6078 Qms Jobs - Page 4

Responsibilities: * Lead QMS implementation and audits * Ensure compliance with ISO standards * Manage CAPA process for non-conformances * Collaborate on continuous improvement initiatives * Develop and maintain quality procedures Health insurance Provident fund Annual bonus

plant quality assurance activities includes , implementation and maintenance of QMS throughout the plant Customer handling for quality related queries, regular customer visits , Customer complaint handling, Supplier audit monisha.m@liveconnections.in

shall be responsible for maintaining and improving all QMS activity, GMP and GLP across the company Handling QMS activities like change control, validations, stability, qualifications, APQR and Risk assessment etc Label artwork review and management Required Candidate profile Assisting HOD in customer complaint analysis and preparation of customer complaint report. Investigation of incidents, deviations, OOS and ensure corrective actions in place.

Min 2yr BPO Quality Manager Exp on the paper, AM/DM cannot apply Manage BPO Quality Team Call Callibration, Audit, Score , CSAT Call/WhatsApp CV Deepshikha 8368531573 Must Knows-English and Telugu Required Candidate profile Work from Office-Hyderabad only not Visakhapatnam neither Bangalore. Apply those who can relocate in Hyderabad Call/WhatsApp CV Deepshikha 8368531573 Must Knows-English and Telugu

A. Execution and Recording: 1. Perform the manufacturing activities as per the BMR and SOP’s. 2. Batch related documents in manufacturing area. 3. Preparation of shift schedule and batch schedule. 4. Readiness related to batch manufacturing. 5. Execution and monitoring of activities in compliance to cGMP. 6. Execution of activities during product change over 7. Checking and timely submission of Batch Manufacturing records to QA. 8. Decontamination and disposable of bio waste. 9. Preparation of MCB/WCB. 10. Automated or manual CIP and SIP of equipment in the manufacturing area. 11. Follow safety norms in the manufacturing area. 12. Self-Inspection of manufacturing area and compliance as per r...

Regular monitoring for yearly plan (SPC'MSA, PPAP, CAPA, training, etc) handling or under Quality MR working or good knowledge of process defect of machine Shop unit Basic knowledge of QMS system ISO and basis knowledge of Maruti audit check sheet Required Candidate profile SAP B1 , MS Office - advance excel, outlook email reply Knowledge of sheet metal processes Problem-solving, communication skills Person can stay nearby to office location (Sarurpur Industrial Area)

Hiring 'Manager - Quality Control' for a leading MedTech company. Position: Manager - Quality Control Location: Bangalore Req. Experience: 6~10 years into quality control Role & Responsibilities:- Lead and manage the Quality team to ensure product and process compliance. Oversee inspections, audits, CAPA, and supplier quality. Support regulatory requirements and drive continuous improvement. Lead, train and mentor quality team members. Overseeing incoming, and final inspection activities. Establish and track KPIs for Quality Team members Assigning the Daily Incoming Quality Control and Final Quality Check tasks and managing them. Represent the quality function at management reviews and strat...

- Provide remote QMS support for global sites, handling OOS, OOT, deviations, incidents and change controls. - Review documentation for compliance & drive continuous improvement. - Ensure timely investigation, analysis & change control initiation. Required Candidate profile - 9+ years of QC/QA experience in regulated pharma co. - Reviewing OOS, OOT, APQR & lab incident investigations, change controls & managing deviations - Strong knowledge of USFDA, EU & Health Canada

Role & responsibilities- Weekly Audit of line for process confirmation of previous actions with kakotora check sheet. Customer complains handling & submits countermeasures. New product feasibility check & required request for design change. New part development as APQP & PPAP requirements. Red bin analysis of Quality concern of customer issues in the supplier & in-house parts & follow up for the 8D report to all concern section. Prepare the major defect/complaints data and analysis of complaints for weekly Quality meeting with President and managers. Product & Process validation /revalidation & Layout inspection as per plan. Poke-yoke, Tools & equipments implementation, verification & monito...

As a Veeva Config Specialist, your role will primarily involve focusing on Veeva Vault Configurations in the life sciences sector. Your key responsibilities will include: - Having 5-8 years of experience in the life sciences sector, with a strong emphasis on Veeva Vault Configurations for any Vault. - Proficiency in implementing, supporting, and administering the Veeva Vault platform, including suites such as CTMS, QMS, Safety, and eTMF. - Defining and implementing global business processes for safety, demonstrating the ability to navigate international regulations and associated business processes. - Conducting tech impact assessments on current features and functionalities in response to n...

Purpose of the Job To support the powder coating operations by assisting in equipment monitoring, Process parameter optimization, Process control. This role is designed to ensure consistent powder coating quality, Minimize VOC emissions & Uphold safety and environmental standards. To maintain production, Quality , Safety documentation. Compliance with safety standards. SAP based inventory tracking. Responsibilities Responsible for PQSCDM & Manpower management , 5S. Ensure all process parameter & Responsible for loss capturing and improvement. Machine startup check, ensure machine readiness before line startup. Coordination with other departement for line related issue. Follow work instructio...

Role & responsibilities :- In-Process & FG Quality : Lead LPAs, internal audits, and ensure process compliance. Review rejections, drive corrective actions, and lead Redbin analysis. Coordinate with cross-functional teams for quality improvements. Conduct pre-dispatch inspections & manage IFM documentation. Strong understanding of process & product audits. Data analysis and report preparation (MPR/MIS). Hands-on in defect analysis and improvement actions. Customer Quality : Handle daily customer quality interactions, mainly with MSIL & TKM. Investigate customer complaints & warranty issues through RCA & CAPA. Coordinate with QREs for rejection control & issue resolution. Manage customer port...

Understanding testable requirements and the development of automation test cases towards product realization. Automation C#, Python, Behave, GitHub workflows Enabling team: responsible for setting up the generic infrastructure for test automation, such as devops/configuration management, DMB, etc. Experience in test design Experience AI/ML Knowledge on agile methodology Performs automation testing within the systems/agile teams throughout the whole development Cycle ensuring built-in quality Adherence to quality gates (QMS) for the test artifact deliverables Familiarity with healthcare regulations and interpretation Good to have: Knowledge on DICOM and Hospital workflows

Sanpurple Inc is looking for Web Design Professional to join our dynamic team and embark on a rewarding career journey. Conceptualizing creative ideas with clients. Testing and improving the design of the website. Establishing design guidelines, standards, and best practices. Maintaining the appearance of websites by enforcing content standards. Designing visual imagery for websites and ensuring that they are in line with branding for clients. Working with different content management systems. Communicating design ideas using user flows, process flows, site maps, and wireframes. Incorporating functionalities and features into websites. Designing sample pages including colors and fonts. Prepa...

Pangea Global Services is looking for Database Researcher to join our dynamic team and embark on a rewarding career journey. Collect, verify, and organize large datasets for research and analytics purposes. Design and manage databases ensuring data integrity, security, and accessibility. Develop automated tools for data extraction and cleansing. Collaborate with analysts to support data - driven decision - making and research insights. Disclaimer : This job description has been sourced from a public domain and may have been modified by Naukri. com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels before app...

FTF PHARMA PRIVATE LIMITED is looking for Quality Assurance Professional to join our dynamic team and embark on a rewarding career journey. A Quality Assurance Professional is responsible for developing and implementing quality assurance policies and procedures, conducting tests, and monitoring production processes to ensure quality and compliance with established standards. They identify defects and issues, collaborate with cross - functional teams, and implement corrective actions to improve product quality. Key Responsibilities : Quality Assurance Planning : Develop and implement QA policies, procedures, and standards. Plan and schedule QA activities, including audits, inspections, and te...

We are looking for a detail-oriented and proactive Quality Assurance Engineer to join our Aerospace team in Hyderabad. The ideal candidate will possess a strong foundation in Quality Management Systems (QMS) , process documentation , and Standard Operating Procedures (SOPs) . This role demands collaboration with cross-functional teams to uphold stringent Aerospace quality standards (AS9100 / ISO 9001) . Key Responsibilities; Develop, implement, and maintain Quality Management Systems (QMS) in compliance with AS9100 / ISO 9001 standards. Prepare, review, and update SOPs , process manuals , and other quality documentation. Conduct internal audits , support external audits, and assist in mainta...

Followings will be the Core Job Responsibilities of the position holder: Ensure the Compliance to laid standards of the current Good Manufacturing Practices. Carrying Qualification of Production equipment and compliance to specifications and validated methods Preparation of Standard Operating Procedures for equipment. Implementation of Quality Management System as per cGMP and international requirement at all levels of Manufacturing. Training and evaluation of the Technicians for their qualifications of specific task to operate specific equipment. Coordination with production Planning department and QA for work order and Batch Record document. To exercise effective control over the environme...

We have a top-tier portfolio of businesses, including Cubic Transportation Systems (CTS) and Cubic Defense (CD). Explore more on Cubic. com. Job Details: Job Summary: Performs data entry, calculating, posting and verifying figures related to the payment of vendor invoices. This position typically works under general supervision and direction. Essential Job Duties and Responsibilities: Maintains invoice, purchase order, and receiver reconciliations. Matches invoices with receivers and compares to purchase orders within SAP and OpenText. Processes invoices for payment by entering data in the computer, checking for mathematical accuracy, taxes that may apply, taking advantage of applicable disc...

Candidate should have experience in New Product development of quality function. Knowledge of PPAP documents & QMS Process Lay out inspection and Drawing reading,Conduct PTR AAR submission and sign off with Customer. Process & product validation. Required Candidate profile Preferred Candidates from : Plastic Injection Moulding Automotive Background.

Responsibilities: Manage the department performance from a purely Operational aspect. Lead, manage and recommend feasible options to reporting manager to ensure that the services provided are consistent , fit for purpose and meet both external and internal requirements; this would include both legal compliance and customer expectations Maintain a set of AISATS data archives. Responsible for every aspect of the QMS/QC function from Audit Planning, Conduct of Audits, & Implementation, Corrective Action & Closure, Monitoring & Verification, Feedback/follow up and re audit where necessary Converts data collected during internal audits into information and provide necessary statistics to Senior M...

Role Purpose The purpose of the role is to provide effective technical support to the process and actively resolve client issues directly or through timely escalation to meet process SLAs. Do Support process by managing transactions as per required quality standards Fielding all incoming help requests from clients via telephone and/or emails in a courteous manner Document all pertinent end user identification information, including name, department, contact information and nature of problem or issue Update own availability in the RAVE system to ensure productivity of the process Record, track, and document all queries received, problem-solving steps taken and total successful and unsuccessfu...

Role Purpose The purpose of the role is to provide effective technical support to the process and actively resolve client issues directly or through timely escalation to meet process SLAs. Do Support process by managing transactions as per required quality standards Fielding all incoming help requests from clients via telephone and/or emails in a courteous manner Document all pertinent end user identification information, including name, department, contact information and nature of problem or issue Update own availability in the RAVE system to ensure productivity of the process Record, track, and document all queries received, problem-solving steps taken and total successful and unsuccessfu...

Role & responsibilities Suggested position: Sr Manager / Manager Education: Post Graduation (Life sciences preferred) Total Exp: 15-17 Years (Biopharma is preferred) Others: Ready to support in different shifts Responsibilities: Mainly responsible to review of Harvest, Drug Substance and Drug Product analytical (Biosimilars) raw data and analytical trends Conduct Gemba walkthroughs in QC department and to ensure quality compliance. Involve in investigations (Deviations, OOS, OOT, Lab incidents) to ensure QMS compliance for QC sections Audit trails and conduct routine monitoring in QC to check effectiveness of the system implemented. Responsible for preparation and review of documents SOPs, P...

Exp : Must have At least 5+ years experience in Quality management system. Skill : Auditing experience in QMS Should have internal auditor certificate of ISO 9001 and IATF 16949. Key Responsibilities: Implement and maintain ISO 9001-compliant Quality Management System. Prepare and control quality documentation (SOPs, manuals, procedures). Conduct internal audits and support external/customer audits. Lead and document Debug Audits to identify and resolve recurring quality issues. Drive corrective and preventive actions (CAPA) for audit findings and process issues. Perform root cause analysis using tools like 8D, Fishbone, and 5-Why. Ensure supplier quality through audits and incoming inspecti...