Quality Control Analyst
About The Position
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. Agilent Technologies, Inc. is looking to add a Quality Control Analyst to its high-performance quality team working at the state-of-the-art, contract API manufacturing facility that specializes in Nucleic Acid Chemistries located in Frederick, Colorado. The world's most revolutionary biopharma companies are partnering with Agilent Technologies to advance the next frontier of medicine. Agilent continues to invest in the 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, life-saving medicines. This position coordinates and conducts routine and non-routine testing to support process water monitoring, environmental monitoring, and compressed gas monitoring. Responsibilities also include testing to support cleaning verification for equipment release to support manufacturing activities. Understanding and experience with Standard Operating Procedures, current Good Manufacturing Practices (cGMPs), and other regulatory requirements are required. The QC Analyst will also work on complex problems to drive improvement. Experience with in-process analysis utilizing analytical instrumentation for UV Analysis, HPLC, and HPLC-MS is preferred. The ability to support occasional weekend and evening work is required. Shift: Monday to Friday, 8:00 am to 4:30 pm
Requirements
- A Bachelor's degree (B.S.) or equivalent in Chemistry or related life sciences field; or equivalent combination of education and experience
- 0-2 years of relevant experience within the Industry
- Exposure and knowledge of FDA regulations and guidelines
- Knowledge of cGMP guidelines or international regulations (i.e., International Committee on Harmonization (ICH) Q7)
- Knowledge of analytical equipment and instrumentation utilized for the testing of in-process samples, raw materials, and microbiological samples
- Proficient with Microsoft Word, Excel, and Chemstation
- The ability to support occasional weekend and evening work is required.
Nice To Haves
- Experience with in-process analysis utilizing analytical instrumentation for UV Analysis, HPLC, and HPLC-MS
- Familiarity with the following laboratory disciplines is highly desired.
- Solution Preparation
- UV analysis
- HPLC
- HPLC-MS
Responsibilities
- Coordinates and conducts routine and non-routine testing to support process water monitoring, environmental monitoring, and compressed gas monitoring.
- Testing to support cleaning verification for equipment release to support manufacturing activities.
- Work on complex problems to drive improvement.
Benefits
- full time weekly schedule
- eligibility for bonus, stock and benefits
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
