Supplier QA Technical Lead Engineer Job at Lam Research (Bangalore)

Supplier/Vendor QA Engineer 3

This position is part of the SET (Supplier Engineering and Technology). SET is a...

Location

Korea (the Republic of) , Osan

Salary:

Not provided

Lam Research

Expiration Date

Until further notice

Requirements

Minimum 5 years’ experience in managing technical programs and projects, preferably in the Semiconductor Industry
Knowledge in EFEM’s (Equipment Front End Modules), BEM’s (Back End Modules) and PM (Process Module) will be an added advantage
Creative thinking and strong problem solving and troubleshooting capabilities, including experience in the areas of electrical/mechanical/test engineering
In-depth understanding of equipment and component manufacturing processes of Semiconductor equipment system(Transfer module & Process module)
Basic understanding for workmanship standard especially, assembly process, cable routing, sheet metal, Machining, welding and powder painting, Vacuum chamber
Skills in understanding of drawing interpretation and electric circuit-diagram(electrical schematic)
Experience in supplier process development & quality management sucha as FMEA, QMS, supplier audit, scorecard, FAIR, Poka-yoke, Kaizen and, etc
Experience in supplier development, transition and qualification to support localization activity including sub-tier supplier qualification
Bachelor of Science in Mechanical/Material or Engineering or equivalent
Bachelor of Science in Electrical/Electronic Engineering or equivalent

Job Responsibility

Influencing decisions and company driven objectives within internal and external groups to achieve company goals
Work with Lam Product Group Engineering organizations and suppliers in development and product transition for TM(Transfer Module : ATM & VTM) and PM(Process Module)
Interfacing with key teams within Lam including technical product groups, account teams and global operations as a representative of SET
Coordinate and support investigation of key quality defects of components from the customers and/or field service team to drive corrective actions and continuous improvement
Developing suppliers to meet Lam quality standards
Act as liaison/technical lead for cross functional projects to include Build Verify and Production Readiness Review
Build manufacturing jigs and fixtures for Electrical/Electronics/Mechanical assembly
Able to provide key technical analysis for problem solving process
Interface with supplier personnel and provide technical solutions to Electrical/Electronic/Mechanical system assembly
Continuously working on process improvement and developing Best Known Methods

Lead Engineer CQV

Discover your exciting role. Exyte is a global leader in design, engineering and...

Location

Germany , Nürnberg

Salary:

Not provided

Exyte Central Europe GmbH

Expiration Date

Until further notice

Requirements

Degree in Biotechnology, Pharmaceutical, Building Services Engineering or Process Engineering or related field
Several years of experience in CQV within life sciences industry, including leadership responsibilities
Strong knowledge of GMP, ISO, 21 CFR, Annex 15, data integrity
Proven ability to lead teams and manage complex projects
Fluent German and good English skills required
High level of quality awareness, efficiency, and accuracy

Job Responsibility

Lead and mentor CQV engineers, ensuring efficient resource allocation and professional development
Define CQV strategies and ensure alignment with project objectives, timelines, and compliance requirements
Supervise commissioning, qualification, and validation activities for HVAC, cleanroom, and clean media systems according to GMP regulations
Approve CQV documentation (specifications, risk analyses, protocols, reports) and ensure regulatory compliance
Act as primary interface between CQV team, clients, technical engineering, automation, QA, and suppliers
Oversee FAT/SAT activities and review supplier documentation
Implement best practices and drive process optimization across projects

What we offer

Your Start at Exyte: Join a two-day onboarding event with new colleagues
Attractive Location: Spacious workspaces with height-adjustable desks
Buddy System: Several weeks of onboarding with your teammates
Work-Life Balance: Option to switch to mobile working at any time
Catering: Free specialty coffees and water dispensers on every floor
Stay Fit: Exyte subsidizes your fitness membership via Qualitrain at over 5,000 locations across Germany

Fulltime

Supplier Quality Engineer

We are seeking a highly motivated and detail-oriented Supplier Quality Engineer ...

Location

Vietnam , Hanoi

Salary:

Not provided

Hewlett Packard Enterprise

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Engineering (Mechanical, Electrical, or related field)
5+ years of experience in supplier quality, ideally within electronics or networking industries
Strong knowledge of electronic and mechanical components used in telecom/networking products
Familiarity with IPC standards, GD&T, APQP, PPAP, and statistical quality tools
Experience with ISO 9001/14001, IATF 16949, or other quality system standards
Strong analytical, communication, and supplier management skills
Ability to travel to supplier sites domestically and internationally

Job Responsibility

Qualify new suppliers through audits and capability assessments
Conduct periodic supplier audits (ISO 9001, IATF 16949, IPC standards, etc.)
Evaluate supplier processes, quality systems, and capacity for continuous improvement
Ensure supplier compliance with engineering specifications, RoHS and environmental/regulatory requirements
Review and approve PPAP, FAI, and quality documentation from suppliers
Lead root cause analysis and corrective action for supplier-related issues (8D, 5 Why, Fishbone)
Work with suppliers to drive zero-defect quality culture and reduce defect rates
Develop incoming inspection plans and criteria for electronic (PCBs, ICs, connectors) and mechanical parts (enclosures, fasteners, thermal parts)
Collaborate with internal engineering teams to interpret technical drawings, schematics, and specifications
Monitor and report supplier quality metrics (PPM, DPPM, on-time delivery)

What we offer

Health & Wellbeing
Personal & Professional Development
Unconditional Inclusion

Fulltime

Senior QA Specialist – Supplier Audits

This role is instrumental in strengthening supplier quality and compliance acros...

Location

United States , California

Salary:

Not provided

Mantell Associates

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Life Sciences, Engineering, Chemistry, or related discipline
Significant experience in supplier quality, audits, and quality systems within a pharmaceutical, biopharmaceutical, or CDMO environment
Strong knowledge of cGMP, ICH, regulatory expectations, and quality risk management principles
Demonstrated ability to lead supplier audits and effectively communicate findings to technical and operational stakeholders
Excellent analytical, report writing, and interpersonal skills with a proactive, solutions-oriented mindset
Ability to travel as required to support supplier audit activities (domestic and, occasionally, international)

Job Responsibility

Plan, execute, and lead supplier audits (on-site and remote) in accordance with cGMP, ISO standards, and internal procedures
Evaluate supplier quality systems, processes, corrective actions, and risk controls to ensure compliance and robust supply continuity
Prepare comprehensive audit reports, findings, and recommendations, and drive closure of audit observations with stakeholders
Support supplier qualification activities, including documentation review, risk assessments, and technical evaluations
Collaborate with Quality, Procurement, Regulatory, and Manufacturing teams to escalate supplier risks and implement mitigation strategies
Maintain audit schedules, quality intelligence, and supplier performance metrics to support continuous improvement
Serve as a subject matter expert on supplier quality expectations, training internal partners as needed

Fulltime

Qa Sr Manager External Supply Quality (Esq) - Supplier Quality Management

In this vital role you will serve as the quality lead and subject matter expert ...

Location

United States , Charlotte; Providence; Boston; Los Angeles

Salary:

144021.45 - 194852.55 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

High school diploma / GED and 12 years of Quality experience OR Associate’s degree and 10 years of Quality experience OR Bachelor’s degree and 8 years of Quality experience OR Master’s degree and 6 years of Quality experience OR Doctorate degree and 2 years of Quality experience
In addition to meeting at least one of the above requirements, you must have a minimum of 2 years experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation or resources
Educational background in Life Sciences
Strong technical knowledge and experience within operations in the pharmaceutical or GMP-regulated industry
Relevant work experience within Drug Substance and Drug Product operations, ideally with single use systems and platforms
5+ years of experience overseeing quality of suppliers
Robust problem-solving and root-cause analysis experience
Strong continuous improvement mentality
Strong compliance, quality, and regulatory knowledge with critical thinking, inquisitive with an end-to-end mentality
Strong communication skills with proficiency in the English language and collaborative cross-functionally behavior

Job Responsibility

Act as the quality lead for supplier relationships, from onboarding through disengagement, ensuring performance through robust proactive monitoring, technical site visits, and continuous improvement
Perform proactive quality management of suppliers, ensuring compliance with global regulatory standards, including but not limited to GDP, GMP, ISO, etc and Amgen’s industry leading expectations
Review and approve quality documentation, including Quality Agreements, deviations, supplier investigations, CAPAs, CAPA EVs, supplier change notifications and change controls, with a sharp eye for risk and compliance
Participate in and/or lead supplier audits and collaborate with internal and external partners to implement corrective and preventive actions
Prepare Amgen sites and suppliers for audits and inspections including development of inspection playbooks
Represent Amgen/ESQ during such audits and inspections - owning our quality story with confidence and clarity
Identify and mitigate risks at the supplier and/or escalate to management
Perform Person in Plant activities, as deemed appropriate
Drive audit commitments to completion
Act as a key quality partner to External Supply, Manufacturing, Supply Chain, Material Sciences, Engineering Technical Authority (ETA), Process Development and other internal functions

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible

Fulltime

Technical R+D Manager, Food/Bev

The Food Research and Development Manager provides technical leadership across t...

Location

United States , Irving

Salary:

Not provided

7-Eleven, Inc

Expiration Date

Until further notice

Requirements

Bachelor's degree in food science, Food Engineering, Chemistry, or related field
6-12 years of relevant work experience
5+ years of project management experience
Strong technical knowledge of food chemistry, microbiology, and processing technologies
Expertise in formulation development, ingredient functionality, and food product optimization
Proficiency in experimental design, product testing methodologies, and data analysis
Understanding food safety principles, HACCP, and regulatory requirements for food products
Experience with sensory evaluation techniques and consumer testing methodologies
Strong project management skills with ability to manage multiple projects simultaneously
Excellent problem-solving abilities with a solutions-oriented approach

Job Responsibility

Lead end-to-end technical research and development and commercialization for innovation, renovation, and maintenance initiatives across the Private Brands portfolio
Apply and continuously improve technical development and commercialization systems that embed food safety, regulatory compliance, QA standards, and shelf-life considerations
Translate product concepts into scalable, manufacturable formulations and processes, ensuring technical readiness for launch
Own product performance over shelf life, including defining test strategies, validating assumptions, and managing technical risk for formulation, process, and supplier changes
Ensure all products comply with applicable food regulations and brand QA standards
Partner closely with QA, Regulatory, Legal, and Sensory to support approvals, audits, testing, and ongoing compliance
Serve as a primary technical partner to co-manufacturers, establishing expectations for quality, performance, and compliance
Identify opportunities for continuous improvement and lead implementation with suppliers and internal teams
Support supplier performance management, including technical input to scorecards, corrective actions, and continuous improvement
Partner with Strategic Sourcing to identify, qualify, and onboard new suppliers through technical evaluations and capability assessments

Fulltime

Sr Project Leader, Technical Cost Out

You will plan, monitor and coordinate project tasks, as well as maintain and upd...

Location

United States , Skaneateles Falls

Salary:

112000.00 - 154000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

5+ years of applied project management experience
Bachelor’s degree in Engineering (Electrical, Mechanical or Biomed preferred)
Applied experience with Microsoft Project as well as other Office Suite applications
Prior SAP experience preferred (including DIRs, BOMs, MMDS, and Engineering Change Requests)
Demonstrated ability to communicate and negotiate with a diverse group of cross-functional stakeholders in Marketing, R&D, QA, Regulatory, Sourcing, and Operations
Well-versed in Medical Device Design Controls
Strong communication skills including experience communicating to senior leadership

Job Responsibility

Managing multiple projects varying in size, complexity and business impact
Leading and/or participating in cost savings ideation events
Developing cost savings ideas into feasible projects
Scoping, planning, and execution of projects
General project management (forming project teams, budgeting, assigning and tracking tasks, identify and mitigating project risks, etc.)
Evaluating and applying regulatory standards
Review of design inputs and outputs
Working with suppliers to implement new designs

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
Medical and dental coverage starting on day one
Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan (RSP)
Flexible Spending Accounts

Fulltime

Senior IT Business Analyst

As a Senior IT Business Analyst, you'll lead and shape analysis on complex, high...

Location

United Kingdom , Cardiff

Salary:

Not provided

Admiral Group Plc

Expiration Date

Until further notice

Requirements

Substantial experience leading business analysis across large‑scale, complex IT and business change, including end‑to‑end technical delivery
Strong understanding of Software Development Lifecycle (SDLC) and change delivery methodologies, with experience working across agile, waterfall and hybrid environments
Experience of business analysis across the delivery lifecycle and across various technology solutions
Excellent written and verbal communication skills, with the ability to engage confidently with stakeholders at all levels across business and technical roles
Strong problem‑solving skills and the confidence to challenge constructively
Proven ability to translate complex business needs into clear, actionable requirements
Confident in leading workshops to elicit requirements, frame problem statements, guide decision‑making and present analysis with stakeholders at all levels
Proficient in creating detailed analysis documentation (e.g. Lean UX canvas, business case, BPMN process models, BRD’s, user stories, functional Specifications etc)
Experience supporting testing activities, including defining acceptance criteria, clarifying requirements, and reviewing test cases
Experience collaborating with Architecture, Developers, QA, Engineering and Delivery teams to support end‑to‑end delivery

Job Responsibility

Lead and shape analysis on complex, high-impact projects and programmes from pre-inception to successful delivery across the Strategic Change Portfolio and IT
Bridge the gap between business needs and technical solutions through effective business analysis that adheres to best-practice and Admirals governance and change controls
Lead analysis at pre-inception to support the business assess their problem statements, opportunities and feasibility of new ideas to help support investment requests
Engage and collaborate with stakeholders at all levels across business and technology to elicit, analyse, validate and manage business and technical requirements
Define project scope, deliverable and success criteria for technical and business change
Translate business needs into clear, actionable requirements, user stories, use cases and functional specifications as appropriate
Track, monitor and report on analysis outcomes and agreed KPIs to ensure that project delivery their expected value and outcomes
Carry out BA activities across the delivery lifecycle, with the ability to select the most appropriate tool from our BA toolkit to execute
Build and maintain effective relationships with Architecture teams to determine optimal solution based on business need
Collaborate with Architecture and delivery teams to determine optimal solutions based on business needs

What we offer

33 days holiday (including bank holidays) when joining, increasing up to 38 days (including bank holidays)
Option to buy or sell up to an additional five days of annual leave
All colleagues eligible for up to £3,600 of free shares each year after one year of service
Disability Confident Leader scheme

Fulltime

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Supplier QA Technical Lead Engineer

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