Hobson Prior International Ltd

Ready to engineer precision in the world of biotech? Join our client's cutting-edge team and play a vital role in developing the instrumentation that powers tomorrow's breakthroughs. Hobson Prior is seeking an Upstream Bioprocessing Team Leader to oversee and manage a team of scientists in a biotechnology manufacturing environment. This role focuses on ensuring safe, compliant, and efficient production of clinical and commercial gene therapies. You will play a key role in leading operations, maintaining quality standards, and fostering a culture of continuous improvement. This is an on-site position with occasional opportunities for remote work. Please note that to be considered for this role you must have the right to work in this location. Responsibilities: Lead and manage a team of up to six bioprocessing scientists, providing training, support, and performance management. Ensure all team activities comply with Good Manufacturing Practices (GMP), data integrity, and documentation standards. Oversee the timely and compliant completion of training for yourself and your team. Manage GMP documentation, including addressing issues, corrective actions, and audit responses promptly and accurately. Collaborate across departments to meet manufacturing schedules and resolve operational challenges. Respond to quality issues during production and ensure the facility remains inspection-ready. Promote safety by identifying risks, implementing controls, and ensuring team members are protected from harm. Communicate goals, progress, and updates effectively within the team. Drive continuous improvement initiatives and coach team members to enhance processes and performance. Maintain high standards for cleanroom behavior, environmental monitoring, and materials handling. Key Skills and Requirements: A degree in Science or Engineering. Strong understanding of manufacturing operations, quality systems, and the process development lifecycle. Experience in regulatory inspections and audit readiness. Ability to lead and develop technical teams in a dynamic environment. Strong organizational skills to manage risks and meet deadlines. Analytical mindset with problem-solving abilities and experience working in cross-functional teams. Commitment to fostering a culture of continuous improvement. For more information, please contact Jessica Taylor . If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page. Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy. By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - .

Hobson Prior is seeking a Senior Clinical Programmer to join our client's team in London. In this role, you will focus on managing project timelines and ensuring quality in clinical programming tasks. You will also engage with clients and support process improvements within the team. Please note that to be considered for this role you must have the right to work in this location. Responsibilities: Oversee project schedules and ensure quality in studies you partially lead. Interact with clients during meetings and audits, providing insights on database programming. Assist in updating standard operating procedures and enhancing processes. Create and support documentation for clinical programming specifications. Manage data transfer agreements with external vendors. Develop validation checks and visualizations to aid data management and reviews. Key Skills and Requirements: Experience in clinical data programming. Ability to understand and present clinical data effectively. Proficiency in SAS for developing or debugging programs. Strong leadership skills in project management. Familiarity with CDISC standards, especially SDTM. Experience in training and mentoring team members. Understanding of clinical trial budgets and tracking activities beyond scope. Experience in participating in sponsor meetings and audits. Ability to contribute to process improvement efforts. If you are interested in learning more or applying to this exciting opportunity then please click 'Apply' and upload a copy of your CV. Alternatively for further details or to talk directly to a life sciences recruitment specialist, please select 'Contact me' at the top of this page. Apply now

Hobson Prior are currently working alongside a fantastic biotech establishment who have an opening for a Good Clinical Practice Compliance Manager to join their team on a contract basis. Our client is focused on converting ground-breaking concepts and findings into remedies for people who suffer from serious diseases. Please note that to be considered for this role you must have the right to work i...... click apply for full job details

Hobson Prior are currently seeking for a Brand and Customer Manager to join a brilliant pharmaceutical establishment on a contract basis. Our client is focused on assisting patients and the population. Please note that to be considered for this role you must have the right to work in this location. Key Responsibilities: For this role, you will be responsible for guiding marketing-led campaigns, guar...... click apply for full job details

Hobson Prior are seeking for a Bioprocessing Scientist to join a Biotech organisation to be located in London on a permanent basis. Our client is determined to develop treatments who can save patients' lives. Please note that to be considered for this role you must have the right to work in this location. Key Responsibilities: Perform production processes, following SOPs and GMP practices to manufac...... click apply for full job details

Hobson Prior are looking to recruit a passionate Research Associate to join our fantastic client on a permanent basis. For more information, please get in touch now! Please note that to be considered for this role you must have the right to work in this location. Key Responsibilities: Creating tissue microarrays...... click apply for full job details

Hobson Prior are currently working with a top pharmaceutical organisation who are focused on the development, manufacturing and commercialising of medicines that will make a real transformation to patients and their family's lives. Our client is seeking a Regulatory Affairs Specialist to join them on a permanent basis. Please note that to be considered for this role you must have the right to work ...... click apply for full job details