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Dingcheng Liu Email & Phone Number
Supplier Quality Engineer (SQE) and Regulatory Affairs
at
Exelint International
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✓ Verified May 2026
3 data sources
Profile completeness 86%
Current company
Role
Supplier Quality Engineer (SQE) and Regulatory Affairs
Location
Los Angeles, California, United States
Company size
Who is Dingcheng Liu? Overview
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Quick answer
Dingcheng Liu is listed as Supplier Quality Engineer (SQE) and Regulatory Affairs at Exelint International, a company with 27 employees, based in Los Angeles, California, United States. AeroLeads shows a matched LinkedIn profile for Dingcheng Liu.
Dingcheng Liu previously worked as Member at Regulatory Affairs Professionals Society (Raps) and Regulatory Intern | D.K. Kim International Center for Regulatory Science at University Of Southern California. Dingcheng Liu holds Master'S Degree, Regulatory Science from University Of Southern California.
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Exelint International
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Profile bio
About Dingcheng Liu
I am a graduate student at University of Southern California pursuing a Master's in Regulatory Science, with a Doctoral of Pharmacy from Taipei Medical University.My Pharmacy background provides me with robust knowledge of diseases and treatments. Hospital rotations have gives me the clinical insights from both healthcare providers and patients, and realize there are numerous unmet medical needs. My experience in Medical Affair has allow me to combine all experience, enhancing my strategic thinking about the industry and competitors while polishing my skills in industry.I intend to pursue my career in Regulatory Affair to address the unmet medical needs and contribute to improving the health of our community.
Current workplace
Dingcheng Liu's current company
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Exelint International
11 roles
Dingcheng Liu work experience
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Member
Current
Sep 2024 - Present
Regulatory Intern | D.K. Kim International Center For Regulatory Science
Current- Reviewed Case report forms CRFs and clinical trial compliance, determined risk-based clinical trial monitoring plan
- Evaluated a 510K submission (eSTAR) and drafted responses to an FDA rejection letter within 180 days
- Determined accessories in a medical device and corrected the labeling
- Utilizing the FDA’s 510K database and registration database to develop a product strategy for a medical device
- Updated regulatory news and policies weekly and conducted regulatory intelligence research
Jan 2024 - Present
Regulatory Affair Intern | Team-Based Regulatory And Quality (Traqs) Experiential Projects
- Formulated a Predetermine Change Control Plan, including the modification, requirement, risk analysis, and test methods according to the FDA guidance and product description
- Proposed design changes for AI/ML device according to the device description and the FDA guidance
- Researched and utilized FDA guidance for machine learning and real-world data guidance (regulatory intelligence)
- Summarized current products that have implemented the AI Change Control Plan according to FDA & ISO guidance
- Document the meeting minutes, deliverables, guidance, and regulatory documents
Jan 2024 - May 2024
Medical Affairs Intern
- Co-organized two national academic seminars containing hundreds of physicians from the US, Vietnam, Singapore, and Taiwan.
- Created Canva materials about the latest research results and updates for the company’s product and distributed nationally
- Integrated worldwide conferences, including ASCO, WCLC, and ESMO, to educate internal sales in a quarterly meeting
- Translated regulations into different languages and updated them with the company
- Sent more than 30+ Medical Veeva Vaults and 10+ Commercial Veeva Vaults
Jul 2023 - Dec 2023
Researcher
- Constructed and conducted a single-center, controlled, retrospective study
- Reviewed and amended the study protocol accordingly and submitted annual reports to the IRB
- Collected study data through the electronic healthcare system and designed the data analysis plan
- Performed statistical analyses using SPSS, version 19 (SPSS, Chicago, IL, USA)
- Drafted an abstract and poster for the 2023 Congress of the Federation of Asian Pharmaceutical Associations (FAPA)
Jul 2022 - May 2023
Hostipal Intern Pharmacist
Training in Liver and Kidney Transplant Center
Mar 2023 - Apr 2023
Hospital Intern Pharmacist
Training in Neonatal/Pediatric Intensive Care Unit
Feb 2023 - Mar 2023
Hospital Intern Pharmacist
Training in Surgical Intensive Care Unit
Jan 2023 - Feb 2023
Hospital Intern Pharmacist
Taipei City Psychiatric Center
Training in Psychiatry center
Dec 2022 - Jan 2023
Hospital Intern Pharmacist
Training in Medical Intensive Care Unit, Infection and Oncology
Jul 2022 - Dec 2022
2 education records
Dingcheng Liu education
Master'S Degree, Regulatory Science
Doctor Of Pharmacy - Pharmd, Doctor Of Pharmacy
FAQ
Frequently asked questions about Dingcheng Liu
Quick answers generated from the profile data available on this page.
What company does Dingcheng Liu work for?
Dingcheng Liu works for Exelint International.
What is Dingcheng Liu's role at Exelint International?
Dingcheng Liu is listed as Supplier Quality Engineer (SQE) and Regulatory Affairs at Exelint International.
Where is Dingcheng Liu based?
Dingcheng Liu is based in Los Angeles, California, United States while working with Exelint International.
What companies has Dingcheng Liu worked for?
Dingcheng Liu has worked for Exelint International, Regulatory Affairs Professionals Society (Raps), University Of Southern California, Dexcom, and Boehringer Ingelheim.
How can I contact Dingcheng Liu?
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What schools did Dingcheng Liu attend?
Dingcheng Liu holds Master'S Degree, Regulatory Science from University Of Southern California.
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