(Sr.) Manager, ITBP - Quality

Job description

Nantong, China | full time | Job ID: 11727 Searched your files Searched your files IT Partner – Quality Domain (China) About the Role: As an IT Partner for the Quality domain, you will play a pivotal role in ensuring seamless IT operations across all BioNTech sites in China. Your expertise will drive the alignment of IT systems with the needs of the Quality department, directly contributing to our mission of revolutionizing medicine. By collaborating with cross-functional teams, you'll ensure that our IT solutions support and enhance critical quality processes, creating a robust foundation for innovation and compliance. You’ll be working in a dynamic and collaborative environment where your technical and strategic insights will shape IT initiatives in the quality domain. From managing projects to ensuring regulatory compliance, your role will be integral to maintaining high standards and achieving operational excellence. Your Contribution: Act as the strategic IT partner for the Quality business unit, providing technical consulting and aligning systems with business objectives Lead end-to-end IT operations across all BioNTech sites in China, ensuring efficiency and effectiveness Manage the full lifecycle of IT projects within the quality domain, including requirements analysis, design, development, testing, and go-live phases Coordinate internal teams (IT, QA, QC, QV) and external vendor resources to drive project success while managing risks and changes Oversee Computerized System Validation (CSV) for GMP systems such as LIMS, Empower chromatography system, and QMS by defining validation strategies Deeply understand and support key quality processes like quality management, documentation management, training management, and laboratory information systems A Good Match: Strong experience in IT operations management within a regulated environment (preferably pharmaceutical or biopharmaceutical industries) In-depth knowledge of quality management systems (e.g., LIMS, Empower chromatography system) and their application in GMP settings Proven track record of leading complex IT projects from inception to completion Expertise in Computerized System Validation (CSV) processes for GMP-compliant environments Excellent communication skills with a collaborative mindset to work effectively across diverse teams Proactive problem-solving abilities with a strategic approach to align technology with business needs Join us at BioNTech as we work together to transform lives through innovative medicine. Your role as an IT Partner will not only support our operational goals but also contribute to advancing healthcare solutions worldwide. Your benefits: BioNTech is committed to the wellbeing of our team members and offers a variety of benefits in support of our diverse employee base. We offer competitive remuneration packages which is determined by the specific role, location of employment and also the selected candidate’s qualifications and experience. Note: The availability, eligibility and design of the listed benefits may vary depending on the location. The final requirements for the individual use of our benefits are based on the company's internal policies and applicable law. How to apply: Apply now by sending us your application documents including Curriculum Vitae, copy of ID, copies of degree certificates and professional certificates, motivation letter as well as your contact details via our online form. Please note: Only applications sent via our online form shall be considered. By submitting your application, you acknowledge that a background check will be conducted as part of the recruitment process in accordance with applicable laws and regulations. If you are considered for the position, BioNTech will conduct the background check through our service provider ‘HireRight’. You will be informed accordingly by your BioNTech-Recruiter. We are looking forward receiving your application.