Manufacturing Representative - Night Shift
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 building and training future team members. This hands-on role involves manufacturing oligonucleotide APIs in a GMP-regulated environment and supporting process transfer and scale-up. The position requires adaptability, problem-solving, and a consistent commitment to quality and safety. Candidates train on a weekday day schedule of 5x8, Monday–Friday, 8 am–5 pm, and then transition to a night shift based on business needs. The role is full-time. The full-time equivalent pay range is $34.00–$53.13 per hour, with eligibility for bonus, stock, and benefits; actual pay depends on work location and job-related skills, experience, and education or training. No travel is required.
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.
- Demonstrated commitment to Agilent’s core values: uncompromising integrity, trust, respect, teamwork, focus, speaking up, and accountability.
- Willingness to work a weekday day schedule during training and transition to night shift based on business needs.
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 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 CAPAs, deviations, and change-control documentation.
- Maintain, calibrate, and troubleshoot critical process equipment.
- Help establish best practices and training materials for future team members.
Benefits
- Eligibility for bonus, stock, and benefits.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
Associate degree
