Job Description
- 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
Bachelor Degree in Pharmacy, Science, Medicine or Chemistry
2 - 5 years of experience in a similar position.