Summary
Avalon Pharma is hiring a Formulation Research and Development Supervisor in Riyadh. The role develops pharmaceutical products, including oral solid dosage forms, oncology products and sterile injectables, and oversees formulation optimization, scale-up, stability studies and registration activities. Duties include maintaining and qualifying laboratory equipment, transferring products to Production, supporting site transfers and assessing technical feasibility and costs. Applicants need a B. Pharma or M. Pharma in Pharmaceutics and 8–14 years of experience in formulation research and technology transfer.
The posting
As published on avalon.com.sa. Pulled from the employer's site and shown as they wrote it.
- Development of new products and registration as per plan and timelines
- Improvement of products quality and productivity
- Formulation Laboratory Maintenance.
- New product technology transfer from R&D to Production.
- Product variation for site transfer.
- Cost evaluation of new products proposed by business development team.
Responsibilties:
- To develop new pharmaceutical products, including oral solid dosage forms, oncology products, and sterile injectable formulations, in accordance with approved development plans, regulatory requirements, and project timelines.
- To establish, maintain, and ensure the readiness of the Formulation R&D laboratory, including general formulation, oncology, and sterile injectable development facilities.
- To support the installation, setup, qualification, calibration, and trial operation of R&D laboratory equipment and instruments.
- To execute formulation development, process optimization, scale-up, stability studies, and registration batch activities for oncology and sterile injectable products.
- To facilitate technology transfer of developed products from R&D to Production and support site transfer activities.
- To evaluate the technical feasibility, formulation composition, manufacturing process, and cost of new products proposed by the Business Development team, including in-licensed and Contract Manufacturing Organization (CMO) products.
- To ensure compliance with applicable GMP, GLP, GDP, data integrity, occupational safety, and product-specific handling requirements during all R&D activities.
- To perform trouble shooting of Existing products & Production support (whenever required).
- Planning for Procurement of RM PM for Process optimization and Registration batches
- Preparation of MFC, PVP/POP & HTS.
- R&D observation sample stability monitoring.
- RM & PM Procurement follow up and Sample submission for testing after receiving.
- Technical support to store personnel for proper entry of RM/PM/RLD.
- Blocked Material list Monitoring and supporting Store Personnel for FIFO.
Education: B. Pharma / M. Pharma (Pharmaceutics)
Experience: 8-14 Year experience in formulation research & technology transfer.