125 Corrective Jobs

As a Quality Assurance Manager for the Pharma Vertical at Cotecna Life Sciences India Pvt Ltd. (Erstwhile Geochem Laboratories), your role will involve the following responsibilities: - Establish, implement, and maintain the Quality Management System in alignment with current GxP activities, including ISO/IEC 17025:2017 standards. - Make independent and timely decisions related to GxP quality and compliance requirements. - Host and provide support during regulatory and customer audits. - Train and mentor staff on GxP regulations, manage GxP and ISO documentation systems, and oversee the training program. - Align Quality Assurance Standard Operating Procedures (SOPs) with guidelines and best ...

As part of Frencken's IMS Division, you will be part of a team that focuses on delivering high-quality, end-to-end manufacturing solutions to various global industries. The division excels in integrating cutting-edge technology with world-class processes to meet the diverse needs of clients. You will have the opportunity to work in a dynamic environment that values innovation, collaboration, and excellence. **Key Responsibilities:** - Oversee the company's overall QC inspection and testing activities. - Prepare countermeasure reports related to product quality claims from customers. - Coordinate the handling of customer complaints. - Implement improvement plans for the QA department. - Monit...

Role Overview: You will be responsible for ensuring the timely production of parts according to the production plan and directions. Your main focus will be on maintaining safety, following correct manufacturing processes, and improving productivity while minimizing rework/rejection. Key Responsibilities: - Ensure 100% safety in all plant activities. - Follow correct manufacturing processes and use appropriate tools/equipment. - Understand and control CNC machine programs. - Work on productivity improvement and minimize rework/rejection. - Maintain proper housekeeping in the work area. - Ensure timely delivery of parts. - Properly use measuring instruments. - Take corrective and preventive ac...

Role Overview: At Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe. As a Sr. Clinical Research Associate Contractor (SrCRA) at Allucent, you will independently control and monitor investigational sites, proactively detect issues, and provide solutions to ensure clinical studies are conducted according to the trial protocol and in compliance with SOPs, applicable regulations, and the principles of Good Clinical Practice. Key Responsibilities: - Govern highest possible quality standards for trial monitoring activities. - Conduct all study...

As a Regulatory and Quality Manager at our company in Noida, you will play a crucial role in ensuring compliance with regulatory requirements and maintaining high product quality standards. Your responsibilities will include: - Implementing the Quality Management System in accordance with regulatory guidelines. - Managing regulatory documentation to ensure accuracy and completeness. - Overseeing the Continual Improvement of Systems and Product Quality Review Process for the Corrective and Preventive Action System. - Ensuring data integrity and implementing Standard Operating Procedures (SOP) and policies. - Evaluating and approving master documents across various departments. - Preparing and...

As the Head of Quality Operations, you will lead and oversee all Quality Assurance, Quality Control, Documentation, and Microbiology operations for the Ahmedabad Manufacturing sites. Your role involves ensuring compliance with cGMP regulations, GLP, and global regulatory requirements while upholding the highest quality standards in manufacturing processes. You will be responsible for implementing and maintaining robust quality systems, driving continuous improvement initiatives, and ensuring adherence to regulatory standards and industry best practices. **Responsibilities:** - Formulate, implement, and maintain quality policies, procedures, and systems to ensure compliance with cGMP, GLP, an...

As the EHS Manager at the Pune Plant, your role will involve leading the Environment, Health & Safety (EHS) agenda at the site. This includes driving compliance, risk management, and fostering a strong safety culture in line with legal requirements and business objectives. Your responsibilities will also encompass overseeing EHS systems, audits, training, and emergency preparedness while promoting continuous improvement and collaboration across functions. Key Responsibilities: - Lead, implement, and strengthen EHS systems, culture, and compliance at the Pune site, aligning safety initiatives with business objectives and legal requirements. - Conduct and lead risk assessments such as PHA, PRA...

Role Overview: You will play a key role in ensuring product reliability, consistency, and compliance with industry standards. Your focus will be on strengthening quality systems, driving process improvements, and supporting cross-functional teams to deliver products that meet customer expectations and regulatory requirements. Key Responsibilities: - Quality Control & Assurance - Inspect raw materials, components, and finished products against defined standards. - Implement and monitor quality systems throughout production. - Develop SOPs, checklists, and other quality documentation. - Lead Root Cause Analysis (RCA) and manage Corrective and Preventive Actions (CAPA). - Process Improvement - ...

As a Quality Assurance Manager, your role will involve developing, implementing, and maintaining the company's quality assurance policies, procedures, and standards. You will lead and manage the QA team to ensure effective inspection, testing, and documentation processes. Your responsibilities will also include overseeing incoming raw material inspection, in-process quality control, and final product verification. It will be your duty to ensure compliance with relevant industry standards, regulatory requirements, and customer specifications. You will conduct internal audits, prepare quality reports, and coordinate with external auditors. Analysing quality performance data, identifying root c...

Role Overview: As an Associate Manager in the Quality Control department at ZLL-SEZ Oncology Injectable, your role is critical and involves planning routine activities, reviewing analytical raw data for accuracy, reporting discrepancies, performing stability analysis, managing key elements of the Quality management system, ensuring timely sampling and testing of materials, coordinating with internal and external teams, and maintaining laboratory resources and equipment. Key Responsibilities: - Plan routine activities of the respective section - Review all analytical raw data, calibration reports, and trend data for accuracy - Report any discrepancies and follow deviation reporting procedures...

As the Head of Quality Assurance and Compliance at our Biopharmaceutical company, your role will be crucial in maintaining the highest standards of quality, compliance, and regulatory adherence across all operations. Reporting directly to the executive leadership team, you will play a vital part in upholding and improving our reputation for excellence in the industry. **Key Responsibilities:** - **Establish and Maintain Quality Systems:** Develop and maintain robust Quality Systems to support cGMP activities, ensuring compliance with regulatory requirements and industry standards. - **Manage Quality Control and Assurance Departments:** Direct and oversee the activities of the Quality Control...

As a Senior Process Engineer/Industrial Engineer Senior Consultant at our firm, your role will involve: - Designing, establishing, and implementing Standard Operating Procedures (SOP), Key Result Areas (KRA), and Key Performance Indicators (KPI) specifically within the apparel manufacturing sector. - Demonstrating innovation and embracing the latest manufacturing principles to achieve the highest standards of efficiency. - Utilizing Lean management tools, efficiency improvement techniques, Root Cause Analysis (RCA), and Corrective and Preventive Action (CAPA) analysis. - Utilizing Artificial Intelligence (AI) tools, creating presentations, and conducting data analysis for project requirement...

An Electrician Technician work in offices or factories, either supervising electricians or as part of a production team. Electrical technicians follow a device's design plan, inspect, construct, and repair electrical systems. Electrical Technician Responsibilities: Assembling, evaluating, testing, and maintaining electrical or electronic wiring, equipment, appliances, and apparatus. Troubleshooting and repairing malfunctioning equipment, appliances, and apparatus. Constructing and fabricating parts, using hand tools and specifications. Reading and interpreting electrical and electronic circuit blueprints, diagrams, and schematics. Advising management on continued use of unsuitable equipment,...

As a Supplier Quality Engineer at Hitachi Energy, your role involves executing supplier qualification and certification processes while continuously monitoring supplier performance through assessments, audits, escape management, performance management, and non-conformity resolution. You will be responsible for ensuring that suppliers have the capability to meet all requirements for work transfer and process change management, including FAI, Resourcing Gate, and Production Part Approval Process (PPAP) acceptance. Key Responsibilities: - Prepare product and module level quality requirements - Co-ordinate with suppliers and internal stakeholders to build confidence in achieving requirements - R...

As a Junior Engineer or Engineer in the Quality Control department of a reputed Engineering Manufacturing Company near Vadodara, you will be responsible for ensuring the quality standards of the products. You should hold a qualification of BE or Diploma in Mechanical or Plastic engineering with 1 to 3 years of relevant experience in industries such as Engineering or Plastic. - Have knowledge of Quality Management Systems (QMS) - Familiarity with Advanced Product Quality Planning (APQP) documents - Handle Non-Conforming (NC) material and perform Root Cause Analysis (RCA) - Conduct Corrective and Preventive Action (CAPA) analysis - Utilize QC tools for investigations - Understand ISO standards...

As an SMT / MLB Failure Analysis Engineer at the position of Asst Manager / Deputy Manager with 10-18 years of experience based in Hosur, your role will involve leading complex failure analysis of MLBs and SMT assemblies using advanced diagnostic tools such as X-ray, SEM, ICT, and AOI. Your responsibilities will include: - Performing root cause analysis on field returns, in-process failures, and customer complaints - Developing and implementing corrective and preventive actions to eliminate recurring issues - Collaborating with design, process, and quality teams to enhance product and process robustness - Analyzing yield trends and driving continuous improvement initiatives - Preparing detai...

The role of SMT / MLB Failure Analysis Engineering involves leading complex failure analysis of MLBs and SMT assemblies using advanced diagnostic tools such as X-ray, SEM, ICT, AOI, etc. You will be responsible for performing root cause analysis on field returns, in-process failures, and customer complaints. Developing and implementing corrective and preventive actions to eliminate recurring issues will be a key part of your role. Collaboration with design, process, and quality teams to improve product and process robustness is essential. Analyzing yield trends and driving continuous improvement initiatives are also part of the job responsibilities. Additionally, preparing detailed technical...

As an In-Process Quality Engineer at our company, you will play a crucial role in ensuring the highest quality standards are maintained throughout the manufacturing process of small and medium power transformers. Your responsibilities will include: - Developing, implementing, and maintaining in-process quality control plans, procedures, and work instructions for manufacturing small and medium power transformers. - Conducting regular inspections, tests, and audits at different stages of the production process to identify and address non-conformities. - Utilizing quality tools and methodologies such as FMEA, 8D, Ishikawa, and SPC for root cause analysis of defects and implementing corrective a...

You will be working as a Shift Safety Officer in the EHSS department at Syngene International Ltd., a global discovery, development, and manufacturing organization. Your primary responsibility will be to ensure adherence to safety practices and procedures for yourself and the team, drive a corporate culture that promotes environment, health, and safety (EHS) in the workplace, and uphold Syngene's quality standards in all operations. You will also be accountable for achieving safety goals, reviewing and tracking safety metrics periodically, and assisting with Emergency Management System and Contractor Management. Your qualifications should include a B.E/B. Tech in chemical engineering and a D...

As a Production Manager at our company in Kolhapur, your role involves optimizing resource utilization to enhance production line efficiency and meet daily targets. You will be responsible for ensuring the implementation of Quality Environment and Safety standards on the assembly lines, in alignment with Operational Control Points (OCPs). Key Responsibilities: - Prepare and maintain IMS documents and records. - Monitor, control, and improve process performance measures, developing improvement plans as necessary. - Train and develop a multi-skilled team of associates. - Investigate accidents, and initiate corrective and preventative actions for safety incidents. - Implement corrective and pre...

As a Production Supervisor in Kolhapur, your role involves optimizing resource utilization to enhance production line efficiency and meet daily targets. You will be responsible for ensuring adherence to Quality, Environment, and Safety standards on assembly lines, as well as executing tasks in alignment with OCPs. Your duties include preparing and managing IMS documents and records, monitoring and enhancing process performance measures, and facilitating the training and development of multi-skilled Team Associates. Key Responsibilities: - Investigate accidents and implement corrective and preventative actions for safety incidents - Implement corrective and preventive actions for quality-rela...

As an experienced professional with a minimum of 6-8 years in Quality assurance and regulatory, this opportunity is tailored for you. With a background in Graduate or Post Graduate studies in Pharmacy, Biochemistry, Biotechnology, or Chemistry, you are well-equipped to excel in this role. Your knowledge of techniques involving quality assurance of pharmaceuticals antibodies/Proteins, along with on-job experience in in vitro MDD/IVD documentation, will be valuable assets. **Key Responsibilities:** - Monitor Implemented Quality Control Systems - Provide training wherever required - Conduct Internal audits at regular intervals - Coordinate Batch failure and OOS Investigations ensuring appropria...

As an experienced candidate with 10 to 15 years of experience, you will be responsible for the following key tasks: - Optimize the utilization of resources to enhance the efficiency of the production line and meet daily targets. - Demonstrate awareness of Quality Environment and Safety standards and ensure their implementation on the respective assembly lines. - Adhere to responsibilities outlined in the Operational Control Plans (OCPs). - Prepare and maintain Integrated Management System (IMS) documents and records. - Monitor, control, and enhance process performance measures while developing improvement plans within your designated area. - Conduct training sessions to enhance the skills of...

As a Discoverant Specialist at Novartis, you will be responsible for supporting the Discoverant System Business Owner within Novartis Technical Operations (NTO). Discoverant is a validated IT solution used across NTO for automated manufacturing data aggregation, advanced analysis, and comprehensive reporting. Your role will involve collaborating with IT teams, manufacturing sites, and the Discoverant Global Business Owner to ensure optimal system setup, seamless change implementations, and ongoing maintenance of the Discoverant platform across the Novartis network. **Key Responsibilities:** - Serve as the primary business-side representative for the implementation, lifecycle management, and ...

You will be responsible for performing Item Attribute Extraction and Content Enrichment. Your key responsibilities will include: - Following the defined process steps - SOP (Statement of Process) and performing the final Quality Check/sign off to the customer - Working on Root Cause Analysis (RCA) and Corrective and Preventive Actions (CAPA) for any Quality issues - Being accountable for the success and quality of the process - Helping to improve the defined processes as more automation is introduced and information is gathered - Maintaining a high degree of confidentiality while meeting strict deadlines - Being flexible to work in any shifts as per business requirements No additional detail...