About Gilead Sciences

Gilead Sciences is a leading biopharmaceutical company dedicated to creating a healthier world for all people. For over 35 years, Gilead has pioneered therapies for some of the world's most challenging diseases, including HIV, viral hepatitis, COVID-19, and cancer. Through its innovative subsidiary Kite, Gilead is at the forefront of cell and gene therapies, particularly in oncology. The company also advances treatments for inflammatory diseases, ensuring broad access to life-changing medicines globally. With a relentless drive for scientific innovation, Gilead fosters collaboration and empowers its teams to tackle bold ambitions in biotechnology.

Role Overview

Kite, a Gilead company, is seeking a highly motivated Associate Director, Process Engineering, External Manufacturing Science & Technology (MSAT) to join the network MSAT unit. Based in Uxbridge, United Kingdom, this role provides technical oversight and leadership for external manufacturing partners producing viral vectors. As the primary technical liaison between Kite and UK-based CMOs, you will ensure robust, compliant, and efficient production for clinical and commercial manufacturing. This position demands strategic thinking, strong influencing skills, and hands-on expertise in a fast-paced biopharma environment.

Key Responsibilities

In this critical role, you will drive technical excellence across external operations. Key responsibilities include serving as Kite’s primary technical point of contact for UK-based CMOs, leading hypercare of manufacturing activities, and providing expertise in deviation resolutions, root cause investigations, and CAPA implementation. You will review trend data, coordinate continuous process verification (CPV), and act as Expert-in-Plant during high-risk operations like PPQ runs and process changes. Additional duties involve onsite technical support, participating in daily huddles, observing operations, and collaborating cross-functionally with internal teams in MSAT, Process Development, Quality, Regulatory, Supply Chain, and Alliance Management.

External Manufacturing Oversight

• Lead technical oversight for viral vector production at CMOs.
• Author impact assessments and oversee remediation plans.
• Ensure business continuity through scenario planning and raw material qualifications.

Onsite Technical Support

• Provide real-time guidance using tools like DMAIC, Ishikawa, and 5 Whys.
• Facilitate communications between UK teams and US-based project groups.

Qualifications & Requirements

To succeed, candidates need a Bachelor's, Master's, or PhD in Biochemical Engineering, Chemical Engineering, Biomedical Engineering, Biotechnology, Biology, Biochemistry, or Chemistry. Experience requirements are 10+ years with a Bachelor's, 8+ years with a Master's, or 5+ years with a PhD in relevant fields. A proven track record in MSAT and tech transfer supporting contract manufacturing is essential, with viral vector process development and GMP manufacturing as strong advantages. Expertise in GMP compliance, process validation (PPQ, Comparability, CPV), cell culture, aseptic processing, risk management (FMEA), project management, and JMP data analysis is required. Excellent communication, presentation skills, and the ability to thrive in a team-oriented, fast-paced setting with minimal direction are crucial. Must be eligible to work in the UK.

Benefits & Perks

Gilead offers a comprehensive benefits package designed to support your well-being and professional success. Enjoy competitive salaries estimated at £90,000–£150,000 annually, performance incentives, and robust health coverage. Additional perks include wellness programs, generous paid time off, and family-friendly policies. As a people leader, you'll benefit from leadership development resources to evolve Gilead's inclusive culture.

Career Growth

At Gilead, career advancement is a priority. This Associate Director role positions you for leadership in biopharma manufacturing, with opportunities to influence global supply chains and innovative therapies. Access mentorship, training in emerging technologies like viral vectors, and cross-functional projects. Gilead's commitment to employee development ensures you can aspire to higher roles while contributing to breakthroughs in HIV treatments, oncology via Kite, and inflammatory diseases.

Why Join Gilead

Joining Gilead means becoming part of a mission-driven team fighting the world's biggest health challenges. Work on cutting-edge viral vector production that powers gene therapies for cancer and beyond. Benefit from a collaborative culture where every voice matters, and innovation thrives. In Uxbridge, UK, you'll engage directly with partners, driving real impact on patients worldwide. Gilead values diversity, inclusion, and empowerment, making it an ideal place for ambitious professionals.

Role FAQs

Q: What is the primary focus of this role?
A: Technical oversight and leadership for external viral vector manufacturing at UK CMOs, ensuring GMP compliance and efficiency.

Q: Is travel required?
A: Yes, onsite support at CMO facilities in the UK, with potential coordination with US teams.

Q: What experience with viral vectors is needed?
A: Strong plus, but proven MSAT and tech transfer experience is essential.

Q: How does this role support Gilead's mission?
A: By enabling reliable production of therapies for HIV, oncology, and inflammatory diseases, improving global access.

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