Quality Assurance

provide QA Validation support to validation activities associated with Quality Control (QC) Laboratory instruments. The main responsibility is review and approval of validation documentation
including specifications, executed protocols, summary reports, deviations, periodic reviews, procedures, and change controls. In addition, this role may provide support to the site’s data integrity
initiative.

Candidate requires strong interpersonal, oral and written
communication skills as there is a high degree of collaboration required between members of QA Validation, Instrument Validation and QC
personnel.
Candidate must be detail oriented as the main job responsibility is review and approval of validation documentation.
Candidate must have at a minimum a BS in biology, engineering or related sciences
with at least 3 years of pharmaceutical or biopharmaceutical experience
in a quality assurance and/or validation role.
Past experience working with QC instrumentation, Labware, Trackwise, and/or
Documentum in the pharma/biopharmaceutical field is preferred but not required.

$30/hr

18 MONTHS