unicon pharma.inc
Location
Hayward, CA | United States
Job description
Description:
Key Responsibilities: Review GMP data for In-Process, Lot Release and Stability studies. Provide on-time, high quality results to meet Manufacturing demands. May be responsible for writing- Quality Records (Deviations, CAPA, Change Control), Forms and Test Methods. Key Requirements: Bachelor or Associates Degree. Preferred area of study in Biochemistry, Chemistry, Microbiology or Related Science field. Working experience running and reviewing assays- ELISA, HPLC, Gas Chromatography, qPCR, Western Blot, FTIR, A280s, CESDS, icIEF, Bioburden, and Wet Chemistry Assays . Some industry experience, preferably in a cGMP environment. Use of Laboratory computer systems and Microsoft Suites (Word, Excel, Powerpoint). Prior use of GMP Quality Systems such as: TrackWise, LIMS and Empower3 preferred. Solid communication skills, both written and verbal. Ability to work independently on assign tasks, within timeframes, as well as work within a team environment. Working experience in process related tasks, data interpretation and independent and team problem solving. May required to work overtime. 3-5 Years ExperienceJob tags
Salary
