Senior R&D Officer

Tabuk Pharmaceuticals Manufacturing Co

Follow approved departmental SOPs.

Follow cGMP and GDPs

Follow all safety precautions as per EHS SOPs.

Monitoring Planning coordinating and controlling the R&D activities and related issues and projects to achieve the target

Responsible for co-ordination and control of respective R&D areas. Reporting to Process Development Manager.

Planning, coordination and control of respective R&D-Tabuk resources to effectively achieve the set production targets & quality standards.

Preparing periodic reports with respect to the activities and achievements to be submitted to Process Development Manager

Follow up activities with Sub-coordinates and analysis the Results for continues improvement

Interaction with concerned departments in the organization on production to ensure

Smooth discharge of technical & administrative responsibilities of the department.

To ensure the compliance and implementation of cGMPs in respective activities of the department.

Maintaining the required standard of health and safety in the department.

Checking of documents such as Process Operating Instructions (POI), SOPs, Validation / Qualification Protocols, Records and other relevant documents.

Organizing training & development of Process Development personnel as per the approved training schedule.

Participating in the internal quality audits for compliance with cGMP requirements.

To provide assistance in scaling up of products.

Technology transfer to production and optimization

To monitor validation of manufacturing process

Prepare & Review of validation batch protocol & reports

To plan for revalidation whenever required

Monitor R&D batches in production