The example in full
Wei Lin Tan
Staff Scientist, Bioanalytical Development
Singapore · weilin.tan@example.com · +65 8200 4417
Summary
Staff scientist with 9 years in bioanalytical R&D, currently leading method development and validation for a clinical-stage portfolio. Runs the assays, owns the regulatory documentation behind them, and keeps enough bench time to stay technically credible with the team.
Experience
Staff Scientist, Bioanalytical Development, Sengkang Therapeutics
06.2022 – Present
- Lead method development, transfer and validation for four clinical programmes, from assay design through regulatory submission support.
- Validated 9 GLP-compliant LC-MS/MS and ELISA methods, all accepted by the regulator without a follow-up query.
- Cut assay turnaround 40% by automating sample preparation on a liquid handler and rewriting the data pipeline in Python.
- Support three IND-enabling packages, authoring the bioanalytical sections and responding to agency questions.
- Supervise four scientists and two research associates, including training, review and technical escalation.
- Chair the monthly cross-functional review with quality, programme management and the clinical team.
Senior Scientist, Aurora Biologics
03.2019 – 05.2022
- Developed and qualified immunoassays for biomarker discovery across six preclinical programmes.
- Introduced electronic lab notebook practice across the department, cutting data reconstruction time during audits.
- Co-authored 4 peer-reviewed papers and two internal white papers.
Scientist, Aurora Biologics
02.2017 – 02.2019
- Ran routine cell-based potency assays and contributed to two method transfers between sites.
Education
- Ph.D. Biochemistry, National University of Singapore — 08.2012 – 12.2016
- B.Sc. (Hons) Life Sciences, National University of Singapore — 08.2008 – 05.2012
Skills
LC-MS/MS method development · Immunoassays (ELISA, MSD) · GLP method validation · Regulatory documentation (IND) · Lab automation (liquid handlers) · Python data analysis · Cell culture · Cross-functional collaboration · Team leadership (6 reports) · Technical writing · Quality & compliance
