Quality Assurance Batch Disposition Associate

  • location: Sanford, NC
  • type: Contract
  • salary: $25 - $29.50 per hour

job description

Quality Assurance Batch Disposition Associate

job summary:
We are searching for a Quality Assurance Batch Disposition Associate in Sanford, NC to work for a leading pharmaceutical company. This is a contract position expected to last 9 months and could be longer.

location: Sanford, North Carolina
job type: Contract
salary: $25.00 - 29.50 per hour
work hours: 8am to 5pm
education: Bachelors
  • Performing Quality review of cGXP documentation procedures/batch records; suggests improvements and conducts continuous improvement activities.
  • Use knowledge of GXPs to be a key contributor or may be able to lead continuous improvement to a process or improve business efficiencies.
  • Reviewing production batch records and have the authorization/approval of procedures and other master production records, certificates of analyses, Board of Health protocols, certificates of compliance and change control assessments.
  • Contributes to the interpretation of cGXPs for the commercial and clinical environment.
  • Independently review working instructions/global procedures for technical content across multiple subject areas, with reference to applicable GXPs and regulatory expectations make value-added comments. Interfaces with other parts of the organization such as research and development groups.
  • Work outside immediate subject area, supporting a wider range of customers of differing subject areas and locations.
  • Resolve issues with minimal assistance from management. Represents Quality Assurance in cross-departmental/cross-site/cross-network meetings/summits.
  • Reviews trending reports and influences /agrees actions with key stakeholders.
  • Provides interpretation of data and reports.

The essential functions of this role include:

  • wearing steel toe shoes
  • Experience level: Experienced
  • Minimum 3 years of experience
  • Education: Bachelors (required)
  • Quality
  • Laboratory
  • Manufacturing
  • cGMP
  • Quality Assurance Review
  • Pharmaceutical
  • Continuous Improvement

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

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