Senior Operations Quality Engineer
- Compensation
- Not disclosed
- Location
- Burlingame, California, United States
- Work setup
- Not specified
- Seniority
- Senior
- Employment
- Contract
- Experience
- Not specified
- Category
- Industrial engineering
- Posted
Skills
Must have
- - Bachelor’s degree in Manufacturing Engineering, Biomedical Engineering, Mechanical Engineering, or a related field (Master’s degree preferred). - 5-7 years minimum professional Engineering experienc
- Neptune Medical is located in Burlingame, CA, near the Millbrae Caltrain and BART Station
- Our job titles may span more than one career level. The starting base salary for this role is between $150,000 and $190,000 depending on experience. The actual base pay is dependent upon many factors,
- Neptune Medical provides equal employment opportunities to all applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, nati
Full description
Neptune Medical is an innovative, venture capital funded medical device startup headquartered in Burlingame, CA. We have already commercialized novel medical devices using our technology. Now the team at Neptune is building something truly unique: a fully flexible medical robot that enables doctors to reach deep into human anatomy. Our robot will disrupt flexible endoscopy and set a new standard in outcomes for decades to come.
TITLE: Sr. Operations Quality EngineerPOSITION SUMMARY:
The Senior Operations Quality Engineer is responsible for supporting volume production, product introductions, and continuous improvements for assembly processes to achieve company initiatives for commercial success, value creation, and operational excellence. The role involves working closely with production, quality control, and cross-functional teams to improve operational efficiency, reduce production costs and ensure product quality standards are met.
The ideal candidate would demonstrate the ability to meet and exceed the below requirements, would show a high level of individual responsibility as well as leadership for the team, and would act with passion and intensity in a fast-paced and collaborative medical device start-up.
ROLES AND RESPONSIBILITIES:Process Design & Improvement
- Identify opportunities for, lead, and implement innovative solutions for quality improvements, cost reduction, scaling production, and production efficiency that reduce risk and optimize production performance.
- Author and maintain inspection documentation, including protocols, reports, Quality Inspection Procedures (QIPs), work instructions (WIs), test methods (TMs) and, if required component/product drawings.
- Review manufacturing documentation, including protocols, reports, manufacturing process instructions (MPIs), lot history records (LHRs), work instructions (WIs), test methods (TMs) and, if required component/product drawings.
- Support and provide expertise regarding validation (IQ/OQ/PQ) activities and similar qualifications and generate detailed technical reports.
Production Support
- Provide technical quality support to the production floor and incoming/in-process quality control areas to address any issues.
- Responsible for sterilization related processes including validation, record verification, etc.
- Leverage statistical methods and software to support data-driven decisions, including for part acceptance and product release.
- Facilitate data collection for key performance indicators (KPIs) to assess project success and address any issues.
- Root cause analysis to investigate yield loss and nonconformances.
- Lead NCR and CAPA efforts.
- Participate in supplier selection and qualification, process transfer to contract manufacturing facilities,