QIAGEN GmbH
JOB ID: JR00000739
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.
About the opportunity
As a (Senior) QA Specialist Supplier Quality Assurance (f/m/d), you will join a cross-functional team responsible for ensuring supplier compliance with ISO 13485 and internal quality standards. You will collaborate with global stakeholders to strengthen supplier performance and uphold QIAGEN's commitment to quality excellence.
This position is planned to be filled with a start date of September 1st at the earliest.
Your tasks include
Drive and monitor supplier compliance within the Chemical & Bioreagents category in line with ISO 13485 and internal quality standards
Execute supplier qualification, evaluation, and re-evaluation activities using the global electronic Quality Management System (eQMS) and other tools
Lead Supplier Corrective and Preventive Actions (SCARs) and ensure timely closure in close collaboration with suppliers and internal stakeholders
Partner with Purchasing, Manufacturing, and R&D to resolve supplier-related issues and implement sustainable improvements
Establish, review, and maintain Quality Agreements with key suppliers
Plan, perform, and support supplier audits to ensure compliance with regulatory and internal requirements
Act as a key quality interface for external partners and ensure transparent communication across all stages of collaboration (approx. 5–10% travel)
Your profile
Bachelor's or Master's degree in a science-related field such as Biology, Chemistry, or Engineering
Initial professional experience (approx. 2–3 years) in Supplier Quality or Quality Assurance within the medical device or diagnostics industry
Solid understanding of ISO 13485 and experience working in a regulated environment
Strong communication and negotiation skills in English (fluent) and German (business level)
Experience with digital systems such as SAP/ARIBA, Salesforce (SFDC), or TrackWise is an advantage
Ability to manage stakeholders effectively in a global, cross-functional environment
A proactive, self-driven, and structured working style with strong analytical thinking skills
What we offer
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.
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