341 Customer Audits Jobs - Page 8

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 respon...

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 activi...

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 improv...

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 M...

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 an...

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 t...

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....

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 manag...

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 retu...

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 improvemen...

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 Man...

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 ...

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...

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 trac...

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 ens...

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 Mat...

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...

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 docume...