💼 About This Role

You'll lead technology transfer and process validation for batch manufacturing in a pharmaceutical environment. You'll serve as the key technical liaison between R&D, Operations, and Quality to ensure seamless scale-up from development to commercial production.

🎯 What You'll Do

• Oversee pilot-scale GMP production and process optimization
• Lead process validation activities including protocol and report writing
• Conduct root cause investigations and contribute to CAPA development
• Collaborate with cross-functional teams to transition products to commercialization

📋 Requirements

• Bachelor's degree in Chemical Engineering or related field
• 3-5 years of experience managing projects from development to commercialization
• Strong data analysis and problem-solving skills
• Technical writing experience (protocols, reports, documentation)

✨ Nice to Have

• Experience in pharmaceutical, cosmetic, or personal care manufacturing
• Understanding of GMP requirements

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter screen· 30 min
2. 2Hiring manager interview· 45 min
3. 3Technical interview· 60 min