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GSK

MSAT OSD Technical Team Lead

Burgos, Spain

Site Name: GSK Aranda de Duero, Burgos
Posted Date: Apr 10 2024

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.

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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

Why Us?

GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organization where people can thrive. Getting ahead means preventing disease as well as treating it, and we aim to positively impact the health of 2.5 billion people by the end of 2030.

Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a workplace where everyone can feel a sense of belonging and thrive as set out in our Equal and Inclusive Treatment of Employees policy. We're committed to being more proactive at all levels so that our workforce reflects the communities we work and hire in, and our GSK leadership reflects our GSK workforce.

If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US).

GSK is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.

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Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit GSK's Transparency Reporting For the Record site.

Client-provided location(s): Burgos, Spain
Job ID: glaxo-392150-en-us
Employment Type: Other