🛠 Tech Stack

💼 About This Role

You'll lead automation strategy and lifecycle management for Ignition SCADA and PLC systems in GMP-regulated biopharma environments. Your work ensures system reliability, compliance, and audit readiness across client engagements. This role offers the opportunity to mentor junior staff and drive digital transformation initiatives.

🎯 What You'll Do

• Lead development and review of automation system documentation.
• Author and execute validation documentation including IOQs and protocols.
• Perform advanced data reviews including alarm rationalization.
• Manage automation change records and coordinate maintenance activities.
• Serve as senior liaison between Facilities, Quality, IT, and external vendors.

📋 Requirements

• 7-11 years in GMP-regulated biotech or pharmaceutical environments.
• Hands-on experience with Ignition SCADA/HMI development and scripting.
• PLC-level programming with Rockwell ControlLogix or CompactLogix.
• Extensive background in GMP documentation, validation, and CSV/SDLC processes.

✨ Nice to Have

• BS or MS in Engineering, Life Sciences, or related technical field.
• Exposure to modern digital or MES-lite stacks such as Ignition Perspective or Sepasoft modules.
• Experience with BAS/BMS, EMS, or process automation platforms.

🎁 Benefits & Perks

• 🏖️ Best Places to Work award winner for third consecutive year
• 📈 Career growth and development opportunities
• 💰 Financial rewards and competitive compensation
• 🌟 Culture of innovation and positive work environment
• 🌍 Global impact in life-saving drug development

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter Screen· 30 min
2. 2Hiring Manager Interview· 60 min
3. 3Technical Interview· 60 min

🚩 Heads Up

• Travel up to 100% to client sites may be required
• Responsibilities list is extensive, potentially indicating role creep