Opportunity Description
Job Title: Specialist Quality ControlJob Description
We are seeking a Specialist in Quality Control for a full-time, on-site position at our facility in Holly Springs, NC. The role involves working within a GMP-regulated biotech or pharmaceutical environment, focusing on maintaining and improving quality systems and QC laboratory operations.
Responsibilities
+ Collaborate with Quality Control and Quality Assurance teams to author and own change control records and deviations using the DQMS Veeva System.
+ Lead investigation teams to collect and report metrics for the systems team.
+ Assist with the review of validation documents to support equipment and computerized system onboarding.
+ Author, revise, and review documents and reports, including SOPs, test methods, safety assessments, trend reports, qualification/validation summary reports, and technical reports.
+ Mentor new deviation owners as required.
+ Support the startup...
We are seeking a Specialist in Quality Control for a full-time, on-site position at our facility in Holly Springs, NC. The role involves working within a GMP-regulated biotech or pharmaceutical environment, focusing on maintaining and improving quality systems and QC laboratory operations.
Responsibilities
+ Collaborate with Quality Control and Quality Assurance teams to author and own change control records and deviations using the DQMS Veeva System.
+ Lead investigation teams to collect and report metrics for the systems team.
+ Assist with the review of validation documents to support equipment and computerized system onboarding.
+ Author, revise, and review documents and reports, including SOPs, test methods, safety assessments, trend reports, qualification/validation summary reports, and technical reports.
+ Mentor new deviation owners as required.
+ Support the startup...
Ready to Apply?
Submit your application for Specialist Quality Control at Actalent
Apply for this Position