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.
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:
Must have solid knowledge of all assembly functionsAssists Manufacturing Engineering as needed with engineering activitiesAssist in finalizing and completing production documentation.Train personnel on manufacturing instructions as requiredPerform all product processing from preparation of raw materials to manufacturing of finished goods.Can operate all production equipment. Assembly of mechanical components, 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 complete 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 regulationsAble 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 Qualifications High School diploma required.Associate degree or equivalent preferred.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 Physical Requirements 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 standardsMust be able to safely move up to 25 lbsThe 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). CompensationWe pay competitively. Base hourly rate range is $23.31 - $28.82. Other paid compensation and benefits may be available.
Additional Information
Sonendo offers a competitive benefits package and a collaborative, motivating work environment where you will be encouraged to innovate continuously; This is a place where you will be encouraged to actively participate, and your ideas can have a direct impact on the success of the organization. If you are interested in applying for this position, please apply online.
No recruiters, please.
Sonendo, Inc. is an Equal Opportunity Employer
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