Resume Checker for Biotechnology & Biomedical Scientists

Pharmaceutical and biotech companies use Greenhouse, Lever, and Workday to screen thousands of candidates. ATS filters are technique-specific — each lab method is a separate keyword. Common biotech resume issues: • "Lab experience" without naming specific techniques (CRISPR, HPLC, mass spectrometry) • Missing GMP/GLP compliance keywords — binary requirements for regulated roles • No regulatory context (FDA, EMA, ICH guidelines) • Scale not specified — bench-scale vs. pilot-scale vs. commercial-scale signals seniority

Our AI checks for: • Techniques: CRISPR-Cas9, PCR/qPCR, gel electrophoresis, Western blot, ELISA, flow cytometry • Analytical: HPLC, mass spectrometry, NMR, UV-Vis, chromatography • Cell biology: cell culture, transfection, iPSC, CHO cells, bioreactor • Regulatory: GMP, GLP, FDA, EMA, ICH, IND filing, NDA, clinical trials • Process: upstream processing, downstream processing, purification, formulation • Software: ELN (Benchling, IDBS), LIMS, JMP, Prism, R, Python • Products: monoclonal antibodies, mRNA, gene therapy, biosimilars, ADC

1. Lead with regulatory compliance — GMP/GLP are binary pass/fail filters at pharma companies 2. List laboratory techniques individually — don't combine them under "lab skills" 3. Specify scale: "50L pilot scale" or "2000L commercial bioreactor" 4. Name analytical instruments with models if possible (Agilent 1260 HPLC, BD FACSAria) 5. Include therapeutic area: oncology, immunology, rare disease, neuroscience 6. Reference ELN and LIMS systems — increasingly weighted in modern lab roles

Research Scientist (Discovery): • Target identification, assay development, HTS, SAR analysis • Molecular biology: cloning, gene editing, protein expression, cell-based assays Process Development: • Upstream: cell line development, media optimisation, bioreactor scale-up • Downstream: chromatography, filtration, formulation, lyophilisation Quality Control / Quality Assurance: • Release testing, stability studies, OOS investigations • GMP documentation: SOPs, batch records, deviation reports, CAPA Regulatory Affairs / Clinical: • IND/NDA submissions, clinical protocol writing, FDA interactions • Phase I-III trial support, data packages, regulatory strategy