Procurment supervisor
Riyadh Pharma
مجموع سنوات الخبرة :14 years, 3 أشهر
• Act as lead procurement professional and responsible for providing expertise and guidance on the most complex procurement issues and negotiation.
• Ensure that the procurement activities are accurate, efficient, timely.
• Professional and expert in procuring of all pharmaceutical industry requirements such as APIs, inactive ingredient, lab requirements, and engineering requirements.
• Primary responsibility is to generate cost saving with minimum 10% of total spend.
• Applied strategic sourcing and category management to drive product sustainability.
• Maintained a word-class, professional ethical relationship with vendors by building trust and keeping open channels of communication.
• Ensured adherence to procurement policy and procedures resulting in the effective procurement.
• Outstanding ability of thinking with the team to achieve cost reduction and business demands.
• Multi-tasking with ability to priorities tasks.
• Responsible of sourcing, effective price negotiation, supplier evaluation, analyses procurement methods, suppliers' contracts, and supply agreements.
Qualify, manage, and approve Riyadh Pharma's Vendors of the Raw materials and packaging materials used
in Riyadh Pharma.
• Evaluate DMF and vendors' qualification documents.
• Timely submitting the vendor qualification documents to Regulatory affairs according to SFDA
guidelines.
• Supervise all analysis activates related to vendor qualification including analysis of RM, finished
Product and dissolution profile.
Supervise routine analysis in raw material and provide technical advice to team members.
• Assuring compliance in all QC laboratory activities.
• SOPs preparation and strong knowledge in pharmacopoeias EP, USP, and BP.
• Transfer, modify, and improve analytical methods.
• Review analyses reports, OOS reports, and Incident reports.
• Perform complex laboratory analyses with supervision.
• Very good knowledge in the validation, method transfer, as well as methods verification.
• Expert in using of analytical instruments, such as GC, HPLC, UV-Vis, FTNIR, IR, Titrations, Viscometer, and
Particle Size Analyser (Malvren).
• Professional in all Quality Control activities including analysis supervising, compliance, and troubleshooting.
Preform all types of chemical analysis of both finished products and raw materials.
• Performs testing for the qualification of working standards.
• Involve in calibration and maintenance of lab instrument.
• Follow cGMP, GLP, and good documentation practices on a daily basis.
.