JOB DESCRIPTION

Join Agilent’s mission to advance scientific discovery and improve lives. As a Manufacturing Quality Assurance Engineer, you’ll play a meaningful role in maintaining the highest standards of quality and compliance in our oligonucleotide production facility. This is a phenomenal opportunity to support real-time manufacturing operations, give to continuous improvement initiatives, and ensure product and process integrity in a GMP-regulated environment.
Shift: Onsite | Wed-Sat 9:00AM – 6:00 PM (10-hour shift)

QUALIFICATIONS

• Bachelor’s or Master’s degree in a relevant scientific or engineering field.
• 1+ year of experience in a quality assurance or regulated manufacturing environment.
• Proven understanding of GMP standards and quality system regulations (e.g., FDA, ISO).
• Experience with batch record review and supporting real-time floor operations preferred.
• Self-motivated, detail-oriented, and collaborative with strong communication skills.
• Oligonucleotide manufacturing experience is a plus.
• Post-graduate certification or license may be required.

• Provide real-time, on-the-floor quality support during manufacturing operations to ensure product compliance with internal standards and external regulations (e.g., FDA, ISO).
• Review executed batch records and in-process documentation to support timely API release.
• Collaborate multi-functionally with Manufacturing, Materials, Quality Control, Engineering, and Facilities teams to address quality issues and drive resolution.
• Contribute to problem-solving efforts and process improvements within defined objectives and growing responsibility.
• Support internal audits, documentation practices, and adherence to GMP and quality system requirements.
• Actively participate in team projects, share expertise, and help mentor less expert team members.