579 Qms Implementation Jobs - Page 3

Role & responsibilities To support the QA department (Maintenance of QMS documents) & CSV Computer System Validation & Training Records. Manage the auditing process and keep detailed records. To collaborate with the QA team to ensure that the different departments meet the quality standards and collaborate in the audits contracted by suppliers and internal auditors. All this under the established standards in terms of SOPs, Good Clinical Practice, and the needs of the client. Provide advice, interpretation, help and training to other departments, in GCP, SOPs, regulatory issues and internal company policies related to Quality Assurance. Manage in the definition of internal tools and remote a...

Hi, We are hiring for Head -Quality & Regulatory | Bangalore Location. Job purpose Implement, maintain and further develop the ZEISS India Management System, aligned with the Corporate ZEISS Management System, maintain the ISO 9001 certification requirements, and the business requirements across the pan-India ZEISS organization. Regulate, control and improve the quality of all processes throughout the business and the final product to meet the quality needs of our customers and other stakeholders. Embed a culture of continuous improvement throughout the company. Lead the team to achieve quality management system targets for customers and business goals. Main Accountabilities Quality Manageme...

Certified Internal Auditor with 3–5 years' experience in QMS deployment, internal/external audits (IATF/ISO), process/product audits, NC closure, improvement projects, BEST culture promotion, and strong know-how in plastic & painting processes.

*Maintain and implement Quality Management System as per ISO 9001/IATF 16949 standards *Conduct internal and supplier audits and ensure closure of non-conformities *Monitor product and process quality, drive root cause analysis and corrective actions

DIWALI OFFER Urgent hiring for the post of Management Representative sheet metal line Interview F2F and immediate joining Location- Faridabad Thanks & Regards UNICK PLACEMENT Nisha Mathur 9266661621 Call and Whatsapp

Need implement & continual improvement in QMS, manage & develop quality team, skill enhancement, coordinate with certification bodies, develop, update & maintain standards, perform SPC & MSA audits, design & deliver QMS related training programs

Experience in Fabrication Heavy Fabrication , Structure Fabrication , PEB Fabrication NDT Qualified ( UT , RT , MPT , DPT ) Most Preferable if same Crane Field Documentation Knowledge as per QMS location- Taluka Bareja, Matar, Gujarat 387530. Required Candidate profile Factory:- Plot 326/B, Opp Govt Borewell, Sarsa Kanera Road, Taluka Bareja, Matar, Gujarat 387530.

Key Responsibilities : 1. Documentation & Compliance Ensure compliance with cGMP, WHO, EU GMP, USFDA, and other regulatory requirements specific to injectable formulations. Review, control, and maintain SOPs, Quality Manuals, and other QMS documents. Control issuance, retrieval, and archival of GMP documents as per SOPs. 2. Deviations & CAPA Investigation and documentation of deviations, incidents, and non-conformances. Identify root causes using tools like 5 Whys / Fishbone analysis. Initiate, track, and ensure timely closure of Corrective and Preventive Actions (CAPA). 3. Change Control Review and manage Change Control records related to injectable manufacturing. Ensure impact assessments ...

Experience: 10+years Job Location: Remote Qualifications: B Tech / M Tech/ MCA or Higher Work Timings: 1:30 PM IST to 10:30 PM IST We are seeking a person with 10+ years of experience in driving the adoption of Integrated Management Systems (Quality Management Systems) across projects and support functions, with hands-on experience in creating awareness, reviewing artifacts with reference to applicable policies, processes, guidelines, checklists, and templates. The person must have valuable experience in ISO27001:2022, ISO9001:2015. Awareness and exposure of SOC2, HIPAA, and ISO42001 are mandatory as an integrated management system is based on required practices in context with the organizat...

Role & responsibilities Maintain and implement QMS and EMS systems within the organization. Maintain quality and environmental Standards as per ISO-9000 (QMS) and ISO 14000 (EMS). Prepare all documents of Audit & provide control copy to each department and where ever applicable. Prepare Audit NC & take corrective & preventive action. Responsible for all Management Representative (MR) activity. Coordinate / collect data from each department and conduct MRM Meeting. Conduct internal Audit and External audit. Responsible for MPI/DP inspection, and coordinated with production team and ensure the results are delivered without delay. Responsible for all RT casting and complete follow up with RT in...

Ensure the effective implementation of Quality Management system compliant to ISO -9001 in each department/division in the plant and monitor the same. Streamlining existing systems for achieving operational efficiency, and Required Candidate profile QC Manager Candidate should have experience in Sheet Metal Call at 9818040604

PUMP ACADEMY PVT. LTD. QMS MANAGER/ENGINEER (ISO, SoPs & TECHNICAL DOCUMENTATION) We are a Bengaluru-based technology company, at the forefront of Industrial IIoT and AI/ML-driven digital transformation through our flagship platform, iPUMPNET, revolutionizing the way Pumping Stations and Treatment Plants are monitored and optimized. We are now expanding our team and invite experienced Quality Management professionals to join us in our journey toward smarter, sustainable water systems. Position: QMS Engineer (ISO, SoPs & Technical Documentation) Location: Bengaluru Qualification: Graduate Engineer with 5–10 years of relevant experience in Quality Management Systems, ISO implementation, proces...

Responsibilities: * Lead quality initiatives * Ensure compliance with ISO standards * Oversee internal audits & inspections * Implement QMS strategies * Develop & maintain quality policies & procedures Food allowance Health insurance Annual bonus Provident fund

You will be responsible for ensuring the quality and compliance of the organization's products and services through effective implementation and maintenance of the Quality Management System (QMS). As the QA/QMS Head, you will play a critical role in establishing and maintaining a robust quality management system to meet regulatory requirements and customer expectations. You will lead the quality assurance team and work closely with cross-functional teams to drive continuous improvement initiatives. - Develop and implement quality assurance policies and procedures - Conduct internal audits to ensure compliance with QMS standards - Coordinate external audits and regulatory inspections - Analyz...

The QA/QC Lead Auditor conducts internal and supplier audits to ensure compliance with ISO/GMP standards, identifies quality gaps, drives corrective actions, and supports continuous improvement in quality systems. Required Candidate profile Conduct internal & supplier audits, ensure ISO/GMP compliance, prepare reports, track CAPA, support certifications, and drive continuous improvement in quality systems. ISO 9001, ISO 13485, GMP pref.

MR (Management Representative) for SSPL. Diploma/BE Mechanical, 5+ yrs exp, male/female, ISO 9001/14001/18001/IMS 45001. Karnataka-based, willing to relocate Shimoga. CTC negotiable, age <50 yrs. Food allowance Health insurance Annual bonus Provident fund

RESPONSIBILITIES GCP Subject Matter Expert - Provide independent and objective quality advice in support of clinical trial activities and in line with current best practice. Provide quality oversight for Amgen programmes for all stages of products in clinical development Ensure quality oversight for the Risk Assessment Categorization Tool (RACT) for each trial to guarantee the proper identification, prioritization, and mitigation of risks to critical data and processes and patient safety, welfare and rights Support the establishment of regional expertise to ensure quality and compliance to local Regulations Support Clinical Trial Teams for all quality management activities, including Deviati...

EZ Rankings is looking for Quality Manager to join our dynamic team and embark on a rewarding career journey Delegating responsibilities and supervising business operations Hiring, training, motivating and coaching employees as they provide attentive, efficient service to customers, assessing employee performance and providing helpful feedback and training opportunities. Resolving conflicts or complaints from customers and employees. Monitoring store activity and ensuring it is properly provisioned and staffed. Analyzing information and processes and developing more effective or efficient processes and strategies. Establishing and achieving business and profit objectives. Maintaining a clean...

1. Should be able to work under guidance of MR to establish implement & maintain quality system as per API specifications, ISO & IATF standards. 2. Should be able to work under guidance of MR for preparing Procedure, Work Instructions & Formats. 3. Coordinate with expernal certification agency for audit. 4. Cordinate with process owners to update reports for system audit, customer audit. 5. Work under guidance of MR to control internal audit & closure of NC. 6. Good communication skill.

Experience in Fabrication Heavy Fabrication , Structure Fabrication , PEB Fabrication NDT Qualified ( UT , RT , MPT , DPT ) Most Preferable if same Crane Field Documentation Knowledge as per QMS location- Taluka Bareja, Matar, Gujarat 387530. Required Candidate profile Factory:- Plot 326/B, Opp Govt Borewell, Sarsa Kanera Road, Taluka Bareja, Matar, Gujarat 387530.

Role & responsibilities I. Ensure timely revision/review of SOPs implemented by keeping a track of documents to maintain the compliance status of quality system II. Review and assess change controls, deviations and CAPAs by coordinating with IPD sub-functions to ensure effective implementation of approved changes/actions III. Prepare the trend of change controls, deviations and CAPAs to identify the areas of improvement and ensure implementation of remedial actions IV. Prepare the plan for internal audits for IPD sub-functions and monitor its implementation to meet regulatory compliance Preferred candidate profile M.Sc Organic Chemistry with minimum 1 year experience in API QMS Recruiter Moh...

The opportunity Manage a team of Tender Quotation Specialists to deliver high quality, competitive offers and timely submissions to Customers. Prepare Bids & proposals during tendering phase. Drive the team to have complete responsibility for the tenders prepared from IN Operation Center with appropriate inputs from the different stakeholders. How You'll Make An Impact Lead a team of Tender Quotation Specialists in the preparation of competitive offers. Responsible for process, tool & QMS implementation actions within the team. Implement LOM Tendering process in-line with the global framework. Ensure tendering processes are followed within the team and ensure close, efficient collaboration w...

1. Documentation of all processes and system and responsible for storage of all ISO 9001:2015 & IATF related Certificates and Documents 2. Implementation of 4M Change Management and Verification of 4M Change Matrix and Records 3. Cust. complaints Required Candidate profile 4. Find the Root cause analysis and Corrective and Preventive Actions and Submit 8D 5. Lead the implementation of 5S in plant effectively. 6. Conducting regular 5S audits. 7. facing external audits

Responsible for maintaining and improving the QMS to meet standards (ISO 9001, ISO 13485, etc.), leading audits, managing CAPAs, and supporting cross-functional teams to ensure compliance and drive quality improvements across the organization.

Roles and Responsibilities Lead and manage CAPA process from initiation to closure. Coordinate root cause investigations and ensure robust corrective actions. Track and report CAPA metrics and trends to management. Drive quality improvement projects and cross-functional collaboration. Ensure timely documentation and regulatory compliance. Facilitate audits and provide CAPA-related evidence. Support risk management and preventive action initiatives. Qualifications Bachelor’s degree in Engineering, Mechanical or related field. 7+ years’ experience in Quality/Regulatory in the medical device industry. Strong knowledge of ISO 13485, 21 CFR 820, EU MDR, and risk management (ISO 14971). Project ma...