Engineer II, Quality Job at MSA BOURGOGNE (Atlacomulco)

Engineer II, Quality

As an innovation leader, we look for ambitious, forward-thinking, open-minded an...

Location

Mexico , Atlacomulco

Salary:

Not provided

MSA BOURGOGNE

Expiration Date

Until further notice

Requirements

2-4 years of experience
Typically requires a college or university degree or the equivalent work experience that provides exposure to fundamental theories, principles and concepts

Job Responsibility

Develops broad knowledge and skills in a specific practice area
Works on small projects or portions of larger projects
Performs moderate design tasks
Prepares portions of project documents
Edits specifications
Performs research and investigations
Assists in determining schedule and budget requirements
Evaluates, selects, and applies standard techniques, procedures, and criteria to perform a task or sequence of tasks for conventional projects with few complex features
Possesses effective oral and written communication skills
Assists with client, customer, or official contacts and communication pertaining to specific assignments or meetings

Fulltime

Engineer II, Quality

Location

India , Verna, Goa

Salary:

Not provided

CommScope

Expiration Date

Until further notice

Requirements

Handling Customer Complaint Independently using 8D Methodology
Create PFMEA, Control Plans and Quality Inspection Plans
Work closely with the NPI team to understand the new products CTQ and controls for ensuring handover from NPI to Mass production
Work with design/development group-Provide input at design reviews, participate in drawing change request reviews
Monitoring Process yields & conducting process capability Study – (CP/CPk Study, SPC, MSA. Etc
Certified Black Belt
Lead Six Sigma projects to reduce scrap, Rework and Inspection cost
Conducting internal audits based on TL9000
Coordinate customer inspection or 3rd party inspection process and documentation
Capable to face customer Audits independently

Job Responsibility

Support the manufacturing process by: working closely with operations and process engineer on process enhancement projects
Recognize customer expectations and implement (or promote) appropriate procedures/awareness to ensure BU satisfaction
Have ownership for controlling and ensuring root cause analysis and preventive actions are implemented
Create and present appropriate quality measures

Quality Engineer II

Aurora’s mission is to deliver the benefits of self-driving technology safely, q...

Location

United States , Mountain View

Salary:

124000.00 - 199000.00 USD / Year

Aurora Innovation

Expiration Date

Until further notice

Requirements

Bachelor of Science in Electrical, Mechanical, Industrial Engineering, or related fields
or equivalent combination of education and experience.
5+ years in quality, supplier quality, or manufacturing - ideally in automotive, aerospace, robotics, or medical devices.
Hands-on experience launching new products and improving quality systems.
Strong experience with supplier audits, APQP, PPAP, and production ramp-ups.
Excellent analytical abilities, technical writing ability and comprehensive understanding of the quality toolbox (SPC, 8D root cause analysis, tolerancing, control and inspection standards, etc.).
Familiar with key quality tools: FMEAs, control plans, SPC, MSA, and capability studies.
Understanding of manufacturing processes for PCBA, electromechanical assemblies, injection molding, casting, and stamping.
Capable of interpreting engineering drawings and using GD&T
Knowledge of ISO 9001, IATF 16949 quality systems

Job Responsibility

Lead the supplier partner and/or CM industrialization process from design through production ramp-up.
Lead the APQP process and manage PPAP through the start of production with supplier partners and/or CM as well as Aurora’s OEM customers.
Lead the development of pFMEA, Control Plan, capability analysis, MSAs, DOEs, etc. in alignment with automotive APQP and PPAP requirements and activities.
Support the development of dFMEAs, PFD, and Work Instructions at supplier partner and/or CM by closely working with Aurora design and NPI teams.
Support supplier partner and/or CM with tooling, equipment, and process qualifications by closely working with Aurora design and NPI teams.
Assess supplier partner and/or CM readiness for each build phase and help manage production risks.
Lead root cause and corrective action efforts for any supplier partner and/or CM related quality issues from production or field returns.
Monitor and report supplier partner and/or CM quality metrics both internally and externally to Aurora’s OEM customers to ensure continuous improvement.
Uses lean tools, statistical techniques and analytical methods to achieve effective problem solving, root cause discovery and corrective action (8D Problem Solving, 5-Why) both internally and externally.
Closely collaborate with other cross-functional teams throughout the industrialization phases to ensure products meet industry and Aurora’s quality standard.

What we offer

annual bonus
equity compensation
benefits

Fulltime

Quality Engineer II

We are seeking a detail-oriented and proactive Quality Engineer with experience ...

Location

United States , Longmont

Salary:

73000.00 - 90000.00 USD / Year

Antech Diagnostics

Expiration Date

Until further notice

Requirements

Bachelor's degree in biotechnology, Biomedical Engineering, Biology, or related field
A minimum of 4-7+ years of quality assurance experience, preferably in a regulated industry or equivalent combination of education and experience
Familiarity with GMP, GLP, QSR, and ISO 9001/13485 standards
Experience managing nonconforming materials, investigations, and dispositions
Proficiency in quality tools such as CAPA, FMEA, Root Cause Analysis, and 8D
Solid documentation, analytical, and communication skills

Job Responsibility

Provide quality engineering support to manufacturing operations, including batch record review, deviation management, and in-process control monitoring
Assist in resolving quality issues on the production floor by collaborating with manufacturing, quality control, and engineering teams
Implement, and maintain quality systems in compliance with standard requirements and regulations (e.g., USDA APHIS, FDA CVM, ISO)
Support validation and qualification of manufacturing equipment, utilities, and processes (IQ/OQ/PQ)
Manage Nonconforming Material Reports (NCMRs), including investigation, segregation, documentation, and disposition of nonconforming products, and leading the Material Review Board
Lead and participate in root cause investigations and implement corrective and preventive actions (CAPA) related to manufacturing deviations and product issues
Collaborate with Operations, R&D and regulatory teams during the development and scale-up of new products
Analyze trends in manufacturing quality data to identify opportunities for continuous improvement and risk reduction
Support lot release testing, stability studies, and regulatory compliance activities
Conduct and support internal and external audits, including USDA CVB and FDA CVM inspections

What we offer

Paid Time Off & Holidays
Medical, Dental, Vision (Multiple Plans Available)
Basic Life (Company Paid) & Supplemental Life
Short and Long Term Disability (Company Paid)
Flexible Spending Accounts/Health Savings Accounts
Paid Parental Leave
401(k) with company match
Tuition/Continuing Education Reimbursement
Life Assistance Program
Pet Care Discounts

Fulltime

Quality Engineer II

We are seeking a detail-oriented and proactive Quality Engineer with experience ...

Location

United States , Rockville

Salary:

70000.00 - 90000.00 USD / Year

Antech Diagnostics

Expiration Date

Until further notice

Requirements

Bachelor's degree in biotechnology, Biomedical Engineering, Biology, or related field
A minimum of 4-7+ years of quality assurance experience, preferably in a regulated industry or equivalent combination of education and experience
Familiarity with GMP, GLP, QSR, and ISO 9001/13485 standards
Experience managing nonconforming materials, investigations, and dispositions
Proficiency in quality tools such as CAPA, FMEA, Root Cause Analysis, and 8D
Solid documentation, analytical, and communication skills
Experience supporting biologics manufacturing in a USDA-licensed facility
Knowledge of aseptic manufacturing and cleanroom compliance requirements
Certified Quality Engineer (CQE) or Six Sigma certification
Experience supporting regulatory inspections (USDA CVB, FDA CVM)

Job Responsibility

Provide quality engineering support to manufacturing operations, including batch record review, deviation management, and in-process control monitoring
Assist in resolving quality issues on the production floor by collaborating with manufacturing, quality control, and engineering teams
Implement, and maintain quality systems in compliance with standard requirements and regulations (e.g., USDA APHIS, FDA CVM, ISO)
Support validation and qualification of manufacturing equipment, utilities, and processes (IQ/OQ/PQ)
Manage Nonconforming Material Reports (NCMRs), including investigation, segregation, documentation, and disposition of nonconforming products, and leading the Material Review Board
Lead and participate in root cause investigations and implement corrective and preventive actions (CAPA) related to manufacturing deviations and product issues
Collaborate with Operations, R&D and regulatory teams during the development and scale-up of new products
Analyze trends in manufacturing quality data to identify opportunities for continuous improvement and risk reduction
Support lot release testing, stability studies, and regulatory compliance activities
Conduct and support internal and external audits, including USDA CVB and FDA CVM inspections

What we offer

Paid Time Off & Holidays
Medical, Dental, Vision (Multiple Plans Available)
Basic Life (Company Paid) & Supplemental Life
Short and Long Term Disability (Company Paid)
Flexible Spending Accounts/Health Savings Accounts
Paid Parental Leave
401(k) with company match
Tuition/Continuing Education Reimbursement
Life Assistance Program
Pet Care Discounts

Fulltime

Quality Engineer II

We are looking for a Quality Engineer II to join our Platform and Integration te...

Location

India , Chennai

Salary:

Not provided

Exasol

Expiration Date

Until further notice

Requirements

6+ years in product engineering and automation testing
Strong expertise in system-level and API-level automation
Experience with automation tools and platforms
Excellent communication skills and ability to work independently
Experience in C++ and Python

Job Responsibility

Design and develop system-level automation tests, especially at the customer use-case level
Lead automation initiatives on development team
Introduce and implement the right automation tools and platforms
Work independently, engaging with cross-functional teams to troubleshoot and resolve issues
Communicate effectively with teams and stakeholders, providing clear documentation and reporting

Fulltime

Quality Engineer II - HW Systems

We’re searching for a Hardware Systems Quality Engineer. The primary objective o...

Location

United States , Pittsburgh

Salary:

112000.00 - 180000.00 USD / Year

Aurora Innovation

Expiration Date

Until further notice

Requirements

Bachelor's Degree in Engineering, Computer Science, or related field
3+ years of experience in quality, autonomous vehicle manufacturing, electro-mechanical assembly operations, robotics or equivalent field experience
Experience with programming and scripting (C++, Python or equivalent)
Experience debugging complex electronic assemblies and/or manufacturing cable assemblies
Ability to understand electrical and mechanical drawings
Strong attention to detail, with excellent written and verbal communication skills
Ability to work in a fast-paced team environment

Job Responsibility

Lead, develop, and support test and inspection plan creation in accordance with required specifications
Perform tests and inspections according to Quality plans and procedures to record & analyze data, document and report results
Create and maintain documentation and records of test operations
Troubleshoot, debug, and perform general root cause analysis for software and hardware faults and defects
Perform cable and harness assembly testing and troubleshooting
Operate inspection and test fixtures or equipment, with ability to train others as required
Support the activities related to non-conforming product(s) and returned material authorization activities (Material Review Board)
Participate in audit and manufacturing process audit activities
Actively participate in continuous improvement activities

What we offer

annual bonus
equity compensation

Fulltime

Quality Engineer II

You will join our client as a Quality Engineer II, helping to reduce defects, ac...

Location

United States , San Fernando

Salary:

Not provided

Van Kaizen

Expiration Date

Until further notice

Requirements

Bachelor’s degree in engineering or a related field
5+ years in quality engineering in manufacturing
At least 2 years in customer-facing roles
Expertise in PFMEA, control plans, SPC, MSA, and Lean/Six Sigma

Job Responsibility

Lead 8D and DMAIC initiatives, champion APQP/PPAP readiness, facilitate FMEA risk assessments, and resolve quality inventory issues quickly
Log and track customer complaints, lead containment actions, perform root-cause analysis, and communicate resolutions to customers
Conduct process audits and Gemba walks to identify issues early
approve reworks and support MRB/NCMR activities for timely disposition
Lead structured problem solving using 8D and DMAIC
drive corrective actions and continuous improvement initiatives
Facilitate PFMEA sessions and ensure compliance with ISO 9001 and transit standards
Track APQP/PPAP deliverables for new product launches and validate process readiness
Collaborate cross-functionally to resolve supplier quality issues and drive corrective actions
Use ERP, MES, and QMS platforms to manage data, prepare quality reports, COPQ trends, and highlight systemic issues

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Engineer II, Quality

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