🛠 Tech Stack

💼 About This Role

You'll lead engineering analyses of inspection and production data to assess product performance and identify quality issues. Your core impact includes conducting quality investigations and implementing corrective actions. This role offers exposure to clinical laboratory regulations in a hybrid work environment.

🎯 What You'll Do

• Leads engineering analyses of inspection and production data to assess product performance.
• Conducts quality investigations, root cause analysis, and corrective actions.
• Develops or updates qualification and inspection criteria and quality procedures.
• Evaluates nonconforming materials and coordinates disposition activities.

📋 Requirements

• Bachelor's degree in Engineering, Quality, or related technical discipline.
• 2–5 years of relevant quality, manufacturing, or engineering experience.
• Knowledge of GMP quality management systems (e.g., ISO 13485).
• Proficiency in root cause analysis and CAPA.

✨ Nice to Have

• Effective project and time management abilities.
• Skilled in statistical analysis and quality tools (SPC, Minitab).
• Ability to work independently and collaboratively.

🎁 Benefits & Perks

• 🏖️ Hybrid work environment
• 💵 Competitive compensation
• 🏥 Health insurance
• 📈 401(k) matching

📨 Hiring Process

Estimated timeline: 3-5 weeks · AI estimate

1. 1Recruiter Phone Screen· 30 min
2. 2Hiring Manager Interview· 45 min
3. 3Technical Interview· 60 min
4. 4Offer· N/A