Process Engineer, Backend Assembly - (E5)

Applied Materials Santa Clara , CA 95051

Posted 2 months ago

This positions is within our Engineered Optics team.

Key Responsibilities

  • Die Singulation Process by laser dicing tool.

  • Die package assembly.

  • Drive innovative techniques to characterize hardware, define methods and new technologies and apply them to characterize hardware, and/or perform hardware characterization on significantly complex systems for a range of programs, within safety guidelines.

  • Design, collect data, analyze and compile reports on significantly complex process engineering experiments for a range of products, within safety guidelines

  • Design and implement new technology, products and analytical instrumentation

  • Train engineers, define and implement new methodologies, define and apply new technologies, and/or troubleshoot and resolve significantly complex process engineering issues/problems for a range of products

  • Develop, plan and execute process engineering projects for a range of products

  • Interact with key customers to resolve significantly complex process engineering issues for a range of products to address our customers High Value Problems (HVP)

  • Generate internal and external documentation for products, presentations, technical reports for integrated products and generate process engineering specifications for integrated products

  • Define and validate film measurement techniques. Train engineers on the techniques and guide them in the interpretation of the data

Functional Knowledge

  • Regarded as the technical expert in laser dicing/die singulation field

  • Demonstrates in-depth and/or breadth of expertise in own discipline and broad knowledge of other disciplines within the function

Business Expertise

  • Anticipates business and regulatory issues; recommends product, process or service improvements

Leadership

  • Leads projects with notable risk and complexity; develops the strategy for project execution

Problem Solving

  • Solves unique and complex problems with broad impact on the business; requires conceptual and innovative thinking to develop solutions

Impact

  • Impacts the direction and resource allocation for program, project or services; works within general functional policies and industry guidelines

Interpersonal Skills

  • Communicates complex ideas, anticipates potential objections and persuades others, often at senior levels, to adopt a different point of view

#Engineered Optics

#LI

Qualifications

Education:

Bachelor's Degree

Skills

Certifications:

Languages:

Years of Experience:

10 - 15 Years

Work Experience:

Additional Information

Travel:

Yes, 20% of the Time

Relocation Eligible:

Yes

Applied Materials is committed to diversity in its workforce including Equal Employment Opportunity for Minorities, Females, Protected Veterans and Individuals with Disabilities.


icon no score

See how you match
to the job

Find your dream job anywhere
with the LiveCareer app.
Mobile App Icon
Download the
LiveCareer app and find
your dream job anywhere
App Store Icon Google Play Icon
lc_ad

Boost your job search productivity with our
free Chrome Extension!

lc_apply_tool GET EXTENSION

Similar Jobs

Want to see jobs matched to your resume? Upload One Now! Remove
Product Development Process Systems Engineer (Verification & Validation)

Techone Resources

Posted Yesterday

VIEW JOBS 6/5/2020 12:00:00 AM 2020-09-03T00:00 Product Development Process Systems Engineer (Verification & Validation) Location: Belmont, CA initially (then, Santa Clara), 15% travel Duration: 1 year (contract to hire possible) Description: Serve as a subject-matter expert on product development related design control SOPs (Standard Operating Procedures, work instructions, work templates and training). Support verification and validation protocol execution, perform data review, and assist in deviation resolution process by using knowledge of deviation management and Quality Implication and Corrective and Preventive Actions (CAPA) to ensure continuous improvement during development, manufacturing, and product release. Generate, review, and approve verification and validation protocols for Medical device applications, including IQ (Installation Qualification), OQ (Operational Qualification) and PQ (Performance Qualification) using experience with system review, verification and validation and knowledge of the medical device development and manufacturing domain. Analyze business, compliance, data Integrity and technical/operational requirements for Medical device and Pharmaceutical Software as a Service product, to support technical and product leaders to create quality management systems (QMS) consistent with compliance requirements. Act as a bridge between cross-functional team members and quality compliance to identify gaps and help resolve questions and open issues for low risk SaaS and medical devices. Author, review, and finalize software test and design verification and validation deliverables including Plan, Requirements, Test Plan, Design, Protocols, Traceability Matrix, Reports, and also help maintaining SOPs and work instructions. Ensure product verification and validation and program deliverables packages are complete as required for audits and regulatory inspections. Assess change control and discrepancy events for system verification, validation systems and automation systems. Work with subject matter experts through quality risk management process and prepare risk management reports documenting system risks, applicable remediation, risk reduction, and critical controls. Will also contribute to the Software Development Lifecycle (SDLC) process engineering. This will include maintaining SOPs, work instructions, training documents and tools to support the process (Jira/Enzyme, Zephyr/ Aha!). Strong interest and knowledge in process and tools development for regulated software development is needed. A medical device or healthcare software background with experience working in a regulated environment is required. Working effectively with the Quality System, Regulatory and Software Engineering functions will be a key success factor. Ensure the applications developed are compliant with FDA (Food and Drug Administration) regulations such as 21 CFR part11, 21 CFR part820 and ISO regulations such as ISO 13485 (Standard for medical devices). MUST-HAVE Qualifications: Bachelor's degree Biomedical Engineering, Computer Science, Technical writing, or a related life science field, and 5 years of post-baccalaureate and progressive in job offered or as Verification & Validation Test Engineer, Validation Analyst, or System Analyst. Must have 3 years of experience with each of the following: * Process system verification and validation in the medical device field * Design control * Computer system validation /Software testing * FDA and ISO standards and regulations * Agile methodology * prior SW development is useful Techone Resources Santa Clara CA

Process Engineer, Backend Assembly - (E5)

Applied Materials