Agilent Technologies

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. The Quality Control Analyst: Conducts routine and non-routine analysis of raw materials and in-process and finished formulations according to standard operating procedures Performs analyses, including biochemical and/or chemical analyses of products, analysis of raw materials, in-process items and finished products to ensure stability according toa established operating procedures Compiles data for documentation of test procedures that may include biochemical and chemical assays, stability program testing and formulation studies Calibrates and maintains lab equipment Participates in the...

Job Description : 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](https://www.agilent.com/){rel="noopener noreferrer" target="_blank"} . We are currently hiring a Document Control II to join our team in Frederick, CO. Responsibilities: Handles the document lifecycle using the site Training and Document Management System (TMS) Maintains all document files as related to Agilent NASD and assists in the archival of documents at the offsite storage location Issues and reconciles controlled documentation including logbooks, notebooks, controlled forms, batch records, and protocols...

Job Description : Job Description Conducts routine and non-routine analysis of raw materials and in-process and finished formulations according to standard operating procedures. Performs analyses, including biochemical and/or chemical analyses of products, analysis of raw materials, in-process items and finished products to ensure stability according to established operating procedures. Compiles data for documentation of test procedures that may include biochemical and chemical assays, stability program testing and formulation studies. Calibrates and maintains lab equipment. Participates in the preparation of investigations, summaries and reports. May develop testing methods. Reviews data obtained for compliance to specifications and reports abnormalities. Revises and updates standard operating procedures as needed. May perform special projects on analytical and instrument problem-solving. Shift schedule: Monday to Friday Shift hours: 1:30 pm to...

Job Description Performs a variety of quality duties to support expansion of Frederick manufacturing operations. Improves documentation, processes and applications to meet agreed-upon objectives. Participates actively in creation and approval of equipment and process SOPs, related documentation, and new product introduction. Supports and implements the transition of products and manufacturing processes from prototype to full production and through the entire life cycle of the product. In a process environment, interfaces with the process materials and adheres to safety guidelines. Partners with material management, quality peers, planning and procurement, manufacturing, and technical services to create and improve products and processes to meet expansion and production timelines, quality policies, and customer expectations. Utilizes digital solutions to optimize and maintain state of the art manufacturing processes. May be required to use continuous improvement...

Job Description Conducts routine and non-routine analysis of raw materials and in-process and finished formulations according to standard operating procedures. Performs analyses, including biochemical and/or chemical analyses of products, analysis of raw materials, in-process items and finished products to ensure stability according to established operating procedures. Compiles data for documentation of test procedures that may include biochemical and chemical assays, stability program testing and formulation studies. Calibrates and maintains lab equipment. Participates in the preparation of investigations, summaries and reports. May develop testing methods. Reviews data obtained for compliance to specifications and reports abnormalities. Revises and updates standard operating procedures as needed. May perform special projects on analytical and instrument problem-solving. Shift Days: Sunday thru Thursday Shift Hours: 8:00 pm to 4:30 am...