Company Description Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable
Job Description Are You Ready to Make It Happen at Mondelēz International? Join our Mission to Lead the Future of Snacking. Make It With Pride. Key Responsibilities: Process Management & Optimization: Develop, implement, and maintain process
JOB DESCRIPTION: Followings will be the Core Job Responsibilities of the position holder: Ensure the Compliance to laid standards of the current Good Manufacturing Practices in the Liquid Manufacturing, Packing and Stick pack. Co-ordination for installation
Job Purpose To lead Quality Assurance operations for the Solid Oral facility and ensure compliance with cGMP, global regulatory requirements, data integrity standards, and Quality Management Systems. Key Responsibilities Ensure compliance with cGMP, Data Integrity, and
Key Responsibilities Technical Operations & Process Excellence Lead scale-up, engineering batches, PPQ batches, process validation, and technology transfer activities. Review and approve validation protocols, reports, and batch manufacturing records. Drive process optimization, troubleshooting, revalidation, batch size
Key Responsibilities Ensure compliance with cGMP, data integrity, and regulatory requirements. Manage Analytical Method Transfer (AMT), Validation (AMV), and Verification activities. Review and approve AMT/AMV protocols, reports, and related documentation. Ensure timely completion of validation, verification,
Job Purpose To lead and manage qualification, validation, and requalification activities for equipment, facilities, utilities, and manufacturing processes, ensuring compliance with cGMP, regulatory requirements, and data integrity standards. Key Responsibilities Ensure cGMP, Data Integrity, and regulatory
////// CONTEXT Within Dedienne Aerospace Group, one of the strategic priority is to develop the after sales services business. The Services Business Unit aim to ensure great customer relationship and maintain tooling serviceability and availability along
Company Description Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable
Company Description Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable
Job description Monitoring of gowning and sanitation practices in area of operation. Monitoring of compliance of standard operation procedure in production & packaging department. Reporting the noncompliance of written SOP of machine operation. Line clearance inspection
Brief Requirements Should have worked on the shop floor and have sound process knowledge in manufacturing Semisolid, Solid oral, Liquids, powder dosage forms, cosmetics and nutraceuticals. Should have thorough understanding of GMP guidelines and regulations applicable
JOB DESCRIPTION: Position : Assistant manager Section : Analytical Quality Assurance Qualification : M.Sc. /B. Pharm. Desirable Experience: 12-14 years Followings will be the responsibilities of the position holder: 1. Quality Management System (QMS): Must be
Job Title Executive Business Unit Global Quality and Compliance Job Grade G12A Location : Baddi At Sun Pharma, we commit to helping you Create your own sunshine — by fostering an environment where you grow at
Key Responsibilities Ensure compliance with cGMP, data integrity, and regulatory requirements. Manage Analytical Method Transfer (AMT), Validation (AMV), and Verification activities. Review and approve AMT/AMV protocols, reports, and related documentation. Ensure timely completion of validation, verification,
Job Description Position : Assistant manager Section : Analytical Quality Assurance Qualification : M.Sc. /B. Pharm. Desirable Experience: 12-14 years Followings will be the responsibilities of the position holder: 1. Quality Management System (QMS): Must be
Key Responsibilities Technical Operations & Process Excellence Lead scale-up, engineering batches, PPQ batches, process validation, and technology transfer activities. Review and approve validation protocols, reports, and batch manufacturing records. Drive process optimization, troubleshooting, revalidation, batch size
Greetings from P360.! About us : P360 is an advanced pharma software company specializing in business technology development and implementation for pharmaceutical and life sciences companies worldwide. We specialize in technology that boosts operational efficiency across
Detailing Engineer - Concrete and Rebar Who We Are: DBM Vircon, a premier construction modeling, detailing and digital engineering company, delivers high-profile projects with state-of-the-art technology, uncompromising detail and millimeter precision. At DBM Vircon we see
Job Purpose To lead Quality Assurance operations for the Solid Oral facility and ensure compliance with cGMP, global regulatory requirements, data integrity standards, and Quality Management Systems. Key Responsibilities Ensure compliance with cGMP, Data Integrity, and