Manufacturing Representative - Night Shift

Agilent Technologies•Frederick, CO

7d•$34 - $53

About The Position

Agilent is expanding its oligonucleotide manufacturing capabilities with a new purpose-built facility. As part of the initial startup team, the Manufacturing Representative will help commission, qualify, and validate new equipment and systems; establish the foundation of the manufacturing operation; and contribute to training future team members. This hands-on role involves manufacturing oligonucleotide APIs in a GMP-regulated environment and supporting process transfer, scale-up, equipment readiness, and operational best practices. The position is suited to someone who learns quickly, anticipates and resolves manufacturing or delivery challenges, and upholds high standards of quality. The role begins with day-shift training on a standard Monday–Friday, 8 a.m.–5 p.m. schedule. After training, the employee will transition to a night shift according to business needs; the listed night-shift options are 1600–0630, either Monday–Wednesday or Wednesday–Friday. This is a full-time position with no end date. The full-time equivalent pay range is $34.00–$53.13 per hour, plus eligibility for bonus, stock, and benefits. Pay within the range depends on work location and job-related skills, experience, and relevant education or training.

Requirements

Associate’s or Bachelor’s degree in a scientific or technical field, or equivalent experience.
At least 1 year of experience in pharmaceutical or GMP manufacturing.
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.
Must be willing to work day shift during training and transition to a night shift based on business needs.
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.
Experience in a chemical processing facility, PSM-regulated environment, clean room environment, or FDA-regulated manufacturing.

Responsibilities

Support commissioning, qualification, and validation (CQV) of new manufacturing equipment and systems.
Manufacture oligonucleotide APIs in a GMP-regulated environment.
Assist with technology transfer and scale-up of new processes from Technical Services to Manufacturing.
Operate and maintain lab instruments, including 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, including CAPAs, deviations, and change controls.
Maintain, calibrate, and troubleshoot critical process equipment.
Help establish best practices and training materials for future team members.