MSAT Drug Product Lead (Parenteral Products) in Barnard Castle

Position Summary

You will manage the Manufacturing Science and Technology (MSAT) Drug Product technical delivery for drug product manufacturing of a defined product or product family (mainly for the GSK sterile injectable Products portfolio), with a primary focus on New Product Introduction (NPI) and successful product launches, including delivering successful right-first-time product qualifications. You will work closely with R&D, manufacturing sites, quality, regulatory and external partners to ensure safe, robust and compliant supply. This role offers visible impact, strong development opportunities and a chance to help GSK unite science, technology and talent to get ahead of disease together.

Responsibilities

• Act as the single technical point of contact for the drug product portfolio, owning technical risk, decision-making and product knowledge.
• Manage and deliver technology transfers to internal sites and external manufacturers, including transfer packages, training and readiness reviews.
• Manage continued process verification, process performance qualification and change management to maintain product robustness and compliance.
• Drive right-first-time execution of product qualification activities (e.g., PPQ/qualification readiness), managing appropriate governance through the relevant stage-gate forums as the program approaches PPQ, ensuring robust data, clear acceptance criteria and effective issue resolution.
• Define and maintain product control strategy and technical risk assessments.
• Translate that knowledge into clear documentation for operations.
• Support regulatory submissions and post-approval inspections by providing technical input, comparability strategies and supporting documentation.
• Manage cross-functional investigations, root cause analysis and corrective actions for complex deviations and quality events.

Expectations

• Work in a matrix environment and build strong relationships across functions and sites.
• Make technical recommendations that balance speed, quality and patient safety.
• Share knowledge through clear documentation, training and mentoring of operational teams.
• Ensure data and documentation meet regulatory and GSK quality standards.
• Drive continuous improvement and apply practical lessons to prevent recurrence.
• Travel to manufacturing sites and partner organisations as required.

Location

The successful applicant can be based at Ware, Barnard Castle or Worthing (UK), or Rosia (Italy) or Wavre (Belgium).

Closing Date

Applications close on Tuesday, 26th of May 2026 (COB).

Basic Qualification

• Degree in a relevant technical, scientific or engineering discipline (e.g., pharmacy, chemistry, chemical/biochemical engineering).
• Knowledge/experience in drug product manufacturing, MSAT, process development or technical transfer roles in the pharmaceutical industry.
• Practical knowledge of risk tools (e.g., FMEA), control strategy development and statistical concepts for CPV.
• Demonstrable experience of technology transfer, process validation or continued process verification.
• Knowledge of good manufacturing practice (GMP) and product lifecycle management principles.
• Experience working in cross-functional teams and managing stakeholder expectations.

Preferred Qualification

• Experience with specific drug product formats such as injectable or oral solid dose.
• Experience preparing technical content for regulatory submissions and supporting inspections.
• Experience managing complex investigations and applying Lean/Six Sigma problem solving (e.g., trained DMAIC facilitator).
• Experience working with contract manufacturing organisations (CMOs) or external partners.
• Demonstrable track record in coaching or managing small technical teams and cross-functional projects.

Salary

Salary ranges for Italy and Belgium are EUR 0–EUR 0. Additional incentives may be offered based on the role level.

Equal Opportunity Employer

GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.