Job Information
Cirtec Medical Sr. Technician, Engineering in Santa Clara, California
Sr. Technician, Engineering
Department: NC2 - Engineering
Location: Santa Clara, CA
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JOB SUMMARY
The Sr. Technician, Engineering is primarily responsible for utilizing state of the art equipment for the development of life changing medical devices. Be able to operate a variety of equipment including, but not limited to; lasers, injection molders, reflow machines as well as an array of test equipment while adhering to the quality requirements of the company. In addition, this position will work with the design and process teams to ideate, create, and build first prototypes. This individual is essential in the maturation of these prototypes and their progress through the development. Lastly, the Sr. Technician, Engineering must feel comfortable providing candid feedback to the development team to ensure success in later phases of the program at a more senior level.
ESSENTIAL RESPONSIBILITIES
Assemble development prototypes in a timely manner, whether independently or coordinating with a larger team of operators and technicians.
Provide candid feedback to engineering team when designs and/or processes can be improved.
Document settings, assembly techniques, etc. in a laboratory notebook using good documentation practices.
Draft initial process flows and manufacturing procedures.
Small scale Engineering Change Order creation and execution.
Perform training to the assembly team when programs mature in the development phases.
Perform DVT in the design lab.
ECN creation and execution.
Place an order (purchase req) for materials through purchasing dept.
Maintain compliance to procedures and regulatory requirements.
Assist in training employees on equipment and assembly skills.
Interact effectively and assist engineering in improving quality and solving problems.
Ability to diagnose and solve problems with jobs in a timely manner.
Reliable, consistent, and punctual attendance is an essential function of the job.
Complies with company, quality, and safety standards, policies, and procedures.
Other duties as required.
This is not a remote position.
An individual in this position must be able to successfully perform the essential duties and responsibilities listed above. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position.
QUALIFICATIONS
3-7 years- experience in the engineering/manufacturing environment for medical devices.
Strong drive to learn, share and teach.
Understanding of and experience with mechanical equipment.
FDA, cGMP principles and practices, (ISO 9001, ISO 13485).
In-depth understanding of one or more manufacturing processes is a plus.
Familiarity with Pro-E / CREO and or SolidWorks is preferred.
Strong computer skills associated with Microsoft software.
Ability to interpret technical drawing, blueprints, specifications, and illustrations.
Must be able to read, write and speak fluent English.
Excellent reading, writing, communication, and organizational skills.
Maintains performance with changing priorities under minimal supervision.
Possess strong team collaboration skills.
Must be able to make clear and accurate decisions.
Strong desire to learn and apply new technology.
WORKING ENVIRONMENT
Work is performed in an office environment. The noise level in the work environment is usually moderate. The work environment characteristics described here are representative of those an individual encounters while performing the essential functions of this position.
PAY RANGE
The pay range for this role is $35 to $40. The successful candidate-s starting base pay will be determined based on job-related skills, experience, qualifications, work location and market conditions. The expected base pay range for this role may be modified based on market conditions.
START YOUR APPLICATION (https://apply.hrmdirect.com/resumedirect/ApplyOnline/Apply.aspx?req_id=3183280&source=3183280-CJB-0)