job Location: Pan India Experience: +1 years Profile Summary: Ensure the quality of training Center and Hostel operations. Their duties include developing and implementing quality control tests, inspecting at various stages and writing reports. The ideal candidate is an exceptionally organized, methodical professional with the experience necessary to take our project to the next level with respect to accuracy, security, and safety. Job Responsibility: Share inspection report and advisories with SRLM/CTSA Carry out the inspection Follow up for compliance supervising the process and make sure to meet standards monitoring all the operations for center coordinating with center manager Document quality assurance activities Develop new standards, with improvements as needed Skills: E SOP certified ms office Min. Education: Graduate Apply Job Type: Contractual Job Location: Pan India Experience: +1 years

Role & responsibilities Requirements: QC Qualification: B.sc (Chemistry) Total Experience: 2-5 years in QC Dept. He should be ready to Travel/visit frequently anywhere in India at Customer locations to attend Customer Complaints and resolve issues, individually. He should be ready to visit our all India 20Microns plants QC and capable for new implementation in QC System as per requirements. He should be capable for problem solving techniques, Root Cause investigation of product failures and CAPA System. Sound knowledge of all types of documentation related to QC. Proficient/fluency in English language. Skills for Microsoft Word, Microsoft Excel & PowerPoint Presentation. He should be ready for Multiple task. Preferred candidate profile

Role & responsibilities (Production): Assist in manufacturing operations of parenteral dosage forms (sterile injections) as per SOPs and GMP guidelines. Monitor and record process parameters during manufacturing and filling operations. Ensure compliance to cGMP, documentation and data integrity norms. Support continuous improvement initiatives in production efficiency and compliance. Role & responsibilities (Engineering): Assist in preventive maintenance and breakdown handling of production equipment Support engineering team in equipment qualification and calibration activities. Monitor Utility systems Maintain proper documentation as per GMP norms. Follow safety protocols and support new initiatives Preferred candidate profile Basic knowledge of sterile/aseptic manufacturing / pharma production equipment Interest in plant maintenance Willingness to work in shifts & controlled environment Good documentation and communication skills Attention to detail and compliance mindset Good observations and analytical skiils

Incoming material quality mgt Continuous improvement in product/process quality CAPA on defects/customer complaints Supplier selection, qualification, development, Performance Mgt/audits Calibration Implement QMS & Improvement at supplier place Required Candidate profile Quality Exp in Machining, Sheetmetal, Welding, Painting & Special Processes-Plating, Galvanizing, Anodizing Ready & Interpret STANDARDS & drawings Data driven Certified Auditor - ISO / IATF SPC & SQC Perks and benefits Exp in IQC in Machine Building/Mechanical Ind MUST