Description
The Quality Control Supervisor will be responsible for the technical management of personnel involved in the development, transfer, and troubleshooting of routine and complex techniques associated with daily QC releases. Additionally, they will provide an in-depth investigative and technological orientation in implementing, executing and interpreting quality procedures and test methods. The Quality Control Supervisor will contribute to overall process and method improvements within the Quality Control laboratory.REQUIREMENTS:
- Bachelor's Degree in Life Sciences discipline and 6 years of experience in CGMP lab environment
OR… - Master's Degree in Life Sciences discipline and 4 year experience in CGMP lab Environment
- Strong ASSAY development experience
- HPLC experience
- Background in Analytical Method Development and Validation
- Experience leading technical groups focused in Analytical Development Experience managing scientific projects and personnel and presenting technical data
- Knowledge of CGMP, ICH, USP, and global compendial regulations and guidance's, particularly as related to analytical and bioanalytical method development and validation
- Experience with Scientific technical writing including authoring and revising SOPs or technical reports
- Experience troubleshooting assay and equipment issues
- Strong working knowledge of laboratory information management systems (LIMS)
This is a great opportunity with a leading biotech company in the San Diego area. This position will go permanent after a predetermined amount of time. Pay scale will be determined on a person-by-person basis.
This position will be filled immediately, please apply ASAP to be considered.
To find out more about Real please visit www.realstaffing.com