David Fabrizius Email & Phone Number

Shawnee, Ks, Us

Hanover, Maryland , Us

New York, New York, Us

Provide Analytical method development, method troubleshooting, and method transfer activities to assure product compliance and safe, efficient manufacture throughout the regulatory process. This is accomplished through direct and collaborative communication both with the customer and with internal expertise in the drug product manufacturing business.Pfizer CentreOne is a global contract manufacturer that focuses on API synthesis and sterile injectables fill-finish. Learn more at www.pfizercentreone.com

Serve as a qualified fast pitch softball umpire. Have worked summers with most age groups from all the way through small college and Junior college levels. Enjoy being able to stay around the great game of fast pitch and be a part of teaching young people the benefits of competition and teamwork.

London, England, Gb

Assist pipelines and terminals with procedural execution, review, revision, and implementation. Provide clarification and interpretation of policy and procedure to front line workers to assure compliance with regulatory and internal guidelines. Provide audit action item closure assistance when needed. Assist with internal auditing as necessary. Serve as overall compliance support to frontline / district management

London, England, Gb

Provide Method Development testing where needed. (HPLC and MS)Operator for GCT Premier Mass Spec for Advanced Characterization group (GC-MS, field ioniazation).Provide troubleshooting for process analytical equipment hardware and software issues.Responsible for analytical testing to support pilot plant refining units in Technology Development group.Provide Advanced Hydrocarbon Characterization testing for process units, pilot units, and projects.Provide SQC charting capabilities as necessary for analytical methods

Supervised 7 union QC Technicians, wrote investigations, monitored production processes, assisted with new product validations, customer complaints, and regulatory inspections.

Los Angeles, Ca, Us

Supervised stability group support both production and R&D products. Responsible for reviewing new product protocols and approving sections of regulatory submissions. Also, responsible for writing investigations, assisting with regulatory and internal audits. Provided reports to management on status of group and interfaced regularly with production in my day to day functions.

Assigned daily / weekly work loads to assure timely release of product. Provided root cause investigations for any out of specification results.Performed mid-year and end of year reviews.Provided daily feedback to production management on product testing status and investigation statusProvided troubleshooting assistance to chemists as needed.

Lake Zurich, Illinois, Us

Supervised In-process, stability, and Finished product groups over the 4 years. Responsible for assigning testing, releasing product, writing non-conformance investigations, assisting with audits, Hiring and firing of personnel.

Supervised 2 QC Technicians on 2nd shift and provided QA support to manufacturing. Also, responsible for keeping customer requirements up to date and accurate. Wrote investigations and was involved in regulatory and internal audits.