Brittany Terry
Sanford
Summary
Dedicated and detail-oriented Senior Bioprocess Technician with over 6 years of experience in biopharmaceutical manufacturing and process optimization. Proven track record in executing and overseeing bioprocessing operations, ensuring compliance with industry standards and regulatory guidelines. Experience with troubleshooting production issues, implementing process improvements, and maintaining high-quality standards throughout the manufacturing lifecycle. Strong leadership capabilities demonstrated through mentoring other technicians and collaborating effectively with cross-functional teams. Seeking to leverage technical expertise and leadership skills to transition into another role, fostering a culture of excellence and driving operational efficiency.
Overview
7
7
years of professional experience
Work History
Senior Bioprocess Technician
Pfizer Pharmaceuticals
07.2020 - Current
- Responsible for coordinating and providing appropriate support for daily routine work dedicated to the production of biological products including innovative medicines and vaccines
- Execute manufacturing operations on the production floor for preparation on manufacturing floor to ensure standard operating procedure (SOP), quality standards, batch records, and good manufacturing practices (GMP) are followed throughout the processes
- Drives troubleshooting, technical support, analysis, and resolution of equipment, automation, and process issues
- Demonstrate expertise in the operation of distributed control systems and other automated instruments
- Manage processes pertinent to the supply of tools through the execution of proper actions, process concerns, necessary areas of repair or maintenance, formulation of tools used in production, and oversee the cleaning and up-keep procedures
- Identify and/or communicate process and compliance concerns in real time
- Transport and maintain products to ensure prompt transfer and availability of products, materials, and other supplies and shipment regulations are met accordingly
- Collaborates in the escalation process through various levels of management when operations, personnel safety, equipment, functionality, product supply and/or quality compliance are at risk
- Operate, service, adjust, clean, and sterilize variety of production related equipment to ensure safety and maintain a clean environment to comply with regulatory requirements and cGMPs
- Certified train the trainer for Drug Product
- Authorize GMP and SOP certifications, updates, and revisions
- Compliance Champion
- Visual management lead for Drug Product, Stage 2
- Responsible for inputting teams schedule in standard work and facilitating team cycle counts
Manufacturing Associate
03.2018 - 12.2019
- Handle biologically and chemically hazardous goods
- Drives the troubleshooting of equipment issues within the process of making the vaccines
- Display knowledge in cGMP, manufacturing operations, batch record review, and Aseptic principles and concepts
- Responsible for providing support on the manufacturing floor for daily routines
Quality Auditor
03.2018 - 12.2019
- Handled sterile goods
- Display knowledge in cGMP and manufacturing operations
- Responsible for providing support on the manufacturing floor for daily routines
- Participated in international shipment audits
- Collaborated with cross functional teams
Education
Bachelor's degree - Manufacturing, Distribution and Logistics
East carolina university
03.2026
Bioworks Certification -
Wake Technical community college
12.2019
Skills
- Scheduling/Planning for production schedule
- Proficient in Filtration
- Trained aseptic filler operator
- Experience with operating GMP and non GMP autoclaves and washer
- Qualified Visual Inspector
- Train the Trainer
- Compliance Champion
- SAP Champion
- Experience with applications like DeltaV
- Experience with applications like LIMS
- Experience with applications like GLIMS
- Experience with applications like SAP
- Experience with applications like PDOCS
- Experience with Microsoft Excel
- Experience with Microsoft Word
- Updated documents for Drug Product
- Ran protocols with the process engineers
- Typically schedules suite activities in DOC
- Go-To person for SAP
- Leads production activities
Activities
- Updated documents for Drug Product
- Ran protocols with the process engineers
- Typically schedules suite activities in DOC
- “Go-To” person for SAP
- Leads production activities
Timeline
Senior Bioprocess Technician
Pfizer Pharmaceuticals
07.2020 - Current
Manufacturing Associate
03.2018 - 12.2019
Quality Auditor
03.2018 - 12.2019
Bachelor's degree - Manufacturing, Distribution and Logistics
East carolina university
Bioworks Certification -
Wake Technical community college
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