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1476 Capa Jobs - Page 39

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10.0 - 15.0 years

10 - 15 Lacs

Bengaluru, Karnataka, India

On-site

Responsibilities: Responsible for supplier & product development of wind farm site WTG lifting and assembly tools involving mechanical, hydraulic, and electrical systems for operator effort reduction Manage supplier quality across life cycle management and resolve issues in a timely manner Handle global/regional suppliers and address defects/issues using quality tools such as 8D/CAPA and process claims based on Envision procedures Collaborate with the product development quality engineering team to identify potential risks and implement mitigation plans Introduce and qualify best-fit new suppliers according to Envision quality requirements for both Indian and international business Manage su...

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10.0 - 15.0 years

12 - 16 Lacs

Bengaluru, Karnataka

Work from Office

Knowledge in quality documentation quality plans PPAP Documents MSA, SPC, Etc. Should have exposure in QMS 9001, EMS-14001, Welding standards -15085,3834. Should conduct process audit, Product audit internal audit & MRM & report to management. Having Good Exposure in customer Complaints Handling & Corrective and Preventive Actions. All In-house rejection analysis and taking CAPA. Closure of CAPA with production team IWE or IWT certificate, heavy engineering or fabrication 10+ years of experience in heavy fabrication engineering companies.

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5.0 - 10.0 years

3 - 8 Lacs

Pune

Work from Office

Dear candidate Hiring for the following requirements with Engineering& Manufacturing industry 1)Maintenance Head/Manager 2)Tool Crib Engineer 3)Production Engineer 4) Maintenance Engineer 5)Quality Engineer 6)CMM Engineer 1) Maintenance Manager (1 no.) (Exp- 12 to 20 yrs) (Qualification: Diploma Engg. or B.E/B.Tech) 1. Leading the Maintenance of the Machine shop (CNC Turning, VMC, HMC, Broaching, Grinding, etc.) 2. Developing and implementing maintenance strategies 3. Conducting routine maintenance checks 4. To check and attend trouble- shooting complex electrical problems and failures 5. Ordering and tracking spare parts and equipment 6. Strong understanding of Engineering principles and kn...

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3.0 - 8.0 years

5 - 9 Lacs

Alwar

Work from Office

Kindly share your resume on sv21@svmanagement.com Responsibilities: Engine assembly process/Product/Torque audit and ensure closer of NC with respective department Able to handle New Technology diesel engines Must have knowledge of Engine testing of advance technology engines as mentioned above Having capability of Engine failure analysis during engine testing Hands on experience on calculating Cp Cpk for torque joints and seal pressing joints Able to handle individual Engine assembly/testing line by own Analyzing engine failure root cause and solutions for resolution of concern Familiar with QMS system and able to maintain records and daily MIS generation Must be able to handle Internal/Ext...

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3.0 - 7.0 years

3 - 7 Lacs

Mumbai

Work from Office

Role Purpose The purpose o central quality analyst role is to conduct quality audits and perform analytics in different areas as defined by central quality team, supporting the project teams in ensuring higher client satisfaction Do 1. Conduct process quality audits as per plan Conduct various process audits as per guidelines and SPOs defined in QMS Prepare findings from the report and share it with the account/ project leadership on daily/ weekly/ monthly, as required Conduct weekly analysis to identify the error trends and for top 2 errors, conduct root cause analysis (RCA) Conduct calibration communication to communicate any changes from the client and conduct refresher trainings to bridg...

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4.0 - 8.0 years

4 - 7 Lacs

Pune

Work from Office

Role Purpose The purpose o central quality analyst role is to conduct quality audits and perform analytics in different areas as defined by central quality team, supporting the project teams in ensuring higher client satisfaction Do 1. Conduct process quality audits as per plan Conduct various process audits as per guidelines and SPOs defined in QMS Prepare findings from the report and share it with the account/ project leadership on daily/ weekly/ monthly, as required Conduct weekly analysis to identify the error trends and for top 2 errors, conduct root cause analysis (RCA) Conduct calibration communication to communicate any changes from the client and conduct refresher trainings to bridg...

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2.0 - 6.0 years

4 - 8 Lacs

Navi Mumbai

Work from Office

Job Overview To lead and execute analytical method validation, transfer, and verification activities in compliance with regulatory and cGMP standards, ensuring robust analytical support for product development, regulatory submissions, and commercial manufacturing. Competencies Plan, perform, and document Analytical Method Validation (AMV) and Analytical Method Transfer (AMT) for raw materials, intermediates, and finished drug products. Prepare and review protocols and reports related to method validation/verification/transfer in alignment with ICH guidelines. Coordinate with R&D, AR&D, QA, RA, and manufacturing units for method transfer and troubleshooting activities. Perform routine and non...

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2.0 - 3.0 years

1 - 5 Lacs

Ahmedabad

Work from Office

Nutrizo Advancis Healthcare Private Limited is looking for IPQA-Chemist to join our dynamic team and embark on a rewarding career journey Conduct in-process quality checks during manufacturing Ensure compliance with GMP and SOP standards Document results and report deviations Coordinate with QA and production teams

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3.0 - 10.0 years

10 - 11 Lacs

Gurugram

Work from Office

NAB is looking for Analyst to join our dynamic team and embark on a rewarding career journey Collect, analyze, and interpret data to support business decision-making and strategy development Identify trends, patterns, and insights through quantitative and qualitative research Prepare detailed reports, dashboards, and presentations for stakeholders Collaborate with cross-functional teams to understand data needs and implement solutions Ensure data integrity, maintain databases, and recommend improvements based on analytical findings Stay updated on industry trends, tools, and best practices to enhance data analysis and reporting capabilities

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0.0 - 5.0 years

1 - 5 Lacs

Mallapur, Hyderabad, Uppal

Work from Office

Dear Candidate, We are conducting walk-in drive on 27th June (Friday) for the positions in our Quality Assurance department. Job Description : Position Name: Fresher/Executive Experience - 0 -5 years Qualification - M.Sc Chemistry /M.Pharma Designation - Executive Walk-in Date: 27th June 2025 (Friday) Time: 09:00 AM to 12.00 PM Chemveda is hiring for Quality Assurance Executive Position Job Responsibilities :- 1. Involves in daily QA activities for SOP compliance. 2. Equipment and Software qualifications Review of USR & SRS, Review of IQ, OQ, PQ document inhouse softwares and maintenance of Equipment and software related back up coordination with other departments. 3. Preparation of refresh ...

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5.0 - 10.0 years

8 - 8 Lacs

Chennai

Work from Office

Role & responsibilities Conduct comprehensive fire safety audits and gap assessments across manufacturing and industrial plants in accordance with factory safety norms. Identify critical non-compliances and recommend corrective actions through structured Corrective and Preventive Action (CAPA) plans. Prepare detailed audit reports, executive presentations, and compliance roadmaps for senior management and as well as safety committees. Conduct regular safety committee meetings and discuss on near miss activities and further scope of improvement in the shop floor. Perform field level inspections on fire suppression systems in and around the factory premises. Conduct regular trainings on genera...

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4.0 - 7.0 years

5 - 8 Lacs

Boisar

Work from Office

Supervise day-to-day operations of the external preparation manufacturing section. Ensure proper execution of batch manufacturing processes as per Batch Manufacturing Records (BMRs) and Standard Operating Procedures (SOPs). Coordinate with Quality Assurance (QA), Quality Control (QC), Warehouse, and Maintenance for smooth operations. Monitor equipment calibration, cleaning, and maintenance to ensure readiness for production. Ensure proper line clearance, area cleaning, and equipment readiness before starting manufacturing operations. Review and maintain manufacturing documentation, including BMRs, logbooks, and deviation reports. Handle in-process checks and ensure process parameters are mai...

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4.0 - 7.0 years

5 - 8 Lacs

Boisar

Work from Office

Operate and monitor compression machines (e.g., Cadmach - ACC). Ensure smooth execution of batch production as per BMR/BPR and SOPs. Carry out in-process checks (IPC) like weight variation, hardness, thickness, friability, etc. Perform machine changeovers, cleaning, and line clearance. Maintain and update Batch Manufacturing Records (BMRs), logbooks, equipment usage logs. Adhere strictly to cGMP, GDP, and safety norms. Participate in audits (internal/external) and handle compliance requirements. Collaborate with QA, maintenance, and validation teams. Report deviations, breakdowns, and implement corrective/preventive actions (CAPA). Suggest and implement process improvements for yield and pro...

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5.0 - 10.0 years

5 - 9 Lacs

Ahmedabad

Work from Office

> Role Objective: A key objective of this profile is to ensure the effective planning, execution, and documentation of validation and calibration activities, in compliance with regulatory standards and internal policies. The role focuses on maintaining high-quality standards, managing internal and external audits, and ensuring adherence to ISO 13485 and other relevant quality management standards. Additionally, the role supports continuous quality improvement initiatives and ensures that validation activities align with business needs and regulatory requirements. > Desired Candidate Profile: Bachelor's or master's degree in engineering, life sciences, or a related field. A minimum of 6 years...

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3.0 - 5.0 years

3 - 5 Lacs

Bengaluru

Work from Office

Job Description: Proffered Profile: Bachelors degree (BE/B tech) with 3-5 years of experience in IT QMS Compliance Specialist ensures alignment of all IT systems, processes, and documentation with internal Quality Management Systems (QMS) and applicable regulatory standards such as GxP, ISO 9001, 21 CFR Part 11, and EU Annex 11. This role plays a key part in audit preparedness, deviation management, and maintaining consistent quality across IT operations and projects. Key Responsibilities: Develop, implement, and maintain IT quality policies, SOPs, and work instructions in accordance with QMS. Ensure compliance of IT systems with relevant regulatory requirements (GxP, 21 CFR Part 11, GDPR, e...

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6.0 - 11.0 years

7 - 11 Lacs

Madhepur

Work from Office

Date 19 Jun 2025 Location: Madhepura, BR, IN Company Alstom We create smart innovations to meet the mobility challenges oftoday and tomorrow. We design and manufacture a complete range of transportation systems, from high-speed trains to electric busesand driverless trains, as well asinfrastructure, signalling and digital mobility solutions. Joining us meansjoininga truly global community ofmore than38 900 people dedicated to solving real-world mobility challenges and achieving international projects with sustainable local impact. NETWORK & LINKS INTERNAL You will report to Warehouse Manager. You have to interact will below person/functions. External Logistics team Production Logistics Team ...

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1.0 - 4.0 years

0 - 3 Lacs

Savli, Vadodara

Work from Office

Role & responsibilities To maintain the QA documents in compliance state and ensure they are all time ready for internal and external audits. Preparation and review of SOPs. To act as training coordinator and oversee implementation & compliance of training matrix. To maintain the vendor approval document. Daily issuance and retrieval of records of other departments. To maintain records of change control, deviations, CAPA, incidents logs, OOS, OOT. To prepare and maintain calibration and validation schedules of equipments as per VMP. Upkeep and follow-up for new product licenses. To prepare APR, trends. Prepare and review of BMR and analytical reports. Upkeep of retain samples and controls sa...

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15.0 - 20.0 years

0 Lacs

Ahmedabad, Gujarat, India

On-site

15-20 yrs in quality for SS seamless pipes, incl. 5 yrs leadership role Expert in metallurgy, NDT, global standards & handling TPIs, audits, customers Job Description Strong knowledge of metallurgical processes, stainless steel grades, cold & hot finishing, and heat treatment expertise in Cold Finished Seamless Tubes Proficient in Hydro, Eddy Current, Ultrasonic, PMI, Mechanical & Chemical Testing manages quality at raw material, in-process, final product, and dispatch stages Hands-on experience with ISO 9001, PED, IBR, ISO 14001, OHSAS 18001, and related quality certifications Proven track record in conducting RCA, implementing CAPA, and handling Third Party Inspections (Lloyds, TUV, BVQI, ...

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5.0 - 10.0 years

3 - 5 Lacs

Greater Noida

Work from Office

Location: Greater Noida, Ecotech-6 Job Description: Quality Engineer Experience 2 to 5 Years Budget 3 LPA to 4 LPA Job Responsibilities: 1. Good Knowledge of AutoCad. 2. Good Knowledge of GD&T. 3. Knowledge of New Product Development 4. Knowledge of Die-Casting Process. 5. Conduct internal audits and support IATF (International Automotive Task Force) audits. 6. Develop and maintain quality documentation, including QMS (Quality Management System) procedures and work instructions. 7. Strong Knowledge in drawing Reading. 8. Limit Sample making. 9. Problem Solving Skills. 10. Deflects Analysis (Customer, In process). Company Name: KHvatec India (Electronic & Automobile Industry) Location: Greate...

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4.0 - 8.0 years

5 - 9 Lacs

Boisar

Work from Office

Monitor all in-process manufacturing and packaging activities on the shop floor. Perform line clearance before manufacturing/packaging starts. Verify batch records and ensure adherence to SOPs and BMR/BPR entries. Check critical control points and parameters during manufacturing. Review batch manufacturing records (BMR), batch packaging records (BPR), and logbooks in real time. Ensure timely and accurate documentation of in-process observations. Escalate any deviation or non-conformance observed during the process. Ensure compliance with cGMP, GDP, and regulatory requirements. Assist in handling deviations, change controls, and CAPAs. Participate in internal audits and regulatory inspections...

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8.0 - 12.0 years

9 - 13 Lacs

Boisar

Work from Office

Oversee line clearance , in-process sampling, and real-time review of batch manufacturing & packaging records (BMR/BPR) Monitor critical process parameters (e.g., weight variation, leak tests), hygiene, documentation, calibration, and equipment qualification Lead investigations for deviations, OOS/OOT results, non-conformities; drive CAPA and root cause analysis Approve/reject batches, handle change-controls and disposals, and manage legal/retention samples Support and participate in internal, external, and regulatory audits/inspections ; ensure audit readiness Prepare, review, and maintain SOPs, protocols (validation, cleaning, process), quality documentation, and MIS reporting

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5.0 - 10.0 years

5 - 9 Lacs

Hyderabad

Work from Office

We are looking for a skilled professional to fill the role of Manager - Corporate Quality with Omega Healthcare Management Services Pvt. Ltd., located in [location to be specified]. The ideal candidate will have 5-10 years of experience and a strong background in quality management, preferably in the healthcare industry. Roles and Responsibility Develop and implement comprehensive quality control processes to ensure high standards of service delivery. Conduct regular audits and assessments to identify areas for improvement and provide recommendations for enhancement. Collaborate with cross-functional teams to develop and implement process improvements that drive quality and efficiency gains....

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8.0 - 12.0 years

8 - 12 Lacs

Boisar

Work from Office

Supervise and coordinate QA lab personnel and activities related to sampling, testing, and reporting of raw materials, in-process samples, and finished products. Ensure compliance with Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and regulatory guidelines (e.g., FDA, ISO, ICH, etc.). Review and approve analytical test results, COAs (Certificates of Analysis), and related documentation. Manage calibration, maintenance, and validation of laboratory instruments (e.g., HPLC, GC, UV-Vis, FTIR). Investigate out-of-specification (OOS), out-of-trend (OOT), and non-conformances; participate in root cause analysis and CAPA implementation. Ensure timely completion of stability s...

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2.0 - 5.0 years

2 - 3 Lacs

Hosur

Work from Office

Job CNC Programming CNC Machine Setting CNC Machine Operation Line Inspection as per Quality Plan CAPA for process rejections Autonomous Maintenance of Machines Produce the part as per Drawing Quality and Quantity as per set norms Maintaining the CNC machines as per check list Documentation Work for the part Active participation in CFT teams for Productivity Improvement. Work Experience DME With 2 to 5 Years of Experience

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3.0 - 4.0 years

3 - 6 Lacs

Hosur

Work from Office

Job Receiving user indents, verifying with approved budget, and floating RFQ to the vendor (minimum 2 to 3 vendors). Preparing a worksheet to validate supplier quotes based on cost, quality, OEM, and delivery lead time Knowledge of SAP for PO release. Create PSR and follow the PSR approvals stage-wise. PO release. Monitoring material delivery against committed vendor dates. Coordinating with the maintenance team for installation and commissioning. Coordinating with the logistics team. Coordinating material in warding and acceptance, and vendor payment. Asset management and handling the Audits Generating and circulating reports to management. Relevant Experience: Mechanical and Electrical, Co...

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