Assistant Manager Npd

Manage QMS activities: Change Control, Deviation, CAPA, OOS, OOT, Lab Events.Conduct Risk Assessments, SOP reviews, and assist in grievance handling.Document & review: Specifications, SOPs, Test Data Sheets, Analytical Test Reports, and Master documents.Review Method Validation Protocols & Reports.Monitor calibration and preventive maintenance...

Role: - Assistant Manager -Vendor Management QM.Location: BaddiCompany: Fresenius Kabi Oncology Ltd.Key Responsibilities:To establish, execute and monitor compliance with the procedure for the selection, qualification, development, maintenance, and discontinuation of External Providers (Suppliers of materials & services).Collection of Supplier audit needs...

Following will be the responsibilities of the position holder: 1. To ensure cGMP compliance at site. 2. Responsible for Vendor Qualification and Management 3. Day-to-day coordination with QA-representative w.r.t. Vendor Qualification/Re-Qualification and Management status. 4. To review vendor documents for Vendor Qualification. 5. To perform the Vendor...

Following will be the responsibilities of the position holder:1. To ensure cGMP compliance at site.2. Responsible for Vendor Qualification and Management3. Day-to-day coordination with QA-representative w.r.t. Vendor Qualification/Re-Qualification and Management status.4. To review vendor documents for Vendor Qualification.5. To perform the Vendor audit and...

Following will be the responsibilities of the position holder: 1. To ensure cGMP compliance at site. 2. Responsible for Vendor Qualification and Management 3. Day-to-day coordination with QA-representative w.r.t. Vendor Qualification/Re-Qualification and Management status.4. To review vendor documents for Vendor Qualification. 5. To perform the Vendor audit...

Following will be the responsibilities of the position holder:To ensure cGMP compliance at site.Responsible for Vendor Qualification and ManagementDay-to-day coordination with QA-representative w.r.t. Vendor Qualification/Re-Qualification and Management status.To review vendor documents for Vendor Qualification.To perform the Vendor audit and its compliance...

Company DescriptionEstablished in 1993, EmmForce is a trusted ISO/TS 16949:2009 certified Indian autoparts manufacturer. Our professionals excel in automotive intelligence through collaborations with OEMs, performance racing enthusiasts, and hardcore reverse engineering. EmmForce is equipped to handle challenging projects with its state-of-the-art integrated...

Accountable for all the compliance regarding activities for production block (OSD). Handling change controls and performing investigations for Deviation, OOS/OOT, Market complaints regarding soft floor. Handling Track wise activities. Performing Risk assessments Preparation of documents like SOP, URS, Protocols, BMR/BPR. Co-ordinating with cross...

Role & responsibilitiesComprehensive Oversight: Manage day-to-day activities in Quality Control .Instrument Expertise: Demonstrate hands-on experience with a variety of QC instruments, including HPLC, Dissolution, and other chemical and analytical tools.Lab Development: Utilize your expertise to develop the lab, ensuring compliance with the latest Revised...

We're Hiring: Deputy General Manager – R&D (Design Engineering)Location: Baddi, Himachal Pradesh  Company: Emmforce Autotech LtdOnly Apply If You Can Design the Drivetrain Parts and assemblies, Not Just Manage the ProcessWe're on the hunt for a senior design engineering leader who lives and breathes mechanical design, materials, and precision...