15 Qualification Activities Jobs

As a member of the Process Engineering (Instrumentation) team at Knovea Pharmaceutical Pvt. Ltd. in Indore, MP, you will be responsible for the following key responsibilities: - Reviewing equipment design qualification documents such as PI&D, FS, DQ, SDS, HDS, IQ, OQ & drawings, and approving them if necessary. - Verifying process equipment instruments according to PI&D and electrical drawings, and commissioning instruments if needed. - Conducting FAT for process equipment when required. - Providing support for installation and commissioning activities. - Assisting in qualification activities for equipment like IQ, OQ & PQ. - Identifying all process equipment and utilities equipment field in...

By clicking the Apply button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description: OBJECTIVES/PURPOSE : Manages technical topics related to the global manufacturing of Drug Product within the scope of VBU Manufacturing Science & Technology. Independently develops and implements continuous improvement activities for current and future manufacturing sites within the Takeda vaccines manufacturing network and drives cha...

As a Line Clearance Officer, your role involves ensuring proper line clearance activities before commencing various operations like dispensing, manufacturing, filling, inspection, sealing, labeling, and packing. You will be responsible for conducting process validation, cleaning validation/verification, hold time study, media fill, and routine batch sampling as per protocol/SOP. Additionally, you will review executed BMRs and BPRs and perform in-process tests at different stages as per batch document/SOP. Your key responsibilities will include: - Reviewing environment monitoring and water trends - Reviewing different types of planner and calibration certificates - Receiving necessary resourc...

As a Production Supervisor, your role involves overseeing various aspects of production operations to ensure smooth functioning and adherence to quality standards. Your key responsibilities include: - Indenting, approving, and receiving batch production records, cleaning records, and packing records based on production requirements. - Raising raw material indents and approving indented raw materials in alignment with production planning. - Maintaining good housekeeping in the plant environment. - Coordinating with cross-functional teams to execute plant operations efficiently. - Monitoring equipment utilization and manpower distribution for optimal productivity. - Initiating, reviewing, and ...

As a Process Incharge for Injectable manufacturing projects, your role will involve reviewing equipment design qualification documents such as PI&D, FS, DQ, SDS, HDS, IQ, OQ, and drawings for approval. You will verify process equipment instruments according to PI&D and electrical drawings for commissioning. Additionally, you will conduct FAT for process equipment when necessary and provide support for installation and commissioning activities. Key Responsibilities: - Verify process equipment instruments based on PI&D and electrical drawings - Conduct FAT for process equipment when required - Provide support for installation & commissioning activities - Assist in qualification activities for ...

As an experienced and dynamic professional in the pharmaceutical industry, you have the opportunity to join Ananta Medicare Ltd in Sri Ganganagar, Rajasthan, specifically in the Quality Assurance Department for Validation activities in a manufacturing facility. Your role will involve hands-on experience in qualification and validation activities for a sterile / Cepha manufacturing setup. Key Responsibilities: - Execution and review of Qualification activities for Equipment, Utilities, and Facilities (URS, DQ, IQ, OQ, PQ). - Preparation and review of validation protocols and reports (Process Validation, Cleaning Validation, Sterilization Validation, HVAC Qualification, etc.). - Coordination w...

Preference to Immediate Joiner Company: Ananta Medicare Ltd, Sri Ganganagar, Rajasthan Ananta Medicare Ltd is looking for an experienced and dynamic professional to join our Quality Assurance Department for Validation activities in a manufacturing facility with hands-on experience in qualification and validation activities for a sterile / Cepha manufacturing setup. Key Responsibilities: Execution and review of Qualification activities for Equipment, Utilities, and Facilities (URS, DQ, IQ, OQ, PQ). Preparation and review of validation protocols and reports (Process Validation, Cleaning Validation, Sterilization Validation, HVAC Qualification, etc.). Coordination with Production, QC, and Engin...

As a Water and HVAC Systems Operator, your primary responsibility will be to efficiently operate and manage the water and HVAC systems in accordance with Standard Operating Procedures (SOP). You will also be in charge of maintaining an inventory of critical spares and chemicals for these systems to ensure smooth operations. Additionally, providing necessary utilities such as Raw water, RO water, WFI, Purified water, pure steam, Compressed air, and Nitrogen to the production department or other users will be part of your daily tasks. Key Responsibilities: - Recording and updating all water and HVAC system data as per SOP guidelines, while adhering to cGMP and GEP standards in all work activit...

As a C&Q Engineer - Senior Executive at Novartis Healthcare Private Limited in Hyderabad, you will be responsible for managing Projects Facility, Process, HVAC, Clean room, and Utility Services Commissioning & Qualifications activities for Pharmaceutical OSD/Injectable/API/Oncology/Biotechnology/Vaccine manufacturing facilities. Your role involves developing Protocols, executing reports, organizing, budgeting, scheduling, and monitoring project performance within required timelines. **Key Responsibilities:** - Prepare, execute, and compile Facility, Process, HVAC, Clean room, and Utility Services Commissioning & Qualifications activities Protocols/reports for Pharmaceutical facilities - Prov...

As a member of the Process Engineering (Instrumentation) team at Knovea Pharmaceutical Pvt. Ltd. in Indore, MP, you will play a crucial role in the pharmaceutical manufacturing industry. Your responsibilities will include: - Reviewing equipment design qualification documents such as PI&D, FS, DQ, SDS, HDS, IQ, OQ, and drawings for approval if necessary. - Verifying process equipment instruments according to PI&D and electrical drawings for commissioning if needed. - Conducting FAT for process equipment as required and providing support for installation and commissioning activities. - Supporting qualification activities for equipment including IQ, OQ, and PQ. - Identifying all field instrumen...

As a responsible team member in the pharmaceutical manufacturing process, your role involves the following key responsibilities: - Conduct line clearance activities before starting various operations such as dispensing, manufacturing, filling, inspection, sealing, labeling, and packing. - Perform process validation, cleaning validation/verification, hold time study, media fill, and routine batch sampling according to protocol/SOP. - Review executed Batch Manufacturing Records (BMRs) and Batch Packaging Records (BPRs). - Perform in-process tests at different stages as per batch documents/SOP. - Review environmental monitoring and water trends. - Review different types of calibration certifica...

As a Process Incharge - Injectable, you will be responsible for overseeing formulation manufacturing projects with an experience requirement of 12-15+ years, including 5-6 years specifically in formulation manufacturing projects. Your key responsibilities will include reviewing equipment design qualification documents such as PI&D, FS, DQ, SDS, HDS, IQ, OQ, and drawings for approval when necessary. You will be tasked with verifying process equipment instruments in alignment with PI&D and electrical drawings, ensuring commissioning of instruments as needed, and conducting Factory Acceptance Tests (FAT) for process equipment where necessary. Additionally, you will provide support for installat...

You are invited to attend a walk-in interview for Zydus Animal Health Unit in Ahmedabad on 03rd August 2025 at Hotel Woodlands, NH 8, Near Tejpal Motors, Balitha, Vapi, Gujarat 396191. The interview timings are from 9:00 AM to 04:00 PM. The job location is Pharmez Matoda, Ahmedabad. In the Manufacturing (OSD) Department, we are looking for candidates for the following roles: 1. Officer/Executive: - Qualification: B. Pharma/M. Pharma - Experience: 2 - 7 years - Responsibilities: - Planning manufacturing batches in coordination with PPMC - Monitoring line clearance, cleaning of equipment, and instruments - Performing qualification activities - Initiating QMS activities such as change control, ...

IQ, OQ and PQ,execution of Facility, Utility, Equipment and Computer system qualification,Client schedules,Report daily activities and work completion status to Sr. Manager, Validation ,SOPs Validation, Qualification,Calibration activities

As a Water and HVAC Systems Operator, your primary responsibility will be to efficiently operate and manage the water and HVAC systems in accordance with Standard Operating Procedures (SOP). You will also be in charge of maintaining an inventory of critical spares and chemicals for these systems to ensure smooth operations. Additionally, providing necessary utilities such as Raw water, RO water, WFI, Purified water, pure steam, Compressed air, and Nitrogen to the production department or other users will be part of your daily tasks. Recording and updating all water and HVAC system data as per SOP guidelines, while adhering to cGMP and GEP standards in all work activities, is crucial for this...