BARRETT (KARL) MANNING

Monmouth Junction, NJ ****2

· 601-***-**** · addyd7@r.postjobfree.com · https://linkedin.com/in/karl-manning-ms-rph

PHAR

PHARMACY MANAGER/PHARMACIST

Pharmacy professional with skills in Pharmaceutics, cGMP, Regulatory Affairs, and Pharmacy Practice/Administration, and Project Management. Passionate about creating and implementing innovative solutions to enhance patient care and safety with respect to the medication use process across the continuum of care (manufacturing to medication use). Education includes Bachelor of Science degree in Pharmacy and a Master of Science degree in Pharmaceutical Sciences from University of Mississippi.

SKILLS

· Microsoft Office (Excel, Word, · Sterile Compounding

Outlook, PowerPoint, Access) · Medication/Drug Safety

· Operations Leadership · Formulary Management

· Regulatory Compliance · Therapeutic Drug Monitoring

· Workflow Management · Risk Management/Mitigation

· Technical and Scientific Writing · Medication Use Review

· Medication Use Process/Procedures · cGMPs/USP 797

· Pharmaceutical Care · Medication Therapy Management

Mentoring/Coaching · Patient Counseling

Team Player · Investigative Skills

Project Management

EXPERIENCE

PharMEDium Services LLC, Dayton, NJ November 2019 – Present

Pharmacist-In-Charge, November 2019 – Present

Managed operations in the classified areas (clean room environment) to ensure compliance to good manufacturing and documentation practices, as well as to FDA, DEA, and state boards of pharmacy regulations.

•Implemented improvements to change room traffic flow by repositioning carts, tables, and benches to match the progression of movements in accordance to the sequence of gloving and gowning.

•Worked with clean room staff to reduce documentation errors by Clean Room personnel by over 60% in one month.

PharMEDium Services LLC, Cleveland, MS April 2010 – July 2019

Pharmacist-In-Charge, October 2011 – July 2019

Managed operations in the classified areas (clean room environment) to ensure compliance to good manufacturing and documentation practices, as well as to FDA, DEA, and state boards of pharmacy regulations.

•Implemented the Partnership of Compounding Excellence to: 1) ensure compliance with Standard Operating Procedures and cGMPs, 2) promote proper aseptic behaviors in the Clean Room environment, 3) promote good documentation practices, 4) facilitate and foster the pharmacist-technician relationship through coaching and feedback.

•Implemented a program which reduced documentation errors by Clean Room personnel by over 90% in one year.

•Consulted on design and implementation of a process change in compounding reducing unnecessary motion and waste in the Clean Room, allowed Label and Packaging to start and end its process sooner, and enabled the Shipping Department to complete orders, resulting in fewer missed shipments

Pharmacist, April 2010 – October 2011

Oversight of compounding functions and operations in a clean room environment and actively monitored the compounding of safe and effective compounded products.

•Implemented final container processing on 3rd Shift as precursor step to implementation of the continuous process in October 2011. This involved training all technicians on 3rd shift on the filling of final containers.

Regency Hospital of Meridian, Meridian, MS February 2006 – March 2010

Director of Pharmacy

•Led the efforts to ensure the pharmacy and the medication use process was compliant with all applicable regulations, laws, policies, goals, and guidelines (including The Joint Commission). Facility received reaccreditation with no recommendations for improvement with respect to the pharmacy or the medication use process.

•Oversaw an $800,000 budget on drugs by promoting safe and effective therapy by working with the physician leadership and staff on antimicrobial stewardship, formulary management, protocols, medication use evaluation, and active clinical communication between pharmacists and physicians.

•Implemented and executed protocols and programs to ensure compliance with National Patient Safety Goal 3E (Anticoagulation). This included appropriate use of heparin and low molecular weight heparins, as well as warfarin monitoring.

•Performed staff pharmacist responsibilities, in addition to DOP and clinical activities (therapeutic drug monitoring, nutrition team, renal dosing, IV-to-PO conversion). Worked on an interdisciplinary basis to help manage drug therapy and outcomes, including discharge planning on medication therapy (including helping to arrange home therapy where warranted).

EDUCATION

Master of Science (MS), Pharmaceutical Sciences

University of Mississippi University, MS

Thesis: "The Effect of PVC Formulations on Loss of Nitroglycerin and Diazepam from Aqueous Solution.”

Bachelor of Science (BS), Pharmacy

University of Mississippi University, MS

ACTIVITIES

Memberships: American Society of Health-Systems Pharmacists;

Mississippi Pharmacists Association

Awards: Advances in Sterile Compounding Award, 2014, Pharmedium Services, LLC.

ACTIVE PHARMACIST LICENSURES

State Permanent License/ Registration No. Date of Issue Expiration Date

Mississippi E-06616 06/06/1979 12/31/2020

Alabama 11340 06/29/1988 12/31/2020

Arkansas PD11827 02/14/2012 12/31/2020

Maryland 21284 09/30/2012 09/30/2020

Idaho P7242 04/21/2015 06/30/2020

Oklahoma 16353 09/21/2015 09/30/2020

Virginia 020*******-**/28/2016 12/31/2020

Michigan 530-***-**** 07/01/2016 06/30/2022

New York 059519 07/25/2014 08/31/2022

New Jersey 28RI04086800 02/28/2020 04/30/2021

(Pending applications in Texas and Nevada)

DRUG SAFETY/PHARMACOVIGILANCE

As Director of Pharmacy and Clinical Manager in hospital pharmacy practice (1990-2010): Monitored adverse drug reactions and medication errors as key indicators as part of the pharmacy and therapeutics committee functions. This included reporting internally and to FDA (MedWatch), performing and writing investigations, communicating with internal and external entities (including pharmaceutical manufacturers), and developing/implementing corrective and preventive actions.

Conducted quality event/deviation and CAPA investigations while at Pharmedium. This included the participation on cross-functional teams. Wrote investigation reports, which included risk analysis, corrective/preventive actions, and effectiveness monitoring.

Participated in multiple FDA, State Board of Pharmacy, State Board of Health, and The Joint Commission inspections during career as a pharmacist, director of pharmacy in hospitals, and as a Pharmacist-In-Charge at Pharmedium.

Helped develop, implement, and champion the Partnership in Compounding Excellence at Pharmedium. This program was developed to foster the mentoring relationship between the pharmacist (coach) and the technician in promoting and executing best practices in four critical areas of focus (area clearance, aseptic technique, good documentation practices, and procedural compliance).

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