Documentation Specialist

**Summary**:This Role provides oversight of all GMP documents ( SOPs, FRMS, WPS) and ensures that all documents are updated, trained and effective in alignment with the department needs**About the Role**:**Major accountabilities**:- Revise existing or create new SOPs in time to support Manufacturing Strategy.- Ensure periodic review is completed on time-...

**Summary**: The Deviations Specialist/ QA Investigator is responsible for managing and executing investigations of deviations and non-conformities within manufacturing and quality control environments. This role ensures root causes are identified, corrective and preventive actions (CAPAs) are implemented effectively, and documentation complies with cGMP and...

**Summary**:The Deviations Specialist/ QA Investigator is responsible for managing and executing investigations of deviations and non-conformities within manufacturing and quality control environments. This role ensures root causes are identified, corrective and preventive actions (CAPAs) are implemented effectively, and documentation complies with cGMP and...

**Summary**: The Specialist, Compliance & Risk Ops role supports the Audit Readiness Team with identifying, investigating, and triaging compliance issues for tracking and resolution. They will be responsible for assessing escalated issues and communicating them to the relevant Audit Readiness Team member(s) or other stakeholders. They will also identify and...

**Summary**:Step into a role where your expertise in facilities and vendor management directly shapes the workplace experience. As a REFS Specialist/Coordinator, you’ll be the central point of contact for cross-site and cluster-level operations, ensuring services align with business needs and deliver exceptional value. You’ll lead projects from concept...

**Summary**:The Deviations Specialist/ QA Investigator is responsible for managing and executing investigations of deviations and non-conformities within manufacturing and quality control environments. This role ensures root causes are identified, corrective and preventive actions (CAPAs) are implemented effectively, and documentation complies with cGMP and...

**Summary**:We are seeking a dynamic and dedicated Rewards Excellence Specialist to join the US Rewards Excellence team in our mission of driving process improvement and superior employee experience.This position is located in the Novartis Corporate Center in Mexico City, which is one of six strategically located corporate centers established by Novartis...

**Summary**:Plan, prepare, and execute time-critical shipments for Radioligand Therapy (RLT) products, ensuring compliance. Coordinate courier bookings, documentation, GPS assignment, and data quality to achieve safe, on-time delivery from our manufacturing sites to destinations worldwide.**About the Role**:**Key responsibilities**:- Plan, prepare, and...

**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...

**Summary**: Job Description Summary The Specialist, Manufacturing Technical Support, provides expert support for all process-specific issues to manufacturing, to ensure execution of processes on-time, continuously improving in quality and productivity, performed in compliance to GMPs, SOPs and applicable guidelines and functional standards. **About the...