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9.0 - 14.0 years

8 - 15 Lacs

Thane, Navi Mumbai, Mumbai (All Areas)

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Directing staff, scheduling production, maintaining equipment, developing relationships with suppliers, and ensuring compliance with health and safety standards. Required Candidate profile Must have skill to manage overall factory activities of production, quality control & assurance, maintenance, stores, dispatch, Admin, HR. Target oriented & able to take factory operation

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7.0 - 10.0 years

5 - 8 Lacs

Palghar,Maharashtra

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Quality Assurance experience in Quality systems such as Testing ISO, Quality Assurance & Control, Internal & External Audit in a medium size plastic processing or similar industry. preferable in Mfg of Electrical Cable or cable accessories. Required Candidate profile Quality In Charge experience in mfg of Electrical Cable or Cable accessories.

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5.0 - 10.0 years

6 - 8 Lacs

Bengaluru

Remote

Roles and Responsibilities Ensure compliance with quality management systems (QMS) and quality control measures (QC) on MEP works. Conduct regular site inspections to identify non-conformities and implement corrective actions. Develop and maintain quality documentation, including test reports, certificates, and records. Collaborate with customers to resolve issues related to product defects or performance concerns. Desired Candidate Profile 5-10 years of experience in QA/QC engineering role for MEP projects. Diploma/B.Tech/B.E. degree in Electrical or Mechanical field from a recognized institution. Strong knowledge of ISO Systems, QAP (Quality Assurance Program), QMS (Quality Management System), QC Inspection, Non Conformity Management, RCA (Root Cause Analysis). Excellent customer coordination skills with ability to handle customer complaints effectively.

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2.0 - 7.0 years

3 - 5 Lacs

Bengaluru

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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!

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1.0 - 3.0 years

0 Lacs

Vasai, Palghar, Mumbai (All Areas)

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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

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4.0 - 5.0 years

2 - 5 Lacs

Gurugram, Manesar

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1. Working as front-line supervisor, Managing the entire line and maintaining key parameter Safety, Quality, Productivity and Cost 2. Able to navigate the potential coflict/IR situation 3. Should have knowledge of minimum of anyone of areas (e.g. PT-ED /Sealer/ Topcoat) Technical/ Functional: 1)Thorough knowledge of automotive 4 wheeler Paint Shop production processes. 2)At least 4-5 years of experience as front line production supervisor. 3)Hands on experience on workstations and tools/equipment (viz. robots) of production line being handled. 4)Good knowledge of MS-Office and excellent computer skills. 5)Good knowledge of ISO systems (ISO-9001:2015, ISO-14001:2015, ISO-45001). Behavioral: 1)Good communication skills (verbal and written communication). 2)Must know how to work as a team member in an IR sensitive environment to achieve KPI targets. 3)Must be flexible to work in any production area as per present/future requirement.

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7.0 - 10.0 years

5 - 7 Lacs

Hosur, Bengaluru

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The ISO Quality control / Assurance is responsible for supporting the Quality Assurance Department with all ISO 9001 related quality assurance requirements for the ISO 9001 Quality Management System (QMS) Internal audit; External/Customer audit.... Required Candidate profile The ISO Quality will ensure the ISO 9001 QMS demonstrates its ability to consistently provide products &services that meet customer & statutory & regulatory Lead investigations of customer complaints

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5.0 - 10.0 years

3 - 5 Lacs

Gummidipoondi, Ponneri, Chennai

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We are looking for a Quality Control Engineer who will be responsible for ensuring the quality of stainless steel tanks, components, and stamped products meet the companys standards and customer expectations. The role involves hands-on inspection, defect analysis, process monitoring, and supporting continuous improvement initiatives. Key Responsibilities: Perform in-process, incoming, and final inspection of stainless steel tanks, stamped components, and assemblies. Use precision instruments such as vernier calipers, micrometers, height gauges , etc., to check dimensions and tolerances. Interpret engineering drawings and manufacturing tolerances (GD&T). Monitor welding quality (TIG/MIG), seam finish, leak testing, and overall product aesthetics. Conduct quality patrols on the shop floor to ensure adherence to SOPs and quality standards. Prepare and maintain quality documentation, inspection reports, rejection logs, and test records . Identify and report non-conformities (NCRs) and work with the production team to resolve quality issues. Support root cause analysis and corrective/preventive actions (CAPA) for recurring issues. Participate in internal audits, ISO documentation, and process control plans . Assist in training production staff on quality standards and visual inspection criteria. Key Skills Required Strong understanding of QA/QC procedures in manufacturing and 5S methodology . Proficient in measurement tools and inspection techniques Extensive knowledge of welding inspection and surface finish quality Familiarity with implementation of ISO 9001:2015 QMS Good knowledge of MS Excel, quality formats, ERP systems and reporting tools. Analytical thinking and problem-solving using 5 Why/Fishbone. Attention to detail and discipline in documentation.

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2.0 - 4.0 years

9 - 12 Lacs

Bhadra

Work from Office

Position- Assistant Manager Job Location - Rajasthan (Bhadra/ Sardarshahar) Qualification - B.E/B.Tech - Mechanical Engineering and MBA preferrable Experience - 2-3 years of experience into Internal Audits and Project Audits Key Responsibilities: Develop and implement an internal audit plan for different functional areas at the corporate and plants level. Conduct detailed audits of various business processes, including project management, operations, maintenance, financial, operational, and compliance areas. Perform transactional audit for key risk areas. Support the external consultants in coordination and review. Visit the different plants, as per the requirement, to assess the effectiveness of internal controls and obtain an action plan from concerned stakeholders, on the issues identified during the visit. Follow up on the status of action plan on the issues identified by consultants as well as by internal team. Conduct comprehensive internal audits of various departments and functions within the organization. Assess the adequacy and effectiveness of the organization's internal controls and risk management processes. Identify and evaluate risks and recommend corrective actions to mitigate them. Identify requirements of policy & procedures and get them developed and then get it implemented. Prepare detailed audit reports that summarize findings, recommendations, and management responses. Follow up on management responses to audit recommendations to ensure timely and effective implementation. Maintain strong relationships with stakeholders. Stay updated on industry best practices, regulatory requirements, and emerging trends in internal audit. Qualifications: Mechanical Engineer plus MBA Minimum 2-3 years of experience in project management/ project audits/ operations audit Experience in leading and managing internal audit teams. Excellent analytical and problem-solving skills. Strong communication and interpersonal skills. Willingness to travel to plants when required Team player with a collaborative attitude and willingness to contribute ideas and support other team members. Prior experience in the renewable energy sector is desirable but not mandatory. Preferred candidate profile 2-3 years of experience into internal audits and project audits , who is open to Relocate to Rajasthan (Bhadra/ Sardarshahar).

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10.0 - 15.0 years

12 - 18 Lacs

Noida

Work from Office

Meeting management QA Targets Skilled in QC tools Responsible for Customer complaint/query QA Improve plan as per last yr defects Controlling internal/external PPM RedBin/RCA/WHY-WHY Analysis Enhance QA Strategy CFT Wiring Harness knowledge is a must

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15.0 - 24.0 years

25 - 35 Lacs

Mumbai, Navi Mumbai

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Hiring Quality Head for Leading PMC in Navi Mumbai Roles and Responsibilities Conduct quality audits, inspections, and reviews to ensure compliance with ISO standards and company policies. Develop and implement effective quality control procedures for construction projects. Lead and manage the QA/QC department, including setting quality goals, SOPs, and best practices. Collaborate with project teams to identify areas for improvement and implement corrective actions. Ensure accurate documentation of quality records, reports, and certificates. To handle multiple projects /To lead department Must have exposure of handling Real Estate, Industrial & Infra projects Desired Candidate Profile Strong knowledge of ISO systems implementation and auditing principles. B.Tech/B.E. degree in Civil from a recognized university. 15-24 years of experience in civil engineering or related field with expertise in QA/QC, quality audit, internal quality auditing, etc. Excellent communication skills with ability to work effectively at all levels within an organization. To apply, please send your resume with following details Mail to: harshala.kadave@gemengserv.com Subject Line: Application for Quality Head @ Mumbai Total Experience: Current CTC: Expected CTC: Current Location: Notice Period: Reason for change:

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2.0 - 7.0 years

2 - 6 Lacs

Khalapur

Work from Office

Inspect raw materials and finished pond liners Conduct tests: tensile, puncture, thickness Maintain QA/QC records and documentation Ensure ISO 9001 & CE compliance Handle audits and identify defects Drive continual quality improvement Required Candidate profile Inspect raw/finished pond liners Perform tests: tensile, puncture, thickness Maintain QA/QC records Ensure ISO 9001 & CE compliance Support audits and implement improvements

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6 - 10 years

3 - 4 Lacs

Coimbatore

Work from Office

Role & responsibilities Should take responsibility on overall quality systems. Preferred candidate profile Should have experience in castings components and machining knowledge.

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5 - 8 years

8 - 9 Lacs

Anantapur

Work from Office

Role & responsibilities To support EHS in plant and to support the day today activities. Government liaison pertaining to factories ,PCB, Fire etc.. Monitoring the work permits and other activities in campus to ensure safe working. Ensuring the safe construction activities in co-ordination with PMC to ensure accident free site. Regular inspection of Fire pump room, service block, HSD yard, LPG and STP. Conducting risk analysis and ensuring the proper solution to avoid the risk & hazard. Record keeping and documentation of EHS related work. Inspection of machines, lifting tools and other equipment's to ensure the compliance and safe working. Checking of firefighting and detection system to ensure the proper working. Training to the workers and service staff. Ensuring the safety induction of workers in co-ordination with PMC. Ensuring contractors safety programme. Preferred candidate profile Should have exposure of Automobile & Metal related safety also. Exposure of OHSAS 45001:2018and any other standards would be an advantage. Knowledge of environment regulation would be an added advantage. Eligibility: Experience - B. Tech Fire & Safety - PG Diploma industrial safety with 4+ years of experience. Qualification in Environment management will be an added advantage. NEBOSH and other credential will be an advantage

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9 - 12 years

10 - 12 Lacs

Tumkur, Mysuru, Bengaluru

Work from Office

Role & responsibilities Overall responsibility for monitoring of implementation, maintenance and improvement of Management Systems (ISO9001, IATF16949, AS9100D, ISO14001, ISO45001) To maintain the integrity of the Management Systems when the changes are planned and implemented such as new rules, standards, core tools, CSR, IATF Sanctioned Interpretations & FAQs To maintain the management system documents and records Liaison with external parties on matters relating to Management Systems such as quotation, agreements, audit plans, auditor travel & accommodation plans. Scheduling and conducting MRM Scheduling and conducting Internal Management System Audits Corrective action follow-up for all non-conformities raised during Certification body and internal management system audits To lead reviewing and implementing Customer Specific Requirements (CSR) To do centralized KPI monitoring related to Quality, Environment and Safety Preferred candidate profile

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