Lead and manage risk and post-market surveillance activities for NeuroPace’s medical device portfolio.
Compensation
$160K-$185K Base - Compensation will be determined based on several factors, including but not limited to skill set, years of experience, and geographic location.
Responsibilities
Serve as a subject matter expert in post-commercialization risk management processes and data-driven safety analytics.
Lead cross-functional efforts and meetings to analyze and synthesize complex data into actionable insights for senior leadership and other key stakeholders.
Maintain ISO 14971-compliant risk files, developing global Post-Market Surveillance plans, and leverage advanced statistical tools to detect emerging performance signals.
Implement, instruct, and support training of staff on risk management remediation directives based on findings and analysis.
Ensure all ongoing maintenance, continuous improvement and remediation efforts meet applicable quality and regulatory standards.
Conduct process engineering research, development, and evaluation in support of Lam’s cutting‑edge semiconductor equipment.
Review and enhance processing techniques and methods applied in the manufacture and fabrication of products.
Work with vendors to develop and optimize materials used in our deposition equipment.
Develop and sustain new processes and process improvements to reduce production costs and increase yields.
Compile and analyze test data to establish next steps in process development and determine appropriate limits and variables for process specifications.
Requirements
PhD in Materials Science, Chemical Engineering, Chemistry or Physics
Lead process engineering for semiconductor equipment and systems, driving innovation and process improvements.
Compensation
CA San Francisco Bay Area Salary Range for this position: $104,000.00 - $231,000.00.
Responsibilities
Conduct process engineering research, development, and evaluation in support of Lam’s cutting-edge semiconductor equipment and systems.
Review and enhance processing techniques and methods applied in the manufacture and fabrication of products.
Develop and sustain new processes and process improvements to reduce production costs and increase yields.
Compile and analyze test data to establish next steps in process development and determine appropriate limits and variables for process specifications.
Collaborate internally to plan, collect data, analyze results, and report on customer demos for existing process applications.
Requirements
Master’s degree in Materials Science, Chemical Engineering, Chemistry or Physics or related field
PhD in related field
Nice to have: Laboratory experience with semiconductor equipment
Nice to have: Surface preparation and analytical techniques
Nice to have: Statistical analysis and problem-solving methodologies
Lead and support global quality assurance initiatives across Victaulic’s manufacturing operations, driving continuous improvement and ensuring compliance with quality standards.
Compensation
Competitive compensation with performance-based incentives
Responsibilities
Implement and maintain global quality procedures and standards
Support product development and launch activities by developing and executing ISIR Plans
Participate in Manufacturing & Quality Readiness Reviews
Analyze manufacturing quality data and lead initiatives to reduce scrap and rework
Develop and implement process controls and statistical methods
Requirements
Bachelor’s degree in Mechanical, Industrial, Manufacturing, Materials, or Quality Engineering, or a related technical discipline
Nice to have: Master’s degree in Engineering, Manufacturing, Quality, or Business Administration
Nice to have: ASQ Certified Quality Engineer (CQE)
Responsible for improving manufacturing processes, supporting production operations, and ensuring products are produced safely, efficiently, and in compliance with quality and regulatory requirements.
Compensation
Potential salary range for this role is $95,000 - $120,000 annually.
Responsibilities
Follow all manufacturing Good Manufacturing Practices (GMP’s) as defined by Viant Medical’s practices, policies and Standard Operating Procedures (SOP’s)
Performs project management responsibilities for assigned manufacturing changes or new product methods, designs of production fixtures, and methods to monitor efficiency
Evaluates existing machinery and processes to recommend improvements that enhance both operator performance and ergonomics/safety of overall production
Optimizes floor layout, material flow, along with implementation of lean concepts; document improvements to manufacturing efficiencies, takt time, floor space utilization and overhead.
Develops or revises technical documentation to specify manufacturing processes; including documentation of equipment qualification, setup and maintenance procedure
Requirements
Bachelor's degree in Engineering, Quality, Manufacturing, or a related technical or scientific field, or equivalent combination of certification and experience
Lead quality engineering initiatives for manufacturers in the Ironwood region, driving continuous improvement and ensuring compliance with industry standards.
Compensation
Salary Range: $69,000 - $103,000 depending on experience
Responsibilities
Analyze defect and scrap data and report trends to plant leadership.
Support gage repeatability and reproducibility studies and calibration schedules.
Train production staff on quality procedures and inspection methods.
Investigate customer complaints and internal nonconformances to find root causes.
Lead corrective and preventive action activities and track them to closure.
Requirements
Bachelor degree in engineering or a related technical field
Nice to have: Auditor training or lead auditor experience
Nice to have: Certified Quality Engineer or similar certification
Nice to have: Experience with PPAP and APQP in an automotive supply chain
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