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Lead, Site MSAT

TieTalent

Hutton Magna

On-site

GBP 60,000 - 90,000

Full time

5 days ago
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Job summary

A leading biopharmaceutical company is seeking a Lead, Site MSAT to oversee their Manufacturing Science and Technology team. This role involves managing product lifecycle, improving supply chains, and developing future leaders in a dynamic environment. The ideal candidate will have extensive experience in biopharmaceutical processes and a strong leadership background.

Benefits

Competitive salary
Bonuses
Healthcare
Pension
Flexible working options

Qualifications

  • Extensive experience in biopharmaceutical process development and technology transfer (over 5 years).
  • Experience with biopharmaceutical product registration (FDA and/or EMEA).
  • Knowledge of GMP, ICH Guidelines, and validation practices.

Responsibilities

  • Oversee the Manufacturing Science and Technology (MSAT) Team.
  • Manage product lifecycle activities including process improvements and regulatory compliance.
  • Lead technical issue resolution and product investigations.

Skills

Leadership
Interpersonal skills
Communication

Job description

TieTalent Hutton Magna, England, United Kingdom

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Location: Hutton Magna, England, United Kingdom

Posted: 1 day ago - Be among the first 25 applicants

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About the Role

Location: Barnard Castle, UK

Posted Date: Apr 29, 2025

The Lead, Site MSAT will oversee the Manufacturing Science and Technology (MSAT) Team at Barnard Castle, focusing on products in New Product Introduction, sterile manufacturing, and dermatological applications. The role involves managing product lifecycle, improving supply chains, and developing technical capabilities and future leaders within the team.

Key Responsibilities
  • Ownership of core technical processes such as Product Lifecycle Management, NPI, Scale Up, and Technical Transfer.
  • Support site initiatives and contribute to strategic planning as a member of the leadership team.
  • Manage product lifecycle activities including process/yield improvements, knowledge management, and regulatory compliance.
  • Lead technical issue resolution and product investigations, ensuring timely escalation and resolution.
  • Participate in the GSK MSAT community for strategic input.
  • Talent management, including succession planning and capability building within the MSAT team.
Qualifications
Basic Qualifications
  • Extensive experience in biopharmaceutical process development and technology transfer, with over 5 years in leadership roles.
  • Experience with biopharmaceutical product registration (FDA and/or EMEA).
  • Knowledge of GMP, ICH Guidelines, and validation practices.
Preferred Qualifications
  • Strong leadership and interpersonal skills.
  • Effective communication skills and good judgment.
Additional Information

Application deadline: May 26, 2025

We offer competitive salary, bonuses, healthcare, pension, and flexible working options. GSK promotes diversity and inclusion and is an equal opportunity employer.

For adjustments or inquiries, contact us via the provided channels. Please review our FAQ for common questions.

About GSK

GSK is a global biopharma company dedicated to uniting science, technology, and talent to combat disease. We focus on vaccines, medicines, and immunology, aiming to make a positive impact on global health while fostering a supportive environment for our employees.

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