Brett Murray Jr.
Clayton,DE
Summary
Accomplished professional with extensive experience in multi-product pharmaceutical process operations, recognized for consistently enhancing efficiencies and adeptly identifying and resolving complex issues while adhering to stringent deadlines in a highly regulated health and safety, GMP, and quality-focused environment. Proven track record of driving operational excellence and contributing to team success through strategic problem-solving and meticulous attention to detail. Seeking a challenging role that offers opportunities for career advancement and professional growth within a dynamic organization.
Overview
25
25
years of professional experience
1
1
Certification
Work History
Aseptic Process Engineer
Pfizer (Carlton National)
02.2023 - 08.2025
- Executed observations and provided coaching to enhance aseptic SVP filing operations.
- Conducted assessments of clean room behaviors, stopper off-loading, and aseptic gowning activities to uphold safety standards.
- Documented essential metrics for management review, emphasizing observations of gowning practices and aseptic techniques.
- Analyzed existing site procedures to uncover potential areas for improvement and optimization.
- Monitored and analyzed CGMP guidelines and regulatory developments to uphold compliance in aseptic manufacturing operations.
- Managed oversight of aseptic process simulations and provided critical support during smoke studies as required.
- Implemented and monitored protocol executions to maintain compliance with approved procedures and regulatory guidelines.
QA - On the Floor
Emergent Biosolutions (ALKU)
08.2022 - 12.2023
- Ensured adherence to quality standards in the manufacturing area throughout filling operations.
- Ensured compliance with aseptic protocols by conducting on-the-floor batch record reviews and auditing processes.
- Led strategic walkthrough of GMP areas to maintain inspection readiness, ensuring facility compliance. Managed documentation follow-up and escalated critical observations to drive improvements.
- Achieved gowning certification and maintained compliance in a Class 100 cleanroom environment for 3-4 hours daily.
- Developed and updated SOPs to ensure compliance with industry standards and best practices.
- Guided production teams in mastering manufacturing processes, focusing on resolving issues uncovered during record reviews and operational evaluations.
- Tracked and reported key performance metrics for quality assurance audits to provide insights for senior management.
- Provided on-the-floor quality assurance support to manufacturing operations, including area clearance and changeover processes.
- Conducted protocol executions to verify compliance with established procedures and regulatory requirements.
- Supported compliance efforts by coordinating document retrieval and providing subject matter expertise during partner audits and regulatory inspections.
Manufacturing Technician
Janssen
09.2013 - 07.2022
- Facilitated special assignment focused on process mapping to identify and analyze facility workflows.
- Conducted observations of essential process steps while facilitating compliance with Good Manufacturing Practices (GMP).
- Executed manufacturing and manufacturing-support processes in strict adherence to standard operating procedures and curriculum guidelines.
- Assisted in adjusting schedules to align with production material receipt and shipping needs. Reviewed visual schedules for clarity and accuracy.
- Sourced and evaluated trend charts while processing data on established procedures to identify improvement opportunities.
- Ensured accurate completion of documentation in SOP logbooks to maintain compliance with GMP standards.
- Performed detailed inspections and repairs on equipment and instruments, focusing on reliability and performance.
- Facilitated training progression by implementing assigned curriculum effectively.
- Maintained comprehensive knowledge of CGMP standards to support regulatory compliance efforts.
- Utilized proper personal protective equipment to maintain safety standards while working in manufacturing and other hazardous settings.
- Maintained cleanliness and safety in work areas. Assisted in identifying and addressing safety hazards. Communicated unsafe behaviors to team members for prompt resolution.
- Oversaw material readiness and logistics to support seamless production operations.
QA- Batch Record Review Specialist
Fibrocell (YOH)
02.2013 - 03.2013
- Streamlined record-keeping processes by maintaining master files and archives for batch records. Enhanced operational efficiency through effective management of analytical test methods and standard operating procedures. Improved training effectiveness by organizing raw material specifications and curricula.
- Executed distribution of updated controlled documents to satellite binders, ensuring compliance with regulatory standards.
- Facilitated issuance of document change requests to all user departments to initiate revisions of controlled documents.
- Oversaw processing of document change requests, maintaining adherence to required formatting for all controlled documents.
- Developed and managed essential logbooks to ensure compliance with quality control standards in manufacturing facilities.
- Managed issuance of batch records and related documentation to ensure compliance with quality control and assurance standards.
- Collaborated with quality assurance team to enhance processes and maintain product integrity as required.
Scientific Process Operator
Janssen (Abacus)
06.2011 - 02.2013
- Oversaw execution of manufacturing processes in alignment with downstream processing standard operating procedures.
- Executed verification and entry of production parameters in accordance with SOP and batch record protocols.
- Extracted and analyzed trend charts and processed data on established procedures.
- Maintained workplace safety by consistently utilizing required personal protective equipment in manufacturing and other hazardous settings.
- Managed and monitored CIP/SIP processes for processing equipment, ensuring compliance with industry hygiene regulations.
- Assisted in conducting chromatography experiments to analyze chemical compounds. Supported laboratory teams in maintaining equipment and preparing samples for analysis. Contributed to data collection and documentation for research projects.
- Supported first line maintenance and calibration of equipment to enhance operational efficiency.
- Facilitated assembly and disassembly of processing equipment to support production workflows.
- Executed strategic initiatives to enhance operational efficiency at Janssen.
Operator
Synthes USA (Aerotek)
05.2010 - 06.2011
- Executed setup and operation of semi-automatic production equipment, facilitating the manufacturing and assembly processes for clinical and commercial products.
- Ensured up-to-date documentation of batch records and data sheets to support quality control processes.
- Administered systematic in-process tests to validate adherence to manufacturing protocols and specifications.
- Conducted weighing of raw materials to maintain quality control standards.
- Ensured adherence to all procedures within a clean room environment.
- Executed maintenance protocols for manufacturing areas to uphold operational standards.
- Finalized quality records, ensuring alignment with manufacturing processes.
- Maintained comprehensive knowledge of legal and policy requirements, consistently demonstrating professionalism and ethical integrity in daily operations.
- Collaborated with compliance team to fulfill program-related tasks as assigned by supervisor or chief compliance officer.
Pharmaceutical Technical Specialist
Medimmune (Aerotek)
11.2009 - 02.2010
- Conducted thorough inspections of products to maintain integrity of aseptic production environment.
- Ensured compliance with FDA regulations and GCP/GLP/GMP standards through meticulous documentation completion.
- Conducted evaluations of manufacturing facility to ensure adherence to environmental monitoring standards.
- Executed detailed inspections on production equipment, ensuring compliance with calibration controls and effective sample handling practices.
Scientific Process Operator
Centecor (About Consulting)
06.2008 - 11.2009
- Oversaw execution of scheduled tasks within a GMP environment in the media manufacturing department.
- Accurately completed documentation in standard operating procedures, logbooks, and Good Manufacturing Practice documents to support regulatory compliance.
- Coordinated with warehouse staff to ensure timely access to necessary materials for uninterrupted production operations.
- Oversaw CIP/SIP operations on vessels to uphold aseptic standards. Coordinated sampling for in-process testing to enhance product quality. Managed the weighing and formulation of buffers and media to streamline production processes.
- Conducted essential measurements to facilitate correct chemical allocation for operations.
- Conducted thorough assembly and testing of filters to ensure effective sterilization of vessels and products.
- Implemented ultra filtration techniques to ensure high-quality filtration standards.
Transportation Specialist
AstraZeneca (About Consulting)
06.2005 - 06.2008
- Streamlined unloading procedures at loading dock to optimize shipment processing times.
- Facilitated delivery of incoming packages to R&D Wilmington Laboratories and various departments.
- Monitored and organized inventory systems to sustain adequate material supplies for operational needs.
- Engaged with relevant vendors to ensure consistent availability of essential inventory items.
- Executed gas cylinder delivery and setup operations efficiently.
- Monitored and updated knowledge of SHE regulations to enhance compliance in daily activities.
Traffic Management Officer
United States Air Force
08.2000 - 05.2004
- Executed military and commercial transportation operations to efficiently relocate personnel, eligible dependents, materials, and property.
- Coordinated and structured traffic management initiatives to optimize flow and reduce congestion.
- Managed and coordinated forward-deployed operations for cargo reception through various transportation modes from the defense transportation system.
- Utilized the defense transportation system and commercial logistics to enhance selection and procurement of government-operated transportation services.
Education
Delaware Technical Community College
Dover, Delaware01.2018
High School -
Glasglow High School
Newark, Delaware01.2000
undefined
Wilmington University
Wilmington, Delaware01.2006
undefined
Lake Region State College
United States Air Force01.2004
Skills
- Manual and/or system-based inventory systems
- Laboratory environments
- Microsoft office applications
- Best Practices Inventories and Cycle Counts
- Time Management
- Leadership
- Writing and Reviewing SOP's
- Knowledge of GLP
- Basic laboratory techniques
- Class 100 and 1000 environments
- Electronic tools
- Air filtering respirators
- Chromatography
- Protein Purification
- Data Entry
- Autoclave
- Environmental monitoring
- Batch Record Review
- Smoke Study
- Communication
- Veeva
- Knowledge of cGMP regulations (21 CFR, parts 210,211,11, and Good Documentation Practices)
- Provide raw material support, including the review and approval of incoming material documentation and release for GMP use
Certification
- Certified Training: Hazardous Waste, Blood Bourne Pathogens, Chemical Spill and Radiation Awareness.
- Certified Dangerous Goods International Training: 49 CFR, IATA.
- Certified Forklift Operator
- Certified Hazmat Training
- Certified Dangerous Goods Shipper
- GMP
- SOP
- Electrical Truck Trained
- CGMP
- Waste Management
- Status Labeling and Documenting
- EZ Buy Certification
Key Skills And Experience
- Experience with manual and/or system-based inventory systems
- Experience in laboratory environments
- Microsoft office applications
- Best Practices Inventories and Cycle Counts
- Time Management
- Leadership
- Writing and Reviewing SOP's
- Knowledge of GLP
- Basic laboratory techniques used in a chemistry lab (pH, pipetting, handling of chemicals)
- Worked in class 100 and 1000 environments.
- Experience in electronic tools such as SAP, LIMs and LMS.
- Air filtering respirators
- Chromatography
- Protein Purification
- Data Entry
- Autoclave
- Environmental monitoring
- Batch Record Review
- Smoke Study
- Communication
- Veeva
- Knowledge of cGMP regulations (21 CFR, parts 210,211,11, and Good Documentation Practices.)
- Provide raw material support, including the review and approval of incoming material documentation and release for GMP use.
Timeline
Aseptic Process Engineer
Pfizer (Carlton National)
02.2023 - 08.2025
QA - On the Floor
Emergent Biosolutions (ALKU)
08.2022 - 12.2023
Manufacturing Technician
Janssen
09.2013 - 07.2022
QA- Batch Record Review Specialist
Fibrocell (YOH)
02.2013 - 03.2013
Scientific Process Operator
Janssen (Abacus)
06.2011 - 02.2013
Operator
Synthes USA (Aerotek)
05.2010 - 06.2011
Pharmaceutical Technical Specialist
Medimmune (Aerotek)
11.2009 - 02.2010
Scientific Process Operator
Centecor (About Consulting)
06.2008 - 11.2009
Transportation Specialist
AstraZeneca (About Consulting)
06.2005 - 06.2008
Traffic Management Officer
United States Air Force
08.2000 - 05.2004
undefined
Wilmington University
undefined
Lake Region State College
Delaware Technical Community College
High School -
Glasglow High School