141 Customer Audits Jobs

The role involves focusing on Product and Service Quality to ensure the highest standards are maintained. You will be required to analyze data impacting service and product quality, conduct initial assessments by visiting the site if necessary, and identify the root cause of issues related to design, suppliers, or manufacturing processes. Collaborating with Cross-Functional teams, you will work towards resolving key quality concerns efficiently, particularly those affecting the Serviceability of Vertiv products. Promptly addressing Service issues and coordinating with relevant teams to implement corrective actions will be a key responsibility. In terms of Customer Quality, you will be responsible for coordinating Customer audits and managing corrective actions. Furthermore, you will play a crucial role in managing Customer Claims effectively. Additionally, you will support the local Supply Chain by offering strategic quality support for Services supplier quality. Collaborating closely with local suppliers and the Service Quality Organization, you will contribute to the development and maintenance of standardized service supplier quality documentation. Monthly reporting on relevant Quality Key Performance Indicators (KPIs) such as Customer claims and Field First Pass Yield will also be part of your responsibilities. This position requires individuals who are legally authorized to work in the United States. Vertiv does not provide sponsorship for this role. Candidates with temporary visas or requiring sponsorship in the future are not eligible for hire. Vertiv is an Equal Opportunity Employer.,

Role & responsibilities Significant experience in Quality Assurance. Responsible for overall quality assurance control & system activities at Plant. Preferred candidate profile B tech Mechanical having minimum 10+ yrs of experience in automobile industry.. Perks and benefits

Pretech Plast Pvt Ltd is a plastics company based in Bengaluru, Karnataka, India, with a legacy of 27 years as a market leader. The company holds various accreditations such as ISO/IATF/AS/SQ/MSIL and is committed to ensuring customer satisfaction through compliant development and production processes. With expanded capacity including CLEAN ROOM MOULDING at Trivandrum, Kerala, India, Pretech Plast Pvt Ltd focuses on quality and innovation. As a Junior MR Post at Pretech Plast Pvt Ltd, located on-site in Bengaluru, India, you will be responsible for tasks related to analytical skills, customer audits, third Party Audits & communication, training, and documentation revisions. Your daily activities will include overseeing compliance obligations, managing document coherence, conducting training sessions, and supporting NPD documentation. You will be involved in Monthly Review meetings, Instruments calibrations, and Required testings for EMS. The ideal candidate should have knowledge of quality management systems and certification, strong interpersonal skills, and the ability to work collaboratively. It is preferred that you are ISO/IATF/AS/EN internal auditor certified, have experience in providing training and conducting workshops, and possess EMS Knowledge as a bonus. Join Pretech Plast Pvt Ltd to contribute to our commitment to quality, compliance, and customer satisfaction through your role as a Junior MR Post.,

Job Title: Assistant Manager - Process QA Location: Sohna Department: Process QA Roles And Responsibilities : 1. Customer Handling & Analyze Customer Complaints, working in CFT approach to fulfill customer requirements. 2. To handle internal and customer audits and closure of audit observations. 3. Face and handle PPAP audits for new products & co-ordinate with NPD team for new part development. 4. Process QA representation in CFT team for control plan/ FMEA review. 5. Perform internal audits as per VDA6.3, IATF16949, ISO18001 and effective closure of the non-conformances 6. Implementation of Statistical process control (SPC) to improve & analyze process capability. 7. Lead continuous improvement initiatives for man head reduction, cost saving through Kaizen, Process & Inspection Automation. 8. To handle Maruti VSA audit and co-ordinate MACE improvement activities 9. Experience in 4M change management and keeping records as per the system requirements 10. To lead the process QA team for analysis of daily rejection data and action plan for top defects, tracking of action effectiveness. 11.Tracking for internal DAR, supplier defect summary, Traceability of shipments, final inspection records. 12. Active participation in Quality Circles at ACMA, QCFI, CII and other platforms 13. Preparation and presentation of monthly MIS and MRM data in front of Top Management 14. Manpower handling for in-process and final inspection areas. Competence Required (Technical & Behavioral): 1. Manpower Handling 2. Analytical skill - Fault Tree Abalysis, Quality Core Tools, VDA 6.3 3. A3 & 8D Compilation 4. IT Literacy - MS Powerpoint (data presentation skill) 5. Auditing skills - IATF 16949, EHS, VSA Audit Minimum Job Requirements : Educational Qualification (Regular): B.E / B.Tech - Mechanical / Automobile Engineering Experience: 7-12 yrs Industry Exposure: Automobile

Roles and Responsibilities Conduct quality audits, inspections, and reviews to ensure compliance with ISO standards and company policies. Develop and implement quality control procedures to maintain high-quality products and services. Collaborate with cross-functional teams to identify areas for improvement and implement corrective actions. Ensure accurate documentation of all quality-related activities, including audit reports, records, and reports. Provide training on quality systems, processes, and procedures to employees at all levels. Desired Candidate Profile 3-8 years of experience in a similar role within the engineering & construction industry. Strong understanding of QMS (Quality Management System) principles and practices. Excellent communication skills for effective collaboration with stakeholders across various functions. Ability to analyze data from customer audits, identify trends, and develop action plans for improvement.

Responsibilities: Lead quality initiatives, drive continuous improvement. Ensure compliance with IATF & ISO standards, implement QMS. Conduct customer audits, PFMEAs, APQPs, Kaizens.

Position Summary: The ideal candidate will be responsible for driving comprehensive Quality Assurance initiatives across in-process inspection, final product quality, and supplier quality systems. This role also includes leading Industry 4.0 digital transformation projects , focusing on machine and process connectivity. The position demands a strategic thinker with a strong foundation in quality systems, statistical analysis, and regulatory compliance, committed to fostering a zero-defect culture and operational excellence. Key Responsibilities: Develop, implement, and sustain quality standards to enhance in-process, supplier, and final product quality; proactively identify quality issues and recommend corrective actions. Analyze rejections and defects using statistical and analytical tools; implement effective countermeasures to eliminate root causes and prevent recurrence. Lead and execute Industry 4.0 digitalization projects , enabling machine and process connectivity to enhance traceability, quality monitoring, and process control. Establish and maintain a robust Quality Management System (QMS) in alignment with corporate standards, ISO 9001:2015, regulatory requirements, and industry best practices. Oversee document control, change management, and supplier quality processes , including supplier audits, development, and performance monitoring. Conduct thorough root cause analysis and CAPA implementation for non-conformances, with a focus on long-term resolution and continuous improvement. Design and manage an effective internal audit program , ensuring team competence through regular training and adherence to quality standards. Execute validation master plans for new and existing equipment, manufacturing processes, sterilization methods, and test protocols, ensuring compliance and reliability. Ensure adherence to cleanroom practices and quality protocols, promoting a culture of accountability and zero defects across all operational teams. Monitor and evaluate process changes , perform statistical process control studies, interface with customers on quality matters, and lead 8D problem-solving processes. Requirements: Strong working knowledge of ISO 9001:2015 , quality management principles, and regulatory frameworks. Proficiency in quality tools and methodologies including 7 QC tools , 8D analysis , Root Cause Analysis , and CAPA . Experience with digital quality systems and Industry 4.0 concepts is highly desirable. Excellent analytical, leadership, and communication skills, with a proactive and results-driven mindset.

Roles and Responsibilities Complaint analysis and complaint resolution within specific time period Lead the investigation of customer non-conformance reports and all responses using the 8D Problem Solving methodology Resolving complaint to logical end and frame preventive actions in process Pokeyokes for complaints and documentation of the corrections and corrective actions in SOPs/ instructions Initiate improvement action based on market feedback wrt packing/aesthetics Visit to customer end for attending complaints Monitoring of product performance trends and other CTQ's parameters, Trigger deviation/need of process correction Data Analysis, Process capability analysis and improvements in the indices of product and process capabilities. Establish Norms of process capability Coordinate with IT/Industry 4.0 team for digitalization of control wrt process CTP and CTQ’s Prepare and update all necessary quality reports as required by customers. Ensure control plans and associated documentation are implemented effectively and maintained Prepare and perform IMS (Integrated Management System) audits to insure that all procedures and instructions related to the IMS are adhered to Participate in defect reduction projects Participate in WCM improvement projects Closely work with PMG for customer feedback • Use of SPC for problem solving

Develop and maintain QMS documentation. Conduct internal audits and support external audits to ensure compliance. Initiate and track corrective and preventive actions. Ensures compliance As per the industry standards (ISO)

Asst. Manager / Dy. Manager Pharma Sales & Marketing (International Marketing, APIs) Posted: July 2025 Grow global API sales for a multi regulator approved manufacturer: develop new domestic & international business, manage key accounts, coordinate samples/docs across Regulatory, R&D & Operations, and support customer audits in a highly regulated cGMP/ICH Q7 environment.

Greetings from SGS India! Opportunity with SGS India for the position of Social Compliance Lead Auditor (APSCA I, APSCA II and APSCA CSCA) | Location - Pan India Company Profile: Established in 1878, SGS transformed grain trading in Europe by offering innovative agricultural inspection services. SGS is the world's leading inspection, verification, testing and certification MNC. We are recognized as the global benchmark for quality and integrity. With more than 96,000 employees, we operate a network of more than 2,700 offices and laboratories around the world. We cater quality services to 9 Businesses in India like Consumer & Retail Services, Oil & Gas, Industrial services, AFL, Minerals etc. Kindly visit our Global Website: www.sgs.com India Website: www.sgsgroup.in Qualification - APSCA Level I, APSCA Level II and APSCA CSCA Location - Pan India Industry/ Sector: TIC (Testing, Inspection and Certification) Scope of job /Activities handled: Conducting Audits across Pan-India for various industry sectors. Auditing, Presentation, Documentation skills. Key Results Areas ( KRAs) & Key Deliverables: Timely Audit As per Accreditation norm Support on Business Kindly share me your updated CVs on fleur.dsouza@sgs.com

Cyano Pharma Pvt Ltd is a leading pharmaceutical organization in INDORE (MP) focused on quality, compliance, and innovation. We are looking for a highly skilled professional with strong expertise in Quality Management Systems (QMS) and Validation & Qualifications to ensure compliance with international regulatory standards (WHO, USFDA, EMA, MHRA). Key Responsibilities: Quality Management System (QMS): - Implement, maintain, and continuously improve the site Quality Management System in line with global regulatory guidelines (WHO, USFDA, EMA, MHRA). - Prepare, review, and update SOPs, quality manuals, and quality policies. - Manage change control, deviation, incident reporting, and risk management systems. - Coordinate and support internal, external, and third-party audits, ensuring timely CAPA implementation and closure. - Monitor and analyze quality metrics to drive continuous improvement initiatives. - Provide training and awareness programs for QMS procedures and GMP compliance across teams. - Act as a key contact for regulatory inspections and customer audits. Validation & Qualifications: - Prepare and execute qualification protocols (IQ/OQ/PQ) for equipment, utilities, facilities, and systems. - Lead process validation, cleaning validation, and computer system validation as per regulatory requirements. - Develop and maintain the Validation Master Plan (VMP). - Ensure periodic requalification and revalidation activities are performed according to schedules. - Review and approve all validation-related documents, including protocols and reports. - Ensure all validation activities comply with cGMP, data integrity, and documentation requirements. - Work closely with cross-functional teams (engineering, production, QC) to ensure smooth validation and qualification processes. Qualifications & Experience: - M.Pharm with 9-10 years of experience in Quality Assurance within the pharmaceutical industry. - Strong hands-on experience in QMS implementation and validation/qualification activities. - In-depth knowledge of global regulatory requirements (WHO, USFDA, EMA, MHRA). - Strong communication, documentation, and audit-handling skills. - Proficiency in MS Office (Word, Excel, PowerPoint) and quality documentation systems. - Location: Indore Benefits: - Competitive salary and performance-based incentives. - Opportunity to work on global compliance and regulatory projects. - Exposure to international audits and career advancement opportunities.,

Responsible for ensuring overall HR compliance with respect to labour and regulatory matters in a manufacturing / factory environment. Handling manpower strength of 1500+ spreading in PAN India. Person with thorough understanding of compliance laws and interpret with diversity of business spread in different geography, as well as providing adequate communication to key managers and employees about such laws. Role & responsibilities Liaison with Govt. Authorities connected to Labour & Regulatory on regular basis. Handling external third-party compliance audits of customers (SMETA, WRAP, SCS, WCA, BSCI, HIGG, etc). Adherence of all related statutory compliance and submission of periodical returns under various laws i.e.: State & Central Pollution Control Board, Hazardous Waste Management, Contract Labour (R&A) Act, Bonus Act, Gratuity Act, EPF Act, ESIC Act, Shops & Commercial Establishment Act, Maternity Benefit Act, and other applicable laws. Contract Labour Management (end to end) Transportation, Canteen, and Security administration. Attending and managing due diligence and internal audit (by EY, PWC, ERM, etc). Monitoring Statutory Compliance as per timeline (monthly/quarterly/half-yearly/annual). Preferred candidate profile Behavioural Result oriented Excellent communication skills Good Interpersonal skills Strong core values & highest level of integrity Quick decision maker Functional Rapport building Good Negotiator Systems approach and methodical working Must be good with handling data & analysis of the same Travelling to PAN India locations

About Apotex Inc. Apotex Inc. is a Canadian-based global health company that produces high-quality, affordable medicines for patients around the world. Apotex employs almost 7,200 people worldwide in manufacturing, R&D, and commercial operations. Apotex medicines are accessible to patients in more than 75 countries globally. Through vertical integration, the Apotex group is focused on the development and sale of generic, biosimilar and specialty products. For more information visit: www.apotex.com . Job Summary Responsible for supporting business processes within Global Business Services, driving program management including but not limited to governance, transition and continuous improvements Job Responsibilities Responsible for operational excellence in line with GBS operating model by driving governance framework as per GBS operating model Drive governance for GBS operational plans Publish operational dashboards. Trend and analyze for governance Track execution of operational actions. Report against plan on outcomes realized from actions Champion Continuous Improvement Initiatives at GBS Drive meeting as per agreed governance framework for all processes Ensure transition excellence by implementing 6D methodology for all process transfers Manage RAID (Risk, Action, Issue, Decision) across GBS for people, process and systems Escalate process risks and issues appropriately collaboratively with the Service Leaders and Operational Leaders Support Quality Management Team for activities as aligned Support regulatory and customer audits, when required Escalate unresolved issues to immediate supervisor Works in a safe manner collaborating as a team member to achieve all outcomes. Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion. Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies. All other relevant duties as assigned. Job Requirements Education Minimum Post Graduate, preferably in the field of Life-sciences Knowledge, Skills and Abilities Excellent communication skills Multitasking and good at analytics Adept with Microsoft office suite of applications Capability to work in a matrix environment Experience 5-8 yrs of similar industry experience At Apotex, we are committed to fostering an inclusive, accessible work environment, where all employees feel valued, respected and supported. Apotex offers accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation.

Preparing & complying with documents as per QMS/API Q1/EMS/OHS Interaction with certification bodies for audit systems,Training to all concerned in management systems as well as customer specific requirements Customers audits for management systems. Required Candidate profile Candidate should have exeprience in QMS Having experience in Oil/Automotive Industry

Job Title: Quality Assurance Engineer / Senior Engineer QMS & Audits Function: Quality Assurance Location: Tirupathi, Andhra Pradesh Experience Required: 4 to 7 Years Education: B.E. / B.Tech in Mechanical Engineering, Industrial & Production, or Total Quality Management MBA or MS in TQM (preferred, not mandatory) Qualifications: Certified Internal Auditor as per ISO 19011 standard for IATF 16949 or AS 9100 D from an authorized institute or organization Industry: Aerospace, Automotive, Precision Engineering, Manufacturing Employment Type: Full Time, Permanent Job Summary: We are looking for a motivated and experienced Quality Assurance Engineer to join our team and strengthen our Quality Management System (QMS) and audit activities. The ideal candidate will have strong expertise in standards like IATF 16949, AS 9100 D, and ISO 9001, and practical knowledge of core quality tools and customer requirements. Key Responsibilities: Develop, maintain, and improve the Management System in compliance with ISO 9001:2015 , AS 9100 D , IATF 16949:2016 , and EHS standards Plan and execute internal system audits, process audits, and product audits , ensuring effective coordination between auditors and auditees Manage excursion handling and corrective actions for internal, supplier, and customer issues Coordinate timely closure of audit observations and non-conformities Organize and maintain internal audit systems, including corrective action reporting Conduct quality system audits and provide training and guidance to internal auditors Coordinate third-party audits, customer audits , and follow up on non-compliance issues Recommend actions for areas not meeting specified quality standards Review, update, and improve procedures, SOPs, and documentation Train shop floor engineers on QMS procedures, core tools, and quality standards Monitor KPIs , track progress, and promote action plans for improvement Plan and conduct audits of machining and raw material suppliers , including verification of compliance Manage documentation control systems and ensure compliance during internal and external audits Plan and coordinate Management Review Meetings (MRM) , prepare agenda, minutes of meeting (MoM), and communicate to stakeholders Candidate Requirements: 47 years of experience in quality management systems or auditing roles within manufacturing companies Strong knowledge of IATF 16949 , AS9100 D , and ISO 9001 requirements Proficiency in quality documentation (Level 2 & 3), and core tools (PPAP, APQP, MSA, SPC, QUA) Ability to perform independent audits and gap analysis Skilled in CAPA , root cause analysis, and compliance follow-up Ability to understand and interpret customer-specific requirements Strong written and verbal communication skills Preferred Skills: Qualified internal auditor for IATF 16949 , AS 9100 D Knowledge of VDA 6.5 audit standards Familiarity with Aero Engine standards (AS 13100) and RM standards Good team coordination and leadership abilities

BASIC INFORMATION ON THE POSITION Position Name: Deputy Manager - ESGC PURPOSE OF THE ROLE To ensure Information Security Management System and Risk management framework including Business continuity are effectively planned & established in line with the business objectives. The job exists to ensure compliance to IS requirements, both from customer and organization. If this role did not exist, ensuring compliance to IS requirements is not possible. KEY RESPONSIBILITIES AND ACCOUNTABILITIES Compliance to client information security requirements as agreed in the MSA by ensuring that requirements are captured, documented, implemented and verified Ensure customer audits are cleared successfully without any critical non-conformances Propose cost effective solution and maintain compliance cost Contain Revenue Leakage by ensuring reduction in revenue leakages resulting from IS incidents and effective implementation of controls Ensure operational excellence through the following: 1. Develop and manage ISMS (Information Security Management System) framework including Business continuity and awareness 2. Identify and implement applicable industry practices (IT act and amendments, Data Privacy and Data Security framework etc) 3. Establish and implement measurement program to assess effectiveness of the framework/system 4. Ensure all internal / external audits are planned and successfully cleared. 5. Monitor and track all internal/external audit findings to closure. Highlight open findings and accepted risks Enable Innovation through Automation and New initiatives Ensure Effective People Management by keeping the team engaged and having diverse workforce, Creating accountability & ownership in the team, handling team members grievances and ensuring team attrition is within targets Ensure Capability Development in the team by upgrading competency (skills) in the team in line with the current industry practices and business objectives including both managerial and technical capability EDUCATION QUALIFICATION Degree: BE/M.tech or MBA Certifications: CISA/ CISM Certification - ISO27001 lead auditors certification MINIMUM EXPERIENCE REQUIRED Overall (in years): 10- 15 years Relevant (in years): 8-12 years DOMAIN/ FUNCTIONAL SKILLS Good understanding of various IS standards, framework such as ISO27001, PCIDSS, HIPAA, NIST, SOC/SSAE16 Standards & ISO27005, ISO 22301 Guidelines - Knowledge of risk management (ISO31000, ISO27005), business processes - Knowledge of IT Security, physical and environmental security and HR security controls - Knowledge of regulatory requirements

To oversee and enhance the Quality Management System (QMS) within a sheet metal manufacturing setup—ensuring compliance with ISO/IATF standards, driving continuous improvement, and supporting customer satisfaction and operational excellence.

Job Overview: We are seeking a highly experienced and certified Compliance & Information Security Manager to lead and oversee our organizations compliance, quality assurance, and cybersecurity initiatives. The ideal candidate will possess a robust background in ISO standards, IT and Security Operations, and internal/external audit coordination across service industries. Key Responsibilities: Lead the implementation, maintenance, and audit of ISO standards, including ISO 27001, ISO 9001, AS9100D, GDPR, DPDP Ensure compliance with SOC 2, HIPAA , and other applicable regulatory frameworks. Collaborate with cross-functional teams to design, review, and implement information security policies and risk mitigation strategies . Manage and prepare for internal and external audits; represent the organization during surveillance and certification audits. Develop and deliver employee training programs related to information security, regulatory compliance, and quality assurance. Identify and address security risks in networks, systems, and applications , and recommend corrective controls. Update and maintain documentation related to compliance and audit standards. Required Qualifications: Bachelors degree in engineering/technology (preferably Computer Science or related discipline). CISA, CISO, CISM, CISSP Certified (any) Desirable Lead Auditor certifications for ISO 9001:2015, ISO 27001:2022 and AS9100D. Strong exposure to GDPR, HIPAA and SOC 2 frameworks. Proficiency in conducting internal, supplier, and customer audits . Experience with tools such as Microsoft Office Suite. Demonstrated ability to lead cross-functional teams, manage compliance projects, and drive process improvement.

Looking for Candidates who will be responsible for : QMS : Lead, maintain, and continually improve the companys Quality Management System in line with IATF 16949 and ISO 9001 requirements. Plan, execute, and monitor internal system audits per audit program; ensure auditor competency and closure of non-conformities. Facilitate management review meetings with actionable insights and data-driven inputs from core business processes. Ensure robust document and record control system as per standard; manage changes and version control across the organization. Ensure readiness for third-party and customer audits; lead responses to NCs and drive certification maintenance and renewals. Define and track KPIs for core and support processes; drive gap analysis and improvements. Oversee application of APQP, PPAP, FMEA, MSA, and SPC in relevant functions; support teams in correct and effective usage. Drive structured change control process for product, process, and system-level changes. Ensure deployment and compliance of Customer-Specific Requirements (CSR) within the QMS. Establish and monitor risk analysis and contingency planning for business continuity. Develop and deliver QMS training; build awareness across functions on quality standards and updates. Drive, Train & Facilitate QC & production for QC circle teams to resolve perennial issues. Localization : Responsible for establishing Quality of parts developed as per management initiatives. Support supplier for understanding current supplier product quality and guide in establishing a similar or supplier quality products. Support in completion of testing and validations of parts as per all applicable engineering standards and facilitate for customer approval as per the requirements stated by customer. Qualifications: Mandatory: B.E./ B.Tech Mechanical Desired: IATF / VDA certification Functional/Technical Competencies Required: IATF 16949, VDA 6.x, APQP, PPAP, FMEA, MSA, SPC, Control plan, VA/VE, Benchmarking, Customer management, Problem solving techniques, 8D approach, MS Office. Behavioural Competencies Required: Stake holder management, Communication, Leadership, Agile mindset, People management, Customer management, Supplier management, Self initiative & Proactive, Process driven approach. Key result areas / job outcomes: Drive and achieve QMS certifications by effective implementation of QMS Completion of internal system audit plan No of QCC projects completed Customer specific QMS implementation & rating / ranking as per customer systems % of parts localised as per management target Interested Candidates can send their CV on alka.p@peoplesource.in. Immediate joiners will be preferred. Alka Pathak Tiwari Senior Recruitment Consultant Email: alka.p@peoplesource.in

You will be responsible for managing ESIC & PF compliance in line with statutory requirements. This includes overseeing new joiner formalities such as employee ID creation and induction. You will be required to prepare audit documents as per client requirements and ensure audits are NC-free. Additionally, you will coordinate labour license applications, renewals, and compliance, as well as follow up on office utility bills including electricity, courier, and water. It will be your responsibility to maintain accurate records for statutory compliance and HR operations. You will support customer audits and ensure readiness of compliance documentation. Site visits will be conducted by you to ensure HR process adherence across locations. Collaboration with internal teams will also be necessary for smooth onboarding and HR service delivery. You should maintain high standards of work quality and IT proficiency while ensuring timely reporting and documentation for all HR activities. Flexibility and mobility across geographic areas may be required. Reporting to the HR Operations Head, you will also support continuous process improvements.,

Overall handling of Quality Procedures & Quality Management System (QMS). Handling & Issuance of NCs, CAPA and Change Control. ISO Audits, PDI, BMR, Audit Documentation, Customer Audits Required Candidate profile BE/ Btech/ Diploma- Mechanical Engineering, Min. 1 year exp as Quality Executive/ Engineer in Medical Devices or Automotive Industry. Prior exp of handling Quality Procedures & QMS, CAPA, Audits.

JOB DESCRIPTION: Production In-charge of Production and dispatch activity. Receipt and storage of raw material in day stock area for the batch as per request slip Carry out the process as per LMR and operation verification All safety rules/precaution to be followed strictly Execution of the production schedules for current and coming months Coordinating internal /external audits and maintaining relevant documents Maintaining cGMP standards, ISO 9001, ISO 14001 & HACCP standards in the plan Making sure that the premises and equipment are maintained and records kept Environmental audits, Customer audits and Regulatory Audits. Knowing about Validation, Qualification,Production Planning, Raw Material Planning, Manpower management. Preferred only API Pharma Experience

Job Purpose To provide quality support to all projects, quality engineers and analysts involved in Manufacturing and Production Operational Activities. Quality Improvement Initiatives To support an environment where Quality Employees support maintaining and improving flow, and create the required Quality behavior within those relationships. To create LEAN / Continuous Improvement thinking within the team, and validated by Improved Performance Results. Work under minimal guidance to ensure TechnipFMC''s Product are manufactured in accordance with TechnipFMCs Quality Management System, Business Processes and Client requirements. Effectively collaborating with various departments and clients to achieve organizational goals and customer satisfaction. Perform Contract Review focusing on quality requirements for systems, products, manufacturing, operations and documentation. This will require engagement with relevant TechnipFMC SME (Welding, NDE, Engineering and etc.) Ensure that project quality requirements are identified and translated to the organization and relevant internal stakeholders (including supply chain). Initiate and align with project the need for additional specifications to address contract/ client requirements in part report Establish Quality and Inspection Test Plan and ensure the requirement are roll out to manufacturing and supply chain. Identify and ensure approval of all quality documentation (TechnipFMC Qspec, WPS, MPQP, etc.) in project to meet client requirements. Ensure effective execution of all inspection and test activities in Inspection Test Plan (ITP) during manufacturing. To establish and report overall status on product Quality Notifications in regular basis as requested by the management. Coordinate Non Conformance Review Board (NRB) to ensure smooth processing of quality nonconformance and to facilitate and monitor QNs close in timely manner in SAP. Facilitate investigations (RCA) on shop floor related issues Quality Notifications, or Quality escapes and drive verified and sustainable solutions Initiate and follow-up required preventive and corrective actions as a result from CSS , Quality Alert. Support process compliance within Product Quality environment through an established Process Verification Programme. Perform Process Verification and validation to ensure process sustainability. Participate in kick-off meetings and pre-production reviews both internally and at Suppliers to ensure understanding and compliance to quality requirements. E Manage Customer issued NCRs and track them through closure. Participate in Internal (QMS) and External Audit (API, DNV, Client, etc.) Perform Final Acceptance of the product and Witness FAT as per part report requirement You are meant for this job if: Bachelors degree in mechanical engineering. Minimum 5 years of experience as Quality Assurance(ability to create FMEAs, control plans, process qualifications, validations) and quality control processes (ability to create inspection methodologies, RTFI , PT LII certified). Working knowledge in curing or welding processes. Ability to be in auditee role during customer audits and certification audits. Excellent communication and negotiation skills to manage CFT and customer. Working knowledge on DMAIC,Lean, 8D, A3 and basic knowledge in quality core tools. Working knowledge in using 7 QC tools. Working knowledge in SAP QM module. Ability to perform statistical analysis in Excel. Working knowledge in powerpoint. Candidate has to be NDE LII (ISO 9712 or equivalent) certified or CSWIP 3.1 certified or CQE certified. Candidates with experience in client facing roles preferred Skills

You will be responsible for initiating, reviewing, and approving various quality management systems such as Change Controls, Deviations, Investigations, CAPA, OOS, and Complaints. You will also handle Return Goods and ensure the smooth functioning of the quality system by performing risk assessments as required. Conducting regular internal audits and reviewing/approving all documents including SOPs, Spec & STPs, Forms, protocols, and reports will be part of your duties. Additionally, you will review annual product quality review reports, provide training on cGMP topics to employees, and support customer audits/visits as well as regulatory audits. You will assist in providing necessary documents for amendments, annual updates, regulatory filings, and CMC supporting documentation. Other tasks may include filling out questionnaires, declarations, quality agreements, and executing any additional responsibilities assigned by the Head of Department.,