2270 Capa Jobs - Page 12

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...

1.Responsible for BMR/BPR review & batch release 2.Incident/deviation investigation, root cause analysis & CAPA implement 3.Identify, evaluate & approve the validation, calibration & provide training to external service providers & ensure cGMP review

Role Purpose The purpose of this role is to conduct audits to ensure quality compliance within the account. Do Conduct process quality audits as per plan Conduct various process audits (1 audit/ agent/ week) as per procedure and guidelines For agents identified in the bottom quartile of performance, conduct 3 audits/ agent/ week Prepare findings from the report and share it with the client and the account 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 bridge any skill gap...

About The Role Skill required: Membership - Life Sciences Regulatory Operations Designation: Health Operations New Associate Qualifications: Any Graduation Years of Experience: 0 to 1 years Accenture is a global professional services company with leading capabilities in digital, cloud and security.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 count...

About The Role Skill required: Membership - Life Sciences Regulatory Operations Designation: Health Operations New Associate Qualifications: Any Graduation Years of Experience: 0 to 1 years Accenture is a global professional services company with leading capabilities in digital, cloud and security.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 count...

Responsibilities: Reliability test development and planning Conduct reliability testing & failure analysis Implement FMEA, CPk, Failure Mode Analysis Perform root cause & defect analyses Experience in electronic product/module is preferable

The opportunity Its an opportunity to work with diverse materials and people, exposure to variety of global and local suppliers and cross function teams, Lot of learnings on materials specification, engineer, quality requirements of a power quality product (Capacitors and associated equipment), greater opportunity to put your thoughts and creativity for continuous improvement, also exposure to digital solutions (manufacturing, supplier management) How youll make an impact Ensuring Quality requirements are met for the incoming materials (Raw materials, Bought out). Quality Documentation for incoming materials. Use of SAP-REIWA for material management. Handling Non-Conformities / Quality Notif...

About Company Job Description Clearance of finished good in SAP as per OQC plan and maintain daily reports/records/MIS Rejecting and returning non-conforming materials to production department for rework/final rejects. Maintain documents of Inspection, reworks, AQL, defects trends analysis Maintain safe and healthy work environment by following defined standards and procedures. Regular feedback to production department about NCs observed and ensure their closures. Issue of SLN (Stop line note) in case of producing non-conformance materials or not following defined SOPs, and control plan and their closures. Handle internal and external CCRs and their closure as per defined SLAs. Ensure CAPA e...

We are seeking a detail-oriented and efficient Data EntryOfficer to join our team The ideal candidate will be responsible foraccurately entering, updating, and maintaining data across various systems anddatabases This role requires a high level of attention to detail,confidentiality, and proficiency in data management tools Key Responsibilities Enter and update data into internal databases and systems with speed and accuracy Verify data for completeness, correctness, and consistency Perform regular data backups and ensure data integrity Maintain confidentiality and security of sensitive information Generate reports and summaries from entered data as required Collaborate with other department...

Issuance of Analytical Data Sheets and Formats. Preparation and Review of specification and standard test procedure. Review of QC Analytical Data. To ensure online documentation in laboratory as Good Documentation Practices. To attend training as per refresher training schedule. To ensure all time audit readiness in the work area. To perform any other work as and when assigned by Head of department.

1. To prepare annual equipment qualification planner with respect to validationmaster plan. 2. To prepare HVAC / compressed air / effectiveness of cleaning validation planner. 3. Preparation of protocols for qualifications of newly procured equipments and ofequipments transferred from other location. 4. Preparation of protocols for re-qualifications of HVAC system. 5. Preparation and execution of re-qualification protocols and reports as per schedule ofvalidation master plan and as on when required. 6. Toperform cleaning validation cleaning verification. 7. Preparationreview of cleaning assessment report. 8. Preparation review of process validation protocols and reports. 9. Preparation revie...

1. Line clearance in dispensing, manufacturing and packing area 2. In -Process Quality Assurance activities, sampling, analysis and AQL during production. 3. To ensure stage wise completeness of BMR during production. 4. Monitoring of environmental conditions in production area. 5. Coordination with other departments for smooth running of the plant. 6. Calibration, verification and maintenance of IPQA instruments. 7. To monitor process as per technical directions. 8. To fill all IPQA sampling logs in time. 9. To ensure deviations are properly documented and CAPA implemented. 10. To withdraw samples at different stages of In-Process and finished product as well as validation samples as per TD...

The Production Line Supervisor is responsible for achieving production targets Also, responsible for operations of the production line including deployment of manpower, line supervision and resolving issues related to production / quality Additionally, the role holder may also take up special projects for improvement activities Educational Qualification / Experience required : -Degree in Engineering - 4 to 7 years of experience in production / assembly line work - Must have experience in handling Blue collar associates Key Responsibilities : 1. Responsible to achieve production targets as per plan 2. Ensure smooth operations of the production process and shift 3. Ensure adherence to producti...

Key Responsibilities: Develop and implement the company's quality strategy, policies, and procedures in line with industry standards and customer expectations. Oversee Quality Assurance (QA) and Quality Control (QC) operations across production, raw materials, in-process, and finished goods. Ensure compliance with relevant quality certifications such as ISO 9001 , ISO/TS 16949 , GMP , HACCP , or industry-specific regulations. Manage audits (internal/external), regulatory inspections, and customer audits. Establish and monitor Key Quality Metrics (KPIs) such as first-pass yield, defect rate, customer complaints, etc. Lead root cause analysis (RCA), corrective and preventive action (CAPA), and...

The opportunity Manufacturing Quality Assurance work includes: Defining and specifying activities, processes, and standards to fulfill the quality requirements for a manufactured material, component, or product. Building and maintaining the infrastructure and systems necessary to consistently ensure the timely delivery of quality products. Auditing, monitoring, and determining the quality of manufacturing processes and/or outputs against defined internal and regulatory standards. Reporting and troubleshooting manufacturing process deviations and defects in finished goods An Experienced Professional (P2) applies practical knowledge of job area typically obtained through advanced education and...

Job Track Description: Performs business support or technical work, using data organizing and coordination skills. Performs tasks based on established procedures. In some areas, requires vocational training, certifications, licensures, or equivalent experience. General Profile Expands skills within an analytical or operational process. Maintains appropriate licenses, training, and certifications. Applies experience and skills to complete assigned work. Works within established procedures and practices. Establishes the appropriate approach for new assignments. Works with a limited degree of supervision. Functional Knowledge Has developed skillset in a range of processes, procedures, and syste...

Job Title: Solar Cell Quality Integrated PV Manufacturing Location : Kavali/Ramayapatnam, Andhra Pradesh (Location near to Nellore, AP) Position: Solar Cell Quality Head About the client : INDOSOL Solar Private Limited is a Special Project Vehicle (SPV) of Shirdi Sai Electricals Limited (SSEL), who is a leading Indian Conglomerate (Manufacturing B2B) in Transformer manufacturing, headquartered in Hyderabad. Having qualified in PLI (Production linked incentive) scheme through MNRE, Government of India is keenly materializing to set-up 10GW Integrated PV manufacturing for the entire value chain (Polysilicon, ingot, wafer, cell, Module & Glass manufacturing). Currently, this position is for the...

As an Officer to Executive in the Production QMS Department at our company located in Bavla, Ahmedabad, your role will involve the following key responsibilities: - Injectable Production Activities: - Execute and oversee the daily manufacturing of injectable products, whether aseptic or terminal sterilized. - Adhere to batch manufacturing records (BMRs) and standard operating procedures (SOPs) throughout the production process. - Collaborate with QA, QC, and Maintenance teams to ensure seamless operations. - Quality System Support: - Manage QMS tasks including handling deviations, CAPA, change control, and updating documentation. - Participate in investigating and resolving quality events re...

Ensure current versions of all GMP documents are in use. Prepare, revise, and control SOPs . Implement and enforce (GDP). Conduct internal audits, maintain summaries and CAPA tracking Support in process validation, equipment qualification etc Required Candidate profile Ensure all QA activities comply with cGMP, regulatory requirements & internal quality standards for API & Specialty manufacturing. Contact Mr Deep at 9867038868, Email Id: ops@empowerrecruitments.com

As a Quality Executive / Quality Engineer in the Electrical Stampings Manufacturing industry at [Chhatral GIDC], your role will involve: - Inspecting and ensuring quality of electrical stampings at various production stages. - Conducting in-process and final inspection as per quality standards. - Maintaining inspection reports and quality documentation. - Handling instruments like micrometer, vernier, height gauge, etc. - Monitoring and reducing rejection and rework levels. - Ensuring adherence to ISO / quality system requirements. - Coordinating with the production team to resolve quality issues. - Supporting the development and implementation of corrective and preventive actions (CAPA). - ...

You will be joining Biocon Biologics, a subsidiary of Biocon Ltd, a global biopharmaceuticals company dedicated to developing high-quality, affordable biosimilars to provide advanced therapies to patients worldwide. As a QMS Compliance Team Member, you will play a crucial role in ensuring manufacturing compliance for biosimilars in the following key responsibilities: **Role 1 Manufacturing Compliance (Biosimilars Compliance):** - Investigate microbial excursions for facility, utility, and process. - Prepare contamination control and strategy documents. - Conduct product quality assessments for microbial contaminations. - Develop risk assessment protocols and reports. - Harmonize procedures a...

About Business JOB DESCRIPTION Adani Group: Adani Group is a diversified organisation in India comprising 10 publicly traded companies. It has created a world class logistics and utility infrastructure portfolio that has a pan-India presence. Adani Group is headquartered in Ahmedabad, in the state of Gujarat, India. Over the years, Adani Group has positioned itself to be the market leader in its logistics and energy businesses focusing on large scale infrastructure development in India with O & M practices benchmarked to global standards. With four IG rated businesses, it is the only Infrastructure Investment Grade issuer in India. Adani Solar: Adani Solar is India's 1st and largest vertical...

Role Overview: As a member of the Quality team in the Industrial Components Division, you will be responsible for quality control activities on various components including mechanical parts, electrical components, and completed units as well as the related documentation. This position requires knowledge of various inspection tools and processes such as dimensional inspections, visual inspections, non-destructive testing methods, leak testing, and functional testing of switchgear modules. You will also be required to have advanced computer skills, strong organizational skills, excellent communication skills, and problem-solving ability with lean six sigma methodology and metallurgical skill. ...

As a Quality Assurance GLP professional at MSCR, your role involves ensuring the highest standards of quality and compliance across clinical research and laboratory operations by leveraging your expertise in ICH-GCP and GLP principles. You will be responsible for various key activities: - Develop and maintain ICH/GCP-compliant processes at MSCR. - Lead internal quality audits, CAPA activities, and quality management reviews. - Conduct study audits to ensure adherence to sponsor protocols, GCP, and regulatory requirements. - Identify non-conformances, recommend corrective measures, and drive continuous quality improvements. - Perform vendor audits, collaborate with production support teams, a...

Role Overview: As an R&D Executive in the Fill and Finish division, your main responsibility will be to prepare Batch Manufacturing Records (BMR), Batch Packaging Records (BPR), Standard Operating Procedures (SOPs), and General Protocols. Additionally, you will be tasked with handling Change Controls, Deviations, Corrective and Preventive Actions (CAPA), Out of Specification (OOS) and Out of Trend (OOT) investigations. Key Responsibilities: - Prepare Batch Manufacturing Records (BMR) - Prepare Batch Packaging Records (BPR) - Develop Standard Operating Procedures (SOPs) - Create General Protocols - Handle Change Controls - Manage Deviations - Implement Corrective and Preventive Actions (CAPA)...