Summary
Location
Manchester
Type
full-time
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About this role
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.
Other facts
About QIAGEN
QIAGEN is the leading global provider of Sample to Insight solutions that enable customers to gain valuable molecular insights from samples containing the building blocks of life.
Our sample technologies isolate and process DNA, RNA and proteins from blood, tissue and other materials. Assay technologies make these biomolecules visible and ready for analysis. Bioinformatics software and knowledge bases interpret data to report relevant, actionable insights. Automation solutions tie these together in seamless and cost-effective workflows.
QIAGEN provides solutions to more than 500,000 customers around the world in Molecular Diagnostics (human healthcare) and Life Sciences (academia, pharma R&D and industrial applications, primarily forensics).
As of December 31 2021 QIAGEN employed more than 6,000 people in over 35 locations worldwide. Further information can be found at www.qiagen.com.
What you'll do
- Drive cross-functional product development projects within a matrix organization, ensuring timely delivery and adherence to quality standards. Collaborate with internal teams and external partners to achieve project goals and maintain transparent communication.
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