Overview At QIAGEN, we are driven by a simple but powerful vision: making improvements in life possible. We’re dedicated to revolutionizing science and healthcare for the better. From our entrepreneurial roots to our current global presence, we've grown into a force for positive change. With thousands of employees across six continents, collaboration is our greatest strength. We’re always striving to identify talented individuals to join our exceptional teams. We have played a pivotal role in shaping modern science and healthcare, and we're just getting started. If you're someone who thrives on new challenges, values diversity and wants to make a tangible difference in people's lives, then QIAGEN is the place for you. At QIAGEN, every day is an opportunity to make a real-life impact. Join us, grow with us, and together, let's shape the future of biological discovery. At QIAGEN Manchester, we are a world-leading centre for molecular diagnostic applications, developing life-changing solutions for precision diagnostics. In collaboration with external pharmaceutical partners you will work with cross-functional QIAGEN teams, leading impactful development projects that shape future companion diagnostics solutions. Your Tasks Drive cross-functional product development projects within a matrix organisation, ensuring delivery on time, within budget, and to the highest quality standards. Collaborate with internal teams and external partners to achieve project goals and maintain transparent communication. Apply QIAGEN’s project management standards and ensure regulatory requirements are met throughout the development lifecycle. Identify and evaluate risks, implement mitigation strategies, and escalate critical issues promptly. Ensure accurate project documentation and reporting for stakeholders. Your Profile Degree in Life Sciences or equivalent experience; project management certification (e.g., PMP®, PRINCE2, APMP) is a plus. Proven experience in the development of diagnostics, or medical devices in a regulated environment. Strong track record in work with cross-functional teams and building effective relationships. Familiarity with Design Controls and regulatory standards (21 CFR 820, ISO 13485, ISO 14971) is desirable. Experience working with external partners on high profile projects. What we offer Attractive pension Private Healthcare and Dentalcare Gym membership contribution A range of retail discounts and offers Enhanced maternity package Flexible working options Bonus/commission 25 days annual leave (potential to increase linked to service) Employee Assistance Program and internal QIAGEN communities Hybrid work (conditional to your role) Our people are the heartbeat of everything we do. Passion drives us as we push boundaries to innovate and evolve. We inspire with our leadership and make an impact with our actions. We cultivate a collaborative, supportive environment where each individual and team can flourish. We champion accountability and encourage entrepreneurial thinking. QIAGEN is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, or disability.