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Job Description
- Managing the new projects since the idea is received till they are launched in the market, by creating a path for each project and monitoring every step and solving any problem that pops out, to make sure the project is launched at the target time and by the target price.
- Send weekly the Critical Path Analysis of each project to all concerned parties to monitor the project progress.
- Keep abreast of the goings-on in the industry.
- Review and recommend changes to current product development processes.
- Make creative recommendations to expand product base and vision.
- Document daily deliveries and shipments to update inventory.
- Search for the best, innovative and cost-effective packs, and providing samples and following up for Marketing’s approval, with attention to split-up cost and budget allowance.
- Tracking the inter-department transactions of Claims, Texts & Artworks, and ensure through revisions that they are complying with both Local and International Regulations.
- Follow up the formulation process with R&D while considering the budget allowance, as well as Marketing approval for a final effective formula. Also follow up stability and compatibility status of each product.
- Track the entire process of placing orders for Packs and Raw materials with Planning and Purchasing Departments.
- Search for new business channels to grab new Toll Manufacturing opportunities.
- Sends weekly reports to the concerned parties and the top management with the all project updates/details.
- Developing sales tools for a product.
- Recommends changes in service and /or policy by evaluating results and competitive developments
- Attend training and develop relevant knowledge, skills and techniques.
- Collaborate with team to achieve better results.
- Planning and overseeing new marketing initiative.
- Conduct research to identify new markets and customer needs.
- Prepare SOPs, quality related repots and change control documentation (PdAs), when appropriate.
- Performing formulation trials using different excipients and different processing methods.
- Carry out in process tests to ensure product compliance with established specs and providing related reports accordingly.
- Check the quality system during manufacturing process in production area.
- Check the document step by step in production area during the manufacturing process
- Record inspection results from manufacturing process
- Monitoring GMP & system implementation on daily basis and providing related reports accordingly.
- Withdrawing IPC & finished samples for QC department as per the established sampling plan.
- Supervise the dispensing process of raw and packaging materials.
- Verify the batch records and logbooks completeness.
- Highlight deviations and establishing of corrective...
- Approve process master documentation.
- Approve product specifications and associated documentation.
- Final product release: review completed batch records and associated deviations.
- Approve quality-related and/or project specific protocols.
- Responsible for evaluation/approval of equipment cleaning.
- Approve equipment qualification protocols and reports.
- Approve process validation protocols and reports.
- Manage site stability program including approval of stability data report.
- Handle clients quality related issues.
- Provide support during Client audits/inspections
- Conduct regular inspections of the operational areas to verify compliance with cGMPs.
- Provide training to staff in cGMPs.
Job Requirements
- B.Sc in Pharmaceutical Sciences is required.
- Language: Very Good English Language proficiency.
- Computer: Good Computer skills proficiency.
- Minimum of 5 years of experience in the area of research development.
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