🛠 Tech Stack

💼 About This Role

You'll coordinate GMP documentation activities to ensure compliance with regulatory guidelines. You'll manage the Document Control System and support audit documentation needs across all facility departments. This role is critical to ByHeart's renewed commitment to safety.

🎯 What You'll Do

• Coordinate GMP compliance activities across departments.
• Review, edit, and release GMP documentation.
• Manage the Document Control System (Intelex).
• Assist with documentation during audits.

📋 Requirements

• 5 years of hands-on QA in GMP manufacturing.
• College degree or BS, preferably in biological science.
• Fast, efficient user of MS Word and Excel.
• Adherence to CGMPs and safety policies.

✨ Nice to Have

• Experience with electronic document control systems.
• Strong troubleshooting and problem-solving skills.
• Attention to detail.

🎁 Benefits & Perks

• 🏖️ Paid time off
• 🩺 Health insurance
• 📈 Retirement plans

📨 Hiring Process

Estimated timeline: 3-5 weeks · AI estimate

1. 1Application Review· 1-2 weeks
2. 2Phone Screen· 30 min
3. 3Interview· 1 hour
4. 4Offer· 1 week