Associate Process Expert

hace 2 semanas


Insurgentes, México Novartis A tiempo completo

**Summary**:This role will author and oversee deviations, investigations, CAPAs, and related reports to ensure closure within the established timelines for the manufacturing department.**About the Role**:**Deviation and Investigation Management**:- Open deviations and assess the criticality of the deviation within required timeframes- Assess impact to any products involved in deviations, ensuring product impact is assessed in alignment with batch release activities- Author investigations- Owning investigations and developing corrective actions- Use process knowledge and root cause investigation tools to identify root causes of product and process deviations.- Ensures robustness (complete, accurate and defendable) of all critical and major investigations- Author and execute any experiments or runs to support investigations- Work cross-functionally to assess and analyze deviations and investigations to determine impact- Work cross-functionally to ensure production continues in a compliant manner in the event of a deviation and document accordingly.**Corrective and Preventive Actions**:- Generation and documentation of effective corrective and preventative actions- Ensures all CAPAs are implemented through GMP systems (e.g. MBR revision, training, etc.)- Monitor and ensure effectiveness checks of CAPAs are conducted- Communicate to the production team any training or awareness events to reinforce quality behaviors.**MES Order Management**:- Generation of manufacturing orders within the MES system, as required.**Training**:- Develop training (as immediate response to unexpected events, for technical document execution, and new products/processes) to the Cell Processing team, as required.- Maintain compliance with training requirements.**Key Performance Indicators**:- Quality measures (e.g., deviations, oos rate)- Schedule adherence to operational model- Opening and closing investigations within time frame- Production right first time- Costs and budget (e.g. overtime)**Ideal Background**:**Education**: Bachelor's degree with 2-5 years of work experience in the pharmaceutical industry or equivalent. An advanced degree is desirable.**Languages**: Fluent in speaking / writing in English**Experience**:- 2-5 years of related pharmaceutical experience preferably in a production, QA, and/ or QC related role preferred. Direct experience working in a GMP and aseptic or sterile environment is required. Cell & gene therapy experience highly desired.- Investigator Certified required- Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing.- Experience with 1QEMDivisionOperationsBusiness UnitInnovative MedicinesLocationMexicoSiteINSURGENTESCompany / Legal EntityMX06 (FCRS = MX006) Novartis Farmacéutica S.A. de C.V.Functional AreaTechnical OperationsJob TypeFull timeEmployment TypeRegularShift WorkNo**Accessibility and accommodation**: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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