47 Corrective Jobs

Role Overview: As a Manager-II in the MSTG department at Dadra, your primary responsibility will be to provide support in the execution and monitoring of trial, scale up, and exhibit process qualification batches. You will be involved in preparing and reviewing new product documents such as material requirement sheets, master formula cards, bill of materials, risk assessment reports, sampling protocols, reports, exhibit batch manufacturing records, and exhibit protocols. Sharing process knowledge with cross-functional departments through presentations to facilitate smooth technology transfer will also be a key aspect of your role. Key Responsibilities: - Review and evaluate product history a...

Role Overview: You should have a minimum of 6-8 years of experience in Quality assurance and regulatory, preferably in the field of pharmaceuticals, antibodies, proteins, IVD/medical devices, or injectables. As a Graduate or Post Graduate in Pharmacy, Biochemistry, Biotechnology, or Chemistry, you will be responsible for ensuring the quality control systems are implemented effectively and participating in various quality assurance activities. Your innovative thinking and leadership skills will be crucial in solving problems related to the Quality Management System. Key Responsibilities: - Monitor and ensure the implementation of Quality Control Systems - Provide training as and when required...

As an Assistant EHS Manager at Givaudan's Pune Plant, you will play a crucial role in leading the Environment, Health & Safety (EHS) agenda. Your responsibilities will include driving compliance, risk management, and fostering a strong safety culture in alignment with legal requirements and business objectives. Based in Ranjangaon, Pune, you will report directly to the EHS Manager. Your key responsibilities will involve leading, implementing, and strengthening EHS systems, culture, and compliance at the Pune site. This includes conducting risk assessments, ensuring statutory compliance, managing hazardous materials, and overseeing environmental monitoring. You will also be responsible for co...

As a Quality and Food Safety Manager, you will be responsible for developing strategies to ensure the smooth functioning of quality and food safety processes, systems, and guidelines for all incoming materials, processes, and finished goods. You will be tasked with developing the budget for the Quality and Food Safety department and monitoring adherence to the set budget. Your role will involve drafting and proposing revisions in the quality assurance policies, processes, systems, and guidelines based on organic quality standards, norms, and statutory requirements. Leading the development of specifications and tolerance limits for incoming, work in progress, and finished goods with criteria ...

As a Quality Manager at our organization in Nagpur, you will be responsible for overseeing and managing the overall quality assurance operations. Your primary goal will be to ensure that products and services meet required standards, quality procedures, and customer expectations. You will play a crucial role in developing, implementing, and maintaining quality management systems while fostering a culture of continuous improvement within the organization. Your key responsibilities will include developing, implementing, and maintaining the organization's Quality Management System (QMS) to ensure compliance with industry standards and regulations such as ISO and Six Sigma. You will lead and man...

The role of the In-Process Quality Assurance Executive is to ensure that all products are manufactured and packaged according to cGMP and regulatory standards. You will collaborate with production teams to monitor and verify product quality throughout the manufacturing process. Your responsibilities will include maintaining quality standards from warehouse to production and packing areas. You will ensure compliance with cGMP and regulatory requirements, identify and resolve quality issues in real-time, and participate in investigations of deviations and non-conformances. Additionally, you will support root cause analysis and corrective actions, maintain accurate documentation, and assist in ...

Over the past 15 years, Medanta has created an unrivalled impact in delivering world-class multi-specialty care for patients in India. With hospitals in Gurgaon, Lucknow, Patna, Indore, and Ranchi, as well as clinics in Defence Colony (South Delhi), Cybercity & Subhash Chowk (Gurgaon), and at the Delhi Airport, Medanta is constantly growing. The organization has also ventured into the Retail vertical through Diagnostics (Laboratory Services) and Pharmacies, along with launching homecare services. Plans are underway to scale up existing facilities, expand into new geographical areas, and identify new avenues within the healthcare eco-system, such as Academics - Medical College. As Medanta con...

The ideal candidate for this role is a critical thinker who will proactively improve the quality systems of the company through internal audits, participation in process improvement programs, and interaction with key partners to obtain constructive feedback. As a quality systems professional, you will be responsible for leading the development, implementation, and continuous improvement (CI) of the Quality Management System (QMS) in line with ISO and other relevant standards. Your role will also involve ensuring company-wide compliance with applicable regulatory and quality standards, planning and conducting internal audits, as well as coordinating external and customer audits. In this posit...

As a Senior Manager - Production at Sun Pharmaceutical Industries Ltd in Mohali, you will be responsible for overseeing the planning and execution of production and packing activities to meet monthly targets. Your key responsibilities will include reviewing daily production activities, ensuring Good Documentation Practices (GDP) are followed, coordinating with various departments for smooth functioning, handling SAP related work, and implementing best practices in compliance with cGMP and safety guidelines. You will be required to review and approve various documents such as SOPs, purchase requisitions, process validation protocols, and equipment qualification reports. Additionally, you will...

The position aims to ensure the timely production of parts in accordance with the production plan and directions provided. As part of the Machine Shop team, you will be responsible for handling various CNC Machines. Your duties will include ensuring 100% safety in all plant activities, adhering to correct manufacturing processes and utilizing tools and equipment appropriately. A key aspect of your role will involve understanding and controlling CNC Machine Programs, with a focus on productivity improvement and minimizing rework/rejection. It will be crucial to maintain proper housekeeping in the work area, deliver parts on time, and make proper use of measuring instruments. Additionally, you...

Join Frencken's IMS Division: Innovating for the Future At Frencken, our Integrated Manufacturing Services (IMS) division is dedicated to providing high-quality, end-to-end manufacturing solutions to various global industries. From precision engineering to complex assembly, IMS excels in merging cutting-edge technology with world-class processes to cater to the diverse requirements of our clients. By becoming a part of the IMS team, you will be joining a dynamic division that thrives on innovation, collaboration, and the pursuit of excellence. Whether you are an engineer, technician, or operations specialist, you will discover endless opportunities to develop and create an impact in industri...

As a Quality Assurance Specialist, your responsibilities will include reviewing all Master Production and Control Record (MPCR) and Batch Packing Records (BPR), as well as Standard Operating Procedures (SOPs). You will need to meticulously review specifications and testing procedures for starting materials, packaging materials, in-process products, finished products, working standards, and stability (Shelf life). Additionally, you will be tasked with reviewing Out-of-Specification (OOS) investigation reports and participating in investigations related to complaints, vendor audits, external testing laboratories audits, and the subsequent Corrective and Preventive Actions (CAPA). You will also...

You are a dedicated and detail-oriented Quality Management System (QMS) Executive responsible for supporting and enhancing the organization's quality framework. Your primary role includes implementing, maintaining, and continuously improving the QMS in line with ISO 9001:2015 and relevant regulatory standards. Your focus will be on ensuring quality compliance across departments and fostering a culture of continuous improvement. Your key responsibilities will involve implementing and maintaining the Quality Management System in alignment with ISO 9001:2015 standards. You will be tasked with developing, reviewing, and controlling quality documents such as SOPs, manuals, work instructions, and ...

As an individual working with the Site Investigations team member (Microbiology) at Dr. Reddys Laboratories Ltd., your primary responsibility is to ensure effective investigations and root cause analysis for microbiology-related deviations, Out of Specification (OOS), and Out of Trend (OOT) results. Your role involves driving these investigations towards closure in a timely manner with adequacy. Key Responsibilities: - Performing root cause analysis for microbiology-related deviations, OOS, and OOT results, including Bioburden, Sterility, and Bacterial Endotoxins Test (BET). - Collaborating with cross-functional teams to ensure timely and adequate closure of investigations. - Conducting tren...

As a Real Time Monitoring Specialist, you will be responsible for various tasks related to data management and connectivity in a dialler environment. Your key responsibilities will include real-time monitoring, data uploading, reporting, and management in the dialler system. You will play a crucial role in ensuring seamless connectivity and enhancing business outcomes through data churning strategy and implementation. Additionally, you will be in charge of DND scrubbing, tracking downtime, monitoring PRI levels, and providing timely responses to escalations. Your role will also involve analyzing connectivity and business improvements, as well as identifying deviations in data behavior and im...

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 t...

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, coordi...

The Technical Writer Change Control Management is responsible for developing, managing, and maintaining documentation related to change control processes within a regulated manufacturing environment. This role ensures documentation accuracy, consistency, and compliance with regulatory and organizational standards. You will leverage your knowledge of science and manufacturing technologies to collaborate effectively with cross-functional teams, streamline documentation workflows, and support the organization's change control management processes. You will develop, revise, and maintain high-quality documentation related to change control processes, ensuring alignment with cGMP and other regulat...

As a Process Improvement Specialist, you will be responsible for designing process workflows, creating corrective and preventive action plans, and establishing design verification procedures. Your role will involve the implementation of a Quality Management System (QMS) and identifying attrition points within the process for improvement. You will be required to develop and implement methods to analyze the quality of end-products, identify issues and flaws in current models and processes, and recommend necessary changes to the relevant department. It will also be part of your responsibilities to pitch ideas for solving potential problems, draft strategies to enhance productivity, and generate...

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 poli...

About the Role: This is a Full-Time job opportunity for an experienced individual with a minimum of 10 to 18 years of relevant experience. The role is based in Chennai, Tamil Nadu and is a requirement for one of the Workassist Hiring Partners. Primary Responsibility: As the Quality and R&D Head, your main responsibility will be to lead the quality and R&D functions of the company. This includes ensuring compliance with various standards such as FSSAI, HACCP, FSSC 22000, GFSI, Kosher, and Halal. Your tasks will involve setting quality policies, conducting audits, managing RCA and CAPA, driving new product innovation, and collaborating with cross-functional teams to enhance efficiency. Additio...

As the Quality Assurance Supervisor, you will be responsible for monitoring in-line, end-line, and final audits to ensure strict adherence to AQL standards. Your key responsibilities will include supervising QA/QC inspectors, providing guidance, and ensuring that daily quality targets are met. You will be required to analyze defect trends, implement corrective and preventive actions (CAPA), and work towards reducing rework rates. Additionally, you will play a crucial role in ensuring the implementation of specific quality manuals and SOPs during production processes. Your role will also involve supporting pre-production activities such as PP meetings, sample reviews, and initial inspections ...

As a Senior Manager Production at our Guwahati location, you will be responsible for overseeing all manufacturing operations to ensure smooth production processes and meeting quality standards. Your role involves planning, coordinating, and directing production activities while ensuring compliance with safety, regulatory, and company policies. Your key responsibilities will include planning and coordinating production and packing activities to achieve monthly targets. You will review daily production activities for various processes such as Granulation, Compression, Coating, Capsule filling, Inspection, Packing, and Nutra section. Ensuring Good Documentation Practices (GDP) at the shop floor...

As a Quality Assurance Specialist, you will be responsible for reviewing paper and electronic batch records to ensure completeness, clarity, and compliance with Good Manufacturing Practices (GMP). Your role will involve assessing the documentation related to raw materials and releasing them for production. You will provide quality support by contributing to the development of Corrective and Preventative Actions (CAPAs) and offering guidance to various departments on GMP aspects. Additionally, you will review and approve quality assurance controlled documents such as Standard Operating Procedures (SOPs), batch records, and work instructions. In this position, you will be tasked with evaluatin...

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 w...