BioPhase Solutions specializes in recruiting top talented professionals for San Diego's Scientific community. We are currently looking for QC Analysts to work for a leading San Diego biotechnology company.
QC Analysts (multiple openings)
Commercial Quality Control is responsible for ensuring preparation and maintenance of high quality of analytical techniques in a cGMP environment to support the needs of the Quality Control Department for commercial pharmaceutical release. Also, execute series of analytical validation protocols and tests to fulfill the quality control requirements for commercial pharmaceutical injectable products.
ESSENTIAL JOB FUNCTIONS
Execute established analytical methods and generate the required data within set timelines.
Work in a strict cGMP compliant laboratory environment.
Review data generated by the laboratory.
Inventory laboratory chemicals, reagents, standards and equipment.
Maintain a rigorous notebook.
Follow SOP and laboratory guidelines for the daily laboratory operation.
Record and archive equipment information regarding, maintenance, use and repair as needed..
Maintain inventory of samples prior and after testing and account for all sample reconciliation after the completion of studies.
Maintain a training record per the cGMP requirements.
Possessing a team oriented attitude and problem solving ability.
Follow project timelines.
BS in chemistry or related field.
Minimum 4 to 6 years of experience Pharmaceutical, Biotechnology or related laboratory environment.
Experience in conducting all/some of the following quantitative analytical techniques: analytical assays for using HPLC, GC, IR, UV and fluorescence spectroscopy, density determination, titrimetric techniques such as Karl-Fisher titration for the water content, viscosity measurement techniques, osmometry, polymer analysis, etc.
Excellent written/oral communication skills, focused self-starter, attention to details, team-oriented but able to work independently and proactively, and ability to multi-task.
Experience in LIMS or Quality Assurance, Quality Control, method validation, method transfer, amino acid analysis, peptide sequencing and cGMP regulations is required.
Experience with Empower software and Microsoft Office as well.