5 cleaning technician jobs found in Frederick, CO

As a * Manufacturing Associate (Associate), * you will check and schedule resources to ensure on-time delivery. You will help to maintain a clean organized site for cGMP production. Your proficiency in maintaining a clean, well-stocked chemical site while having a positive collaborative attitude will be key to the success of this position. You will have an opportunity to become skilled in the use of a wide range of lab instruments, including but not limited to spectrophotometers, conductivity meters and auto-pipettors, all of which are essential to meeting our customers' requirements. Having the ability to learn quickly on the job, anticipate and resolve potential manufacturing and delivery issues and maintaining the highest level of quality are critical. Schedule: The schedule will be Day 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. Key responsibilities...

Job Description : Job Description Agilent is expanding on its oligonucleotide manufacturing capabilities with a new, purpose-built facility, designed to support the growing demand and innovation in therapeutic development- and we're looking for Manufacturing Associates to help bring it to life! As part of the initial startup team, you'll play a key role in commissioning, qualifying, and validating new equipment and systems. This role offers a unique opportunity to help establish the foundation of a world-class manufacturing operation and contribute to building and training future team members. We value employees who can quickly learn on the job, proactively anticipate and resolve manufacturing or delivery challenges, and consistently uphold the highest standards of quality. This is a hands-on, high-impact position ideal for someone who thrives in dynamic environments, enjoys solving complex problems, and wants to be part of something transformative. Key...

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. This role will perform a variety of technical support duties in GMP manufacturing, utility, and laboratory areas. The primary focus will be support of equipment used in the manufacturing of Oligonucleotides. Supports the operation and execution of the Process Maintenance & Engineering organization: Functions as the administrator of Computerized Maintenance Management System (CMMS): Facilitates and administers CMMS (Blue Mountain Regulatory Asset Manager) New Equipment setup. Supporting configuration of Maintenance Plans, PM's, Calibrations, Spare Parts (Master Data & Bill of Materials)...

What's it like to work at Agilent in Manufacturing? Watch the video" 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. Cleaning Validation Manager. You've established your people management and leadership ability. Here is where you take it further. You will manage a team of validation engineers, driving their performance in the design of validation policies and processes, to improve quality, production and profitability. You will also have the opportunity to develop strategies and multi-year implementation plans for new product introductions and continuous improvement. Responsible for all aspects of the...

Job Description : Job Description Want to take your knowledge and experience further? Ready to provide technical leadership and make key decisions? This is your opportunity - not only to join a committed, professional, and forward-thinking team but also to lead in the design and implementation of complex manufacturing processes and transform broad concepts into structured results-focused projects. Join a growing team with this exciting new opportunity for an advanced level Process Engineer at our Frederick, Colorado GMP facility. Work in our dynamic, fast-paced, API-Biopharma manufacturing environment with the ability to contribute to the growing industry of oligonucleotide (DNA-RNA) based therapeutics. Responsibilities may include but are not limited to: Support design and construction activities for capital projects from concept design through validation of new processes. Including working hand in hand with A&E and all other cross functional teams....