Transversal Support Project Manager Technical Life
Il y a 2 mois
**Site Name**: Belgium-Wavre
**Posted Date**: Mar 27 2023
The current approved GSK vaccine portfolio includes around 50 different products. The product portfolio needs continuous process and product maintenance in order to keep the products in a compliant state at all times and keep continuous improvements of the manufacturing process and analytical methods.
The Technical Life Cycle Management (TLCM) owns and provides strong technical oversight of our commercial products and End to End processes and throughout their life cycle across the global GSK network.
The Transversal Support Manager TLCM:
- ensures continuous exchange of knowledge between the different manufacturing units with the GIO & Quality network.
- leads specific projects according to GSK Vaccines standards in an efficient, timely and cost-efficient way.
- brings technical support to secondary sites in the resolution of Transversal Support deviation, recurrent deviation, or troubleshooting.
- supports and coordinates all activities related to Transversal Support Projects within TLCM including the management of operational activities linked to Transversal Support and transactional flows of master data.
This role will give YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following:
- The Transversal Support Manager Technical Life Cycle Management is responsible to support the Technical Life Cycle Team (TLCT) and the preparation of the technical life cycle plan (TLCP) for processes. She/ he can act as a back-up of the TLCM Transversal Support Leader.
- The Transversal Support Manager Technical Life Cycle Management is responsible of leading multidisciplinary taskforce, complex projects in order to support proactive/reactive technical lifecycle management and continuous improvement. This responsibility includes the preparation of business case and overall budget definition, implementation of efficient governance, monitoring of project progress and escalation to appropriate governing bodies (i.e., TLCTs, TLCPs, QMT, ad hoc Corporate governances, project steercos).
- The Transversal Support Manager Technical Life Cycle Management is responsible to interpret and understand cross-departmental regulatory impact related to Secondary Transversal projects and provide guidance on markets evolutions and associated impacts on SKU portfolio
- The Transversal Support Manager Technical Life Cycle Management is responsible to support TLCM Transversal Support leader in providing product and process expertise for contact with authorities (i.e., type C meeting) and for the technical revision of CMC/Labelling parts of the regulatory dossiers.
- The Transversal Support Manager Technical Life Cycle Management is the single point of contact for the different manufacturing units, QA, QC, GVSC and RA regarding knowledge management, continuous improvement, and project management for Transversal project.
- The Transversal Support Manager Technical Life Cycle Management supports cross-departmental Transversal Support operational activities related to Secondary Transversal projects by coordinating operations with Tech resolutions and E2E Supply Chain
- The Transversal Support Manager Technical Life Cycle Management is responsible to feed and maintain the knowledge management in his / her field of responsibility and to ensure continuous exchange and update with the production units and with the GIO & Quality network
- The Transversal Support Manager Technical Life Cycle Management is responsible to ensure the Business process and master data maintenance
**Why you?**:
**Basic Qualifications**:
We are looking for professionals with these required skills to achieve our goals:
- University degree in Supply-Chain, Business, Engineering or Natural or Data Sciences/ Programming
- Minimum 5 years experiences in an international pharmaceutical environment
- Solid understanding of regulatory, supply-chain and vaccines production processes
- Demonstrated data analytics & computer skills (SAP/APO, MS Office, PowerBI, etc)
- Fluent in French & English (written and spoken)
**Preferred Qualifications**:
If you have the following characteristics, it would be a plus:
- Minimum 5 years applicable experience in biopharmaceutical manufacturing and / or experience in project management with impact in Packaging, Regulatory, Logistics & Distribution, Master Data Management, Supply Chain within a biological environment
- Demonstrated project and stakeholders Management skills
- Proven experience in project management
- Excellent understanding of the framework within which a pharmaceutical product has to be maintained in compliance: Authorities / Scientific / Business
**Why GSK?**:
Our values and expectations are at the heart of everything we do and form an important part of our culture.
- Managing individual performance.
- Creating a performance culture and driving results, prioritisation, execution, delivering performance.
- S
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