Quality Assurance
Globalchannelmanagementinc
Apply to this jobGlobal 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.
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
Summary
Review and approve validation documentation for QC instruments in pharma/biopharma
Job title
Quality Assurance
Experience level
3+ years
Industry
technology
Location requirements
Andover, MA, US; on-site role, no remote work
Salary
$30/hr
Management role
No
Required skills
Preferred skills
Specializations
Structured locations inferred from the posting.
Andover, MA, USA