Enable next‑gen solutions through direct engagement with OSATs and Fabless accounts, owning PVD solutions and driving qualification, ramp, and continuous improvement for advanced packaging.
Locations (2)
Singapore, Singapore
Tampines, Singapore
Responsibilities
Act as technical owner for PVD solutions at assigned OSATs and Fabless accounts
Understand customers and Fabless stakeholders technical roadmap
Partner with Fabless packaging architects to define material stacks, reliability criteria, and integration flows
Lead joint qualification programs involving Fabless and OSAT stakeholders
Establish process‑of‑record for advanced packaging applications
Requirements
Bachelor’s or Master’s in Materials Science, Physics, Chemical Engineering, or related field; PhD preferred
Nice to have: Hybrid bonding or chiplet integration through PVD underlayers
Nice to have: Familiarity with APAC OSAT ecosystem and Fabless packaging roadmaps
Focus on monitoring and optimizing the chemical and physical parameters of the manufacturing process to ensure product quality, tracking production data, and adjusting equipment settings.
Compensation
The current base salary range for this role is between $26.00 - $33.00/hour.
Responsibilities
Performing Recipe Set-Up, including understanding recipe structures, inputting parameters, and verifying the setup through initial wafer evaluations.
Adjusting parameters within the Recipe Spec to maintain standards and managing the history of these changes.
Identifying key factors and performing sensitivity analysis on parameters to derive and verify optimal process conditions.
Defining the Process Window, setting upper/lower limits, and performing margin analysis to ensure stability.
Monitoring process quality and stability, and responding to abnormalities in the production flow.
Requirements
Associate’s degree (AAS/AS) or technical certificate in Electronics
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
Advanced Quality Engineer opportunity within manufacturing companies in the Warren area, focusing on continuous improvement, root cause analysis, and quality metrics.
Locations (5)
Warren, Michigan, United States
Sterling Heights, Michigan, United States
Madison Heights, Michigan, United States
Royal Oak, Michigan, United States
Roseville, Michigan, United States
Compensation
Salary Range: $86,000 - $127,000 depending on experience
The Process Engineer will be responsible for optimizing manufacturing processes, improving efficiency, and ensuring product quality.
Compensation
Starting Pay / Salary Range
$85,000.00 - $122,200.00 / year
Responsibilities
Design, develop, and implement new manufacturing processes and optimize existing ones to enhance productivity, reduce costs, and improve product quality.
Conduct process analysis, identify bottlenecks, and propose solutions to improve operational efficiency and throughput.
Develop and execute process validation protocols, including IQ, OQ, and PQ, to ensure compliance with industry standards and internal procedures.
Monitor process performance using statistical process control (SPC) and other analytical tools, troubleshoot deviations, and implement corrective actions.
Collaborate with cross-functional teams including R&D, production, quality assurance, and maintenance to support new product introductions and continuous improvement initiatives.
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