Manufacturing Engineer

Responsibilities

• Transfer and scale-up new processes from Chemical Development into Manufacturing
• Write and review process documentation, including master batch records, data capture forms, and automated equipment methods
• Manage change control records (CC), risk assessments (RA), CAPA, and effectiveness verification (EV) to maintain cGMP compliance
• Provide real-time troubleshooting and problem-solving for manufacturing processes and equipment
• Lead or participate in investigations of major process deviations and assist Quality Assurance with root cause identification
• Coordinate the revision of Standard Operating Procedures (SOPs) to support new process implementation
• Review and approve technical transfer documents to ensure compatibility with manufacturing systems

Requirements

• Bachelor's degree in chemistry, biology, engineering, or a related life science field
• 2+ years of relevant professional experience
• Proven technical writing experience

Preferred Qualifications

• Prior experience in a GMP manufacturing facility
• Experience with large-scale pharmaceutical or biopharmaceutical manufacturing unit operations
• Experience coordinating and participating in interdepartmental project teams
• Knowledge of regulatory agencies and associated audits

About the Company

Agilent is a global leader in laboratory and clinical technologies, passionate about bringing great science to life. We provide advanced instruments, software, and consumables that support cutting-edge life science research, patient diagnostics, and the safety of food, water, and pharmaceuticals. With over 50 years of expertise and 18,000 employees worldwide, we work collaboratively to provide trusted answers to the world's most critical scientific challenges.