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Senior Supplier Relationship Manager
Il y a 2 mois
Site Name:
Belgium-Rixensart, UK - Hertfordshire - Ware RD, USA - North Carolina - Zebulon
Posted Date:
Jun
**_
About the role_**As a Senior Relationship Manager, you will provide effective functional management of the External Pack Ops (EPO), External Shipping (EST) and Supply Chain Assistant (SCA) teams globally.
You will also provide leadership and strategic direction for the labelling and packaging of Phase I - IV clinical trials supplies within CSC and any associate CMO facilities.
In doing so:
- Implement and manage an effective CMO network to be used by GSK Pharma for all clinical supply chain activities to include: Encapsulation/Overcapsulation of comparators; label creation; primary and secondary packaging; warehouse and distribution / logistics depot management; cold chain and temperature excursion management throughout the process
- Deliver supply chain efficiency through continued business process improvement
- Strong focus and drive to continuously improve and deliver business change activities aligned to quality and strategic priorities
- Provide and maintain high quality processes which are fit for clinical packaging purposes and are fully compliant with regulatory expectations always
_ About the responsibilities_:
- Manage a team accountable for determining and implementing the strategies of the Third Party Network, being the recognized central point of contact for all CMOs and external service providers
- Ultimate ownership and oversight of all EPO/SCA SOPs and associated business processes
- Empower accountability with the relevant leaders and individuals within the organisation, but take ultimate accountability for all Third Party Management operational decisions
- Delivery of all Key Performance Indicators with focus on CMO capacity utilization, on time delivery, productivity and supply chain efficiency.
- Meet the total global supply chain demand by optimizing operational capacity utilization at each CMO.
- Implement and manage Third Party governance structure for internal providers and external CMOs, ensuring crossfunctional alignment
- Resolve and report on supply chain issues at the Senior Director and VP and levels within CSC.
- Drive a program of business improvement activities within all applicable functional areas, inline with measured performance and customer expectations
- Create and maintain a safe work environment conducive to the development, retention and recruitment of staff at the highest level
_ Some specific activities _
- Overall accountability for a complex operations that not only involves multiple activities with CMOs
- Requirement to interact and influence PD Directors and project leads, senior managers in the Clinical, IT, Regulatory, Quality Environments; third party CROs and CMOs; other senior members of the CSC organization
- Must lead, constructively challenge, and work in many forums and teams of a matrixed organization with people of varied skills and educational levels to ensure the strategic direction of packaging operations are consistently delivered
- The role requires and understanding of key objectives, strategies and complexities of the global R&D organization
- Needs to maintain credibility across a breadth of scientific, operational and geographic business units, networking internally and externally at the senior executive level
- Capable of interacting independently with regulatory agencies on issues relevant to support areas
_ About you_:
- Degree in pharmacy/chemistry or a related scientific field or equivalent experience
- Experience in clinical trials supplies packaging and distribution or other relevant area
- Proven ability to work by leading multiple matrix teams concurrently in a cohesive & effective way
- Demonstrated experience managing resources and budgets
- Ability to organize and manage a diverse, crossfunctional group with constantly changing demands
- Excellent oral and written communication, interpersonal and negotiation skills
- Demonstrated ability to effectively allocate resources and manage multiple complex projects to fixed timelines
- Able to respond rapidly to arising situations globally
- In depth working knowledge of GMP and country specific regulations and serves as an expert resource to the staff and customer groups; high degree of accuracy and attention to detail especially about the completion of regulatory and GMP documentation
- Possesses necessary computer skills and general computer literacy
- Knowledgeable of and able to assess new technological advances that can improve processes
- Experienced with the packaging and distribution of clinical trials supplies using IVR (interactive voice response) technology
If you have a disability and require assistance during the course of the selection process, you will have the opportunity to let us know what specific assistance you require in order to make suitable arrangements.
