Job Description

Agilent's Manufacturing team is seeking a Quality Assurance Engineer to join their team! The QA Engineer ensures that high quality products are designed, engineered and manufactured by Agilent, in conformance with required standards and regulations. In this position, quality, product regulation, and compliance positions may be in either the field or factory. In the field, they will act as a liaison between customers, distributors, authorities and Agilent's Factory Quality/Product Regulation & Compliance team.

Day-to-day responsibilities include working on quality department assignments with clearly defined objectives such as:

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 | Mon-Thurs, 8:00 PM - 6:30 AM (10-hour shift; flexible with discussion)

Key Responsibilities

• 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.
• Role requires this team member participates in an on call rotational schedule as part of the engineering quality team.

Qualifications

Job Posting Qualifications

• Bachelor's or Master's degree in a relevant scientific or engineering field.
• 2+ 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.

Additional Details

This job has a full time weekly schedule. Applications for this job will be accepted until at least June 30, 2026 or until the job is no longer posted.

The full-time equivalent pay range for this position is $82,480.00 - $128,875.00/yr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locations

Travel Required:
No

Shift:
Day

Duration:
No End Date

Job Function:
Quality/Regulatory