1+ years of related experience in a pharmaceutical manufacturing environment preferred but not required
Previous knowledge of oligonucleotide synthesis, purification, UF, conjugation, and lyophilization is advantageous
Detail oriented and can perform technical duties following standard operating procedures and general laboratory safety rules
Ability to work both independently and in a team setting on a variety of projects and use individual discretion to meet required project objectives and deadlines
Excellent math, documentation, communication and operational trouble shooting skills
Mechanically inclined
Ability to work as a successful member of a team working to establish priorities, scheduling, and procedures that collectively will meet department goals and project deadlines
Ability to work in a clean room environment
Previous experience in a FDA regulated manufacturing environment highly desired
Additional Details
This job has a full time weekly schedule. Applications for this job will be accepted until at least June 15, 2026 or until the job is no longer posted.
Travel Required:
No
Shift:
Morning
Duration:
No End Date
Job Function:
Manufacturing
Benefits
Equity / stock optionsPerformance bonus
Additional Information
Job Description
Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications and expertise. Agilent enables customers to gain the answers and insights they seek so they can do what they do best: improve the world around us. Information about Agilent is available at www.agilent.com .
The world's most revolutionary biopharma companies are partnering with Agilent Technologies to advance the next frontier of medicine. Agilent continues to invest in capacity and expansion of its Colorado operations. Join our team of professionals dedicated to the development and commercialization of nucleic acid therapeutics for life changing, lifesaving medicines.
Key responsibilities include:
Actively involved in the manufacturing of oligonucleotide APIs in a GMP environment.
Actively involved in aspects of technology transfer and scale-up of oligonucleotide manufacturing processes delivered from Manufacturing Technical Services into Manufacturing.
Write and revise standard operating procedures according to regulatory and procedural guidelines.
Work with Validation and Engineering personnel to validate new equipment and facilities.
Work with Manufacturing Management and Quality to resolve manufacturing problems including drafting quality documentation (CAPA, deviation, change control, etc.).
Maintain, calibrate, and trouble shoot critical process equipment.
Shift details:
The schedule will be Night shift (4:30 PM - 5:00 AM) working a Pitman schedule: of 2 days working, 2 days off, 3 days working, 2 days off, 2 days working, then 3 days off.
Agilent · CO Frederick