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WHAT
IN
Quality Control Supervisor
Job
TEVA Pharmaceuticals
US
-
Forest,
Virginia
Job Code - 09-4277
Position - See job description
Job First Active on: Monday, November 02, 2009
APPLY TO THIS JOB (You will be applying directly to TEVA Pharmaceuticals for this position!)
JOB DESCRIPTION: Quality Control Supervisor
* To direct efforts for laboratory auditing, as well as, validation and method improvement activities to support business needs.
* Manage groups and provide feedback on systems to promote continuous improvement and highlight compliance concerns
* Assess auditing practices and procedures to maintain consistent performance in the auditing function.
* Perform Analyst reviews
* Work with Lab Management, QA, and Operations to coordinate staff efforts and to solve problems.
* Perform Change Controls and SOP revisions to address and improve laboratory systems.
* Assess auditing practices and procedures to maintain consistent performance in the auditing function.
* Responsible for meeting the assigned deadlines for QC Laboratory.
* Responsible for the ensuring that laboratory documentation and notebooks meet compliance standards.
* Responsible for reporting group progress to management.
REQUIREMENTS - QUALIFICATIONS: Quality Control Supervisor
* BS Degree in Chemistry or related quantitative scientific discipline
* Minimum of 5 years of cGMP Laboratory experience
* Familiarity with laboratory information management systems
* Proven technical writing skills, including reports, change controls, and SOP revisions.
* Proven ability to communicate problems and required resolution in a positive manner.
* Proven ability to recognize problems with equipment, methods, software, procedures and resolve the issues.
* Ability to monitor and improve the technical skills of staff.
* Proven expertise in chromatographic analysis, analytical instrumentation theory and practice and wet chemistry techniques.
TEVA Pharmaceuticals
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