MSAT OSD Technical Team Lead

Encontrado en: beBee jobs ES - hace 2 semanas

Aranda de Duero, Burgos, España GSK A tiempo completo
Nome della sede: GSK Aranda de Duero, Burgos
Data di apertura: Apr

MSAT OSD Technical Team Lead

Are you energized by a highly technical manufacturing role that allows you to accelerate business improvement efficiency and shape maximize product quality?

If so, this Manufacturing Science and Technology (MSAT) OSD Technical Team Lead role could be an ideal opportunity to explore.

As a MSAT OSD Technical Team Lead, you will Implement and maintain the control strategy for a variety of drug products substance production. You will be responsible for driving the production process lifecycle management for next generation and continuous improvement of biologics specialty and critical to patients drug products substance manufacturing.

This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

  • Provide technical oversight maximizing value and robustness of our products and processes end-to-end, across sites, and throughout their lifecycle.
  • Develop and lead a highly competent team of Product Owners, Process Engineers, Platform Experts, Documentation and Validation Specialists Technologists and Technicians to deliver projects, mitigate discharge risks, implement changes and maintain knowledge management systems for the site.
  • Function as Single Point of Contact (SPOC) for Technical Lifecycle Management Team (TLCT) and ensure strong collaboration with the global Manufacturing Science and Technology (MSAT) organization. Acquire, maintain and manage product knowledge throughout the product lifecycle.
  • Lead process robustness and yield improvement projects. Provide Global Product and Process Expertise (Task Force, Trouble Shooting). Promote and monitor technical standards throughout the product lifecycle and ensure they are adhered to.
  • Industrializing and Transferring newly developed and commercialized products within the GSK Pharma Supply Chain and other third party companies sites as applicable. Key focus areas are project and risk management, technical due diligence and embedding quality and technical capabilities to ensure robust, cost-effective manufacturing processes.
  • Provide and coordinate technical activities and support to the Value Stream manufacturing operations in alignment with groups within the Value Stream, and coordinate technical activities.

Basic Qualifications:

We are looking for professionals with these required skills to achieve our goals:

  • Bachelor's degree in engineering, pharmacy, biochemistry or chemistry
  • Solid experience in Good Manufacturing Practices (GMP) regulated pharma/biotech environment.
  • Experience developing Risk Based process control strategies and Continuous Process Verification, specifically in OSD products
  • Experience with root cause analysis and evaluating variables influencing process performance
  • Experience in Process/Product Transfers and industrialization from R&D and/or between manufacturing plants
  • Experience in Team management.

Preferred Qualifications:

If you have the following characteristics, it would be a plus:

  • Ability to problem solve and identify technical/scientific solutions to resolve process-related issues.
  • Strong interpersonal and relationship building skills.
  • Ability to influence and gain support on complex issues.
  • English C1

End date: 30/04/2024

Se è necessaria accoglienza specifica o altro tipo di assistenza per presentare una domanda di lavoro presso GSK/ViiV Healthcare, contattare il centro servizi HR al numero gratuito negli Stati Uniti) o al numero fuori dagli Stati Uniti).

GSK/ViiV è un datore di lavoro favorevole alle pari opportunità. Tutti i candidati qualificati riceveranno uguale considerazione per l'impiego a prescindere da razza, colore, nazionalità, religione, sesso, gravidanza, stato civile, orientamento sessuale, identità/espressione di genere, età, disabilità, informazioni genetiche, servizio militare, stato di veterano protetto stato o qualsiasi altra classe protetta federale, statale o locale.

Avviso importante per le imprese/agenzie per l'occupazione

GSK non accetta referenze da parte di aziende e/o agenzie di collocamento in relazione alle offerte di lavoro pubblicate su questo sito. Tutte le aziende/agenzie di collocamento sono tenute a contattare l'ufficio commerciale e il reparto generale/risorse umane di GSK per ottenere un'autorizzazione scritta prima di segnalare eventuali candidati a GSK. L'ottenimento della previa autorizzazione scritta è una condizione sospensiva rispetto a qualsiasi accordo (verbale o scritto) tra l'azienda/agenzia di collocamento e GSK. In assenza di tale autorizzazione scritta ottenuta, qualsiasi azione intrapresa dall'azienda/agenzia di collocamento verrà considerata eseguita senza il consenso o l'accordo contrattuale di GSK. GSK non sarà quindi responsabile per eventuali commissioni derivanti da tali azioni o commissioni derivanti da eventuali segnalazioni da parte di aziende/agenzie di lavoro in relazione alle offerte di lavoro pubblicate su questo sito.

Tenere presente che se si è un operatore sanitario o un operatore sanitario autorizzato negli Stati Uniti come definito dalle leggi dello stato che rilascia la licenza, a GSK potrebbe essere richiesto di registrare e segnalare le spese sostenute da GSK per conto dell'operatore sanitario nel caso in cui esso venga convocato per un colloquio per lavoro. Questa registrazione dei trasferimenti di valore applicabili è necessaria per garantire la conformità di GSK a tutti i requisiti di trasparenza federali e statali degli Stati Uniti. Per ulteriori informazioni, visitare il sito Transparency Reporting For the Record di GSK.

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