💼 About This Role

You'll lead cGMP commissioning and qualification projects for life sciences clients in Australia. You'll manage mid- to large-scale projects ensuring compliance and timely delivery. This role offers exposure to cutting-edge therapies and employee-ownership culture.

🎯 What You'll Do

• Manage mid-sized to large CQV projects for process equipment and clean utilities.
• Lead design review, site acceptance, and equipment installation.
• Write, review, and approve CQV documents per 21 CFR standards.
• Allocate project resources and track progress against schedule.

📋 Requirements

• 5+ years of Commissioning, Qualification, Validation experience in life sciences.
• BS or MS in a relevant science or engineering field or equivalent experience.
• Sound technical knowledge of TGA and global regulatory requirements.
• Proficient in cGMP standards.

✨ Nice to Have

• Automation PM experience.
• Experience in biotech, aseptic processing, fill/finish, OSD, or gene therapy.

🎁 Benefits & Perks

• 💰 Highly Competitive Salary
• 📚 Continuing education (internal and external)
• 🔬 Cutting-edge projects in a highly evolving field
• 🏢 Employee-ownership culture