Manufacturing Representative - Day Shift

Agilent Technologies•Frederick, MD

14d•$32 - $50

About The Position

Agilent is expanding on its oligonucleotide manufacturing capabilities with a new, purpose-built facility, designed to support the growing demand and innovation in therapeutic development— and we’re looking for Manufacturing Associates to help bring it to life! As part of the initial startup team, you’ll play a key role in commissioning, qualifying, and validating new equipment and systems. This role offers a unique opportunity to help establish the foundation of a world-class manufacturing operation and contribute to building and training future team members. We value employees who can quickly learn on the job, proactively anticipate and resolve manufacturing or delivery challenges, and consistently uphold the highest standards of quality. This is a hands-on, high-impact position ideal for someone who thrives in dynamic environments, enjoys solving complex problems, and wants to be part of something transformative.

Requirements

Associate’s or Bachelor’s degree in a scientific or technical field, or equivalent experience.
1+ years of experience in pharmaceutical or GMP manufacturing experience
Strong attention to detail and ability to follow SOPs and safety protocols.
Excellent documentation, math, and troubleshooting skills.
Mechanically inclined and comfortable working with complex equipment.
Demonstrated commitment to Agilent’s core values: uncompromising integrity, trust, respect, teamwork, focus, speaking up and accountability.

Nice To Haves

Familiarity with oligonucleotide synthesis, HPLC, UFDF, and lyophilization is a plus.
Experience in a chemical processing facility/PSM regulated environments/ clean room environments, or FDA-regulated manufacturing highly desired.

Responsibilities

Support commissioning, qualification, and validation (CQV) of new manufacturing equipment and systems.
Manufacture oligonucleotide APIs in a GMP-regulated environment.
Assist with tech-transfer and scale-up of new processes from Technical Services to Manufacturing.
Operate and maintain lab instruments such as spectrophotometers, conductivity meters, and auto-pipettors.
Write and revise SOPs and other documentation in compliance with regulatory standards.
Collaborate with Engineering, Validation, and Quality teams to resolve technical issues and support documentation (CAPAs, deviations, change controls).
Maintain, calibrate, and troubleshoot critical process equipment.
Help establish best practices and training materials for future team members.