Samantha Jacot
San Marcos,CA
Summary
Reliable and efficient manufacturing and quality associate offering experience within FDA regulated environments. Dedicated professional providing exceptional support with necessary functions throughout manufacturing research and quality control processes.
Overview
5
5
years of professional experience
Work History
Manufacturing Associate
Singular Genomics
03.2023 - 08.2023
- Responsible for the manufacture of flow cell slides under good manufacturing practice (GMPs) conditions.
- Performed Surface Analysis testing for flow cell slides for Quality Control team
- Execute process recipes, follow standard operating procedures (SOPs), and monitor equipment and processes.
- Set up, operate equipment, and monitor production processes, including clean-in-place (CIP) and steam-in-place (SIP) operations and report production in written and electronic documents in accordance with good manufacturing practice (GMPs) and good documentation procedures (GDPs).
Quality Control Scientist
Thermo Fisher Scientific Inc.
06.2022 - 03.2023
- Responsible for testing incoming raw materials and perform incoming inspections for material release under good manufacturing practice (GMPs) conditions while following standard operating procedures (SOPs).
- Perform material movements and transfer raw materials/chemicals into, out of, across production areas and warehouses.
- Perform basic laboratory tasks, such as monitor pH, conductivity, test product samples, etc.
- Investigate deviations an out-of-specification instances through CAPAs and author reports.
Production Chemist
Bachem
01.2021 - 06.2022
- Downstream manufacturing performing purification processes through chromatography, crystallization, and in-process test methods on active pharmaceutical ingredients (APIs) under good manufacturing practice (GMPs) while following standard operating procedures (SOPs).
- Actively installing, operating, and maintaining tangential flow filtration systems and AKTAs.
- Use of analytical HPLC to characterize pharmaceutical drug products and intermediates.
Specimen Processing Specialist
Sequenom
10.2018 - 01.2021
- Accessioned data into the Laboratory Information Management System.
- Screened patient samples for reproductive risks using comprehensive carrier screening tests.
- Worked daily with human samples which include whole blood and amniotic fluid.
Education
Bachelor of Science - Biology
California State University - San Marcos
San Marcos, CA2016
Skills
- Professional experience in Manufacturing under GMP protocol
- Policy Implementation
- Strong attention to detail
- Excellent analytical, organizational and communication skills
- Proven ability to prioritize and handle multiple tasks
- Microsoft Office (Excel, Powerpoint, Word)
- Database Management
- Congenial and enthusiastic contributor, collaborator and supporter of team goals
- Manufacturing and Production
- Records Accuracy
- Time Management
Timeline
Manufacturing Associate
Singular Genomics
03.2023 - 08.2023
Quality Control Scientist
Thermo Fisher Scientific Inc.
06.2022 - 03.2023
Production Chemist
Bachem
01.2021 - 06.2022
Specimen Processing Specialist
Sequenom
10.2018 - 01.2021
Bachelor of Science - Biology
California State University - San Marcos
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