Local Msat Italy Head

1 settimana fa

Trieste, Friuli Venezia Giulia, Italia GSK A tempo pieno

Site Name:
Italy - Rosia

Posted Date:
Apr

This is a site-based role at Rosia, Italy.


As a member of Site Leadership Team, she/he will Lead the MSAT organization which provides technical, operational, and scientific expertise to site manufacturing operations to deliver continuous process performance verification and improvement throughout the lifecycle of the processes and products and ensure site readiness to attract new product platforms.

This is a critical role, with a high degree of trust and visibility among senior leaders across the organization. Working with a diverse supply chain you will be a key contributor to the site and wider GSC.

Ready to shape the future of healthcare?

In this role you will:

  • Lead and develop the Local MSAT resources in Rosia and be a team member in the Site Leadership Team. Develop people and organizations to match evolving requirements. Manage people development and succession planning, training programs and career/succession opportunities in Rosia and within the global network, in line with GSK expectations and GSK values, to prepare them for growing GSK ambition.
  • Lead Products Lifecycle in Rosia in close collaboration and coordination with the respective Manufacturing Process Units leaders. Coordinate in a timely manner and shopfloor their continuous improvements and troubleshooting requests.
  • Support operations by leading crossfunctional root cause analysis and problem solving on technical/process issues by GPS approach (e.g., RR, DMAIC for major deviations/investigations).
  • Oversee, support and challenge local process robustness monitoring & trending through Continued Process Verification owned by the respective Product Stewards.
  • Ensure the maintenance of process and cleaning validation status according to Site Validation Master Plans (VMPs), annual revalidation plans and any other validation activity required from Health Authorities, New Product Introductions and Process Improvements.
  • Ensure that all the technical projects, including New Product Introduction, major changes and product improvement projects requiring multidisciplinary teams are adequately resourced and are delivered in compliance to the regulations and to the Site target.
  • Promote the introduction of new manufacturing technologies and Digital & Data Analytics by providing technical leadership on various technical governance committees and decisionmaking bodies and support the preparation and implementation in the site.
  • Lead the lifecycle of Incoming Materials (e.g SuS qualification, L&E, BCT)
  • Manage the L-MSAT budgets in line with expectations.
  • Building a

Learning Organization:

Ensures development and deployment of highly specialist technical skills and knowledge to meet the needs of the site's product portfolio and strategy.

Foster knowledge transfer within site, between sites and across the network.

  • Ensure compliance with regulations and company standard operating procedures (SOPs).
  • Responsible for Italian law (D.Lgs 81/08) compliance, policies and GSK standards; ensure a cultural change in terms of safety & linked behaviors in the team; people safety and health as mandatory and primary objectives as manager; lead by example and in agreement with local SOP (e.g. PPE, risk assessment evaluation, L1 Audit); ensure correct waste management according to our internal procedures.
Please take a copy of the Job Description, as this will not be available post closure of the advert.

Why you?

Required qualifications and skills:

  • Degree Qualified preferably in Science/Engineering/ Pharmaceutical Technology or equivalent experience
  • Considerable experience in Supply chain or in manufacturing area
  • Significant experience in TRD or MSAT organizations
  • Proven underpinning scientific knowledge of Vaccines manufacturing and analytical testing
  • Sound experience of data handling and applied statistics.
  • Has an understanding of the complexities of transformational projects and change management projects
  • Fluent in English and proficient in site local language
  • Able to deal with ambiguity and have an agile mindset working in a complex site.

Preferred qualifications and skills:

  • MSc/Ph. D in Science/Engineering/ Pharmaceutical Technology
  • Strong ability to influence and clearly communicate across a wide variety of stakeholders and personal resilience
  • Proactive, independent, and highly performance focused
  • Ability to bring objective viewpoints and potential solutions to challenges across different functions and business areas
  • Excellent interpersonal and communication skills.


We make and supply medicines and vaccines all around the globe and our teams own every production stage, from creating quality products at our manufacturing sites to designing effective supply forecasting and regulatory inspections; all powered by digital, data and analytics.

We operate at impressive scale, producing over 1.7 billion packs of medicine and 767 vaccine d

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