Mf01-062725 Cqv Scientist For Biotech Manufacturing Equipment
Validation & Engineering Group
- Barceloneta, PR
- Permanente
- Tiempo completo
Minimum of 3 years of experience in direct pharmaceutical, medical device or preferably (biotechnology) industries.
Must be fully bilingual (English / Spanish) with excellent oral skills.
Experience in developing Systems Development Life Cycle (SDLC) documents such as VP, URS, DS, RA, IQ, OQ, PQ, TMX and so forth. Includes execution of protocols IOPQ, managing deviations, and reports generation.
Preferably experience in the Biotech industry.
Technical writing skills and investigations processes.
Available to work extended hours, possibility of weekends and holidays.
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