Executive - Production Documentation Biocon

3.0 - 7.0 years

0 Lacs

andhra pradesh

On-site

You will be responsible for: - Handling QMS activities such as CCF, Deviations, and OOS - Preparing and reviewing SOPs, EOPs, OCPs, BMR, and production-related documents - Reviewing batch reports and participating in productivity improvements and batch failure investigations - Creating AIM and HIRA register - Conducting HAZOP study - Coordinating with QA for validation, qualification, and Audit preparedness - Ensuring adherence to Standard Operating Procedures and product specifications - Following Good Manufacturing Practices and Good Documentation Practices - Reviewing all completed documents for completeness and signatures - Performing data entry in Quality records Qualifications required...

Posted 4 weeks ago

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Assistant Manager - Production Documentation Biocon

8.0 - 10.0 years

0 Lacs

visakhapatnam, andhra pradesh, india

On-site

Handling of QMS activities (CCF, Deviations and OOS etc.) Preparation and review of SOPs, EOPs, OCPs, BMR and production related documents. Review of batch reports and Involvements on productivity improvements and batch failure investigations. Preparation of AIM and HIRA register. Preparation of HAZOP study. To coordinate with QA for all the validation, qualification, and Audit preparedness. Adherence to Standard Operating Procedures, product specifications. Adherence to Good manufacturing Practices and Good Documentation Practices. Review All completed documents and ensuring that completeness and signed. Real time data entry in Quality records. Handling of e-BMR (SAP) activities. Sound know...

Posted 2 months ago

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Assistant Manager - Production Documentation Biocon

8.0 - 12.0 years

0 Lacs

andhra pradesh

On-site

As an experienced professional in the field of Quality Management Systems (QMS), you will be responsible for various key activities including handling of Corrective and Preventive Actions (CCF), Deviations, Out of Specification (OOS) incidents, and more. Your role will involve the preparation and thorough review of Standard Operating Procedures (SOPs), Equipment Operating Procedures (EOPs), Operational Control Plans (OCPs), Batch Manufacturing Records (BMR), and other crucial production documents. In addition, you will play a significant part in reviewing batch reports, identifying opportunities for productivity enhancements, and conducting investigations into batch failures. Your expertise ...

Posted 3 months ago

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Executive - Production Documentation Biocon

3.0 - 7.0 years

0 Lacs

andhra pradesh

On-site

As a candidate for this role, you will be responsible for handling various Quality Management System (QMS) activities such as managing Corrective and Preventive Actions (CCF), deviations, and Out of Specification (OOS) incidents. Your duties will include preparing and reviewing Standard Operating Procedures (SOPs), Equipment Operating Procedures (EOPs), Operating Control Plans (OCPs), Batch Manufacturing Records (BMR), and other production-related documents. Additionally, you will be required to review batch reports, participate in productivity improvement initiatives, and investigate batch failures. You will also be responsible for creating and maintaining the Asset Integrity Management (AI...

Posted 3 months ago

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