Head Global Packaging, Labelling, Distribution
il y a 1 semaine
Site Name:
UK - Hertfordshire - Stevenage, Belgium-Wavre, USA - North Carolina - Research Triangle Park, USA - Pennsylvania - Philadelphia
Posted Date:
Jun
GSK is a place where outstanding people do amazing things. As a science-led global healthcare company, we exist to help people do more, feel better, live longer. Our goal is to be one of the most innovative, best performing, and trusted healthcare companies.
Are you interested in a highly visible, global leadership role that allows you to lead a team of key functional expertise areas while being part of the Global Clinical Supply Chain leadership team to contribute to the advancement of a robust and innovative R&D pipeline? If so, this new role is an exciting move to explore.
The Head of Packaging, Labelling, Distribution and Comparators (PLDC) is a critical new leadership role within Clinical Supply Chain, responsible for the strategic direction and operational oversight of the Clinical Packaging, Labelling, Distribution, Comparators and Collaborations, supporting Phase I through IV GSK sponsored clinical studies as well as investigator sponsored trials and compassionate use programs for all Medicine and Vaccine portfolios across Infectious Disease, Specialty Care and Oncology.
This is a highly technical, dynamic, and impactful role where you will be working alongside a collaborative team of fellow CSC leaders, all with a shared focus on delivering our Ambition for Patients.
It is a high priority to accelerate the integration of silks and capabilities across Medicines and Vaccines, driving the digital and operational modernization of the clinical supply chain.
And in parallel support the development of individuals and teams ensuring their knowledge and capability is most efficiently deployed on priorities for the business and our patients.
Reporting to VP Clinical Supply Chain the role is to drive acceleration of the Clinical Supply Chain Packaging, Labelling, Distribution, Comparators and Collaborations by utilizing science, technology, and talent.
Key Responsibilities:
The role is accountable for the strategic direction and operational oversight of the R&D Global Clinical Supply Chain Packaging, Labelling, Distribution, Comparators and Collaborations functions by:
- Effectively leading, developing, motivating, inspiring a global team of ~90 FTE, including 5-8 direct reports and leadership team heading up five functional areas.
- Leading and embedding a Packaging, Labelling, Distribution, Comparators and Collaborations function that supports the GSK Vaccine and Medicine portfolio, including GxP internal operations and oversight of external PLDC operations
- Providing Leadership and coordination across line, region, and countrybased professionals to ensure consistency of approach and Supply Continuity.
- Effectively leading the safety, quality, and performance of all internal and external operations to deliver IMP, Comparators and Ancillaries (where required) to Clinical depots and sites.
- Providing leadership and partnership with colleagues in Clinical Development, GSC, CSC, MDS and the CMC board to deliver and accelerate the GSK Portfolio.
- Develop and deliver the Clinical Supply Chain strategy with the CSCLT to deliver the GSK R&D ambition.
- Ensure deployment of modernised Digital platform in support of the modernisation of clinical supply chain
- Ensure all supply solutions are effectively planned and compliantly executed RFT, meeting OTD targets driving efficient utilization of FTEs, fixed assets, and revenue expenditure
Job related Experience:
- Highly credible with broader CMC community and with senior stakeholders across GSK, with strong knowledge of CMC, Clinical operations, QA, regulatory, and cross modality therapeutic landscapes.
- Proven record of being able to influence internal and external stakeholders on challenging medicine development, reimbursement, and productstewardship issues
- Able to operate effectively in a range of external settings, such as working with codevelopment partners, consulting with external experts, or representing GSK at highprofile regulatory meetings
Basic Qualifications:
- Bachelor's Degree in Science, engineering or businessrelated discipline or a related field with applicable experience
- Extensive years in industry with several years of demonstrated leadership and influence
- Senior leader experience within the Pharmaceutical Industry, ideally in development and /or supply CMC activities supporting a range of different modalities
- Demonstrable global functional leadership capability
- Expert knowledge of cross modality clinical demand drivers and critical success factors
- Demonstrable understanding of clinical trial and supply Regulation and QA/ QP accountabilities
- Proficient knowledge of GSK portfolio and priorities
- Proficient knowledge of cross modality drug product development, manufacturing and supply
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