Descripción del Empleo:
The candidate will be responsible for leading, generate and execute documentation for Process Validation Protocols. Must support development, characterization, process validation and product transfer activities related to new product introduction. Must have experience on biotechnology industry. Must have excellent knowledge of all stages of the FDA Process Validation Guidance and Process lifecycle. Fully Bilingual (English/Spanish) and excellent Technical Writing Skills.
Must be available to work on the west coast of USA.
Position Type – W2 starting with a minimum of 6 months contract
Experience – At least 5 years in Biotechnology, Pharmaceutical or Medical Devices. Knowledge in regulations and guidelines such as FDA, GMP, OSHA, ISO and ISPE.
Systems – MS Word, MS Excel and MS Power Point
Submit Resume to – **********