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
Job details are sourced from the employer's original posting.
Open job postingAbout the company
Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at same requiring the best "talent " for the job.