🛠 Tech Stack

💼 About This Role

You'll support the international roll-out of a prostate cancer imaging agent by developing and validating analytical methods in a GMP-regulated radiochemistry lab. Your work ensures product quality and regulatory compliance for a fast-growing radiopharmaceutical company.

🎯 What You'll Do

• Conduct analytical testing (HPLC, TLC, spectroscopy) on radiopharmaceuticals.
• Lead technical transfer of analytical methods from vendors to GMP.
• Plan and execute experiments to support research objectives.
• Maintain compliance with safety, GLP, and regulatory requirements.

📋 Requirements

• BS + 5 years, MS + 3 years, or PhD + 2 years experience.
• Proficient use of Open Lab or similar analytical chemistry software.
• Experience writing and reviewing SOPs and reports.
• Operate in a regulated GMP environment.

✨ Nice to Have

• Experience handling radioactive material.
• Experience with HPLC or ICP instrument maintenance.
• Hosting or supporting external audits.

🎁 Benefits & Perks

• 💰 Competitive salary and annual performance bonuses.
• 📈 Equity-based incentive program.
• 🏖️ Generous vacation and paid wellness days.
• 📚 Support for learning and development.
• 🌍 Hybrid and remote work options.