6078 Qms Jobs - Page 5

The Quality Auditor will be responsible for conducting systematic inspections and audits across production processes, components, and finished goods. The role ensures that all products meet required quality standards and comply with internal procedures, customer specifications, and regulatory norms. Perform incoming, in-process, and final product audits based on defined checklists and standards Conduct process audits within the production line to ensure compliance with SOPs and work instructions Report non-conformities and assist in root cause analysis & corrective actions Maintain audit records, quality reports, and inspection data Verify calibration status of measuring & inspection equipme...

Department Global Regulatory Reporting Reports To Global Regulatory Reporting Senior Manager About your team Regulatory Reporting is a department within Global Asset Management Delivery responsible for submitting various shareholding reports as required by law and financial regulations in Europe, Middle East, Asian and African jurisdictions The group is also responsible for all of Fidelitys post trade reporting obligations like EMIR, ASIC, MIFID Transaction and Trade reporting The Regulatory Reporting function is a global team based in Dublin, Dalian, and Gurgaon covering all relevant regions Types of regulatory filings include substantial shareholder requirements, takeovers, short-selling, ...

Role & responsibilities Ensure proper documentation and control of records related to incidents, deviations, change controls, and other QMS-related activities. Maintain and update records as per established SOPs and regulatory requirements. Oversee day-to-day warehouse activities, including material receipt, storage, issuance, and handling. Manage material handling activities through RF and GRN systems in SAP. Ensure proper segregation, identification, and traceability of materials. Coordinate with Sales and Supply Chain teams to ensure smooth and timely dispatch of goods. Prepare packing lists, consignment checklists, and related dispatch documents in line with SOPs.. Competencies Strong or...

1.Manager- 10+yrs exp 2.Asst Manager- 10+yrs exp Review of audit trail for chromatographic and non chromatographic systems 3.Sr.Executive- 7+yrs exp ONLY MALE CANDIDATES ARE PREFFERED

Role & responsibilities Setting Quality Standards Developing Quality Control Processes Monitoring and Auditing Continuous Improvement Training & Development Data Analysis Supplier Quality Management Customer Feedback Regulatory Compliance Cross-functional Collaboration Documentation Problem Solving Resource Management Representation Risk Management:

Should have exposure in ensuring compliance, documentation, preparing / reviewing SOPs, assisting in submission of regulatory documents, coordination with cross functional teams.

Oversee and manage all quality operations in plastic injection molding Handle customer complaints Hands-on experience with PPAP, FMEA, SPC, MSA, 8D Reports, CAPA. Exposure to ISO 9001 / IATF 16949 standards Required Candidate profile Lead internal audits and support external audits (customer & certification). Ensure calibration and maintenance of measuring instruments and gauges.

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 | Labelling & Packing Division :- Formulation Interview Date:-08-11-2025 (Sunday) Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur | MSNF-V R.K.Puram Venue Location :- Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbubnagar, Telangana 509001) Contact No:- 040-304338954 Note:- Candidate should bring Update Resume , Increment Letter, Paysli...

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 | Labelling & Packing Division :- Formulation Interview Date:-09-11-2025 (Sunday) 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, Ce...

Responsibilities: * Develop quality plans & procedures * Conduct regular audits & inspections * Collaborate with cross-functional teams on improvement initiatives * Ensure compliance with QMS standards. * Wind Experience Quality candidate Male only. Office cab/shuttle Health insurance Free meal Cafeteria Travel allowance Employee state insurance Life insurance Retention bonus Provident fund Job/soft skill training

Role & responsibilities Job Title: Quality Assurance (QA) Officer Department: Quality Assurance Location: Piplaj , Ahmedabad Job Responsibilities: 1. Quality Compliance & Documentation: Ensure compliance with cGMP, GLP, and company SOPs across all departments. Review and control of Batch Manufacturing Records (BMRs) and Batch Packing Records (BPRs) . Ensure proper documentation and archival of all QA records as per GDP (Good Documentation Practices) . Review and preparation of Annual Product Quality Reports (APQRs) . Review and maintain calibration and validation documentation for all instruments and equipment. Review and maintain records for documentation issuance, retrieval, and control. 2...

Quality Compliance Manager What you will do Lets do this! Lets change the world! We are hiring a Quality Compliance Manager, which will operate within the General Medicine & Obesity Quality Therapeutic Area. In this vital role you will provide proactive end to end quality support for the development and implementation of a risk-based quality assurance strategy that advances quality by design principles for the full clinical development program. (protocol development, database lock, and regulatory submissions/ approvals). Reporting to the Quality Compliance Associate Director, you will oversee quality management and ensure compliance for global and local clinical trials by supporting study te...

Walk In Drive For Production OSD In Formulation Division @ Kothur Department:- Production OSD Qualification :-ITI | BA | Diploma | BSC | B Pharmacy | M Sc | M Pharmacy Experience :- 2 To 8 Years Skills :- Operator: Compression | Coating | Granulation | Capsule Filling Manufacturing: Supervisor | Shift IN charge Packing operators: Cartonator | Auto Cartonator | Packing Supervisor | Blister Packing | Bottle Packing Division :- Formulation Interview Date:- 08-11-2025 Interview Time :- 9.00AM TO 2.00PM Work Location:- MSNF-II , Kothur Venue Location:- Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbubnagar, Telangana 509001) Note:- Candidate should bring Update Resume , ...

1.Dy.Manager - ( QMS/VALIDATION) Exp-10-15+yrs in a pharmaceutical or analytical lab,especially validation,transfer and verification activity The analytical method validation specialist is responsible for developing,validating and transferring analytical methods to ensure they meet regulatory standards(ICH,USP,FDA,EMA) 2.Asst Manager-( QMS/VALIDATION) Exp-10-15+yrs in a pharmaceutical or analytical lab,especially validation,transfer and verification activity The analytical method validation specialist is responsible for developing,validating and transferring analytical methods to ensure they meet regulatory standards(ICH,USP,FDA,EMA) 3. Executive/Sr.Executive- 3 to 6+yrs Validation Execution...

Greetings! & very warm welcome to BEST-FIT Recruitment Riders, We are BEST-FIT Recruitment Riders feel immense pleasure to search and provide you with better carrier opportunities to aid you in achieving your aspirations. BEST-FIT Recruitment Rider is a highly specialized Recruitment & Executive Search Partner for Pharmaceutical, Biotech, CRO, Chemicals, Medical Devices & Turnkey Pharma Projects Engineering-Construction Design Sectors. We are searching & recruiting highly qualified professionals for Middle-Senior-Upper-Management and Executive jobs. (Eg: Managers, VP, President, CFO & CEO). Also offering customized recruitment services by Headhunting & Executive Search for Middle & Top manag...

Responsibilities: Experience interacting with global regulatory agencies FDA., Knowledge of QMS Prepare and submit regulatory documentation to authorities across global markets Promotional approval for medical devices and pharmaceutical products

As a Managing Representative (QMS) at Shahnaz Bright Steel Industries Pvt. Ltd., you will play a crucial role in maintaining and improving the company's Quality Management System (QMS). Your responsibilities will include ensuring compliance with ISO 9001 / IATF 16949 standards across all departments, coordinating internal and external audits, tracking closure of Non-Conformities (NCs) and Corrective Action Reports (CARs), conducting Management Review Meetings (MRM), and supporting customer-specific documentation such as PPAP, FMEA, and control plans. Key Responsibilities: - Ensure compliance with ISO 9001 / IATF 16949 standards. - Maintain quality manuals, SOPs, and work instructions (WIs). ...

As a Quality Assurance professional at the cutting-edge electrical cables and wires manufacturer serving aerospace and defence clients, your role will involve overseeing all quality management activities to ensure compliance with aerospace and defence standards (AS9100/MIL/QMS). You will be responsible for developing, implementing, and continuously improving the company's quality systems and certification programs. Your duties will include conducting thorough process audits, root cause analyses, and corrective actions to enhance process reliability. Collaborating with production, procurement, and engineering teams will be essential to ensure material, process, and documentation compliance. U...

As an Assistant Manager - Quality at Voltaira group, you will be responsible for promoting quality achievement and performance improvement throughout the organization. Your key tasks will include: - Interacting effectively with Production and Development teams to maintain product supply and help introduce new products. - Working with purchasing staff to establish quality requirements from external suppliers and ensuring tests and procedures are properly understood and carried out. - Supervising quality staff and inspectors in carrying out tests and checks. - Managing and maintaining the Company's quality inspection and product release programs for incoming and in-process materials, component...

As a System Executive (IT) at the Manufacturing Company located in GIDC, Manjusar, Savli, your role will involve the following responsibilities and qualifications: **Role Overview:** You will be responsible for network maintenance and managing all communication equipment such as Telephone, EPABEX system, Fax, Cellular Phone, ERP system, CCTV camera, Firewall, user profile configuration, Server, and antivirus. Additionally, you should be able to develop software as per the company's requirements and provide training to employees on computer applications. Your role will also include handling ISO, QMS, and EMS documentations. **Key Responsibilities:** - Network maintenance - Managing communicat...

We are looking for competent, dynamic and motivated candidates for Manufacturing- QMS Injectable department for Amneal Pharmaceutical Pvt. Ltd ( Injectable units, SEZ-Matoda Plant,Ahmedabad) Job Description Key Responsibilities: Responsible for preparation & review of the master documents of sterile manufacturing for parenteral facility. Responsible for preparation and review of protocols and reports based on the requirements. Responsible for document management and preparation like BMRs, BPRs, master SOPs etc. Responsible for the handling of change control, deviations, CAPA, investigation etc. Responsible to give training to all the subordinates, technicians and operators of the department....

Responsible for overall Quality Assurance & Control in Gear Division. Expertise in gear manufacturing, machining, metrology lab, vendor audits, customer complaints, QA/QC systems, and ensuring PPM & process compliance across all operations.

1. Store Management: Maintain and control inventory of raw materials, consumables, and finished goods. Ensure compliance with STORE SOP (SOP/STR/02/00) and related documentation. Handle material inward/outward entries, delivery challans, and stock registers. Coordinate with production, QA, and dispatch teams for timely availability of materials. Maintain records for lot traceability, shelf-life items, and calibration tools as per QMS requirements. Ensure periodic physical verification and reconciliation of inventory. 2. Purchase & Procurement: Raise purchase requests as per material requirement and reorder levels. Identify, evaluate, and negotiate with vendors for cost-effective procurement....

Responsibilities: Manage client relationships, drive revenue expansion Execute business negotiations Manage and track new business opportunities and sales targets. Participate in marketing efforts to promote business opportunities. Annual bonus Provident fund Health insurance

Join us as a Quality Automation Specialist In this key role, youll be undertaking and enabling automated testing activities in all delivery models Well look to you to support teams to develop quality solutions and enable continuous integration and assurance of defect free deployment of customer value Youll be working closely with feature teams and a variety of stakeholders, giving you great exposure to professional development opportunities We're offering this role at associate level What you'll do Joining us in a highly collaborative role, youll be contributing to the transformation of testing using quality processes, tools, and methodologies, significantly improving control, accuracy and i...