ten23 health is a human-centric and sustainable strategic partner of choice for the pharmaceutical industry and biotech start-ups for the development, manufacture, and testing of tomorrow’s medicines. We support our clients in developing differentiated, stable, usable, and safe injectable treatments for patients. 80–100% FTE I Basel We are looking for a Paralegal supports the legal and business teams by drafting, reviewing, and tracking a high volume of commercial contracts. They ensure compliance with strict pharmaceutical regulations (FDA, EMA, cGMP) and safeguard proprietary client data and technology. Unlike general paralegals, this role requires a deep understanding of the tech transfer process, manufacturing liabilities, and intellectual property (IP) boundaries in a business-to-business (B2B) setting. Your responsibilities will include, Contract Management & Drafting Draft and negotiate foundational agreements: Handle Master Services Agreements (MSAs), Statements of Work (SOWs), Non-Disclosure Agreements (NDAs), and Quality Agreements. Manage the contract lifecycle: Oversee the legal database from initial intake and drafting through approvals, electronic signatures, and expiration alerts. Standardize templates: Create, Maintain and update standard contract templates to adapt to changing pharmaceutical laws and corporate policies. Regulatory & Corporate Compliance Support cGMP compliance: Ensure all contract terms align with Current Good Manufacturing Practices (cGMP) and health authority regulations. Audit preparation: Assist internal quality teams in prepping documentation for client audits or regulatory inspections (e.g., FDA inspections). Corporate governance: Assist with corporate secretarial duties, including organizing board minutes, maintaining entity registrations, and managing operational licenses. IP Protection & Technical Support Safeguard intellectual property: Ensure contracts clearly distinguish between "Background IP" (what the client or CDMO owned before working together) and "Foreground IP" (new formulations or methods developed during the DP process). Tech transfer documentation: Review legal documentation related to the transfer of manufacturing processes from the client to the CDMO facility. Day-to-Day Tasks Reviewing a new SOW for a client's phase clinical trial drug product batch filling to ensure the timelines, pricing, and liabilities match the master agreement. Liaising between the Quality Assurance (QA) team and the client's legal counsel to resolve a dispute over a clause in a Quality Agreement. Tracking corporate filings for multiple manufacturing sites and labs to keep facility licenses current. Managing the legal intake portal, prioritizing contract requests based on manufacturing timelines and slot availability. We are looking for a motivated and committed professional who is ready to actively grow with us, combining in-depth technical knowledge with a pronounced cooperative spirit. The ideal candidate possesses: Bachelor’s degree or an Associate’s degree with a Paralegal Certificate. 3 years minimum in-house legal experience, ideally within a CDMO, CRO (Contract Research Organization), or a broader life sciences/biotech environment. Proficiency with tools like Ironclad, Conga, or DocuSign CLM. Basic understanding of the drug development lifecycle, specifically "Drug Product" (vials, cartridges, syringes, tech transfers) versus "Drug Substance" (API manufacturing). Familiarity with FDA 21 CFR regulations and global equivalents. Essential for catching conflicting terms between MSAs and Quality Agreements. Ability to act as a bridge between scientific, quality, business development, and legal teams.