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4.0 - 6.0 years

3 - 7 Lacs

gummidipoondi, sullurpeta, chennai

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Role Overview: We are looking for a Quality Assurance Engineer (Incoming & Supplier Quality) to ensure that all supplied parts, raw materials, and components meet the required quality standards. The role involves inspection of incoming materials, coordination with suppliers on quality issues, supplier audits, and driving continuous improvement in the supply base Key Responsibilities: Inspect and verify incoming raw materials, components, and parts using precision instruments (Profile Projector, VernierCalipers , Micrometers , Height Gauges, CMM, etc.). Review supplier quality documents including material test certificates, PPAP, and inspection reports. Manage supplier quality performance, tr...

Posted 14 hours ago

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2.0 - 3.0 years

1 - 4 Lacs

tarapur

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Familiar with GMP guidelines and batch manufacturing processes. Skills: MS Office and effective communication. Responsible for managing daily production activities and documentation. Required Candidate profile Experience: 2-3 years in Pharma/API Qualification: B.Sc / M.Sc in Chemistry Experience in Oncology production preferred.

Posted 15 hours ago

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10.0 - 15.0 years

0 - 0 Lacs

vadodara

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Role & respo Job Title: Senior Manager Quality Control (QC) Location: Waghodia, Gujarat Key Responsibilities: Quality Leadership: Lead the QC function to ensure raw materials, intermediates, and finished products meet internal and external specifications. Establish and enforce quality control protocols in line with industry standards (ISO, GMP, HACCP, etc.). Team Management: Supervise and mentor a team of QC officers, chemists, and analysts. Conduct training programs to enhance technical and regulatory knowledge. Compliance & Documentation: Ensure adherence to regulatory requirements from FDA, BIS, CPCB, and other authorities. Maintain comprehensive documentation including COAs, SOPs, CAPA r...

Posted 15 hours ago

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5.0 - 7.0 years

19 - 25 Lacs

hyderabad

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A Quality Auditor is responsible for ensuring that all aspects of the Company's Quality Management System adhere to regulatory standards and established quality guidelines. This role is crucial for maintaining the integrity of clinical trial data and protecting the safety of participants. Key Responsibilities * Conducting/Host Audits: Perform internal and host external audits. These audits verify compliance with Good Clinical Practice (GCP) guidelines, Good Documentation Practices (GDP), company standard operating procedures (SOPs), and other relevant regulations. Write up an audit report and track findings. * Quality Management: Evaluate and help maintain the company's quality management sy...

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1.0 - 6.0 years

2 - 6 Lacs

vadodara

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Role & responsibilities Sampling and analysis of Raw Materials, In-process samples, Finished Products , and Stability samples as per SOP and test methods. Preparation and standardization of volumetric solutions, reagents , and reference standards . Performing routine chemical, instrumental (HPLC, GC, UV, FTIR), and microbiological testing (for applicable roles). Equipment/instrument calibration and maintenance logs. Participation in method validation , stability studies, and process validation activities. Adherence to Good Laboratory Practices (GLP) and regulatory standards. Supporting internal and external regulatory audits (like USFDA, WHO-GMP). Reporting deviations, OOS results, and non-c...

Posted 16 hours ago

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0.0 - 1.0 years

3 - 6 Lacs

bengaluru

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Role Description The Financial Operations Analyst reports to and works closely with the Service Lines Regional and National Financial Operations Leaders, as well as within the firms other core Finance functions (Centralized Billing, Planning & Investment, Enterprise Reporting & Analytics) to provide consistent and collaborative support and analysis. The role requires strong analytical and communication skills and the ability to support multiple leaders simultaneously. Areas of Responsibility: Support our client-facing professionals to optimize engagement efficiency and profitability through active project management (a thorough understanding of the business of our business is paramount); thi...

Posted 16 hours ago

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0.0 - 2.0 years

1 - 3 Lacs

manesar

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Role & responsibilities Responsible for the control and maintenance of all laboratory documents. Ensure adherence to the Quality Policy and compliance with ISO/IEC 17025 requirements. Prepare and maintain updated lists of certified reference standards and working standards. Conduct induction training sessions for newly joined laboratory personnel. Review and verify analytical test reports to ensure accuracy and compliance with established standards. Prepare and regularly update the SOP/STP list, equipment list, and calibration schedules for all laboratory equipment. Develop and maintain preventive maintenance schedules for laboratory equipment. Prepare and update training schedules as per th...

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2.0 - 3.0 years

1 - 5 Lacs

tarapur

Work from Office

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

Posted 16 hours ago

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6.0 - 8.0 years

10 - 20 Lacs

pune, chennai, bengaluru

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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...

Posted 18 hours ago

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2.0 - 7.0 years

4 - 6 Lacs

chennai

Work from Office

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 ...

Posted 18 hours ago

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0.0 - 2.0 years

2 - 3 Lacs

ahmedabad

Work from Office

• 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.

Posted 18 hours ago

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10.0 - 20.0 years

10 - 20 Lacs

pune, bengaluru

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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...

Posted 20 hours ago

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3.0 - 6.0 years

3 - 6 Lacs

pune

Work from Office

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

Posted 22 hours ago

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2.0 - 6.0 years

0 Lacs

indore, madhya pradesh

On-site

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....

Posted 1 day ago

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5.0 - 9.0 years

0 Lacs

palghar, maharashtra

On-site

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. -...

Posted 1 day ago

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4.0 - 8.0 years

0 Lacs

karnataka

On-site

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...

Posted 1 day ago

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1.0 - 3.0 years

2 - 6 Lacs

bengaluru

Work from Office

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...

Posted 1 day ago

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3.0 - 7.0 years

3 - 4 Lacs

bengaluru

Work from Office

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...

Posted 1 day ago

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4.0 - 6.0 years

3 - 5 Lacs

hyderabad

Work from Office

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...

Posted 1 day ago

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2.0 - 5.0 years

2 - 4 Lacs

gandhinagar, kadi, ahmedabad

Work from Office

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

Posted 1 day ago

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7.0 - 11.0 years

7 - 10 Lacs

hyderabad

Work from Office

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,...

Posted 1 day ago

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6.0 - 11.0 years

7 - 11 Lacs

hyderabad

Work from Office

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,...

Posted 1 day ago

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10.0 - 15.0 years

12 - 14 Lacs

dadra & nagar haveli

Work from Office

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...

Posted 1 day ago

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8.0 - 12.0 years

4 - 6 Lacs

warangal, hyderabad

Work from Office

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...

Posted 1 day ago

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2.0 - 7.0 years

2 - 7 Lacs

vadodara, gujarat, india

On-site

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...

Posted 1 day ago

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