Manufacturing Associate, Representative (Night Shift)
Quick Summary
Actively involved in the manufacturing of oligonucleotide APIs in a GMP environment.
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.
Responsibilities
~1 min read- →
Actively involved in the manufacturing of oligonucleotide APIs in a GMP environment.
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Actively involved in aspects of technology transfer and scale-up of oligonucleotide manufacturing processes delivered from Manufacturing Technical Services into Manufacturing.
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Write and revise standard operating procedures according to regulatory and procedural guidelines.
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Work with Validation and Engineering personnel to validate new equipment and facilities.
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Work with Manufacturing Management and Quality to resolve manufacturing problems including drafting quality documentation (CAPA, deviation, change control, etc.).
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Maintain, calibrate, and trouble shoot critical process equipment.
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.
Requirements
~1 min readHSD or higher education
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
Location & Eligibility
Listing Details
- Posted
- June 11, 2026
- First seen
- July 6, 2026
- Last seen
- July 6, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 13%
- Scored at
- July 6, 2026
Signal breakdown
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