Results-driven manufacturing professional with extensive experience in regulated environments, quality systems, documentation, and process support. Known for strong problem-solving skills, attention to detail, and the ability to develop solutions that improve safety, efficiency, and compliance.
Work History
Senior Bioprocess Technician
7 Months
Pfizer | 11.2025 - 06.2026
Execute buffer preparation activities in accordance with GMP requirements, batch records, SOPs, and established manufacturing schedules.
Perform process monitoring and in-process testing, including pH, conductivity, and visual inspections..
Operate and monitor mixing vessels, tanks, and related process equipment to ensure accurate solution preparation and process reliability.
Complete batch records, logbooks, and production documentation with a high level of accuracy and compliance.
Utilize SAP and manufacturing systems to process inventory transactions, material movements, and production-related documentation.
Conduct equipment setup, cleaning, sanitization, and pre-use inspections to maintain operational readiness and regulatory compliance.
Partner with Manufacturing, Quality Assurance, Warehouse, and Process Engineering teams to support production goals and timely batch execution.
Prepare, dispense and verify manufacturing solutions, media, and process buffers in support of monoclonal antibody (mAbs)
Manufacturing Associate IV
7 Months
Biogen | 03.2025 - 10.2025
Perform small-scale purification processes including filtration and chromatography for sample preparation and process development.
Key documentation includes batch records, SLRs, and equipment logbooks.
Prepare and handle buffers and solutions used in manufacturing processes.
Operate and maintain equipment in wash and sterile environments to ensure aseptic conditions.
Senior Process Technician
2 Years 8 Months
Pfizer | 01.2023 - 09.2025
Facilitated Corrective and Preventive Action (CAPA) initiatives, resulting in a 20% reduction in process deviations and non-conformances.
Led the updating of Standard Operating Procedures (SOPs) and Master Batch Records (MBRs), ensuring alignment with current regulatory requirements and industry best practices.
Managed material procurement through SAP, optimizing inventory levels and ensuring uninterrupted production activities.
Executed high-density filling operations with precision and accuracy, meeting stringent quality standards and production targets consistently.
Obtain and stock supplies as directed through SAP and assist with cycle counts and materials management within the assigned functional area.
Document Owner of Master Batch Record
Ensure Downstream processing area SOPs/Job Aids were updated when changes were revised.
Senior Associate, Manufacturing
8 Months
Abzena | 05.2022 - 01.2023
Executed operations within a stringent cGMP manufacturing environment, ensuring compliance with regulatory standards.
Collaborated cross-functionally to review and create SOPs, master batch records, and specifications, ensuring alignment with cGMP requirements.
Developed and authored Standard Operating Procedures (SOPs) from the ground up by reviewing equipment manuals, collaborating with equipment vendors, and partnering with cross-functional teams to ensure accuracy, compliance, and alignment with cGMP requirements.
Bioprocess Technician IV
1 Year 10 Months
Pfizer | 07.2020 - 05.2022
Maintained documentation, including training records, batch records, and logs, ensuring compliance with regulatory standards.
Collaborated cross-functionally with technology transfer teams, lab scientists, supply chain, quality, and engineering to support manufacturing processes.
Demonstrated expertise in downstream purification processes, serving as the document owner for Downstream Purification Master Batch Record.
Facilitated startup activities and provided assistance to engineers and automation teams, ensuring seamless operations.
Qualified trainer on Downstream equipment such as Harvest, Affinity Chromotography, AEX, Viral Filtration and UF/DF skids through Delta V.
Filling Technician- Inspection
2 Years 6 Months
Novo Nordisk, Inc. | 01.2018 - 07.2020
Achieved a 95% inspection accuracy rate, ensuring product quality and reducing the likelihood of defective products reaching the market.
Authored and reviewed SOPs, actively participating in event response and equipment maintenance.
Collaborated with engineering teams to identify and address equipment maintenance needs, resulting in a 30% reduction in equipment downtime.
Provided training to colleagues and contributed to continuous learning initiatives, ensuring adherence to quality standards throughout production processes.
Production Operator -Packaging
1 Year 8 Months
Merck (Manpower) | 05.2016 - 01.2018
Conducted setup, adjustment, and operation of packaging equipment, maintaining a clean and efficient work environment.
Implemented lean manufacturing principles in packaging operations, resulting in a 15% reduction in material waste and increased operational efficiency.
Participated in continuous improvement initiatives, contributing to a 10% increase in overall production output through the identification and implementation of process optimizations.
Production Operator -Filling
1 Year 10 Months
Hospira, a Pfizer company (Kelly Services) | 07.2014 - 05.2016
Achieved 100% compliance with aseptic gowning procedures, ensuring product integrity and adherence to regulatory requirements.
Collaborated with quality assurance teams to implement process improvements, resulting in a 15% reduction in non-conformances and deviations.
Received recognition for outstanding performance in maintaining production line cleanliness and organization.
Education
Medical Billing & Coding - Associate's degree
Ultimate Medical Academy-Tampa | Tampa, FL | 09.2017
High School Diploma
Beddingfield High School | Wilson County, NC | 06.2008
Skills
Production batch record review
Teamwork
DeltaV
Single-use Technology
Medical coding - Medical coding experience (Less than 1 year)
SAP
Time management
CGMP
Compliance
Human-machine interface (HMI) systems
Master batch record
Certification
Bioworks, HIPPA, April 2026 to April 2028, HIPPA Awareness certified, BBP, April 2026 to April 2028, Bloodborne Pathogen certified
Personal Information
Work Permit: Authorized to work in the US for any employer