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Legal Counsel - Pharmaceutical Manufacturing

10 hours, 36 minutes ago
United States
Full-time
Mid Level
Legal Counsel
Legal
Apply Now
Telix Pharmaceuticals

Telix Pharmaceuticals

Telix Pharmaceuticals is a global biopharmaceutical firm dedicated to the development and commercialization of diagnostic and therapeutic products that utilize targeted radiation, aiming to enhance treatment decisions and provide personalized therapies...

Pharmaceuticals
201-500
Founded 2015
View All Jobs 31

Description

  • Draft, review, and negotiate manufacturing services agreements, MSAs, quality agreements, supply contracts, statements of work, and change orders.
  • Identify cGMP, import/export, manufacturing-regulatory, and facility-compliance issues, escalating complex matters as appropriate.
  • Manage first-line contract disputes, warranty claims, quality matters, and service-level remediation issues.
  • Develop and improve contract templates, clause libraries, playbooks, and fallback positions with Legal Enablement.
  • Partner with Operations, Quality, Procurement, Finance, and Commercial teams on manufacturing contracting matters.
  • Use and enhance contracting intake workflows, escalation matrices, and process tools for high-volume agreements.
  • Monitor pharmaceutical manufacturing regulations, industry practices, and developments in quality and supply-chain law.
  • Support procurement, isotope supply, logistics, distribution, and other operational services agreements as assigned.

Requirements

  • Juris Doctor (JD), Bachelor of Laws (LLB), or equivalent legal qualification, with admission or eligibility to practice in the relevant jurisdiction.
  • 6+ years of legal experience in commercial, manufacturing, supply chain, or transactional law.
  • Experience in pharmaceutical, biotechnology, medical device, or healthcare sectors preferred.
  • Strong contract drafting and negotiation skills and experience managing high volumes of commercial contracts.
  • Experience with manufacturing services agreements, supply-chain contracts, quality agreements, or services contracting.
  • Familiarity with cGMP, FDA/TGA manufacturing compliance, or pharmaceutical quality frameworks (preferred).
  • Prior in-house experience preferred; relevant life sciences transactional law-firm experience considered.
  • Strong commercial judgment, attention to detail, communication, and cross-functional collaboration skills.
  • Ability to work effectively in a dynamic environment under supervision while developing greater autonomy.
  • Commitment to quality, safety, ethical conduct, process improvement, and continuous learning.

Benefits

  • Competitive salary.
  • Annual performance-based bonus.
  • Equity-based incentive program.
  • Generous vacation.
  • Paid wellness days.
  • Learning and development support.
  • Hybrid and remote work opportunities.

Interested in this position?

Apply directly on the company website

Apply Now

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