Analyst 1, QC Chemistry
About The Position
The Analyst 1, QC Chemistry works with direction to execute QC Analytical Chemistry methods used in biological product manufacturing, including chromatography, spectroscopy, electrophoresis, wet chemistry, glycan analysis, sub-visible particle analysis, peptide mapping, and physical appearance, etc. The Analyst 1, QC Chemistry, adheres to GMP-compliant laboratory operations in accordance with regulatory guidelines and standard operating procedures. This role generates analytical results and identifies laboratory exceptions, invalid assays, deviations. The Analyst 1, QC Chemistry is primarily responsible for executing routine analytical methods in support of manufacturing.
Requirements
- Bachelor’s Degree in Chemistry, Biochemistry, Biological Sciences, or related science field with 1- 3 years relevant experience.
- 1+ years laboratory experience.
- 1-3 years GMP laboratory experience.
- Experience with physical and chemical analytical testing methods used in biological product manufacturing including spectroscopy (UV, UV-Vis, FTIR), wet chemistry, and physical appearance.
Nice To Haves
- Experience with physical and chemical analytical testing methods used in biological product manufacturing including chromatography (GC, HPLC, UPLC, SEC), spectroscopy (UV, UV-Vis, FTIR), electrophoresis (non-reducing and reducing CESDS, imaged capillary isoelectric focusing (icIEF)), wet chemistry, glycan analysis, sub-visible particle analysis, peptide mapping, and physical appearance, etc. with cellular and molecular analytical testing methods
- Experience with LIMS software.
Responsibilities
- Executes physical and chemical analytical testing methods used in biological product manufacturing, including chromatography (GC, HPLC, UPLC, SEC), spectroscopy (UV, UV-Vis), electrophoresis (non-reducing and reducing CE-SDS, imaged capillary isoelectric focusing (icIEF)), wet chemistry, glycan analysis, sub-visible particle analysis, peptide mapping, and physical appearance, etc.
- Ensures analytical testing of in-process, drug substance (DS), drug product (DP), and stability samples is performed according to standard operating procedures.
- Ensures analytical testing data is captured in LIMS software and data integrity is maintained.
- Reports assay performance and assists with implementing improvements that ensure quality and efficiency within QC Chemistry.
- Identifies excursions and deviations.
- Coordinates and supports QC Chemistry lab activities as needed.
- Works cross-functionally with other QC departments, Manufacturing, Process Science, and Quality Assurance stakeholders to achieve customer and FUJIFILM Biotechnologies objectives.
- Performs other duties, as assigned.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Number of Employees
501-1,000 employees
