MSAT OSD Technical Team Lead - Aranda de Duero, España - GSK

Descripción

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

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