12/2013 to CurrentSalt Lake City, Utah

04/2010 to 10/2012Salt Lake City, Texas

10/2002 to 08/2008Salt Lake City, Utah

MR YASIR BUTT

Professional SummaryExperienced professional with excellent client and project management skills. Action-oriented with strong ability tocommunicate effectively with technology, executive, and business audiences. Strong web based sales skills.

Core QualificationsOperations management.Change management.Training and development.Reports generation and analysis.Multi-Task Management.Client Relations.Online Sales.Public Speaking Multilingual.Power-point Presentations.Customer Engagement.Customer Engagement.Familiarity with Agile Project Management.

GLP/GCP Phase 1-3 Bioanalysis.CFR 21 part 11 and 58.HPLC/MS/MS and GC/MS/MS operations.Quality Assurance.Quality Control/CAPA.GLP Site/Study Directed Audits.CRO GLP/GCP Monitoring.EMEA, FDA, MHLW GLP Regulations.Corrective And Preventative Actions (CAPAs).Regulatory Pharmacovigilance.

Experience (2000-2013)Project Management TeamTandem Labs

Project Management/Study outsourced Project Management on Projects Outsourced to organization frominternational Pharmaceutical companies developing drugs for multiple therapies (TK and PK).Responsibility for full project cycle from quote submission, financial grant initiation, sample shipmentarrangement/notification, validation, sample analysis, QC'd/QA'd data critique, CAPAs, report review andapproval/finalization.

Study Monitor (Project Manager Outsourced Research Studies)Alcon Labs/Novartis

Project Management/Study outsourced Project Management on Projects Outsourced to CROs (TK and PK)including full project cycle quote submission, financial grant initiation, sample shipment arrangement/notification,validation, sample analysis, QC'd/QA'd data critique, report review and approval/finalization.Prepared weekly update to update stakeholders on project status and completion.GLP/GCP Protocols, GLP/GCP Study Monitoring.Oversaw data technical laboratory reports, analytical methods from CROs conducting outsourced studies.Communicated with Project Managers in CROs to represent Alcon and provide study over sight.Participated in contract lab conference calls for project delivery dates oversight and updates as well astroubleshooting.Assisted in directed study/Facilities QA audits of CROs for contract and GLP/GCP regulation compliance.Addressed QA findings and review/input to QA observations, and CAPAs.

CRO Technical Staff Trainer GLP/GCP Phase 1Tandem Labs

Responsible for assessing and developing standardized Laboratory "Best Practices".Part of the Company Presidential Award 2003 "going above and beyond call of duty award" winning Team thatgenerated over 1 million dollars in revenue in one month for the division.Trained New staff on GLP/GCP laboratory functions including wet lab techniques, GLP/GCP Phase 1, OSHA,Analyst and Watson LIMS use.

5060 S Ellerby Ct, Salt Lake City, Utah 84117 | H: (801) 815-0170 | C: (801) 815-0170 | retaane@gmail.com

12/2000 to 10/2002Salt Lake City, Utah

1995Mobile, Alabama, USA

Trained new staff on electronic lab notebook (Velquest) functions.Served in cross functional team on CFR 21 part 11 software systems as a user and release tester for differentmodules.Utilized LC/MS/MS and GC/MS/MS testing for complex bio-analysis for all phases of GLP/Research DrugDevelopment for International Pharmaceutical companies.Lead studies audited by FDA/Clients without 483 citations.Met with clients during audits to update and discuss technical aspects of current and forecasted Projects.Helped the Director in formulating/amending Standard Operating Procedures.Participated in contract lab conference calls for Project delivery dates and updates as well as troubleshooting.Proficient in MDS Sciex API 5000, 4000, 3000 MS/MS operations and data analysis.

Research ScientistNorthwest Toxicology

Performed (complex analytical) tests to identify drugs of abuse in Urine and Tissue.Handled, forensic samples including blood, hair and oral fluids.Utilized complex testing GC/MS, Thin Layer Chromatography (Toxi-Lab), GC/FID techniques.Maintained and Troubleshot Instruments.Performed rigorous revisions of generated data, including Chain of Custody documentation, QA and QC data per(SAMHSA and CAP, FRA) regulations.Functioned in Senior Scientist Capacity in the department; duties included but not limited to: training new staff,revisions of Standard operating Procedures, research and method development.Worked alone, and with the manager of the department to implement new procedures, efficiency parameters andguidelines (to satisfy protocols).

EducationBachelor of Science: Medical TechnologyUniversity of South Alabama Mobile

Professional Development•DiSC and Customer Service (8 Contact Hours) Alabama Reference Labs, Montgomery Alabama.•Business Writing (12 Contact Hours) Alcon Labs, Fort Worth Texas.•How To Communicate with Professionalism (12 Contact Hours) Alcon Labs, Fort Worth Texas.•Velquest Operator Training CFR 21 Part 11 Software Tandem Labs, Salt Lake City Utah.•Managing Multiple Projects, Objectives and Deadlines (SkillPath) Tandem Labs, Salt Lake City Utah.•Secrets and Development in GC and GC/MS (Agilent Technologies) Tandem Labs, Salt Lake City Utah.

Computer and Software ProficiencyPharma/Medical Device IT Platforms (CFR 21 Part 11)

WatsonAnalyst.Velquest (SamrtLab).

Health Care Patient Information LIMS.Antrim.Cerner.HL7

Operating Systems.Windows (95, 98, 2000, XP, Vista, 7 and 8).Apple IOS 5 and 6.

Productivity.Microsoft Office Suite (Power Point emphasis)Adobe Acrobat 9 Pro.Intuit Quick Base.