33 Preventive Actions Jobs

As the Manager of Environment, Health & Safety at ENNOVI Mobility Solutions India Pvt Ltd, your role will involve establishing and maintaining an effective documented Environmental, Energy, Health and Safety, Chemical management system as per standard requirements. Your main responsibilities will include coordinating and assisting the concerned offices in the implementation of IMS, ensuring all staff understand their roles and responsibilities through security awareness training, managing IMS incidents and responses, implementing corrective and preventive actions against identified or potential non-conformities, and developing Environmental, Energy, Health and Safety infrastructure to meet the business needs of the organization. You will also be responsible for providing IMS advice and assistance as required, including project or customer-specific consultation, implementing Environmental, Energy, Health and Safety policies and standards, planning and conducting regular internal audits and compliance audits, reporting performance of IMS to top management, conducting Management Reviews at scheduled intervals, reviewing IMS annually or as required, coordinating with certifying authorities, and devising, testing, and reviewing Environmental, Energy, Health and Safety requirements in mock drills, Emergency Evacuation Plans, and Crisis Management Plans. To qualify for this role, you should have a Diploma in Industrial Safety, a bachelor's degree in a related field such as environmental science, occupational health and safety, or public health, Safety certifications in ISO14001, 45001, and 50001 (Mandatory), knowledge in stamping, molding, plating (an added advantage), relevant EHS experience in an industrial or manufacturing environment only, and a minimum of 15 to 18 years of experience. Join us at ENNOVI as we work towards a future of electrification and innovation, offering a dynamic, collaborative, and inclusive culture that encourages continuous learning, professional growth, and a sense of purpose. Be a part of our team that champions sustainability initiatives and fosters a winning team environment. To learn more about us, visit www.ennovi.com.,

The Senior Quality Auditor provides support to the audit program and clinical projects to ensure compliance with regulations and Precision procedures. You will be responsible for offering oversight and subject matter expertise to quality and compliance activities, aiding project teams throughout all phases of a clinical study. Your essential job functions will include supporting the Quality Management System by managing SOPs, training, and CAPA. You will be required to process and maintain documentation for controlled documents as needed. Additionally, you will develop and conduct training for employees and consultants. Hosting client/sponsor audits, supporting regulatory inspections, coordinating and conducting assessments of vendors, including audits, conducting internal audits of quality systems, investigator site audits, and trial master file audits are all part of your responsibilities. You will also participate in computer systems validation projects and systems change control processes. Providing QA consultation and support to assigned project teams internally and externally, managing reported quality issues and associated corrective and preventive actions, monitoring quality systems, and identifying compliance risks for QA management are crucial aspects of your role. It is essential to maintain Q&C trackers, databases, metrics, and files. You must adhere to applicable regulations and standards, including local regulations (US FDA and EU), ICH guidelines, and company policies and procedures. Other tasks as required should also be handled effectively. **Qualifications:** **Minimum Required:** - 4 years of industry experience - Clinical research experience in a non-QA role (e.g., clinical research associate experience) - Working knowledge of GCP/ICH guidelines and FDA regulations and standards **Other Required:** - Bachelor's degree in a science, healthcare, or related field of study; relevant experience may be considered - Willingness to travel up to 25% domestically and/or internationally **Preferred:** - Experience in CRO, Pharmaceutical, and/or Medical device industry - QA certification preferred (e.g., CQA, SQA, etc.) - Familiarity with electronic clinical trial systems (e.g., EDC, CTMS, IxRS, ePRO, etc.) **Skills:** - Strong interpersonal and problem-solving skills - Effective verbal and written communication - Proficiency in computer skills **Competencies:** - Proficient in GCP/ICH guidelines, FDA regulations, and industry standards - Intermediate proficiency in Microsoft Word, Excel, and PowerPoint - Customer service-oriented - Collaborative, flexible, and detail-oriented - Ability to work independently and in a team environment - Prioritization and multitasking abilities - Results-oriented, accountable, motivated, and flexible - Consistent with Precision Values and Company Principles - Excellent verbal and written communication skills - Fluency in English language Please note that any data provided as part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please refer to our CA Privacy Notice. If you need a reasonable accommodation to complete the application process or require an alternative method for applying due to a disability, please contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com.,

The QC Engineer plays a critical role in ensuring that products meet specified quality standards and customer expectations during the manufacturing process. They are responsible for developing and implementing quality control systems, procedures, and processes to maintain consistency and adherence to standards. Conducting thorough inspections and tests on raw materials, components, and finished products is a key responsibility of QC Engineers to identify any defects or deviations from specifications. By analyzing data from inspections and tests, they can pinpoint trends, root causes of quality problems, and areas for improvement. Collaboration with cross-functional teams is essential for QC Engineers to implement corrective and preventive actions to address quality issues and prevent their recurrence. They are also responsible for maintaining detailed records of inspections, tests, and corrective actions and preparing reports to document quality performance and identify areas for enhancement. In addition, QC Engineers collaborate with various departments such as production, engineering, and supply chain to ensure that quality standards are met throughout the entire process. They stay updated with industry trends, new technologies, and regulatory requirements related to quality control to continuously enhance processes and procedures. This is a full-time job suitable for freshers with benefits including health insurance and a performance bonus. The work schedule is during the day shift and the work location is in person.,

You are a passionate, dedicated, and detail-oriented professional, and an exciting opportunity awaits you to join the Quality Assurance Team at Zydus Takeda Healthcare Private Limited in Turbhe, Navi Mumbai. This joint venture between Zydus Lifesciences and Takeda Pharmaceuticals is committed to maintaining the highest level of quality and safety in its products. As a Senior Executive / Executive in Quality Assurance, based in Navi Mumbai, you will play a crucial role in In-Process Quality Assurance (IPQA). Your responsibilities will include monitoring and controlling the quality of products during the production process to ensure compliance with regulatory standards and company quality policies. Your contributions to the role will involve conducting real-time monitoring of production processes, performing routine inspections and in-process checks, collaborating with production and quality control teams to address quality issues promptly, identifying deviations and implementing corrective and preventive actions. Additionally, you will be responsible for documenting quality-related activities, reviewing Batch Manufacturing Records (BMRs) and Analytical data, as well as participating in internal audits and inspections to ensure compliance with GMP, SOPs, and regulatory requirements. To excel in this role, you should hold a Post Graduate or Graduate degree in Science or Pharmacy from a reputable institute, possess hands-on experience and knowledge of Quality Management System, and demonstrate a strong understanding of GMP, FDA regulations, and industry standards such as ICH and cGMP. The ideal candidate will have a minimum of 6 to 8 years of experience in a pharma manufacturing plant, preferably an API Manufacturing Plant, with experience in IPQA in rotational shifts. Proficiency in quality management software and tools like Trackwise, SAP, etc., will be an added advantage. Desired skills for this position include excellent observational and attention-to-detail skills, the ability to work effectively in a team-oriented, fast-paced environment, strong problem-solving and decision-making capabilities, good documentation and record-keeping skills, and a continuous improvement mindset with the ability to handle multiple tasks efficiently. If you are ready to make a meaningful contribution to the quality assurance processes in a dynamic pharmaceutical environment, we invite you to apply for this role and be part of our dedicated team in Navi Mumbai.,

As a Quality Control (QC) Engineer, your primary responsibility will be to ensure that products consistently meet specified quality standards and exceed customer expectations throughout the manufacturing process. You will play a crucial role in developing and implementing quality control systems, procedures, and processes to maintain consistency and adherence to standards. Conducting thorough inspections and tests on raw materials, components, and finished products will be a key part of your duties to identify any defects or deviations from specifications. Your role will also involve analyzing data obtained from inspections and tests to identify trends, root causes of quality issues, and areas for improvement. Working closely with cross-functional teams, you will be responsible for implementing corrective and preventive actions to address identified quality issues and prevent their recurrence. Maintaining detailed records of inspections, tests, and corrective actions, as well as preparing reports to document quality performance and identify areas for enhancement, will be essential. Collaboration with various departments such as production, engineering, and supply chain will be required to ensure that quality standards are met at every stage of the process. It is imperative to stay updated with industry trends, new technologies, and regulatory requirements related to quality control to continuously enhance processes and procedures. In some instances, you may also need to train and mentor junior engineers or technicians in quality control procedures. Additionally, you may be involved in auditing quality management systems to ensure compliance and effectiveness. Your role may also require you to liaise with customers to address quality-related concerns and ensure their satisfaction. This is a full-time position that will require you to work day shifts in person at the specified work location. As a QC Engineer, you will be entitled to benefits such as Provident Fund.,

The position of SME Grinding and Honing (Process Engineer/Process Expert) at SKF's Ahmedabad Manufacturing Plant reports to the General Manager Manufacturing Engineering and Quality. As an individual contributor, your role will involve driving process improvements, supporting new product development, and ensuring the smooth execution of grinding and honing operations during the factory expansion phase. You will be responsible for serving as the technical expert for grinding and honing operations, leading the installation and validation of new machines, defining and optimizing process parameters, conducting process trials and capability studies, troubleshooting process issues, collaborating with cross-functional teams, training engineers and operators, driving continuous improvement initiatives, supporting CAPEX planning, reducing cycle times, introducing new abrasives and tools, participating in documentation for new and existing products, leading technology improvement projects, managing machine qualification activities, implementing Engineering Change Requests, and releasing and maintaining process documentation. Your success in this role will be measured by metrics such as cycle time improvement, successful development and launch of new products, productivity and OEE improvements, and timely installation and qualification of new machines and equipment. To excel in this position, you should have a B.Tech in Mechanical/Production/Industrial Engineering with a minimum of 8-10 years of relevant experience in manufacturing engineering, specifically in grinding and honing operations. Active involvement in factory expansion projects is essential for this role. Your technical competencies should include process knowledge, technology focus, statistical knowledge, project management skills, structured problem-solving abilities, exposure to Industry 4.0 applications, and proficiency in SPS (SKF Production System). On the behavioral side, you should demonstrate patience, curiosity, collaboration, effective communication, accountability, strong analytical and problem-solving skills, ability to work independently, and adaptability with a continuous improvement mindset. If you are interested in this opportunity, please share your updated profile with supriya.joshi@skf.com.,

As a Quality Control Reviewer at TAPI, you will play a crucial role in ensuring the quality and compliance of our pharmaceutical products. Your primary responsibilities will include reviewing various documents such as batch records, test results, deviations, and corrective actions to determine the disposition of batches. You will also be responsible for monitoring manufacturing and packaging processes, investigating any errors or deviations, and implementing corrective and preventive actions as necessary. Your role will involve collaborating with internal and external stakeholders to address quality and compliance issues, facilitate batch reviews, and ensure the timely shipment and receipt of materials. Additionally, you will be involved in the review of R&D product development, validation of manufacturing processes, and support for Regulatory Affairs activities. To be successful in this role, you should have a Bachelor's or Master's degree in Chemistry or Chemical Engineering, along with a minimum of 7 to 10 years of experience in the API or Pharma industry. Your attention to detail, analytical skills, and ability to work effectively in a team will be critical for ensuring the quality and compliance of our products. Join us at TAPI and be part of a team that is dedicated to advancing global health. If you are ready to contribute to our mission, innovate, and drive excellence, we invite you to apply for this exciting opportunity. Shape the future of pharmaceuticals with us at TAPI. Apply now, and our talent acquisition team will contact you soon to discuss your application.,

The Manager Supplier Quality (Solar) is responsible for ensuring that all components and materials sourced from suppliers meet the company's quality standards and project requirements. This role involves evaluating and auditing suppliers, implementing quality assurance processes, supporting supplier development, and driving continuous improvement within the solar supply chain. Key Responsibilities Develop and implement supplier quality strategies aligned with solar project goals (modules, inverters, structures, cables, etc.). Evaluate and approve new suppliers through audits, quality assessments, and qualification procedures. Conduct regular supplier audits (ISO 9001, IEC certifications, etc.) to ensure compliance with internal and regulatory standards. Work closely with procurement and engineering teams to ensure that quality requirements are embedded in supplier contracts. Manage incoming inspection and quality control processes for supplier-delivered materials. Lead root cause analysis and corrective/preventive actions (RCA/CAPA) for supplier-related quality issues. Maintain and report supplier performance metrics (PPM, NCRs, OTIF, etc.). Support NPI (New Product Introduction) by qualifying new components and establishing incoming quality plans. Drive continuous improvement initiatives with strategic suppliers. Ensure compliance with industry-specific standards (IEC, UL, BIS, ISO, etc.) relevant to solar components. Qualifications And Skills Bachelors degree in Engineering (Electrical, Mechanical, or related). Masters preferred.,

The Supervisor role involves the preparation, review, revision, control, and implementation of standard operating procedures, Change Control, and Corrective and Preventive Actions (CAPA) within the Sterile manufacturing department. You will be responsible for activities related to document preparation such as CCF, SOP, Investigation, Risk Assessment, and Protocol. Key Responsibilities: - Oversee the preparation, review, revision, control, and implementation of standard operating procedures, Change Control, and CAPA within the Sterile manufacturing department. - Manage document preparation including CCF, SOP, Investigation, Risk Assessment, and Protocol. Skills Required: - Quality Management Systems: Mastery - CAPA (Corrective and Preventive Actions): Mastery - Regulatory Compliance: Expert - Change Control Management: Expert - Report Writing: Expert - Audit & Inspection Readiness (Internal & External Audits): Expert - Capability Development: Expert - Manufacturing Process and Equipment Understanding: Expert - Communication & Collaboration: Expert Qualifications: - M.Sc B.Pharm / M.Pharm Experience: - 8 - 11 years In this role, your expertise in Quality Management Systems, CAPA, Regulatory Compliance, Change Control Management, Report Writing, Audit & Inspection Readiness, Capability Development, Manufacturing Process and Equipment Understanding, and Communication & Collaboration will be essential. Your experience of 8-11 years will be valuable in successfully executing the responsibilities of this position.,

As a Lead QMS at Ai Health Highway, you will play a crucial role in implementing Quality Management System (QMS), ISO13485, EU MDR, and US FDA (510k) Risk Management processes for our cutting-edge medical devices. Your responsibilities will include creating device master records, updating technical documentation, and collaborating with internal and external stakeholders to establish a robust quality management and regulatory framework for our product pipeline. You will work closely with engineering and manufacturing teams to develop verification test strategies to ensure the safety and reliability of our products. Additionally, you will be involved in developing product requirements, supporting validation programs for new product development, and providing inputs for regulatory guidelines and procedures. Your expertise in risk assessment for medical devices, as per ISO13485/ISO 14971 CE certification, will be essential in this role. You will also be responsible for reviewing device labelling and advertising materials for compliance with regulations, liaising with external consultants, and assisting in documentation preparation for US FDA (510k) and EU-CE Marking regulatory submissions. To be successful in this position, you should have 3 to 5 years of experience in the Medical Device QMS and regulatory domain, along with a BTech/BE in Electronics/Electrical/CS or Bio-Medical Engineering. Strong skills in documentation, review, reporting, and excellent interpersonal communication are required. Experience in managing non-conformance, corrective action preventive actions, deviation, and conducting QMS training will be beneficial. Join us at Ai Health Highway in our mission to reduce premature deaths due to Non-Communicable Diseases by 30% by 2030. Your expertise and dedication will contribute significantly to our goal of revolutionizing healthcare with innovative medical devices.,

Jaidev Pharma Placement is a renowned organization with a rich history spanning over two decades in Pharmaceutical Sales. With additional expertise in recruitment, hiring, and training, we deliver top-tier human resources services nationwide. Our core competencies lie in strategic planning, business analysis, and crafting holistic improvement strategies tailored to meet the unique needs of our clients. At Jaidev Pharma Placement, we are dedicated to sourcing exceptional talent at competitive rates, prioritizing the long-term growth of our employees and contributing to the prosperity of our clientele. As a QA Head based in Roorkee, you will assume a full-time on-site position with a primary focus on overseeing all quality assurance operations. Your responsibilities will encompass ensuring adherence to industry standards and regulations, executing audits, and supervising quality control procedures. Your daily duties will involve the development and implementation of quality management systems, collaboration with production and various departments, as well as leadership of a team of QA professionals. In this crucial role, you will be instrumental in upholding product quality standards and driving continuous process enhancement within the organization. The ideal candidate for this role should possess a solid background in quality assurance, quality control, and compliance management within the pharmaceutical sector. A robust understanding of industry regulations, standards, and quality management systems is essential. Furthermore, exceptional leadership skills, adept team management capabilities, and effective communication abilities are prerequisites for this position. Proficiency in conducting audits, overseeing inspections, and managing corrective and preventive actions is highly valued. Experience in formulating and executing quality assurance protocols and processes is crucial, along with the capacity to collaborate efficiently with diverse departments and stakeholders. A Bachelor's or Master's degree in Pharmaceutical Sciences, Chemistry, or a related field is required, while relevant certifications in Quality Assurance or related disciplines are considered advantageous for this role.,

As the Quality Assurance Manager, your primary responsibilities will include overseeing the quality assurance procedures, protocols, and standards for steel production processes at the SMS Plant. You will be responsible for ensuring compliance with national and international quality standards, industry regulations, and customer specifications. Your role will involve implementing strategies for continual improvement, defect reduction, and process optimization. Your duties will also include leading the inspection and testing of raw materials, intermediate products, and finished products in the SMS, Rolling Mill, and Bright Bar processes. You will be expected to analyze production processes, identify potential quality issues, and ensure high-quality output at every stage of production. Reviewing and approving inspection reports, test results, and product certifications will be part of your daily tasks. In case of quality-related problems, you will lead investigations and implement corrective and preventive actions to address root causes and avoid recurrence. It will be crucial for you to document all quality issues, findings, and actions taken effectively. Additionally, you will act as the main point of contact for quality-related matters with customers, vendors, and regulatory authorities. Your role will involve monitoring customer feedback and quality complaints to ensure timely resolution and customer satisfaction. By analyzing customer complaints, you will be able to identify systemic issues and take corrective actions to enhance product quality and service. Leading internal and external audits, inspections, and certification processes will also be part of your responsibilities. Ensuring regulatory compliance and maintaining documentation for industry certifications will be essential. You will be required to prepare and present regular quality reports for senior management, highlighting performance, trends, and areas for improvement. Your contribution will play a vital role in maintaining high standards of quality and customer satisfaction within the steel production processes.,

As an Executive - Quality Assurance at our Site in Dahej, Bharuch, you will be responsible for overseeing the QA | QC activities. Your main responsibilities will include developing annual QA plans and budgets, monitoring and improving QA processes, executing QA requirements, enhancing customer satisfaction, resolving issues, implementing Root Cause Analysis (RCA) and Corrective and Preventive Actions (CAPA), maintaining documentation and compliance, as well as fostering team development and growth. Your key responsibilities will involve collaborating with the Head of Department (HoD) to develop and submit annual QA requirements for budgeting, ensuring proper resource allocation for smooth QA operations, monitoring QA processes to identify inefficiencies and gaps, proactively working with cross-functional teams to address issues, overseeing critical QA functions such as managing customer complaints and conducting qualifications and validations, ensuring all QA activities meet internal standards and customer expectations, driving customer satisfaction enhancement, acting as a key point of contact for resolving customer concerns, reporting and monitoring deviations, following up on corrective actions, overseeing RCA and CAPA implementation for critical deviations, ensuring compliance with regulatory and internal requirements, reviewing key documentation, and fostering the professional development of QA team members. To excel in this role, you should have an MSc in Chemistry, with a minimum of 10-15 years of experience in the chemicals industry for MSc holders and a minimum of 2 years plus for Ph.D. holders. You should possess in-depth knowledge of QA principles, regulatory guidelines, and industry standards, as well as proven experience in managing QA functions, addressing customer complaints, and resolving critical deviations. Strong leadership and communication skills, along with a focus on team development and cross-functional collaboration, will be essential for success in this position.,

As a Quality Assurance and Quality Control professional, you will be responsible for developing and implementing strategies, policies, and procedures to enhance operational excellence and ensure stakeholder and client satisfaction across existing accounts. Your key responsibilities will involve conducting regular audits, inspections, and performance evaluations to identify areas for improvement and minimize risk within the defined governance structure. You will collaborate closely with the JBS Transitions and Operations team to align quality assurance practices with the JBS QMF framework. Working across various operations teams, you will play a crucial role in supporting the implementation of quality frameworks across multiple transitions simultaneously. In this role, you will be instrumental in fostering a culture of quality within the organization by raising awareness, providing training, and instilling a customer-centric mindset. Your analytical skills will be put to use as you analyze data, identify trends, and utilize insights to drive decision-making and implement necessary corrective and preventive actions. Collaboration with cross-functional teams will be essential to establish quality control measures and ensure adherence to compliance standards. You will also be responsible for monitoring and reporting on the progress of quality framework deployment to senior management, highlighting any areas of concern and proposing effective solutions. Staying informed about industry trends, best practices, and regulatory requirements within the Real Estate Industry and the processes supported by JBS will be a key part of your role to ensure that the quality management practices remain up-to-date and aligned with industry standards.,

As the Head of Quality and Sustainability for our global logistics organization, you will have a strategic role in influencing senior leadership decisions and ensuring adherence to quality standards, sustainability goals, and regulatory requirements. You will be responsible for enhancing our Quality Management System (QMS) and internal quality policies to promote a culture of continuous improvement and operational excellence across the GCC region. Your key responsibilities will include: - Acting as the voice of quality in the leadership team and driving quality outcomes. - Developing partnerships with global quality leaders to deploy best-in-class quality systems. - Creating and executing the quality strategy, vision, roadmap, and objectives aligned with business goals. - Ensuring compliance with industry standards and regulatory requirements. - Leading operational excellence initiatives to enhance quality, customer satisfaction, and business performance. - Establishing processes for quality assurance, quality control, audits, inspections, and corrective/preventive actions. - Owning audit readiness, certification, and regulatory compliance. - Developing KPIs and dashboards to monitor and report on quality performance. - Fostering a quality-centric culture and continuous learning at all organizational levels. - Collaborating with stakeholders to align on quality expectations and embedding quality into processes. - Building and leading a high-performing quality team and conducting training programs. - Proactively assessing risks and implementing risk management strategies. In terms of sustainability and ESG execution, you will be responsible for localizing and driving the sustainability framework in India, ensuring compliance with environmental regulations, promoting energy efficiency, waste reduction, and leading sustainability reporting efforts. Key qualifications and experience required for this role include a bachelor's or master's degree in engineering, Quality Management, Environment Science, or related field, along with 15+ years of progressive experience in quality, sustainability, or EHS roles. Strong knowledge of quality systems, compliance standards, and industry regulations is essential, as well as experience in leading quality transformations and large teams. Personal attributes such as strategic thinking, effective communication, data-driven decision-making, and visionary leadership style are key for success in this role. If you are interested in this opportunity, please share your updated resume at jeena.sunil@evokehr.com or connect on -9274682913.,

You will be responsible for managing the monitoring, measurement, and review of internal processes, especially those that affect the quality of the organization's products. You will lead a team of quality engineers and inspectors to ensure that organizational goals are met. Reporting to top management on the performance of the Quality Management System (QMS) and identifying areas for improvement will be a key aspect of your role. Your duties will include ensuring timely inspection of monitoring and measuring devices, overseeing the inspection of materials at incoming, in-process, and final stages to ensure compliance with requirements. You will also be required to ensure digital recording of all inspections, maintain accurate documentation, and perform statistical analysis. As an interdepartmental coordinator, you will facilitate smooth workflow within the organization. Developing effective quality control processes by understanding customer needs and requirements, reviewing non-conforming products, and implementing corrective and preventive actions will be part of your responsibilities. Providing training as per the training plan and monitoring its effectiveness will also be crucial. Additionally, you will conduct periodic management review meetings and drive initiatives to reduce departmental overtime. This is a full-time, permanent position with a flexible schedule and day shift. A diploma is required for this role, and experience in CNC for at least 2 years is preferred. The work location is in person.,

You are a highly skilled and experienced Quality Engineer with a strong background in the inspection, testing, and quality assurance of pressure vessels, heat exchangers, nodulizers, and other critical equipment utilized in refinery, oil & gas, and industrial settings. Your role involves ensuring the safety, reliability, and compliance of essential equipment by conducting inspections, quality control assessments, and non-destructive testing (NDT) in accordance with international standards such as ASME, API, and ASNT. Your responsibilities include reviewing and approving weld procedures, monitoring equipment performance, performing root cause analysis for quality issues, preparing inspection reports, and coordinating with vendors to maintain quality standards. Additionally, you will lead audits, provide technical guidance to junior engineers, and stay updated on industry standards to ensure continuous compliance. To qualify for this position, you should hold a Diploma or Bachelor's degree in mechanical engineering, Metallurgical Engineering, or a related field, along with a minimum of 4+ years of experience in quality assurance, inspection, and testing of pressure vessels and related equipment. Proficiency in NDT techniques, knowledge of industry codes and standards, strong analytical skills, and excellent communication abilities are essential for this role. Experience in a refinery or oil & gas environment and certifications in Quality Assurance are highly desirable. Preferred skills include experience with equipment like separators, filters, columns, and reactors, advanced proficiency in inspection software, and familiarity with industry-specific project management and risk assessment techniques. This is a full-time position that requires in-person work at the designated location. Application Questions: - Do you have experience in pressure vessel inspection and working with international standards (ASME, API, ASNT) - Do you have experience in performing non-destructive testing (NDT) such as ultrasonic, radiographic, magnetic particle, and dye penetrant tests on pressure vessels and associated equipment Experience: Quality Engineer: 4 years (Required),

You are an experienced and detail-oriented Quality Manager with a background in quality control/assurance, specifically in heavy fabrication, sheet metal, or container manufacturing. In this role at Transafe Services Limited (TSL) located in Dharuhera (HR), you will be responsible for overseeing quality assurance and control at a container manufacturing facility within the Container Manufacturing (Heavy Fabrication & Sheet Metal) industry. Your primary objective will be to ensure compliance with ISO 9001:2015, ISO 45001:2018 (currently under upgradation), and industry-specific standards while fostering continuous improvement in manufacturing processes. Key responsibilities include developing, implementing, and maintaining Quality Management Systems (QMS) in alignment with ISO standards, conducting various audits to ensure quality adherence, leading inspections and testing procedures, handling Non-Conformance Reports (NCRs) and implementing corrective and preventive actions (CAPA), developing Standard Operating Procedures (SOPs) and Work Instructions, collaborating with production and design teams to optimize processes, training and mentoring the Quality Control (QC) and Quality Assurance (QA) team, maintaining quality records and compliance documents, ensuring customer specifications and regulatory requirements are met, and addressing customer complaints through root cause analysis for defect reduction. To excel in this role, you must hold a Bachelors/Masters degree in Mechanical Engineering, Production Engineering, or a related field, along with a minimum of 7 years of relevant experience in quality control/assurance within the specified industries. You should possess in-depth knowledge of ISO standards, welding practices, and industrial safety regulations, as well as experience in Non-Destructive Testing (NDT), material testing, and welding inspections. Proficiency in quality tools such as 8D, 5S, Six Sigma, Root Cause Analysis (RCA), and Failure Mode and Effects Analysis (FMEA) is essential. Strong leadership, analytical, and problem-solving skills, coupled with excellent communication abilities and the capacity to collaborate effectively with cross-functional teams, are also key attributes required for this position.,

You will be responsible for overseeing all aspects of quality management and ensuring the highest level of compliance across projects. This includes driving the validation process, supporting the authoring, reviewing, and approving of CSV deliverables, coordinating with project managers to align project outputs with quality standards, and managing change control processes for tool updates and deployments. Additionally, you will evaluate data and QM processes for improvements, support audits and inspections for compliance, oversee root cause analysis and corrective actions, and provide training on quality standards and procedures. Minimum Requirements: - Minimum of 10 years experience in Quality Management, preferably in Pharma or regulated industries. - Proven experience in managing GxP/non GxP projects from requirement definition to retirement. - Working experience in all lifecycle stages of IT systems, including System retirement. - Ability to drive innovative validation strategies and knowledge of IT systems in the Pharma industry. - Exceptional leadership and interpersonal skills with attention to detail. - Bachelor's degree in IT, Pharmacy, or related field. Novartis is committed to diversity and inclusion in the workplace, creating an outstanding work environment that reflects the patients and communities served. The company also provides accessibility and accommodation for individuals with disabilities, aiming to support reasonable accommodations during the recruitment process. If you are interested in staying connected with Novartis for future career opportunities, you can join the Novartis Network. Additionally, you can learn more about the benefits and rewards offered by Novartis in the Novartis Life Handbook.,

As a Quality Control (QC) professional, you will be responsible for conducting routine inspections, calibrations, and validations of medical devices and hospital equipment. Your role will involve monitoring and documenting the performance and safety metrics of equipment, as well as maintaining and updating equipment service history and maintenance logs. It will be essential to ensure that preventive maintenance is conducted on schedule and properly documented. In the area of Regulatory & Compliance, you will play a crucial role in ensuring that the equipment complies with national and international regulations such as CDSCO, AERB, and BIS. You will be responsible for supporting the documentation and filing for certifications, licenses, and renewals, as well as reviewing and approving technical specifications from suppliers/vendors. Your Technical Support responsibilities will include providing troubleshooting support for technical and operational issues related to biomedical equipment. You will need to coordinate with vendors, engineers, and OEMs for repair, replacement, and calibration tasks. Additionally, you will be involved in evaluating new medical technologies and supporting procurement processes while ensuring adherence to ISO 13485, NABH, CE, and other relevant regulatory and safety standards. As part of your role, you will be required to conduct root cause analysis and implement corrective and preventive actions (CAPA) for product/process deviations. You will assist in internal and external audits and ensure timely closure of non-conformities. This is a Full-time job opportunity that offers health insurance benefits, a Day shift, Fixed shift, Morning shift schedule, and a Yearly bonus. The preferred educational qualification for this position is a Bachelor's degree, and the preferred total work experience required is 1 year. If you are looking for a challenging role where you can contribute to ensuring the quality and compliance of medical equipment while providing technical support and maintaining regulatory standards, this position might be the right fit for you.,

You will be responsible for ensuring quality compliance in all civil engineering aspects of green hydrogen projects, which includes structural, architectural, and geotechnical works. Your role will involve site quality control, inspection, documentation, and coordination with internal teams, contractors, and consultants to guarantee adherence to technical specifications and international standards. Your key responsibilities will include monitoring and ensuring quality compliance of all civil works such as foundations, structural steel, RCC, roads, and stormwater drainage across green hydrogen facilities. You will need to review and implement Quality Assurance/Quality Control (QA/QC) plans in accordance with project specifications and ISO standards, as well as conduct inspections and tests of civil works at various stages. Moreover, you will be responsible for ensuring proper documentation of quality records including inspection reports, test results, NCRs (Non-Conformance Reports), method statements, and material approvals. You will also assist in third-party inspection (TPI) coordination, audits, and compliance closure, and collaborate with design, HSE, and project management teams to resolve quality issues. Additionally, you will support root cause analysis and corrective/preventive actions for civil quality issues, ensure materials and workmanship comply with codes (IS codes, ASTM, BS, etc.) and green hydrogen-specific guidelines, and maintain a strong focus on sustainability, green construction practices, and safety. Reviewing contractor and supplier submittals related to civil works will also be part of your responsibilities.,

As a Quality Control Supervisor, your primary responsibility will be to supervise and coordinate quality control activities throughout production processes. You will be required to monitor and enforce quality assurance standards to ensure they meet the company's requirements. Conducting inspections, audits, and process evaluations to identify defects and root causes will be an essential part of your role, along with training and guiding workers on quality control procedures. You will also be responsible for implementing corrective and preventive actions to enhance product quality, working closely with production teams to minimize defects and optimize processes. Maintaining quality documentation, reports, and compliance records will be crucial, as well as assisting in preparing for external audits and customer inspections. Driving a culture of continuous improvement and quality awareness among employees will be a key focus area. To qualify for this position, you should have 2-5 years of experience in a similar role. Academic qualifications required include a Diploma in Polymer Technology or an MSC in Chemistry. This is a full-time, permanent position with benefits such as cell phone reimbursement, flexible schedule, health insurance, leave encashment, life insurance, paid sick time, and provident fund. The work schedule includes day shifts, fixed shifts, and weekend availability. Performance bonuses and yearly bonuses are also part of the compensation package. The work location for this role is in-person, where you will be actively involved in ensuring quality control standards are met and maintained across production processes.,

As a Quality Management Specialist at API, you will be responsible for executing technical onsite audits to ensure adherence to established standards and procedures. Your role will involve evaluating factory processes, products, and systems to guarantee they meet the required quality criteria. You will meticulously review documentation, including procedures and working instructions, to ensure accuracy, completeness, and compliance with standards. During audits, you will be expected to detect errors, deviations, non-conformities, and areas for improvement, providing clear and actionable feedback to relevant factory stakeholders. Your responsibilities will also include preparing detailed audit reports summarizing findings, observations, and recommendations, which will be presented to factory management and stakeholders to highlight risks and areas for enhancement. Tracking corrective and preventive actions (CAPAs) to ensure timely issue resolution, providing remote desktop control for review of corrections and evidence, and conducting follow-up audits to verify the implementation of corrective actions will also be part of your duties. You will play a crucial role in ensuring that non-conformities are effectively and sustainably resolved while communicating with clients before and after technical audits for additional audit approach or follow-up. Your qualifications for this role include a Bachelors or Masters degree in Engineering, along with a minimum of 5 years of experience in a similar position within the quality industry, preferably in consumer goods. Familiarity with sectors such as furniture, plastic products, metal, toys, children's products, or electronics is desirable. Extensive audit experience and a solid understanding of international standards, particularly ISO-9001 and ISO-19011, are essential for this role. Moreover, you are expected to possess strong leadership skills, a problem-solving attitude, and excellent analytical and communication skills, with fluency in English. Your role will involve collaborating with cross-functional teams to ensure operational effectiveness and resolution of audit issues, while maintaining compliance with ethical standards and professional guidelines, as well as upholding the confidentiality of audit information. In this role, you will lead audit result measurement and analysis and prepare monthly or seasonal audit performance reports. You will be tasked with identifying potential risks and providing recommendations to improve company processes and controls. Your contribution to API will be vital in driving success in competitive markets and ensuring the delivery of safe and sustainable products to consumers.,

The Quality Control (QC) professional is responsible for inspecting, testing, and evaluating products or materials to ensure they meet the company's quality standards and regulatory requirements. This role helps maintain customer satisfaction by ensuring only high-quality goods reach the market. Key Responsibilities: - Conduct in-process, final product, and incoming material inspections. - Perform routine tests and inspections using various equipment and tools. - Record and report quality issues or non-conformities accurately and promptly. - Maintain documentation in accordance with company standards and regulatory compliance. - Assist in root cause analysis and implementation of corrective/preventive actions (CAPA). - Collaborate with production, engineering, and procurement teams to resolve quality-related problems. - Monitor and maintain calibration of testing equipment. - Support audits and regulatory inspections (if applicable). - Follow Good Manufacturing Practices (GMP) and safety protocols at all times. Qualifications: - High school diploma or equivalent; Bachelor's degree or diploma in quality management, engineering, or related field preferred. - Prior experience in quality control or inspection (1-3 years minimum, depending on the level). - Strong understanding of quality assurance methodologies, tools, and standards (e.g., ISO 9001). - Familiarity with statistical process control (SPC) and Six Sigma (a plus). - Attention to detail and good organizational skills.,

The job involves maximizing the availability and reliability of material handling systems and equipment at a Bio energy site by utilizing specialized expertise across equipment groups. You will be responsible for ensuring Health, Safety, and Environmental compliance, as well as cost-effective maintenance through audits, budgeting, and IMS documentation. Additionally, you will need to maintain the reliability of rotary equipment and material handling systems through PM/CM schedules, condition monitoring, and Root Cause Analysis (RCA). Optimizing spare parts and inventory management using SAP systems and preservation practices will also be a crucial aspect of the role to ensure smooth Operations and Maintenance (O&M). Furthermore, you will be expected to drive performance improvement and enhance team capability through Total Productive Maintenance (TPM), training, benchmarking, and coordination with the Center of Excellence (CoE). Key Responsibilities include: - Ensuring HSE, statutory compliance, and cost-effective maintenance - Maintaining reliability of rotary equipment and material handling systems - Optimizing spare parts and inventory management - Driving performance improvement and team capability Critical Competencies required for the role involve reducing maintenance costs and improving equipment availability, safety, and reliability through proactive actions and audits. You will also need to enhance manpower productivity and minimize production losses by balancing reliability with operational needs. Compliance with Root Cause Analysis (RCA), Reliability Centered Maintenance (RCM), Condition Monitoring (CM), and training protocols while harmonizing standards across vendors and systems is essential. Maintaining inventory control and implementing corrective/preventive actions aligned with organizational policies are also critical competencies. The Ideal Background for this position includes a Bachelor's degree in mechanical engineering, along with 3-8 years of experience, including at least 3 years in the field of Solid/Material handling equipment. Key Metrics that will be measured include: - Maintenance Cost Reduction - Equipment Availability & Reliability - Operational Efficiency & Downtime Control - Inventory & Spare Parts Management - Compliance & Safety Performance,