6082 Qms Jobs - Page 31

Roles & Responsibility: To ensure proper Coordination and receive the production plan & arrangement of all resources accordingly. To ensure Testing and control as per documents to produce 100% safe products. To ensure compliance of Cleaning and Sanitation program as per matrix. To ensure that targets of Quality Measures are achieved. To ensure that the goals of FSSC and QMS are achieved. To ensure Calibration of lab and process measuring instrument as per defined frequency. To ensure the effective implementation of defined PRPs, OPRP and CCP. Initiate Effective corrective action against identified gaps in any external and internal audits. Monitor & achieve the target of Sugar, Concentrate, p...

Walk In Drive For Production-Injectables In Formulation Division @ Corporate Office Department :- Production-Injectables Qualification :- BSc | B Pharmacy | ITI | Diploma | B.Tech Experience:- 2 to 8 Years Skills :- Vial Filling | Vial Washing | Autoclave | Lyophilizer | Compounding | Packing | Visual Inspection | QMS | Division :- Formulation Interview Date:-25-10-2025 Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur | MSNF-V R.K.Puram Venue Location :- MSN Corporate, H. No. 2-91/10 & 11 /MSN, Whitefields, Kondapur, 500084 Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Payslips, Bank Statement, Certificates, Aadhar Card & Pan...

Oversee quality operations in foundry and machine shop. Handle QC tools, GD&T, CMM, PPAP, and QMS. Lead vendor development, root cause analysis, and continuous improvement. Ensure compliance with ISO 9001:2015 and support team training & audits.

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 the Commissioning & Qualification Manager at NNE, you will have the opportunity to work on projects that are shaping the future of sustainable and intelligent pharma facilities. NNE values its employees and offers exciting career opportunities in a passionate and high-powered working environment. You will be joining the Commissioning and Qualification team, part of the Project Management team dedicated to delivering the largest Biopharmaceutical facility to customers. **Main Roles & Responsibilities:** - Work with highly skilled Senior Engineers and Engineers in Denmark and India - Participate in making complex biopharma/Large API facilities - Drive projects with Science and Risk based Va...

In this role, you will be responsible for Veeva development experience in Audits, Deviations, and Exceptions. Your main tasks will include developing and maintaining solution architecture, system administration, security, and procedures across the Veeva Vault Platform. You will support all assigned development activities for the Veeva Vault implementation program under the leadership of the client Quality Veeva team. It will be your responsibility to coordinate with Business analysts to outline the business requirements and ensure that IT security and Data Integrity requirements are properly outlined for the solution. Additionally, you will need to coordinate with the Validation team to prep...

we are hiring for Veeva Configuration Specialist for cognizant for bhubaneswar location. If interested please share your updated resume to [HIDDEN TEXT] Title: Veeva Configuration Specialist Job Description : Experience level : 3 to 12 years Notice : Immediate to 90 Days. Location : Bhuvaneswar. Shortlisted candidates will have interview in Bhuvaneswar Cognizant on 25th oct. Job Description Veeva Vault Clinical Operations Suite QMS & RIM, CTMS & Safety Mandatory- Vault Platform/QMS certified. Key Responsibilities: Deep technical expertise in configuring Veeva Vault, especially QMS modules Hands-on experience with Veeva Vault platform configurations Ability to interpret business requirements ...

As a Senior Engineer in Strategic Sourcing & Supply Chain Management at Kagal, your role involves planning and procuring material in alignment with MRP/BPR requirements. You will be responsible for monitoring the daily delivery performance of suppliers using BPR signals and implementing Quality Management System (QMS) and Environment, Health, and Safety (EHS) standards in procurement processes. Additionally, you will be in charge of monitoring and controlling inventory, coordinating with the production team, stores, and RQA for unloading and inspection, as well as communicating quality issues to suppliers and organizing sorting and rework activities. Qualifications required for this position...

As an Executive/ Sr. Executive in Quality Management System (Analytical Assurance), your role will involve leading the Out of Specification investigations and managing core QMS activities related to QC. Your responsibilities will include: - Triggering out of specification investigations when test results fall outside predefined specifications. You will be required to design and conduct tests to confirm or eliminate suspected root causes. - Handling QMS documents such as Incidents & Deviations. - Evaluating change control & CAPA processes. - Reviewing analytical documents like worksheets, specifications, methods of analysis, stability protocols & summary reports, and logbooks from the Quality...

To raise and get approval of UPD / PD / Change control and get approval from authorities. Handle LMS related activities and their timely completion. To do and arrange CFT meeting of related to QMS. To receive the market complaints and get closer timely after discussion with CFT team. To review and arrangement of all GMP format requirement like formats / log etc. Prepare yearly calibration schedule and their completion timely. To implement and monitor the CAPA. To complete the schedule training / on job training . To maintain / follow the cGMP / GQS guideline requirements.. To handle change control, deviation and other GMP compliance related documents and ensure that all compliance related do...

Are you ready for a new beginning We need your talent, knowledge and dedication to better our world with biology. Our purpose points the way In Novonesis, we know that solutions rooted in biology can help solve humanity's biggest challenges. Since we began more than a century ago, this has been our guide. It's how we've gotten so far. And it's how we'll impact the future. Now, more than ever, the world needs change. And with biosolutions, the possibilities for transformation are endless. We're here to better our world with biology. Tasks And Responsibilities Order Handling & Processing Manage Customer interface to receive orders, its changes and provide timely order confirmation. Process the...

Why Quark Software: At Quark, we've been revolutionizing graphic design, digital publishing, and content automation since 1981. With over four decades of expertise, we empower organizations to master their content lifecycle through cutting-edge design, automation, and intelligence. Our software solutions enable customers to create, manage, publish, and analyse their content with unrivalled effectiveness. As we embark on an exciting new era of growth, we're on the lookout for exceptional individuals to join our Global team. Why Choose Quark: Quark is entering a transformative phase of growth, driven by visionary leadership focused on research and development and customer success. Our culture ...

Role & responsibilities Lead the plant quality function, including incoming quality, in-process quality, final inspection, and customer quality. Ensure compliance with IATF 16949, ISO 9001, and other customer-specific requirements. Manage customer audits, third-party audits, and internal quality system audits. Drive implementation of APQP, PPAP, FMEA, MSA, SPC and other core quality tools across the plant. Address and resolve customer complaints, including root cause analysis (RCA) and corrective/preventive actions (CAPA). Ensure proper documentation and control of quality processes and records. Monitor and improve key quality KPIs such as rejection rate, customer PPM, cost of poor quality (...

Job Description Job Title: General Manager Quality Location: Head Office Company: Vform Tecnopacks Ltd Website: www.vform.in Job Overview: The GM – Quality will lead the entire Quality function at Vform Tecnopacks Ltd, ensuring all products and processes meet consistent standards. This role involves developing and implementing quality systems, driving continuous improvement, and managing the Quality team. The GM – Quality reports directly to top management (CMD/CEO). Key Responsibilities: Lead and supervise Quality Managers; monitor team performance. Implement, maintain, and improve Quality Management Systems (QMS, FSSC, GMP). Ensure all products meet quality and compliance standards before ...

We are seeking a highly motivated and detail-oriented Quality Engineer to join our team. The successful candidate will be responsible for ensuring that products and processes meet established quality standards through testing, inspection, and process improvement. You will work cross-functionally with engineering, production, and supply chain teams to identify and resolve quality issues. Develop and implement quality control systems and inspection processes. Monitor and analyze quality performance metrics. Conduct root cause analysis and implement corrective/preventive actions (CAPA). Work with suppliers to resolve quality issues and ensure compliance with standards. Participate in internal a...

As a member of the Central Quality department, your role involves: - Conducting Vendor Audit & Compliances - Reviewing Procurement bill of material (PBOM) - Initiating and evaluating change control, Corrective and Preventive Actions (CAPA) through track wise software - Evaluating Certificate of Suitability (CEP) updation, Drug Master File (DMF) notification, and Vendor notification for implementation at formulation sites - Reviewing Quality Management System (QMS) documents of all sites - Auditing formulation sites as per self-inspection plan - Preparing Audit planner for Active Pharmaceuticals Ingredients, Excipients, packing materials, Key Starting Materials (KSM)/Intermediates, Sterile ar...

RESPONSIBILITIES: Complete technical/scientific understanding on purification/downstream process of biopharmaceutical products Expertise in downstream process lab scale/pilot scale/ manufacturing scale equipment handling e.g., chromatography system, TFF system, filtration process, centrifugation, etc. Knowledge of execution of small-scale purification process using scale down model. Handling and working knowledge of lab instruments e.g., UV spectroscopy, Solo VPE, pH and conductivity meter, turbidity meter. Knowledge of downstream process scale-up strategies Process data collection, basic data analysis skill. Effectively work and communicate with team, CFTs and partners for planning and exec...

Key missions of the position: Managing Product Quality Activities Hand on experience in Brakes system, Air Generation Compressor & Motor Managing Customer Requirements & Deliverables Achieving Departmental & Company KPIs Main responsibilities: Having good knowledge in Product Management concepts Understanding the needs of Customers on Quality Perspective Maintaining Product Deliverables with internal & external teams Communications with Internal & External stakeholders Must have effective team management skills Well versed with Quality assurance processes & systems Having good knowledge in Basic Mechanical Engineering Concepts Having good analytical skills Managing Internal & External Non-Co...

Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients that is what Vantive aspires to deliver. We believe Vantive will not only build our leadership in the kidney care space, it will also offer meanin...

Job Description A. Job Purpose Assistant - Quality will support the QM to execute the quality management system and conduct engineering audits in the FTO. Monitor training and engineering operations to check compliance with regulatory requirements and industry best practices. B. Key Accountabilities Assistant - Quality will support the Quality Manager to: o Define the quality organization and procedures necessary to comply with regulations o Preparing and implementing quality audit program o Ensures availability of skills and resources necessary to implement the quality system or the organisation review system o implement by performing the necessary audits and inspections. o Implement monito...

1.Role & responsibilities Preparation and review of Standard Operating Procedures. Issuance, review of OOS,OOT,Deviation,CAPA,Change Control & its Management. To impart internal trainings to DCAL Employees. Review of the Instrument qualifications and re-qualifications protocols of Quality control. Preparation & review of quality risk assessment documents. Review and approval of analytical data related to QA release. Review & Approval of Specification STP, Raw data sheet etc. To review laboratory investigations related to complaints and deviations and to ensure CAPA related to QC are completed within timeline. Internal Audit and External audit Compliance To support RA for analytical assistanc...

The opportunity: In the role of an Application Engineer, employee will contribute to Hitachi energys Network Control projects both in India and abroad. Network Control Systems are advanced real-time system for managing operations in a modern control center. It provides monitoring and control capabilities in an integrated software platform. How youll make an impact: Installation, configuration and verification of Hitachi energys Network Control software & third party software. Preparation/modifications of product technical documents with project specific requirements. Data collection, mapping, cleansing and data loads into Hitachi energys ES products. Building displays and generating reports ...

We are looking for a skilled Food & Beverages Manager to join our team in the Hotels & Restaurants industry. The ideal candidate will have 5-10 years of experience in managing food and beverage operations, with a strong background in hospitality. Roles and Responsibility Oversee daily food and beverage operations to ensure high-quality service and customer satisfaction. Develop and implement menus, recipes, and promotions to drive sales and revenue growth. Manage inventory, supplies, and vendor relationships to minimize costs and maximize profits. Train and supervise staff members to enhance their skills and performance. Conduct market research and analyze consumer trends to stay ahead of co...

Roles and Responsibility Develop and implement effective supplier quality management strategies to ensure high-quality products. Conduct regular audits and assessments to evaluate supplier performance and identify areas for improvement. Collaborate with cross-functional teams to resolve issues and improve overall supply chain efficiency. Analyze data and metrics to measure supplier performance and make informed decisions. Provide training and coaching to suppliers to enhance their quality management capabilities. Ensure compliance with industry standards and regulatory requirements. Job Requirements Proven experience in supplier quality management, preferably in the recruitment and staffing ...

So what does a Quality Manager really do? Think of yourself as a champion for operational excellence. You will closely monitor program metrics, provide insights and analysis, offer recommendations, and help manage the implementation of service and process improvement programs and efforts. Your contribution will help ensure program metrics and service level requirements for quality are met consistently. You will also take the lead in conducting quality audits, report on findings, and propose new systems and policies for continuous improvement. Consider yourself a consultant to stakeholders, a mentor and guide to Teams, and an important asset to our passionate pursuit for quality . Imagine you...