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3.0 - 7.0 years
0 Lacs
karnataka
On-site
Role Overview: As an IPQA Executive at Syngene International Limited in Bengaluru, you will play a crucial role in the GMP IPQA team. Your primary responsibility will be to provide independent assurance to the quality of various stages of the process, ensuring the integrity of the process by overseeing equipment cleaning before and after processes and providing line clearance for different process steps. Your role will focus on ensuring process quality and the final product's manufacturing without any quality concerns post-process completion. Key Responsibilities: - Prepare, revise, and review procedures such as SOPs, protocols, reports, calibration schedules, and other related documents. - ...
Posted 1 month ago
5.0 - 10.0 years
0 Lacs
andhra pradesh
On-site
As a member of Pfizer's quality assurance team, you will play a crucial role in ensuring the delivery of safe and effective products to patients. Your commitment to quality, compliance, and patient-centric approach will directly impact the lives of those who rely on our products. Your responsibilities will include evaluating and reviewing clinical and commercial drug batches to ensure they meet established specifications. You will conduct rigorous sampling and statistical process control procedures to identify deviations from standards and approve investigations and change control activities to maintain compliance with configuration management policies. In this role, you will contribute to m...
Posted 2 months ago
15.0 - 18.0 years
15 - 20 Lacs
Bengaluru, Ramanagara
Work from Office
Role & responsibilities Dy.Manager / Manager Production Preferred candidate profile Responcible for Tablet Granulation, Coating & compression, Laser drilling machine , Responsible for sieve, screen, FBE finger bag inventory records, Should Have exposure with Exhibit batches, validation batches , Responsible for Production dept. and process improvement and development. Responsible for manufacturing of new products coordinating with R&D department. Resolve the Quality issues or any delay by coordinating with other departments. Preparation of Batch Manufacturing Record (BMR) from R&D guideline. Investigate the incidents and deviations in production area. Manpower handling and time management. s...
Posted 3 months ago
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