ManufacturingRepresentative-WeekendShift

## **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](http://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 HOURS:** Friday-Sunday 4:30am to 5:30 pm ## ## **Qualifications** * BS in chemistry, biology, biochemistry, science or equivalent or equivalent combination of education and or experience preferred but not required * 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 * D