235 Qms Implementation Jobs - Page 8

Managing and implementing QMS with deep expertise in ISO 9001, ISO 14001, ISO 45001, and IATF 16949. Experience in Automotive manufacturing is a must. Drive continuous improvement initiatives, focusing on reducing waste & improving efficiency. Required Candidate profile Implement (CAPA) based on audits, customer feedback, and internal analysis. Exp of Export related compliances like Sedex, BSCI etc, with excellent communication skills. Must have dealt with customers

PTRC- PERFICIO TESTING AND RESEARCH CENTRE is looking for Quality Manager to join our dynamic team and embark on a rewarding career journey Develop and implement quality management systems and processes. Conduct quality audits and inspections. Monitor and analyze quality performance metrics. Collaborate with cross-functional teams to address quality issues. Provide training and support on quality standards and procedures. Ensure compliance with regulatory and quality standards. Stay updated with industry trends and best practices in quality management. Leadership Skills Retail Knowledge Communication Skills Problem-Solving Abilities

QA Head Seeking a QA Head to ensure skincare products meet regulatory, safety, and quality standards. Work closely with manufacturing, R&D, and QC teams. Requirement: 4+ years of QA experience, preferably in cosmetics or pharma manufacturing. Required Candidate profile Skincare manufacturing & QC expertise Knowledge of FDA, GMP, ISO regulations Attention to detail & procedural compliance Strong analytical, problem-solving & com skills Ability to train & improve Jr.

Formulate & implement a comprehensive Quality Assurance Strategy for textile operations. Ensure adherence to global standards including IATF ,OEKO-TEX, ISO, etc. Lead certification and compliance efforts including documentation, audits, & renewals

Role & responsibilities Greetings from Randstad India !! We are looking to fill a Asst Manager- Quality position at our client. MNC Company is known for designing furniture in commercial places. Below are the details about this role, Position Summary- Looking for an Asst. Manager Quality with 5 to 8 years of experience in managing Quality Management Systems (QMS) and EHS compliance. The role involves conducting internal and third-party audits, ensuring timely NCR closures, and managing ISO 9001, 14001 & 45001 documentation. Responsibilities include organizing MRM, employee training, and instrument calibration. Proficiency in audits, documentation, and MS Office is essential. Mechanical engineering qualification (D.M.E./B.E.) is required. below is the detailed job description. - Qualifications and Key Skills and for this role, DME/B.E./B. Tech in Mechanical. Experience in ISO 9001, ISO 45001 and ISO 14001, Knowledge of QMS, Health, safety and environmental system documentation Ensure quality management and EHS systems, conduct internal and third-party audits & its effective closure Prepare system requirements documentation and MRM reports Experience in handling audits, customer complaints, and root cause analysis Proficient in quality tools like 7 QC Tools, FMEA, CAPA, and SPC Preferred candidate profile Any Manufacturing company Preferred : Retail Manufacturing company

Min. exp. 3 years /5 years - Max. exp. 7 to 10 years for BE/Diploma holder having exp in SCADA system of Solar plant. Experience in commissioning, O&M of SCADA system, trouble shooting of SCADA system (any one) of OEM - EMERSON/ABB/SIEMENS/GE/TRINITY / BRODERSEN /any other make Strong knowledge about components, systems, system architecture, Logic navigation, ethernet system, etc. Note: Experience candidate from Thermal power station with Instrumentation & Control Background also preferred Roles and Responsibilities : We are having multiple site (Solar O&M) with different types of SCADA supplier/systems. Candidate to support site in-charge/site team for O&M/maintenance/trouble shooting of SCADA system/trouble shooting of field components. Should able to read/interpret SCADA supplier documents. Ensure 100 % availability of SCADA system. Reduce outages/non-availability of readings/equipment status in HMI Regular back up/historian back up Report Generation Candidate to travel site for regular monitoring/guidance to site team. Remote support to site team for trouble shooting. Recommend suitable upgrade for old components/system of SCADA. Regular PM/ BD Quality Management System Implementation. Adherence to EHS Requirements Adherence to O&M manual requirements Maintaining equipment warranty/ guarantee Job location : Multiple site- PAN India 75 % travel (minimum). Candidate can operate from any central office of organization.

Job Title: Asst. Manager / Sr. Engineer Operation & Maintenance (Solar) / Site In-charge Experience : Min. 7 years to 10 years exp in Solar Operation & Maintenance. ( at least should have handled single plant capacity of 50 MW solar power plant, experience in electrical equipment testing and commissioning is mandatory) Job Description: Daily monitoring the functions of all electrical equipment s. All reports to be maintain as per site requirement. Subcontractor Management. Regular trainings to subordinates for their development as per site Store/Spares Management. Schedule and execute the Planned Preventive Maintenance (PPM) Attending of Breakdown maintenance at minimal duration. Annual testing of Electrical Equipment Reporting to Project Manager.- DGR, Maintenance Report, Breakdown/ RCA report Quality Management System Implementation. Adherence to EHS Requirements Adherence to O&M manual requirements Maintaining equipment warranty/ guarantee. Ensuring Contractual KPI Generation, PR Stake holder management Internal : Reporting manager, supply chain, F&A, Engineering, External : Client , Vendor / sub-contractor Candidate will work as Site In-charge. Should lead a team of minimum 15 plus team members (Engineers, Technician) Strong knowledge of Electrical equipment operation & maintenance philosophy Experience in Electrical Testing & Commissioning preferred Strong in Maintenance planning of SOLAR plant Soft skills : Should be good in MS- Excel, word, ppt ; Communication : transparent & clear (verbal); Basic email communications Able to manage the site Understand O&M contract T&C Able to manage site budge

Job Title: Asst. Manager / Sr. Engineer Operation & Maintenance (Solar) / Site In-charge Experience : Min. 7 years to 10 years exp in Solar Operation & Maintenance. (at least should have handled single plant capacity of 50 MW solar power plant, experience in electrical equipment testing and commissioning is mandatory) Job Description: Daily monitoring the functions of all electrical equipment s. All reports to be maintain as per site requirement. Subcontractor Management. Regular trainings to subordinates for their development as per site Store/Spares Management. Schedule and execute the Planned Preventive Maintenance (PPM) Attending of Breakdown maintenance at minimal duration. Annual testing of Electrical Equipment Reporting to Project Manager.- DGR, Maintenance Report, Breakdown/ RCA report Quality Management System Implementation. Adherence to EHS Requirements Adherence to O&M manual requirements Maintaining equipment warranty/ guarantee. Ensuring Contractual KPI Generation, PR Stake holder management Internal : Reporting manager, supply chain, F&A, Engineering, External : Client , Vendor / sub-contractor Candidate will work as Site In-charge. Should lead a team of minimum 15 plus team members (Engineers, Technician) Strong knowledge of Electrical equipment operation & maintenance philosophy Experience in Electrical Testing & Commissioning preferred Strong in Maintenance planning of SOLAR plant Soft skills : Should be good in MS- Excel, word, ppt ; Communication : transparent & clear (verbal); Basic email communications Able to manage the site Understand O&M contract T&C

1. Quality Management System (QMS) Implementation - Develop, implement, and maintain the companys QMS in compliance with ISO Standards - Conduct internal audits to ensure adherence to QMS procedures. 2. Documentation & Control - Review and approve supplier/vendor QA documents. - Ensure traceability and documentation of materials, welding activities, NDT reports, and inspection logs. 3. Supplier & Vendor Evaluation - Conduct QA audits and assessments of vendors, subcontractors, and suppliers. - Review and verify vendor quality documents, manufacturing records, and material test certificates (MTCs). - Ensure all bought-out items comply with technical and quality standards. 4. Compliance & Codes - Ensure compliance with national and international codes and standards such as ASME, PED, API, ASTM, ISO, and client specifications. - Support compliance during audits by third-party inspection agencies (TPIs) and clients. 5. Non-Conformance & Corrective Actions - Identify, document, and track non-conformities (NCRs) and issue corrective/preventive actions (CAPA). - Follow up on close-out of NCRs and ensure root cause analysis is carried out effectively.

Job Title: Quality and Regulatory Manager (Medical Devices) Reports to: Director of Quality / Head of Operations Job Summary The Quality and Regulatory Manager is responsible for ensuring that all medical device products comply with global regulatory requirements (e.g., US FDA, EU MDR, ISO 13485), maintaining effective quality management systems, and facilitating successful regulatory submissions. The role involves leading internal and external audits, managing documentation, and supporting cross-functional teams to ensure the safety, efficacy, and compliance of medical devices throughout the product lifecycle. Key Responsibilities Quality Management System (QMS): Develop, implement, and maintain the QMS in accordance with ISO 13485, FDA 21 CFR Part 820, and other applicable regulations. Lead internal and external audits, and manage corrective and preventive action (CAPA) processes. Ensure proper documentation, control, and retention of quality records and regulatory files. Oversee product nonconformance investigations and ensure timely closure of deviations. Regulatory Affairs: Prepare, compile, and submit regulatory filings (510(k), CE Mark Technical Files, etc.) for new and existing products in global markets. Monitor and interpret global regulatory changes, ensuring the company remains in compliance. Serve as primary contact for regulatory agencies and notified bodies during inspections and audits. Develop and maintain product registration dossiers and technical documentation. Risk Management: Lead risk management activities in accordance with ISO 14971, including hazard analysis and post-market surveillance. Support product recalls, field safety corrective actions, and complaint investigations. Training & Continuous Improvement: Train and mentor staff on quality and regulatory requirements. Drive continuous improvement initiatives for product and process quality. Cross-Functional Support: Collaborate with R&D, Manufacturing, Supply Chain, and Marketing to ensure compliance in product design, labeling, packaging, and advertising. Support new product development teams with regulatory strategy and submission pathways. Qualifications & Requirements Bachelors or Master’s degree in Engineering, Life Sciences, Pharmacy, or related field. Minimum 2 years’ experience in quality and/or regulatory roles in the medical device industry. Strong knowledge of ISO 13485, FDA 21 CFR Part 820, EU MDR/IVDR, and related standards/regulations. Experience preparing regulatory submissions (510(k), PMA, CE Mark, etc.). Lead Auditor certification for ISO 13485 (preferred). Excellent written and verbal communication skills. Strong organizational and project management abilities. Key Competencies Detail-oriented and analytical. Problem-solving and decision-making skills. Ability to work cross-functionally and lead teams. Up-to-date with global regulatory trends and requirements. Location: [Insert location] Employment Type: [Full-time/Part-time/Contract] Let me know if you want to add anything about company culture, reporting structure, or specific product lines!

Strong Online Testing & Analysis knowledge Strong Sampling & Methodology knowledge Instrument Calibration & Validation Documentation & Label Method Development & Validation Strong SOP & QMS Compliance Candidates from Herbal/Phyto industry is required

Establish control quality budgets for investments, personnel, laboratories & measuring equipment control within the plant. To maintain and improve the QM system, Quality awareness and practices. Required Candidate profile Establish Quality education and training like Core tools and Technical topics. Experience with Quality tools- APQP/ SPC/MSA/FMEA/PPAP and customer specific requirements across Automotive Industry.

Job Description: We are looking for a detail-oriented and proactive ISO 9001 Compliance Specialist to lead our efforts in achieving ISO 9001 certification. The ideal candidate will have extensive knowledge of ISO 9001 standards and experience in preparing manuals, developing processes, and ensuring overall compliance. Key Responsibilities: Develop and implement ISO 9001 compliant processes and procedures. Prepare and maintain the ISO 9001 Quality Manual. Conduct internal audits to ensure compliance with ISO 9001 standards. Provide training and support to staff on ISO 9001 requirements. Identify areas for improvement and implement corrective actions. Liaise with external auditors and certification bodies. Ensure continuous improvement of the Quality Management System (QMS). Qualifications: Bachelor's degree in Engineering, Quality Management, or a related field. Proven experience in ISO 9001 implementation and compliance. Strong understanding of ISO 9001 standards and requirements. Excellent organizational and project management skills. Ability to work independently and as part of a team. Strong communication and interpersonal skills. Certification in Quality Management or related field is a plus. What We Offer: Competitive salary and benefits package. Opportunity to work with a dynamic and innovative team. Professional development and growth opportunities. A supportive and collaborative work environment. How to Apply: Interested candidates are invited to submit their resume and cover letter detailing their experience and qualifications to WhatsApp +919820274179 or email: info@samaaaerospace.aero

KRA's: Quality check of all raw materials, in-process and finished goods on a FIFO basis QMS Implementation Audit Documentation Internal/ external as well as 3rd party/ regulatory audit compliances Required Candidate profile 5+ years of experience in Quality [quality inspection, auditing, testing, reporting] in a medical device/ pharmaceutical manufacturing co. Should be ready to travel or relocate to Taloja Navi Mumbai

KRA's: Ensure SOPs are followed & quality standards are met Quality check of raw materials, in-process & finished goods on a FIFO basis QMS Implementation Audit Documentation Audit facilitation - Internal/ external & 3rd party/ regulatory audits Required Candidate profile 5+ years of experience in Quality [quality inspection, auditing, testing, reporting] in a pharma/ medical device mfg. co Ready to relocate to Medchal, Hyderabad Accommodation & food will be provided Perks and benefits Accommodation and Food provided

Looking for Senior Manager-Corporate Quality Assurance with 8 to 15 yrs of relevant experience in QMS- Wooden furniture for Wooden Furniture Export House, Moradabad, UP. - Must have sound experience in QMS with wooden furniture exports house/Buying house, Liaison Offices, etc. - CTC: 10 to 14LPA - Email: jobs@rjcube.com Job Descriptions: To ensure that Quality of products, processes and services are established, monitored and maintained within the plant. Quality objectives are established, monitored and maintained against the defined Goals. Work closely with Production & NPD team in determining best methods to accomplish desired results. Specifically aware about Exports Buyers like TARGET / H&M / WSI / RUSTA / IKEA / PB etc To establish Strong Customer Base while performing Internal / External Audits & Plant Improvements. Develop and maintain Quality Standards and check procedures throughout the facility. Analyzing the rejections / rework / statistical data to take corrective and preventive actions to eliminate the root cause of the problems in order to prevent the recurrence of the problem. Develop a plan, promote, facilitate, and organizes training activities for all respective persons related to product quality and standards in quality assurance. Responsible for quality inspection failing; final inspection, in-process/inline quality audit, and inspection. Responsible for customer (buyer) quality claim and all technical audits and implementation of customer technical requirements. Ensure people/ process adhere to Company norms /standards, 5S, QC & improvement activities etc. Skills / Knowledge: Know about: Wood Manufacturing Process and physical characteristics of wood Knowledge of solid woods, Metal & Veneer natural manufacturing defects and characteristics. Good comm skills Proficient with MS Office. Critical thinking and problem-solving skills Ed. Qualification: Graduation / Graduation (Wood Technology) / B.Sc. Wood Technology / B. Tech (Mechanical) B. Tech (Wood Technology) / MBA (Preferred)

QMS develop implement & maintain QMS that meets industry standards (e.d ISO 9001 IATF 16949) Quality Process, Product Quality Process Control Quality Planning, Supplier management, inspection testing, training development, technical knowledge strong Required Candidate profile Should have good experience electronics plant ( PCBA (SMT ). Individual handling of overall SMT PCBA.

Responsibilities: * Lead quality audits, document processes, manage PPAPs & MSA. * Implement QMS, oversee APQP, execute SPC & SPM. * Ensure compliance with industry standards, drive continuous improvement. * Document Consultant Annual bonus Provident fund Performance bonus Travel allowance

Any Graduate or DE / BE (Electrical/Mechanical) 5 - 7 Years Expertise in ISO standards,quality management systems,auditing procedures, documentation control,process improvement methodologies,leadership abilities, & effective communication skills.

Urgent opening for Quality Manager.Candidate should have hand on experience on QMS / Testing methodologies.technical documentation. OHSAS, EMS. Audit based on ISO.

Role & responsibilities Design and implement documentation for the ISO 9001:2015 Quality Management System (QMS) in relation to product standards. Fulfill the requirements outlined by the ISO 45001:2018 Occupational Health and Safety Management System (OHSMS). Assess and confirm safety clearances while ensuring compliance with safety protocols during testing and commissioning processes. Offer continuous support and direction to departmental teams to improve awareness and compliance with QMS and OHSMS standards, reinforcing a safety- and quality-driven culture. Perform internal audits across departments to verify conformity with established QMS and OHSMS procedures. Represent management in contract reviews, identifying quality-related risks and proposing appropriate mitigation plans. Develop the Manufacturing Quality Assurance Plan (MQAP) and author key documents, including Standard Operating Procedures (SOPs) for quality and safety systems. Define inspection criteria and implement Inspection and Test Plans (ITPs) to ensure product quality during the manufacturing lifecycle. Lead quality discussions and coordinate with relevant teams to resolve technical concerns, respond to customer queries, and address complaints. Monitor stage-wise and final product inspections, collaborating closely with Quality Engineers. Coordinate and manage customer and supplier inspections to ensure compliance with quality standards. Carry out safety assessments and confirm adherence to legal and regulatory safety requirements in manufacturing. Maintain proper documentation, conduct data analysis, and compile reports for top management review. Preferred candidate profile Role : Senior QMS Manager Experience - 5+ Degree: BE (Electrical Engineering or Mechanical). Software: MS Office, MS Excel.

Job Description Position: Quality Assurance Experience: 6 - 10 years of relevant experience Location : Gurugram Company Preference: Preferably from an Agency/ Liaison office / Buying House / Export House Product Category: Hand Tools, Hard Lines, Soft Lines Skills: You will support leadership for Quality Assurance functions for the assigned category to meet the brand requirement. Roles and Responsibilities Partners with merchandising to develop clear quality expectations for all branded products. Collaborate with product development and sourcing to ensure technical specifications are adequate and vendors can deliver on quality expectations. Proactively drive quality by communicating quality expectations to vendors before production, gauging vendors ability to deliver expected quality, and addressing potential issues before quality problems arise. Reviewing the Digital Dashboard and discussing Score Card with the vendors. Responsible for understanding, interpreting, and reviewing samples based on the international test standards (ASTM, ISO, and EN, etc.) related to the etc. To supervise QA inspector services to ensure that customers quality standards are met. Production control- Provide QA advice to factories before and during the manufacturing process. Supervise the sample inspections-Check samples against product specifications to ensure that they meet customers’ quality standards. Develop associated audit programs wherever necessary. Risk analysis during the development stage. To provide technical advice and support relating to ensure that customers’ specifications are met. Desired Candidate Profile Education: Mechanical Or Industrial Engineer Strong product and material knowledge with good development skills, and familiar with merchandising and product development process Able to work under pressure, result-oriented, good communication skills in speaking and writing to communicate with buyer /seller. Ability to build strong relationships with cross-functional teams and communicate effectively with internal and external parties. Well-organized individual, able to manage multiple tasks, strong problem-solving skills, able to meet deadlines. Well-versed with MS team applications like Outlook and PowerPoint Frequent travel is required. If this sounds like you, Apply Now!

Team Lease Services Ltd. Role & responsibilities 2) Budget for the role - 22K NTH 3) Contract Duration - 12 Months 4) Detailed JD -Planning, materials management,Good Analytical skills & Excel skills,Receiving,distribution of materials,Materials Reconciliation reporting,Collaborating & stock monitoring, GRN creation 5) Number of Positions -1 6) Minimum Experience Required -2 Years 7) Shift timings(If Applicable) -N/A 8) Is WFH available? -N/A 9) Work location (full Address) - Binola FC (2140) 10) Qualification Preference - Graduate 11) Gender Preference - Male Preferred candidate profile

Manage Customer Complaints,8D Reports,7 QC Tools, Documentation related to PPAP for all new developments Drive End to End QMS ISO/IATF Build new team & deploy across all verticals of production

**Key Responsibilities:** - Lead a team of QA professionals to ensure consistent delivery of high-quality [products/processes]. - Design and implement QA strategies, policies, and procedures to enhance efficiency. - Oversee end-to-end quality assurance processes, including audits and compliance checks. - Collaborate with R&D, production, and other departments to align quality objectives. - Monitor KPIs and metrics to drive continuous improvement in quality standards. - Provide training and mentorship to junior QA team members. - Ensure compliance with industry regulations and standards. **Skills Required:** - Proven leadership and team management skills. - Expertise in [specific QA tools, frameworks, or standards relevant to the industry]. - Strong problem-solving and decision-making abilities. - Excellent organizational and interpersonal skills.