Sara Asmar

About Sara Asmar

With a masters degree in toxicology and valuable work experience in a production/laboratory setting including substantial hands-on exposures to many different tasks and tests within this specialty, I am fully prepared to move into a similar or higher level of responsibility in a supervisory-managerial capacity or in a substantial, more senior level technical role.Some of the work skills I offer are listed below: • Operations: possess a background in laboratory and manufacturing operations and testing control; prepare, review, execute and summarize validation protocols (IQ, OQ, PQ, PV and/or CV) for manufacturing, packaging and automated inspection equipment• Staff supervision: skilled in the supervision and control of employees under my authority• Scheduling: determine priority scheduling for analytical projects and for employees• Employee training: have gained experience in the orientation and training of my staff; taught an undergraduate class in microbiology• Writing: create protocols, standard operating procedures, acceptance criteria and sampling procedures• Records management: maintain the flow of a very broad range of computerized and manual records and reports for the firm; precise and accurate with technical record keeping• New procedures: responsible for the design of new systems of operation, and in the improvement of existing work procedures • Calibration: responsible for maintaining all test equipment, including all calibration work• Coordination: coordinate scheduling of cleaning validation activities between manufacturing and quality control personnel• Quality assurance: actively contribute to the maintenance of product quality standards• Analysis: capable of performing instrumental analysis using HPLC, UV/VIS and spectrophotometer• Interaction: act as a liaison between laboratory technicians and various other managers• Compliance: ensure strict compliance with all federal, state and local regulations and policies

Experience

1. Validation Engineer Iii

   Catalent

   Oct 2022 — Present · US

Education

• Kansas State University

  Masters, Pathobiology / Toxicology

Skills

• Hplc
• Software Documentation
• Regulatory Affairs
• Pharmaceutical Industry
• Sop
• Quality Control
• Fda
• Gmp
• 21 Cfr Part 11
• Glp
• Microbiology
• Validation
• Quality Assurance
• Six Sigma
• Gxp
• Quality Auditing
• Uv/Vis
• Cleaning Validation
• Quality Management
• Capa
• Manufacturing
• Pharmaceutics
• Quality System
• V&V
• Project Management
• Training
• Testing