Pharma Contracts Paralegal — IP, cGMP & Compliance

ten23 health; Basel; Vor Ort; CHF 90.000 - 130.000; Vollzeit

Benefits dieser Stelle

Career development opportunity

Flexible working arrangements

Learning culture & training options

Competitive pension plan

Annual bonus

Zusammenfassung

ten23 health in Basel seeks an experienced Paralegal to support the legal and business teams in drafting, reviewing, and tracking a high volume of commercial contracts. You will ensure compliance with cGMP and pharma regulations, manage IP boundaries, and navigate tech transfer and manufacturing liabilities in a B2B setting.

The role emphasizes collaboration across QA, quality, and regulatory functions, with responsibilities spanning MSAs, SOWs, NDAs, and quality agreements, and ensuring

Qualifikationen

• Bachelor’s degree or Associate’s degree with a Paralegal Certificate.
• 3 years minimum in-house legal experience, ideally in a CDMO/CRO or life sciences environment.
• Proficiency with Ironclad, Conga, or DocuSign CLM.
• Familiarity with FDA 21 CFR regulations and global equivalents.
• Ability to bridge scientific, quality, business development, and legal teams.

Aufgaben

• Draft and negotiate foundational agreements: MSAs, SOWs, NDAs, and Quality Agreements.
• Manage the contract lifecycle from intake to approvals, signatures, and expirations.
• Standardize and update contract templates to reflect evolving pharma laws.
• Support cGMP compliance and regulatory inspections readiness.
• Protect IP by distinguishing Background IP and Foreground IP.
• Review tech transfer documentation between client and CDMO.
• Coordinate with QA and legal to resolve contract disputes.
• Track corporate filings and maintain facility licenses.

Jobbeschreibung

ten23 health in Basel seeks an experienced Paralegal to support the legal and business teams in drafting, reviewing, and tracking a high volume of commercial contracts. You will ensure compliance with cGMP and pharma regulations, manage IP boundaries, and navigate tech transfer and manufacturing liabilities in a B2B setting.

The role emphasizes collaboration across QA, quality, and regulatory functions, with responsibilities spanning MSAs, SOWs, NDAs, and quality agreements, and ensuring