**Summary**:
We are seeking for someone who can support all GxP activities in the Quality department. Administers Quality Systems/ Processes including documentation, metrics and monitoring of actions.
**About the Role**:
**Main accountabilities**:
- Maintains 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 inspections
**Requirements**:
- QC/ QA in pharmaceutical ind./ biotech with environmental monitoring &.
- Functional Breadth.
- Collaborating across boundaries
- 2y at least as Control Quality Analyst.
- English.
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 accommodation**:
Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

📌 Quality Control Specialist (Baja California Sur)
🏢 Novartis
📍 Baja California Sur