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Quality Control Specialist
hace 3 meses
About the RoleMaintains applicable Standard Operating Procedures (SOPs), GxP compliant documentation and records within the Novartis Quality Management System.
Ensures the integrity of all Quality Systems records and data, as applicable and teamwork of own team with other functions and departments.
Ensures an adequate level of education, GxP knowledge.Updates and maintains relevant information in electronic systems (e.g.
Change Control, Documentation, Training).Follow up and monitoring of e.g. CAPAs, actions, metrics, Quality plan).Supports Quality Audits and Health Authority inspection.
Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable)
Customer happiness -Punctuality rate Jobs done on time, following the specified cycle time -Consistent compliance with GMP and Health, Safety and Environment guidelines and Standard Operating Procedures -No complaints with regulatory inspectionsRequirements:
QC/ QA in pharmaceutical ind./ biotech with environmental monitoring &.Functional Breadth.2y at least as Control Quality Analyst.
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Division Operations
Business Unit Pharmaceuticals
Location Mexico
Site INSURGENTES
Company / Legal Entity MX06 (FCRS = MX006) Novartis Farmacéutica S.A. de C.V.
Functional Area Quality
Job Type Full time
Employment Type Regular
Shift Work No
Accessibility and accommodationNovartis is committed to work with and provide reasonable accommodation to individuals with disabilities.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to
and let us know the nature of your request and your contact information.
Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.
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