428 Qms Implementation Jobs - Page 9

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 rotary equipment, ensuring compliance with engineering standards and project specifications. Oversee and verify NDE processes, including ultrasonic, radiographic, magnetic particle, and dye penetrant testing. Monitor and improve welding processes, including qualifications, procedures, and inspection protocols. Collaborate with cross-functional teams to address quality issues, implement corrective actions, and promote continuous improvement. Review technical documents, specifications, and procedures for compliance with quality standards. Provide training and guidance on QMS, NDE, welding, Static rotary equipment and quality assurance practices. Maintain records and documentation to support audits and regulatory inspections.

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 processing, conduct audits and inspections to identify areas of improvements in production operations, laboratory practices, warehouse management, organic certifications and provide recommendation for corrective actions. Prepare and disseminate pre-audit documentation and checklists to relevant department. Able to handle multiple functionalities of units with smooth and effective 4. Lead the end-to-end process for obtaining renewing certifications as per NPOP, NOP and EU standards. 5. Requirements like FFL, Regenerative agriculture, GAP, GFCP etc. certification for the farming for organic lands. 6. To ensure and lead along with cross- functional teams for impact- driven projects towards achieving sustainable development of farmers and our supply- chain security, implement governance mechanism with external partners, including Agro vendors, Contract farming, Certification body and developing strategy and monitor in-season implementation maintaining the right process checks and balances in place 7. Application of domain knowledge (Technology transfer/ innovation) who shall be responsible for the timely and right execution of product development activities including product development, supporting pilot and plant trials, Technology transfer activities, specification, protocols, reports, master documents control and ensure for smooth commercialization of product 8. To manage the day-to-day activities of software application for release, strong understanding in data management, problem- solving skills, proactive approach to the newer challenges Preferred candidate profile B.Sc./M.Sc. (Agri) or equivalent education with proven experience in certifications. Should have experience of working in an commercial organization of scale. Min 4 years experience in the field of organic certifications with different agencies. Should be able to have demonstrated leadership abilities, market intelligence and successful handling of new projects.

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 sectors. Youll have the opportunity to work closely with cross-functional teams including design, production, and supplier quality, contributing to continuous improvement initiatives and quality assurance strategies. Main/ Essential Task : Review and close rejection/rework cases daily; ensure documentation and approvals. Analyze major defects; coordinate action plans with cross-functional teams. Review setup approvals and inspection reports to ensure product compliance. Handle customer complaints with 8D reports and ensure timely resolution. Coordinate with SQA on supplier-related issues and complaint closures. Track and validate corrective actions for effectiveness (internal & supplier). Maintain housekeeping and ensure proper flow of materials and documentation. Present rejection/rework summaries in MMR/MRM reviews. Ensure availability of gauges, instruments, SOPs, WIs, and drawings at all workstations. Monitor adherence to process SOPs and quality standards. Plan daily/weekly shift allocations and manage manpower effectively. Conduct inspector skill assessments; plan and execute training needs. Skills Required : APQP, PPAP, FMEA, SPC & MSA. Internal Auditor for IATF16949/AS9100/ISO9001 VSM, 5S & Kaizen. 8D, CAPA Process Optimization & Improvement Data Analysis & Waste Reduction Supplier Development Audit Management - Process, Customer, Certification & Vendor Working location : Dobaspete, Bangalore Interested candidate can WhatsApp their resume to 9742708222.

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 impurities. Harmonization of Cleaning and validation procedures across all sites of Lupin. Work Experience 10-12 years Education Masters in Science Competencies Collaboration Customer Centricity Developing Talent Innovation & Creativity Process Excellence Result Orientation Stakeholder Management Strategic Agility

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 stakeholders to facilitate delivery and compliance with the quality strategy. Automotive Quality Management System Auditing experience and managing audit programmer Preferred candidate profile Knowledge of Process & Product audit is an advantage. Excellent written, verbal and presentation skills Excellent organizational and follow-up skills Competent in problem solving, team building, planning and decision making. Ability to manage a variety of cross-functional team members. IATF Internal/ Lead Auditor Certification (Preference).

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 action as needed. Desired Candidate Profile 14-20 years of experience in Quality Assurance & Regulatory Affairs with expertise in QMS implementation. Strong understanding of pharmaceutical regulations such as FDA, GMP, ISO 9001:2015 etc. Bachelor's degree in Pharmacy (B.Pharma) or Master's degree in Pharmacy (M.Pharma).

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 feedback and suggest improvements for continuous process and product quality. Preferred candidate profile 1. Diploma / B.Tech in Mechanical. 2. Experience in a automotive manufacturing company preferred. 3. Must have good communication skills. 4. Familiar with mechanical drawings and basic GD&T (Geometric Dimensioning & Tolerancing). 5. Knowledge of tools like Vernier, micrometer, height gauge, and other inspection tools. 6. Basic understanding of ISO 9001 / IATF 16949 quality systems. 7. Good communication and documentation skills. 8. Attention to detail and strong problem-solving skills. 9. Familiarity with PPAP, FMEA, CAPA processes. (preferred)

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 CIF, FOB, Ex-Factory & other Inco terms etc. 12. Knowledge of Local Transportation arrangement for procurement. 13. Knowledge of Shipment / Courier tracking. 14. Knowledge of Negotiate pricing & terms with the vendors and set guideline. Knowledge of Consists of planning, Directing, or coordinating the buyer activities. 15. Excellent math abilities and working experience of Data analysis/Statistical method/ Graphical Presentation, Outstanding communication with leadership skills.

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 track record of dedication & reliability A team player who is equally capable of working alone Fluent in both written and spoken English Knowledge /Experience in peptides Qualifications M.Sc. (Chemistry)/B. Pharm./ M.Pharm.

Accountable for ensuring the smooth functioning of the Quality function of the organization and availability of QMS and Tools on the intranet. Hands on experience in ensuring the effective implementation of the Organizational Quality processes. Health insurance Provident fund

Job description ISO Consultant Job Type: Full-time, Permanent, Freelance Remuneration :- 6,00,000 to 12,00,000 per year for ISO , 6,00,000 to 12,00,000 per year for ZED , 18,00,000 for each MCLS cluster of 10 clients for Intermediate and Advance level, which is done in 18 to 24 months. Total Remuneration 12,00,000 to 24,00,000 per year. Hybrid Working – Visit to the client’s factory is required at your & client’s mutual convenience. Schedule : Flexible shift Education: ( Any of the following) 1. Any Gradutate with knowledge of ISO consultancy/ISO Auditing/ Quality Related fields 2. Any Graduate with minimum 8 years industrial experience in manufacturing. 3. Diploma with 10 years industrial experience in manufacturing 4. BE/BTech with 8 years industrial experience in manufacturing 5. Knowledge of ISO &/or Lean tools implementation/Documentation/Consultancy/Systems/Quality related fields shall get additional weightage Place of Posting:- Shall be required to cover industries near your residence to provide onsite/ Offsite consultancy in factories. Roles and Responsibilities :- 1. To provide onsite and offsite consultancy to the MSME manufacturing clients for doing ISO 9001/14001/45001 consultancy at client’s site and offsite. 2. Same Consultants shall be trained to provide ZED consultancy of the Central government scheme of Zero Defect Zero Effect (ZED) promoted by Ministry of MSME. 3. Same consultants shall also be trained to provide consultancy for lean tools under MCLS MSME Competitive (Lean) Scheme promoted by government of India. Training :- 1. The candidate shall be trained by our company so that he can pass an online examination of Quality Council of India (QCI) to become a national level approved ZED certified consultant and subsequently trained to become national level approved MCLS certified consultant. 2. After clearing the online exam, the consultant shall be allotted MSME manufacturing clients by our company for implementation of ZED scheme. 3. ZED consultant shall be required to implement the ZED &/or lean techniques / modules to help the client obtain ZED/MCLS certification as per the guidance of our company. 4. Consultant shall be provided regular training, support and guidance from the head office so that the ZED/MCLS modules can be implemented properly at client’s factory and ZED &/or lean certificate is delivered in time. Perks and Benefits: 1. Performance incentives Like New Laptop, New Mobile, New Inverter for your residence after starting at least 3 projects as per company norms. 2. No outstation travel required 3. Cell phone reimbursement 4. Flexible schedule 5. Internet reimbursement ABOUT THE COMPANY – BMCPL Boon Management Consultants Pvt. Ltd. (BMCPL) is a consultancy organization (Incorporated in 2005) that specializes in providing services for improvement of systems including capacity building, implementation of lean tools, ZED Consultancy etc. BMCPL is providing consultancy and training services to it’s clients all over India through our consultants located pan India. Besides many private and services sector clients , we are providing services to government/semi-government organizations. Some of our government clients are 33 ZILLA PARISHADS, RURAL DEVELOPMENT DEPARTMENT- GOVERNMENT OF MAHARASHTRA, OFFICE OF GOVERNOR OF MAHARASHTRA, etc. For the ZILLA parishad project done by us, RURAL DEVELOPMENT DEPARTMENT (RDD) has won National Award. MoMSME has selected Quality Council of India (QCI) which is an autonomous body under Govt. of India for implementing and Monitoring ZED scheme across India. QCI has selected BMCPL as a ZED consulting organization and also for MCLS consulting organization for pan India operations. About the ZED Scheme: The Ministry of MSME has selected the Quality Council of India (QCI), an autonomous body under Govt. of India to implement and Monitor the ZED (Zero Defect Zero Effect ) scheme across India. QCI has selected BMCPL as a ZED consulting organization for pan-India operations. The majority of the fees for this project shall be paid by govt. (Ministry of MSME/QCI) and negligible cost shall be borne by the client.The details of the scheme can be seen on govt. website zed.msme.gov.in Till date Boon has trained 150+ ZED consultants and 40+ MCLS consultants from different parts of India Like Maharashtra, West Bengal , Gujrat, Telangana, Tamil Nadu, AP, Karnataka, etc. The consultants have passed the Quality Council of India Examination and have received ZED Consultant certificate. BMCPL has 700+ MSME clients who have taken Pledge to become a ZED certified organisation. Out of this 500+ MSME clients have already received ZED Bronze certification, 200+ clients have received ZED Silver certification and others are in process to get ZED Silver/Gold certification. BMCPL has 100+ MSME clients who have taken pledge to do MCLS and out of this more than 50 MSME clients have received MCLS BASIC level certificate.

Roles and Responsibilities Ensure compliance with quality management systems (QMS) through implementation, maintenance, and continuous improvement of ISO documentation. Prepare SOPs for various processes such as BMR, CAPA, Change Control, Cleaning Validation, etc. Conduct qualification testing and validation protocol execution to ensure product quality and regulatory requirements. Develop and maintain accurate records of test results, reports, and certificates related to quality assurance activities. Collaborate with cross-functional teams to identify areas for improvement in quality control processes. Desired Candidate Profile 5-10 years of experience in pharmaceutical industry with expertise in QMS implementation. Strong understanding of GMP regulations and industry standards like ISO 9001:2015. Proficiency in preparing documents like BMR, SOPs, Capas, Change Control procedures. Experience with cleaning validation process validation protocol execution.