Assembly Technician II - Temporary
Listed on 2026-01-27
-
Manufacturing / Production
Manufacturing Production, Manufacturing Engineer, Quality Engineering
Sonendo, Inc. is a medical technology company with a unique mission to lead the transformation of dentistry through Sound Science®. We are currently building a high-performance team with a passion for creativity and innovation that is committed to collaboration and integrity. We believe our success is based on developing disruptive technologies, and we strive to achieve excellence in our products and services by attracting energetic, entrepreneurial individuals who are committed to this vision.
Applications accepted starting 1/19/26. The Final date to receive applications is subject to change. To apply, please submit your application through job boards, our company website, or call for assistance.
Essential Duties And ResponsibilitiesPrepare and assemble mechanical systems per Standard Operating Procedures (SOPs), Test methods (TMs), Protocols or Engineering Requests to support Operations, R&D and Quality Department. Duties and responsibilities include, but are not limited to:
- Perform all product processing from preparation of raw materials to manufacturing of finished goods.
- Can operate all production equipment.
- Assembly of mechanical components, assembly of fluidic systems, inspection, packaging, labeling, parts preparation, cleaning, and assembly.
- Operate microscopes and other analytical instruments.
- Maintain proper documentation for quality and compliance with GMP requirements.
- Complete appropriate paperwork necessary for maintaining good records.
- Utilize clean room, laboratory and manufacturing equipment and special tools and fixtures. Complete all training courses and some hands‑on trainings.
- Complete required document(s) of the product you produce.
- Interface with personnel within manufacturing and other internal departments.
- Adhere to applicable GMP and ISO rules and regulations.
- Able to work independently and as well as a team player.
- Perform miscellaneous task as assigned by supervisor.
- Maintain compliance with Quality System procedures and company policies.
- High School diploma and preferably 2-4 years’ experience in medical devices manufacturing.
- Must be familiar with FDA/GMP regulations.
- Able to read and write English language, work instructions and technical drawings (including schematics), specifications and forms.
- Must be able to use lab equipment and basic hand tools such as microscope, oven, DI water system, sealer, screwdriver, and wrench.
- Must be proficient in using production equipment and computers in the cleanroom.
- Must have the ability to confidently navigate thru QCBD and have an understanding to use QAD Software Systems.
- Ability to safely and successfully perform the essential job functions consistent with the ADA, FMLA and other federal, state and local standards, including meeting qualitative and/or quantitative productivity standards.
- Ability to maintain regular, punctual attendance consistent with the ADA, FMLA and other federal, state and local standards.
- Must be able to safely move up to 25 lbs.
- The ability to communicate information and ideas so others will understand. Must be able to exchange accurate information in these situations.
- Must be able to remain in a stationary position for 50% of the time.
- Must be able to occasionally move about inside the office to access file cabinets, office machinery, etc.
- The ability to observe details at close range (within a few feet of the observer).
We pay competitively. Base hourly rate range is $22.00 - $24.00.
Additional InformationSonendo, Inc. fosters a collaborative, innovative workplace where every team member’s ideas contribute to our success.
We are an Equal Opportunity Employer.
No recruiters, please.
#J-18808-Ljbffr(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).