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 compliance
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 changes, equipment changes, and alternate
About CloudLabs: CloudLabs Inc was founded in 2014 with the mission to provide exceptional IT & Business consulting services at a competitive price, to help clients realize the best value from their investments. Within a short
Looking for 30-45 days/joiners only. Job Title: Sr. Data Analyst (Risk & Compliance) Experience: 10+ years Location: Remote Join our client and be part of bringing our clients world-changing ideas to life. At our client, you
Tiger Analytics is a leading global Data and Analytics consulting firm. With data and technology at the core of our solutions, we are solving some of the toughest problems out there for Fortune 500 companies. Our
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
Join the team shaping the future of enterprise AI. About Moveworks and 89 Solutions 89 Solutions is a pure play Moveworks partner delivering enterprise-grade AI solutions that transform employee support and productivity. With a proven record
Penguin Ai: Were Not Just Building AI, Were Revolutionizing Healthcare. Seeking a UM Policy Review Nurse to Make Clinical Judgement Scale! Your Role: Clinical Guardian. Policy Translator. Human-in-the-loop Expert. Location: Hyderabad Type: Full-time. Travel: Occasional (For
Job Description Followings will be the responsibilities of the position holder: 1. Preparation and review of qualification and Validation documents (URS, DQ, IQ, OQ, PQ, etc.) for ODF Facility. 2. Preparation and updation of Validation Master Plan, CVMP,
JOB DESCRIPTION: Followings will be the responsibilities of the position holder: 1. Preparation and review of qualification and Validation documents (URS, DQ, IQ, OQ, PQ, etc.) for ODF Facility. 2. Preparation and updation of Validation Master Plan, CVMP,
Followings will be the responsibilities of the position holder : Preparation and review of qualification and Validation documents (URS, DQ, IQ, OQ, PQ, etc.) for ODF Facility. Preparation and updation of Validation Master Plan, CVMP, SMF, Quality Manual
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
Minimum Qualification : M. Pharma/ B. Pharma/M.Sc. Candiate shall be well versed with manufacturing and packaging operations, Compression Machines, Isolators, Blenders, Bulk packing lines, & Process Validation. Followings will be the responsibilities of the position holder : To
Objective: To ensure efficient and optimized utilization of production and packing lines for Oral Solid Dosage (OSD) forms by coordinating machine loading, balancing workflows, and managing dependencies related to QC release, client schedules, and communication with
Responsibilities To ensure that quality systems are developed, implemented and maintained. To ensure that the raw material suppliers are qualified as per the applicable procedures. Oversee investigations of all non-conformances (Incidents, deviations, OOS, market complaints, errors,
Job Description Version. no. : 01 The Job Responsibilities of the position holder are : Responsible for performing the analytical activities as per Analytical competency matrix (Format No.BDI-QCSG004F23) and On job training and Practical Demonstration for
Key Responsibilities Ensure trouble-free operation and maintenance of process and utility equipment. Plan and monitor preventive maintenance activities to minimize downtime. Handle equipment breakdowns, RCA, and CAPA implementation. Lead equipment qualification, validation, calibration, and requalification activities. Review SOPs,
Job Title: SAP MDG Functional Consultant Location: Chennai (5 Days Work From Office) Experience: 7–8 Years Employment Type: Full-Time Job Summary We are seeking an experienced SAP MDG Functional Consultant with 7–8 years of SAP expertise
About Position: The Senior Informix DBA will be responsible for end-to-end administration of IBM Informix database environments across production, non-production, DR, and legacy application platforms of CAP. The candidate should have strong experience in managing Informix
About the Company Avensys is a reputed global IT professional services company headquartered in Singapore. Our service spectrum includes enterprise solution consulting, business intelligence, business process automation and managed services. Given our decade of success, we have