Casey Poirier Email and Phone Number
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Leveraging over 10 years of technical experience from QC Chemistry, QC Microbiology, and Validation in the Pharmaceutical Industry to provide personalized account management with STERIS Corporation | Life Sciences Division. Help clients create and maintain clean and sterile environments through our equipment, formulated cleaning chemistries, and service solutions.
Steris Corporation
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Account ManagerSteris Corporation Aug 2018 - PresentMentor, Oh, Us-Provide contamination control solutions and technical support for the Pharmaceutical, Biotechnology, and Research & Laboratory, Medical Device, Cosmetic, Dietary Supplements, Food & Beverage, and Veterinary Medicine industries-Offer full product line-up of detergents, surface disinfectants & cleaners, biological & chemical indicators for sterilization, and hand hygiene -Help meet demanding regulatory requirements, maximize production time, validate processes, and increase speed to market-Provide exceptional service and support through technical consultations such as: conference calls, webinars, phone/email support, onsite cleaning trials & cleaning optimization, training, audits, trouble-shooting, validation support, and much more-Quality customer support and personalized account management -
Lead Validation EngineerStallergenes Greer Dec 2017 - Aug 2018Baar, Switzerland, Ch• Coordinated the implementation and scheduling of validation testing with affected departments and personnel• Created, populated, and maintained databases for tracking validation & calibration activities • Oversaw and managed the site process simulation program • Organized and coordinated all cleaning validation activities -
Cleaning Validation EngineerStallergenes Greer Jun 2016 - Dec 2017Baar, Switzerland, Ch• Prepared process validation, equipment qualification, and cleaning validation protocols including design, testing procedures, and evaluation criteria for the manufacture of commercial sterile diluents and allergenic extracts• Initiated and executed media fill process simulations to assess the state of process control in aseptic production• Conducted engineering studies to develop process and cleaning improvement strategies• Provided factory acceptance test (FAT) coverage on new aseptic filling equipment and assist in mediating issues with vendors• Investigated and resolved process deviations and assessed/implemented CAPAs in aseptic manufacturing -
Cleaning Validation EngineerBestco Jun 2015 - Jun 2016Mooresville, Nc, Us• Independently led a cleaning validation program for the manufacture of dietary supplements and OTC products •Created cleaning cycle development strategies for a variety of equipment including: process vessels, clean-in-place systems, packaging equipment, parts washers, and production facilities.•Wrote validation protocols and reports in support of the site’s validation program•Investigated and troubleshot problems which occur during cleaning•Responsible for planning and execution of onsite cleaning validation programs compliant with USFDA requirements.•Prepared and reviewed completed validation packages by compiling and analyzing validation data for submittal for review and approval by Quality Assurance•Coordinated with Sales, Innovations (R&D), Process Engineers and Quality to define the cleaning project plan for new product launches and create efficient product changeovers -
Validation EngineerG&W Laboratories May 2014 - Jun 2015South Plainfield, Nj, Us•Analyzed equipment lifecycle review data, identified gaps, and completed reports•Initiated and executed process protocols including initiation of all execution documents, labels, instructions etc., as well as collection, documentation and delivery of samples to QC lab•Qualified in aseptic technique to collect surface samples for API/CIP and Micro in cleaning validations•Supported product transfer activities•Observed and investigated processes in compounding and packaging to improve current practices and procedures•Executed and compiled reports for temperature/humidity studies using Dataloggers•Initiated and implemented (IQ/OQ/PQ) equipment protocols•Active member on Environmental, Health and Safety and First Aid team -
Quality Control Microbiologist IiG&W Laboratories Jun 2011 - May 2014South Plainfield, Nj, Us•Oversaw scheduling of high-priority finished product and stability samples for multiple analysts to meet target dates•Aseptically collected settling plate and surface contact environmental monitoring samples to make sure products are manufactured in a clean facility•Collected and tested water for pharmaceutical purposes from all distribution ports (total count, coliforms, free chlorine, conductivity and total organic carbon) in accordance with USP <1231> •Performed antibiotic assay testing using agar diffusion method in accordance with USP <81> -
Quality Control Chemist IiG&W Laboratories May 2010 - Jun 2011South Plainfield, Nj, Us•Completed HPLC and GC testing on high-volume finished product samples consisting of suspensions, creams, ointments, and suppositories•Worked diligently to decrease cycle times and increase productivity by developing a schedule to manage and organize testing•Aided other analysts in troubleshooting instrumentation errors•Followed Standard Operating Procedures and Validation Protocols -
Quality Control Chemist IHarmony Labs Aug 2009 - May 2010•Performed established HPLC and GC methods on finished products and stability samples•Tested for actives and excipients in OTC, Rx, and cosmetic skin care products from acne treatments to sunscreens for potency as well as other USP/FCC specifications•Maintained accurate and organized documentation of analyses in lab notebooks and computer databases•Ordered supplies for finished product, ICP, raw materials, stability, R & D and pesticides labs•Utilized Waters Empower 2 Software to review and report data
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Quality Control TechnicianHarmony Labs Oct 2008 - Aug 2009•Checked in and prepared samples •Contacted outside vendors to compile test methods and order reagents/supplies •Gathered records for customer and FDA audits•Created matrices for testing turnaround time information•Performed analytical and wet chemistry testing using USP, FCC, BP and manufacturer methods•Prepared and standardized test solutions•Operated FTIR, UV-Vis, Karl Fisher, Waters HPLC, and Agilent GC equipment•Followed GMP, GLP, and SOP regulations
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Certified Pharmacy TechnicianCvs Pharmacy, Indian Trail Pharmacy And Costco Pharmacy Jan 2005 - Oct 2008•Filled high-volume of prescriptions in a fast-paced environment with excellent multi-tasking skills•Maintained patient records and handled insurance claims with professionalism•Communicated directly with patients, doctors, insurance providers, and pharmacists to fill prescriptions with accuracy and efficiency•Learned about many drugs and their indications•Counseled customers about diabetic supplies and medical equipment•Managed inventory of OTC and prescription medications•Compounded various formulations of medications •Followed state and federal pharmacy laws
Casey Poirier Education Details
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Wingate UniversityGeneral -
Strayer UniversityProject Management -
University Of North Carolina At CharlotteLean Six Sigma Green Belt Certification
Frequently Asked Questions about Casey Poirier
What company does Casey Poirier work for?
Casey Poirier works for Steris Corporation
What is Casey Poirier's role at the current company?
Casey Poirier's current role is President Elect, PDA Southeast Chapter Board of Directors, Formulated Chemistries & Sterility Assurance Products Account Manager | Life Sciences at STERIS Corporation.
What is Casey Poirier's email address?
Casey Poirier's email address is ca****@****ris.com
What is Casey Poirier's direct phone number?
Casey Poirier's direct phone number is +170495*****
What schools did Casey Poirier attend?
Casey Poirier attended Wingate University, Strayer University, University Of North Carolina At Charlotte.
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