🛠 Tech Stack

💼 About This Role

You'll support GMP compliance for oral solid dosage drug products by reviewing production records, analytical data, and internal QA documentation. You'll conduct investigations, support audits, and ensure regulatory standards are met. This role offers generous PTO, low-cost health benefits, and a vested 5% 401(k) contribution.

🎯 What You'll Do

• Review and approve batch production and QC records
• Initiate and oversee investigations and CAPAs
• Support internal and client audits and regulatory inspections
• Manage controlled document issuance and archival

📋 Requirements

• Bachelor's degree in a scientific discipline
• 3 years GMP experience in QC or QA for Associate II
• Knowledge of FDA regulations for clinical trial materials
• Pharmaceutical manufacturing experience required

✨ Nice to Have

• Commercial GMP knowledge
• Oral solid dosage experience

🎁 Benefits & Perks

• 🏖️ Generous PTO accrual
• 🏥 Low-cost health benefits
• 💰 5% 401(k) contribution (no match or vesting required)

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Phone Screen· 30 min
2. 2Hiring Manager Interview· 45 min
3. 3On-site Interview· 2 hours