Director / Senior Director of MSAT (Manufacturing Sciences and Technology) London, England
Job description
ABOUT US
At Quell we seek to deliver truly innovative, life-changing therapies for our patients. Our vision as a company is to build a major global biopharmaceutical company bringing transformational and valued therapies for a range of autoimmune and inflammatory diseases, as well as preventing rejection in organ transplantation, based on modular engineered Tregs.
OUR COMPANY
Quell Therapeutics Ltd ("Quell"), the world leader in the development of engineered T-regulatory (Treg) cell therapies for serious medical conditions driven by the immune system, announced it has raised $156 million in an oversubscribed Series B financing. The financing round was co-led by Jeito Capital, Ridgeback Capital Investments, SV Health Investors and Fidelity Management & Research Company LLC with participation from founding investor Syncona. New investors include British Patient Capital through its Future Fund: Breakthrough program, Janus Henderson Investors, Monashee Investment Management, Point72 and funds managed by Tekla Capital Management LLC
THE ROLE
Director / Senior Director of MSAT (Manufacturing Sciences and Technology)
As the Director / Senior Director of MSAT, you will provide strategic direction and leadership to the MSAT team in alignment with Quell's vision and values of Collaboration, Innovation, Respect, Accountability, and Integrity. The role involves overseeing the development and implementation of manufacturing processes for cell therapies and ensuring cross-functional collaboration with various teams.
MAIN RESPONSIBILITIES
- Strategy and Leadership:
- Develop and execute the strategic vision for MSAT, aligning with the overall company and Manufacturing Operations objectives.
- Provide strong leadership and guidance to a multidisciplinary team, fostering a culture of innovation, collaboration, and continuous improvement.
- Foster cross-functional partnerships with R&D, Process Development, Analytical Development, Quality Assurance, Regulatory Affairs, Supply Chain, and Manufacturing to drive efficient and seamless operations.
- Develop and manage the department's budget and resources.
- Technology Transfer and Manufacturing Support
- Oversee technology transfer activities to external manufacturing sites, ensuring seamless integration of processes and technologies.
- Provide technical expertise and support to manufacturing teams, troubleshooting complex issues, and driving process improvements.
- Collaborate closely with CMC and Quality teams to ensure compliance with cGMP regulations and standards.
- Continuous Improvement and Innovation:
- Identify opportunities for process improvements, automation, and innovation to enhance manufacturing efficiency, productivity, and quality.
- Stay up-to-date with industry trends, emerging technologies, and regulatory requirements related to cell therapy manufacturing.
- Implement best practices and establish metrics to measure and monitor manufacturing performance.
- Other duties as assigned
EXPERIENCE WE ARE LOOKING FOR
- Extensive experience in MSAT in the biopharmaceutical industry, with a focus on cell and gene therapy.
- Proven track record of successful leadership and people management.
- Strong strategic thinking, problem-solving, and decision-making skills.
TECHNICAL SKILLS REQUIRED
- Profound knowledge of cell and gene therapy manufacturing processes.
- Experience with technology transfer and process validation.
- Knowledge of risk management strategies in biopharmaceutical production.
- Familiarity with regulatory standards and quality systems in the biopharmaceutical industry.
DESIRABLES
- PhD degree in biological sciences, chemical engineering, or related field.
- Strong background in process development, technology transfer, and scale-up of cell therapy manufacturing processes.
- Demonstrated leadership experience, including managing and developing high-performing teams.
- In-depth knowledge of cGMP regulations, quality systems, and regulatory requirements for cell therapy manufacturing.
- Understanding of the latest advancements and technologies in the cell and gene therapy field.
- Proven track record of successful process optimization, troubleshooting, and continuous improvement initiatives.
- Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams and external partners.
- Strong strategic thinking, problem-solving, and decision-making abilities.
- Previous experience in a startup or high-growth environment.
PERSONAL QUALITIES
- A strong team player who embodies Quell's values of Collaboration, Innovation, Respect, Accountability, and Integrity.
- Able to inspire, motivate, and lead teams.
- Excellent interpersonal and communication skills.
- Hands-on and detail-oriented, with an ability to manage multiple projects and priorities.
BENEFITS
- Holidays: 25 days per year
- Life Assurance: 4 x base salary
- Group Personal Pension: Auto enrolled at 6% employer contribution, 3% employee contribution
- Private Medical Insurance for your whole family
- Annual Bonus
PERKS
- Fantastic collaborative environment at Translation & Innovation Hub
- Click here for Virtual Tour
- $156 Million Investment including brand new lab equipment, innovative methods, and exposure to cutting edge technology
- Flexible working
- Fast paced and progressive company looking for future leaders and innovators
