QC Supervisor NeuroPace
THIS JOB HAS EXPIRED Job Description:
Supervise receiving, in-process and final quality control inspectors. Work with Materials, Manufacturing and Engineering to determine and set inspection priorities to meet company needs.
Supervise Quality Control personnel and inspection activities by ensuring that appropriate instructions, tools and equipment are provided for inspection activities and that QC inspectors work load is prioritized to meet production schedules.
Provide training to new hires and other QC inspectors on use of equipment, and how to appropriately review documentation and determine inspection requirements for parts. Make sure that quality control employees are trained in the processes that they will be performing.
Supervise the quality control staff including hiring additional inspectors as needed. Perform annual performance reviews and ensure group works together well as a team.
Suggest and implement areas for improvement and increased efficiency as manufacturing volume increases.
Interface and communicate with other departments such as manufacturing, engineering or planning personnel to ensure production/engineering requirements are met. Interface with engineering to establish inspection criteria and assure requirements are clear, determine acceptance of parts, and resolve issues.
Ensure compliance of the quality control department with required regulations (including FDA QSR and ISO 13485) and maintain compliant documentation within the guidelines of the FDA QSR for good manufacturing practices.
Performs QC inspection activities as required as well as other duties and responsibilities.
Assist in coordinating requirements for and conducting reliability studies for inspection methods (e.g. Gage R&R).
Strong oral and written communication skills; the ability to effectively interface and supervise QC Inspectors from a wide variety of disciplines. Proven experience in a supervisory role preferred.
Demonstrated ability to coordinate QC and manufacturing operations with co-workers and set priorities to meet production schedules.
10 years experience with medical device in-process and/or receiving inspection in an FDA/ISO environment. Thorough knowledge and understanding of Quality Systems Requirements and ISO 13485. Previous FDA and ISO audit experience a plus.
Experience with inspection of electromechanical components and assemblies and weld/soldering workmanship to IPC standards is strongly preferred.
Minimum A.A. degree or equivalent degree.
NeuroPace is an equal opportunity employer offering a competitive compensation and benefits package including medical, dental, vision, 401(k), and stock options.
||1375 Shorebird Way |
Mountain View, CA 94043
THIS JOB HAS EXPIRED