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3.0 - 7.0 years
0 Lacs
pune, maharashtra
On-site
Role Overview: You will be responsible for assisting in the development and release of standardized manufacturing documentation, such as workmanship standards, work instructions, drawings, and BOMs. Additionally, you will coordinate with suppliers, develop new suppliers, and conduct audits. Your role will also involve handling knowledge of imports, shipment terms, customs clearance, local vendor management, material ordering, and tracking. Understanding engineering drawings, Oracle systems, and bill of materials will be crucial for this position. You will need to adhere to established manufacturing procedures, provide support for plant-to-plant product transfers, and contribute to new produc...
Posted 3 weeks ago
8.0 - 12.0 years
0 Lacs
hyderabad, telangana
On-site
Role Overview: Azurity Pharmaceuticals, a specialty pharmaceutical company, is seeking a motivated individual to join their Technical Operations team. As a key player in managing technical process strategy, this role involves overseeing product deliverables in alignment with company objectives. You will lead a team to achieve project milestones supporting process scale-ups, technical transfers, and investigation of deviations for commercial products. Key Responsibilities: - Manage manufacturing planning and execution, including qualification and validation activities for both development and commercial products. - Develop and review controlled documentation for late-stage development, qualif...
Posted 1 month ago
8.0 - 10.0 years
0 Lacs
india
On-site
Location: India Contract: 12 months with possible extension Are you looking for a unique opportunity to drive quality excellence in pharmaceutical manufacturing Kelly FSP is seeking an experienced Senior Supplier Quality Assurance professional to actively support supplier selection, qualification, product transfers, process validations, and provide comprehensive quality oversight for API manufacturers. This position is part of an important API Restructuring Project. Key Responsibilities: Support the selection and qualification of suppliers through due diligence and audits. Provide quality oversight for product transfers and process validations, including equipment qualification. Ensure all p...
Posted 1 month ago
8.0 - 12.0 years
0 Lacs
hyderabad, telangana
On-site
As a member of the Technical Operations team at Azurity Pharmaceuticals, you will play a crucial role in managing and overseeing technical process strategy, CMO and CDMO management, and the execution of product deliverables. Your dedication and expertise will contribute to the success of Azurity in providing innovative products to underserved patients. Here are the key responsibilities and qualifications required for this role: **Key Responsibilities:** - Manage the planning and execution of manufacturing for both development and commercial products, including qualification and validation activities. - Develop, review, and approve controlled documentation related to late-stage development, q...
Posted 3 months ago
5.0 - 9.0 years
0 Lacs
pune, maharashtra
On-site
As an individual in this role, you will be responsible for supporting the development and release of standardized manufacturing documentation, including workmanship standards, work instructions, drawings, and Bill of Materials (BOMs). You will also be involved in coordinating with suppliers, developing new supplier relationships, and conducting audits. Your duties will include handling knowledge of imports, shipment terms, and customs clearance. Additionally, you will need to have hands-on experience with local vendors, material ordering, and tracking. Understanding engineering drawings, Oracle systems, and Bill of Materials will be essential for this position. You will be required to adhere...
Posted 4 months ago
3.0 - 7.0 years
0 Lacs
pune, maharashtra
On-site
The job involves working as a Packaging Design Engineer for Medical Devices. Your responsibilities will include Packaging Material Qualification and Testing, understanding Production methods specific to the Packaging industry, and applying expertise in executing activities like DFMEA, PFMEA, PPAP, and DFM&A. It is essential to have knowledge of Medical Device Standards such as FDA, EU MDR, ASTM, ISO, and IEC. Additionally, familiarity with Medical Device Product/Site Transfers will be beneficial for this role.,
Posted 5 months ago
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