Manufacturing Quality Engineer (Nights)

Agilent seeks a Manufacturing Quality Engineer to support launch and operations of a new oligonucleotide manufacturing facility. The role involves quality assurance oversight, batch record review, documentation compliance, and cross-functional collaboration in a cGMP-regulated environment.

Responsibilities

• Provide quality assurance guidance and support for process, data, and product quality in cGMP manufacturing
• Review batch records and supporting cGMP documentation for compliance with procedures and regulatory requirements
• Review and approve quality-related documentation for Manufacturing, Materials Management, and other site functions
• Support validation activities, change control, nonconformance investigations, and CAPA initiatives
• Maintain documentation in electronic quality systems and utilize SAP, LIMS, and related business platforms

Requirements

• Bachelor's degree in science, engineering, or related field
• Minimum 2 years quality assurance experience in cGMP-regulated environment
• Batch record review and GMP documentation review experience
• Knowledge of quality systems: deviations, CAPAs, change controls, document management
• Cross-functional operations support in regulated manufacturing
• Strong attention to detail, communication, and problem-solving skills
• Ability to work day shift for 3–6 months during training period

Compensation: $67,760–$105,875 per year plus bonus, stock, and benefits eligibility