Cleanroom Operator

Centrillion Technologies, Inc.•Palo Alto, CA

9d•$20 - $25•Onsite

About The Position

Centrillion Technology, Inc. is on the cutting edge of genetics and biotechnology, spearheading innovations in spatial genomics, ultra-long DNA sequencing, rapid on-chip sequencing, viral sequencing, genotyping, and synthetic biology. Our advanced technologies and high-density DNA chips are revolutionizing genomic research, making groundbreaking discoveries more accessible and affordable. Our team of experts in science, engineering, and business is dedicated to making these breakthroughs accessible and affordable, and to unlocking the full potential of the genome. With our commitment to innovation and collaboration, we are leading the way in shaping the future of life sciences. Join us at Centrillion and be a part of our mission to bring the power of genomics to the world. With opportunities for growth and advancement, a supportive and inclusive work culture, and the chance to work on exciting and impactful projects, Centrillion is the place for those passionate about genetics and biotechnology. Help us make a lasting impact on the world through our innovative technologies. Job Summary: Centrillion is seeking a Cleanroom Operator to join a multidisciplinary research team developing new technologies. The successful candidate will be responsible for executing production processes using an automated synthesizer in a GMP-compliant cleanroom environment. The operator will prepare, and load working substrates onto the synthesizer and transfer them between various processing and analytical instruments throughout the manufacturing workflow. This role requires precise adherence to standard operating procedures (SOPs), consistent documentation, attention to detail, and timely communication of any deviations or equipment issues to ensure high-quality, reproducible production.

Requirements

High school diploma or equivalent
At least 1 year of hands-on experience in a cleanroom, manufacturing, or laboratory setting.
Strong attention to detail with the ability to follow SOPs precisely and document activities in real time.
Comfortable working in a GMP-controlled cleanroom environment with appropriate PPE.
Ability to stand for extended periods and lift up to 30 lbs.
Adequate proficiency with Excel or spreadsheet software for basic data entry, organization, and analysis.
Ability to take initiative, including asking for and offering help when needed; performs work independently without being prompted.

Responsibilities

Prepare the cleanroom environment by staging materials, resources, and prescriptions to eliminate potential errors and ensure operations follow Good Manufacturing Practices (GMP).
Maintain a sterile environment by properly gowning, cleaning the room, and following all cleanroom protocols and behaviors.
Monitor supply levels and assist with inventory tracking, notifying appropriate personnel for ordering consumables as needed.
Maintain the work area and equipment in a clean and orderly condition, ensuring readiness for production at all times.
Perform routine cleaning, setup, calibration, and preventive maintenance of equipment according to standard operating procedures (SOPs).
Follow detailed batch records and SOPs precisely for all production steps including reagent preparation, oligo synthesis, and final processing.
Identify and report defective materials or questionable equipment conditions to the department supervisor promptly.
Record and analyze QC data, including in-process and final product measurements; report any out-of-specification results or unusual trends to the supervisor or quality team immediately.
Contribute to safety and quality initiatives by following established guidelines and participating in safety training and audits.
Communicate the operational status and any safety, quality, or process concerns to management in a timely and proactive manner.