581 Qms Implementation Jobs - Page 15

Job Responsibilities: 1) Manage and control all documentation related to the Integrated Management System (IMS), including policies, procedures, manuals, and records. 2) Coordinate activities related to the implementation and maintenance of IMS across departments and teams within the organization. 3) Assist in the implementation of IMS standards (ISO 9001, ISO 14001, ISO 45001) within the organization, ensuring compliance and continuous improvement. 4) Coordinate training sessions related to IMS and other relevant topics for employees within the organization. 5) Assist in maintaining and improving the quality management system (QMS) as per ISO 9001 standards. 6) Support the implementation an...

Job Overview: As the Assistant Manager - QMS, you will be responsible for supporting the implementation, maintenance, and continuous improvement of the Quality Management System (QMS) in accordance with IATF 16949:2016 standards. You will ensure that all quality processes meet customer and regulatory requirements, and you will play a critical role in preparing and participating in internal and external audits. Key Responsibilities: QMS Implementation & Maintenance: Candidate should be able to lead plant QMS & CI activities. Assist in the development, implementation, and monitoring of the QMS to ensure compliance with IATF 16949:2016 standards, ISO 9001:2015 Standards. Ensure that QMS process...

Quality Head is a person who looks after the quality of product & assures its understanding customer specific requirement, handles QMS & audits, take follow up of internal documents training evidences & customer complaints. Required Candidate profile Customer complaint its resolvement & loss due to sales return. Handling standard documents CSR, Audit with No NC. Note : All local candidate from Saphale ,Virar,Nallasopara,Naigaon ,MiraRoad ,Borivali

Quality Head is a person who looks after the quality of product & assures its understanding customer specific requirement, handles QMS & audits, take follow up of internal documents training evidences & customer complaints. Required Candidate profile Customer complaint its resolvement & loss due to sales return. Handling standard documents CSR, Audit with No NC. Note : All local candidate from Saphale ,Virar,Nallasopara,Naigaon ,MiraRoad ,Borivali

Participate in internal and external audits (USFDA, EDQM, WHO, MHRA, etc.),Ensure compliance with GMP, ICH, and regulatory guidelines in API manufacturing.Conduct in-process checks and ensure batch release activities are done per quality procedures. Required Candidate profile Experience of QMS software Exposure to regulatory audits and good Manufacturing practices. Strong communication and documentation skills. Sound knowledge of regulatory guidelines ICH, WHO, USFDA

Roles and Responsibilities Ensure compliance with ISO standards through implementation, documentation, and auditing processes. Conduct internal process audits to identify areas for improvement and implement corrective actions (CAPAs). Manage vendor audits, MRM systems, PPAP documentation, IATF certification requirements. Develop and maintain quality management systems (QMS) policies, procedures, and guidelines. Collaborate with cross-functional teams to ensure effective communication and coordination.

experienced Quality Head to lead and oversee the quality assurance and control processes at our manufacturing facility in Papparambakkam. andidate will have a strong background in quality management, with in-depth knowledge of ISO and IATF standards.

Title: Mechanical QMS Location: Bangalore Contract: FTC for 2 yrs Job Summary: We are seeking an experienced Mechanical QMS Engineer to join our dynamic team. The ideal candidate will have a strong background in quality management systems, specifically ISO 9001:2015, with hands-on expertise in static and rotary equipment, non-destructive testing (NDE), and welding processes. This role will be pivotal in ensuring that all mechanical equipment meets the highest quality standards, supporting both operational excellence and compliance. Key Responsibilities: Develop, implement, and maintain QMS in accordance with ISO 9001:2015 standards. Conduct quality audits and inspections for static and rotar...

Role & responsibilities 1. Spearhead and deliver end to end organic certification requirements of the company with close participation with agriculture team, processing teams and finished goods team. 2. Management of Regulatory Authorities: Interact with regulatory agencies, responding to inquiries and submissions. Represent the company during inspections and audits 3. Experience in smooth implementation of Quality Management System (QMS), Vendor due diligence, strengthen contract manufacturing units and implementing robust compliance measures. Ensure compliance with company policies and procedures related to Quality assurance, develop, and implement effective QA process for herbal processin...

An ISO Lead Auditor is a certified professional responsible for leading and managing an audit of an organization's management system against specific ISO standards. He must get membership from IAF to the company Call or Whatsapp resume to: 7710336699 Required Candidate profile ISO ISO Auditor Lead ISO Implementation ISO Audit ISO Documentation ISO Systems ISO Consultant ISO 27001 Lead Auditor Lead Auditor ISO QMS QMS Implementation Accreditation NABL NABH Quality Control

Greetings! We are looking for a highly motivated and detail-oriented Sr. Quality Engineer professional to join our QAD team. In this role, you will play a critical part in ensuring the quality and compliance of manufacturing processes, components, and final products across various projects. As an experienced Sr. quality engineer, you will be responsible for overseeing inspection activities, analyzing quality data, driving root cause analysis, and implementing corrective and preventive actions. You will also support the development and maintenance of quality documentation, procedures, and control plans to ensure adherence to industry standards, especially in the automotive and aerospace secto...

Strategic planning to resolve all quality issues observed & received in existing and new products. continually improving of product ,Process and System. implementations of techniques ,Audits and Quality management Systems, Customer handling.

Quality Planning & Execution, Provide support for all supplier quality related activities. receiving Inspection Operations. Supplier Quality Management Quality Systems & Audit Management Quality inspection of raw/incoming materials Required Candidate profile Conduct Inspection and clearance of child parts lots at receipt stage as per MISP, Implement action plan for key gaps highlighted through Dashboards (PPM/COPQ/QPR)

CUSTOMER INTERACTION DURING DEVELOPMENT CYCLE CUSTOMER AUDIT / LINE AUDIT CLOSURES SUBMISSION PROBLEM SOLVING DURING DEVELOPMENT COUNTERMEASURE SUBMISSION TO CUSTOMER CUSTOMER SATISFACTION PPAP SUBMISSION TIMELY CLOSURE OF PROJECT MILESTONE

Job Description Responsible for Toxicological assessment of genotoxic and nitrosamine impurities. Responsible to support the development of nitrosamine and other genotoxic impurity risk assessment and carryover limits. To support the site management team in reviewing cleaning, nitrosamine and genotoxic impurity and keep sites up to date according to current regulatory requirement /expectation. Reviewing Permissible Daily Intake, Occupational Exposure Limits, Toxicological Justification, Quality Risk Assessment document. Responsible for preparation and revision of corporate procedures like SOP related to the assessment of potential carryover or cross-contamination of genotoxic/carcinogenic im...

Responsibilities: * Lead ISO/IATF compliance program * Conduct internal audits & preventive actions * Manage QMS implementation & maintenance * Ensure engineering standards in foundry operations * Oversee quality system management Office cab/shuttle Food allowance

Role & responsibilities Contribute to the creation and implementation of best practice capacity planning vision, strategy, policies, processes, and procedures to aid and improve operational performance Contribute to new business initiatives, projects, review and communicate the impact on Quality Management Systems (QMS). Develop the Management Systems strategy and the management arrangements for key milestones, demonstrating solid progress against plan. Contribute to the creation and implementation of best practice capacity planning vision, strategy, policies, processes and procedures to aid and improve operational performance, Work collaboratively, negotiate, and engage with key stakeholder...

Roles and Responsibilities Develop and implement quality management systems (QMS) policies, procedures, and guidelines to ensure compliance with regulatory requirements. Conduct internal audits to identify areas for improvement and implement corrective actions to address non-conformities. Prepare and maintain accurate records of quality documentation, including standard operating procedures, work instructions, and training materials. Collaborate with cross-functional teams to develop new products or processes that meet customer needs while ensuring adherence to quality standards. Ensure ongoing monitoring of production processes to detect deviations from specifications and take corrective ac...

Role & responsibilities 1. Conduct incoming inspection of raw materials and components as per quality standards. 2. Perform in-process and final inspections on manufactured parts/products. 3. Use various measuring tools and equipment such as Vernier calipers, micrometers, gauges, etc. 4. Identify and report any non-conformities and assist in root cause analysis (RCA). 5. Collaborate with production and design teams to ensure quality issues are addressed promptly. 6. Support audits (internal and external) and assist in documentation such as 4M change records, inspection reports, control plans, etc. 7. Ensure adherence to 5S, ISO/IATF quality standards, and safety guidelines. 8. Provide feedba...

QMS professional in the valve mfg industry needs a strong understanding of API std & application to valve design, manufacturing, & testing . knowledge of API 600, API 602, API Q1,also experience with QC procedures, testing , & documentation .

Being a Biotech graduate having one - two - three years experience in biotech manufacturing industries in all department reputed biotech industries required urgently in Vapi and Daman surrounding area. Required Candidate profile BSC Bio / Msc Biotech / B. tech Biotech / Fresher or experience 1 / 2 / 3 years.

Manage the Quality Assurance function at manufacturing site Ensure compliance with ISO, GMP & REACH standard Develop, implement & monitor Quality Management Systems including SOPs, documentation & CAPA systems Handle customer complaints, conduct RCA Required Candidate profile 8–12 years of experience in QA, preferably in specialty chemicals Knowledge of analytical instruments, QC processes & technical documentation Strong knowledge - ISO 9001, GMP & other quality standards

Testing of all Dairy product Follow by SOPs Manual Ex. Milk quality, Ghee, Butter, Curd, G.J. Mix Powder, Colostrum Powder, Milk Powder (SMP, WMP), Whey Powder (DM-40, DM-70, WPP, WPC- 35, WPC-80, WPI-90) & its record as well as result.

Job Description: - 1. Working Knowledge with Documentation of Purchase Dept. 2. Working Knowledge of P.O making in Excel and in ERP/Software. 3. Working Knowledge of Materials Management. 4. Working Knowledge of making All type of P.O like job work, Domestic & International. 5. Knowledge of Measurement / Conversion. 6. Knowledge of Quote arrangement and Quotation compare and rate approval. 7. Knowledge of Supplier Management Systems as per ISO,QMS. 8. Knowledge of Follow up with Domestic & International Client/Supplier. 9. Knowledge of Supplier Evolution and Performance. 10. Knowledge of Packing, Consumable, House-keeping, Machinery & Raw Materials. 11. Knowledge of P.O Payment terms like CI...

Job Overview To ensure effective quality assurance activities related to batch release, review of analytical data, batch records, QMS elements, and compliance with regulatory standards to support timely product release. Roles & Responsibilities: Batch Release Management Hands on analytical experience Review of QC Analytical Data including electronic data review Review of Batch Records including audit trail review Preparation and Review of APR Responsible for review of QC activities Initiation and review of QMS elements (Deviation/Change Control/OOS/OOT/CAPA) Dispatch and Line clearance Cleaning Validation Competencies Quick learner with excellent communication skills Punctual with proven tra...