Analytical Chemist

Description du poste

Our client, an innovative biotech company operating on a lean, virtual structure in Basel, is seeking a highly autonomous Analytical Chemist Responsible Person for an urgent 6-month mission. This is a 100% desk-based / virtual oversight role. The company has no internal laboratory facilities. You will not perform hands-on lab work, but will entirely manage external partners and data. Key Responsibilities: CDMO Oversight: Act as the primary analytical responsible person for the tracking, troubleshooting, and weekly management of external CDMOs (including managing technical transfers). Phase-Appropriate Strategy: Define and execute analytical strategies according to ICH guidelines for both Drug Substance (API) and Drug Product from preclinical through Phase I/II programs. Data & Documentation: Review and evaluate raw HPLC / MS data coming from external partners. Author and review quality documentation, method validation protocols, stability studies, and release records. Cross-functional Collaboration: Work closely within a flat structure alongside Process Chemists to ensure seamless project advancement. Requirements: Core Scientific Expertise: Deep professional background strictly in Small Molecules / Synthetic Chemistry (API and Final Product). Education: PhD with 4-7 years of industry experience, or MSc with 6-10+ years of experience in the pharmaceutical or biotech sector. CDMO Management: Minimum of 2 years of direct, hands-on experience in outsourcing, tech transfer, and managing external contract manufacturing organizations (CDMOs/CROs). Technical Data Review: Strong proficiency in evaluating HPLC / MS data and phase-appropriate validation protocols without needing laboratory access. Soft Skills & Availability: High level of independence, excellent communication skills in English (100% fluency required), and immediate availability to start. Luciana Sardo