supplier quality manager

Howmet Aerospace

<div><div><b>Job Summary:</b></div><ul><li>
Lead and manage the global supplier quality function, ensuring consistent compliance with ISO 9001 and IATF 16949 standards across all supplier operations.</li><li>
Develop, implement and continuously improve supplier quality systems, audits, and performance metrics to drive product quality, risk mitigation, and process reliability.</li><li>
Collaborate cross-functionally with global procurement, engineering, and manufacturing teams to resolve supplier issues, support new product launches, and ensure alignment with customer and regulatory requirements.
</li></ul><div><b>Key Responsibilities:</b></div><ul><li>
Develop and implement global supplier quality standards aligned with ISO 9001 and IATF 16949 to ensure consistent quality across the supply base.</li><li>
Lead supplier audits and assessments, including initial qualification, periodic surveillance, and performance evaluations to ensure compliance and continuous improvement.</li><li>
Drive corrective and preventive actions (CAPA) with suppliers for non-conformances, ensuring timely resolution and long-term quality improvements.</li><li>
Establish and monitor supplier quality KPIs, such as PPM, on-time delivery, and audit scores, to track performance and initiate improvement plans.</li><li>
Collaborate with internal teams (procurement, engineering, manufacturing, etc.) to align supplier quality objectives with business and customer requirements.</li><li>
Support new product development (APQP/PPAP) by ensuring supplier readiness, capability studies, and documentation in line with IATF 1649 standards and the organization&rsquo;s specific needs.</li><li>
Manage supplier risk assessments and drive strategic initiatives to mitigate quality risks and ensure supply chain resilience.</li><li>
Provide leadership, training, and mentoring to local Quality teams, fostering a culture of accountability and continuous improvement.</li><li>
Implement, develop, and manage receiving inspection processes to ensure incoming materials meet specifications and support robust quality control at point of entry.</li><li>
Lead and manage supplier-related crisis situations, coordinating rapid containment, root cause analysis, and long-term resolution plans to protect customer satisfaction and business continuity.</li></ul><div><b>
Basic Qualifications:</b></div><ul><li>
Bachelor&rsquo;s degree (BS) from an accredited university in Engineering, Quality, Supply Chain, or related technical field.</li><li>
Minimum of 5 years&rsquo; experience in supplier quality or quality management roles within a manufacturing environment.</li><li>
Extensive knowledge of Quality Management Systems such as ISO9001 or IATF16949 and production systems.</li><li>
Proficiency in quality tools and methodologies, including root cause analysis, 8D, CAPA, SPC, and MSA.</li><li>
Demonstrated ability to manage global suppliers and work across cultures, time zones, and functions.</li><li>
Strong leadership and crisis management skills, with track record of resolving complex supplier quality issues.</li><li>
Excellent communication, negotiation, and interpersonal skills to influence both internal stakeholders and external suppliers.</li><li>
Willingness to travel domestic and internationally as needed (typically 20-40%).</li><li>
Employees must be legally authorized to work in the United States. Verification of employment eligibility will be required at the time of hire. Visa sponsorship is not available for this position.</li></ul><div></div><div><b><br>
Preferred Qualifications:</b></div><ul><li>
Master&rsquo;s degree in related fields.</li><li>
Certified Lead Auditor for ISO 9001, IATF 16949 and/or VDA 6.3.</li><li>
Knowledge and experience in metallurgical processes including casting.</li><li>
Experience managing remote or global teams.</li><li>
Knowledge of Regulatory landscape related to transportation and automotive products.</li><li>
Familiarity with sustainability and compliance standards (e.g., RoHS, REACH, Conflict Minerals).</li><li>
Automotive manufacturing background is preferred.</li><li>
Certification in Six Sigma (Green Belt or higher) or Lean Manufacturing principles.</li></ul></div><div></div>

Global Supplier Quality Manager

SaniSure

<div><p><b>Job Summary</b></p><p>
The Supplier Quality Engineer (SQE) is responsible for ensuring that externally sourced materials, components, and services meet applicable regulatory, quality, and performance requirements for medical device manufacturing. This role partners cross-functionally with Supply Chain, Manufacturing, R&amp;D, and Regulatory Affairs to qualify, monitor, and continuously improve supplier performance in compliance with FDA 21 CFR Part 820 (QMSR), ISO 13485, and other global regulatory standards.</p><p><b>
Essential Functions</b></p><ul><li>
Supplier Qualification and Onboarding<ul><li>
Lead supplier selection and qualification activities, including:<ul><li>
Supplier audits (on-site and remote)</li><li>
Quality system assessments</li><li>
Technical capability evaluations</li></ul></li><li>
Approve supplier validation documentation and quality agreements</li><li>
Establish supplier quality requirements and acceptance criteria</li><li>
Ensure suppliers meet ISO 13485 and FDA QSR/QMSR expectations<ul><li>
Supplier Auditing and Oversight o Plan and execute supplier audits in accordance with risk-based audit schedules</li></ul></li><li>
Evaluate compliance to:<ul><li>
21 CFR Part 820</li><li>
ISO 13485</li><li>
ISO 14971 (as applicable)</li><li>
ISO 11135 / 11137 (for sterilization suppliers, if applicable)</li></ul></li><li>
Document audit findings and drive timely corrective actions</li><li>
Assess supplier readiness for regulatory inspections<ul><li>
Supplier Performance Monitoring</li></ul></li><li>
Establish and maintain supplier scorecards and KPIs</li><li>
Analyze supplier quality trends (PPM, NCRs, SCARs, OTD, etc.)</li><li>
Drive continuous improvement initiatives with suppliers</li><li>
Conduct quarterly business reviews as needed<ul><li>
Nonconformance &amp;CAPA Management</li></ul></li><li>
Lead supplier corrective action requests (SCARs)</li><li>
Investigate supplier-related nonconformances and complaints</li><li>
Perform root cause analysis (5-Why, Fishbone, etc.)</li><li>
Verify effectiveness of corrective and preventive actions</li><li>
Escalate critical quality issues appropriately</li><li>
Validation and Change Management Support</li><li>
Support supplier-related validation activities, including:<ul><li>
Process validation (IQ/OQ/PQ)</li><li>
Sterilization validation oversight</li><li>
Packaging validation support</li></ul></li><li>
Review and approve supplier change notifications</li><li>
Perform risk assessments for supplier changes</li><li>
Ensure proper implementation through change control processes</li><li>
Ensure compliance with biocompatibility, material, and regulatory requirements</li><li>
Support regulatory submissions requiring supplier documentation<ul><li>
Risk Management</li></ul></li><li>
Participate in supplier risk assessments</li><li>
Support DFMEA/PFMEA related to supplied components</li><li>
Ensure critical suppliers are identified and controlled appropriately<ul><li>
Cross-Functional Collaboration</li></ul></li><li>
Partner with:<ul><li>
Engineering during new product development</li><li>
Operations during scale-up and product transfer</li></ul></li><li>
Provide supplier quality input during design reviews</li></ul></li><li>
Perform additional job duties as assigned.</li></ul><p><b>
Education</b></p><ul><li>
Bachelor&rsquo;s degree in biological sciences, engineering, or a related field.</li></ul><p><b>
Required Experience &amp; Competencies</b></p><ul><li>
Minimum 5 years of quality experience in a regulated industry</li><li>
Strong knowledge of: FDA 21 CFR Part 820 (QMSR), ISO 13485, Risk Management (ISO 14971), CAPA systems, Supplier auditing practices</li><li>
Experience conducting supplier audits independently</li><li>
Experience managing SCARs and supplier performance metrics</li><li>
Strong technical writing and analytical skills</li><li>
ASQ Auditor, Lead auditor certification for 13485 preferred</li></ul></div>

Supplier Quality Engineer

Stellar Consulting Solutions, LLC

<div>
 <p>
  <strong>
   Role: Supplier Quality Analyst
  </strong>
 </p>
 <p>
  <strong>
   Location: Irvine, CA(Onsite)
  </strong>
 </p>
 <p>
  <strong>
   Duration: 6+Months(Contract#w2)
  </strong>
 </p>
 <p>
  <strong>
   Client: Medical
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  Education Bachelor Engineering or Quality
 </p>
 <p>
  Windchill / PLM Will red line Doc's
 </p>
 <p>
  Doc control , Validating systems , Updating supplier change request , reveiwing Quality Agreements
 </p>
 <p>
  <strong>
   Job Summary
  </strong>
 </p>
 <p>
  The Supplier Quality Analyst is responsible for ensuring that suppliers of materials, components, and services used in medical devices consistently meet quality, regulatory, and risk requirements. This role supports compliance with FDA Quality System Regulation (21 CFR 820), ISO 13485 through supplier performance monitoring, corrective action management, and risk-based supplier controls.
 </p>
 <p>
  <strong>
   Key Responsibilities
  </strong>
 </p>
 <ul>
  <li>
   Manage and maintain supplier qualification, monitoring, and re-evaluation activities in accordance with 21 CFR 820.50 (Purchasing Controls) and ISO 13485.
  </li>
  <li>
   Monitor supplier quality performance using KPIs such as defect rates, corrective action trends, and supplier risk levels.
  </li>
  <li>
   Maintain approved supplier lists (ASL) and supplier quality records per document control requirements.
  </li>
  <li>
   Issue, track, and evaluate Supplier change requests.
  </li>
  <li>
   Escalate supplier quality risks and support remediation and improvement plans.
  </li>
  <li>
   Review and support supplier-initiated or internally driven changes that may impact product quality or compliance (materials, processes, manufacturing location).
  </li>
  <li>
   Collaborate with Engineering and Regulatory Affairs to assess supplier changes requiring validation, verification, or regulatory impact evaluation.
  </li>
  <li>
   Provide supplier quality input for management reviews and quality metrics.
  </li>
  <li>
   Ensure supplier quality documentation is accurate, complete, and maintained in the electronic Quality Management System (eQMS).
  </li>
  <li>
   Ensure supplier activities comply with internal procedures, regulatory requirements, and quality system expectations.
  </li>
 </ul>
 <p>
  <strong>
   Required Qualifications
  </strong>
 </p>
 <ul>
  <li>
   Bachelor&rsquo;s degree in Engineering, Quality, or a related field; or equivalent experience.
  </li>
  <li>
   2&ndash;5 years of experience in Supplier Quality, Quality Assurance, or Manufacturing within a medical device or other regulated environment.
  </li>
  <li>
   Working knowledge of 21 CFR 820, ISO 13485, and supplier control requirements.
  </li>
  <li>
   Proficiency in Microsoft Excel and data analysis.
  </li>
 </ul>
 <p>
  <strong>
   Key Skills &amp; Competencies
  </strong>
 </p>
 <ul>
  <li>
   Strong understanding of regulated quality systems
  </li>
  <li>
   Analytical, detail-oriented problem-solving mindset
  </li>
  <li>
   Clear written and verbal communication
  </li>
  <li>
   Ability to influence suppliers and internal stakeholders
  </li>
  <li>
   Strong organizational and time-management skills.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  kindly share resume at gaurav@stellarconsulting.com or call me at 678-935-7045 to discuss more!
 </p>
</div>


Supplier Quality Assurance

Fluidstack

<div>
 <strong>
  About Fluidstack
  <br/>
  <br/>
 </strong>
 We exist to make humanity more free. For most of human history, you farmed or you starved. Technology gave people more time for the things they wanted to do, instead of things they had to do. Powerful AI will be the biggest lever for human choice we've ever built - but only if models are aligned with what humanity actually wants. There are groups building AI who don't share these goals. Whoever deploys frontier compute infrastructure fastest will decide whether AI expands human freedom or shrinks it.
 <br/>
 <br/>
 We're singularly focused on delivering 10 to 100s of GWs of compute faster than anyone else, rethinking every layer of the stack. We acquire power, design and build data centers, and operate them - with teams spanning hardware and software. Speed and scale are our key differentiators. Come be a part of building civilization-scale infrastructure for AI.
 <br/>
 <br/>
 <strong>
  We hire people who care deeply about this problem space. If that is you, please apply!
  <br/>
  <br/>
 </strong>
 <strong>
  About The Role
  <br/>
  <br/>
 </strong>
 We are looking for a Lead Supplier Quality Engineer to ensure the highest standards across our in-house manufacturing operations and external data center construction projects. As a people manager and subject matter expert, you will build and lead a team of quality engineers while sitting at the intersection of manufacturing production and large-scale infrastructure, owning quality from supplier selection through delivery.
 <br/>
 <br/>
 <strong>
  Responsibilities
  <br/>
  <br/>
 </strong>
 <em>
  <strong>
   Leadership &amp; Management
   <br/>
   <br/>
  </strong>
 </em>
 <ul>
  <li>
   Lead, mentor, and grow a team of supplier quality engineers across manufacturing and data center infrastructure disciplines
  </li>
  <li>
   Set team priorities, manage workload distribution, and drive a culture of quality and continuous improvement
  </li>
  <li>
   Serve as the organizational subject matter expert (SME) on supplier quality, providing guidance to cross-functional stakeholders including procurement, engineering, and construction teams
  </li>
  <li>
   Represent the supplier quality function in leadership reviews, program planning, and executive escalations
  </li>
  <li>
   Develop and manage KPI's and Metrics
  </li>
  <li>
   Support customer executive business reviews
  </li>
  <li>
   Role reports to VP, supply chain. Communication at the founder level will be required.
   <br/>
   <br/>
  </li>
 </ul>
 <em>
  <strong>
   Supplier Quality &amp; Operations
   <br/>
   <br/>
  </strong>
 </em>
 <ul>
  <li>
   Lead supplier qualification, audits, and ongoing performance management for both manufactured components and data center building materials/systems
  </li>
  <li>
   Develop and enforce quality control plans, inspection criteria, and acceptance standards for in-house production lines
  </li>
  <li>
   Partner with external data center general contractors and subcontractors to establish quality expectations and monitor compliance throughout construction
  </li>
  <li>
   Drive root cause analysis and corrective/preventive action (CAPA) processes for non-conformances across manufacturing and infrastructure suppliers
  </li>
  <li>
   Define and track supplier KPIs (defect rates, on-time delivery, audit scores); escalate and remediate underperforming suppliers
  </li>
  <li>
   Collaborate with procurement and engineering teams during new supplier onboarding and new product/facility introduction
  </li>
  <li>
   Support tier-two supplier development initiatives, including capability assessments and capacity planning
  </li>
  <li>
   Maintain quality documentation in compliance with relevant standards (ISO 9001, IPC, ASHRAE, etc.)
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   8+ years of supplier quality, manufacturing quality, or construction quality engineering experience, with at least 2 years in a lead or management role
  </li>
  <li>
   Demonstrated experience managing and developing engineering teams
  </li>
  <li>
   Familiarity with data center infrastructure (MEP systems, structural, electrical) strongly preferred
  </li>
  <li>
   Proficiency in quality tools: FMEA, control plans, SPC, 8D, PPAP
  </li>
  <li>
   Experience conducting supplier audits and managing corrective action workflows
  </li>
  <li>
   Proven ability to influence without authority across suppliers, contractors, and internal teams
  </li>
  <li>
   Bachelor's degree in Mechanical, Electrical, Industrial Engineering, or related field
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Preferred
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Experience in hyperscale or cloud infrastructure environments
  </li>
  <li>
   Certified Quality Engineer (CQE) or Six Sigma certification (Black Belt preferred)
  </li>
  <li>
   First principles mentality
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Salary &amp; Benefits
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Competitive total compensation package (salary + equity).
  </li>
  <li>
   Retirement or pension plan, in line with local norms.
  </li>
  <li>
   Health, dental, and vision insurance.
  </li>
  <li>
   Generous PTO policy, in line with local norms.
   <br/>
   <br/>
  </li>
 </ul>
 The base salary range for this position is $150,000 - $220,000 per year, depending on experience, skills, qualifications, and location. This range represents our good faith estimate of the compensation for this role at the time of posting. Total compensation may also include equity in the form of stock options.
 <br/>
 <br/>
 We are committed to pay equity and transparency.
 <br/>
 <br/>
 Fluidstack is an Equal Employment Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability and protected veterans&rsquo; status, or any other characteristic protected by law. Fluidstack will consider for employment qualified applicants with arrest and conviction records pursuant to applicable law.
 <br/>
 <br/>
 <em>
  You will receive a confirmation email once your application has successfully been accepted. If there is an error with your submission and you
  <strong>
   did not
  </strong>
  receive a confirmation email, please email careers@fluidstack.io with your resume/CV, the role you've applied for, and the date you submitted your application-- someone from our recruiting team will be in touch.
  <br/>
  <br/>
 </em>
 Compensation Range: $175K - $250K
 <br/>
 <br/>
</div>


Supplier Quality Engineer, Lead

Reckitt

<div></div><div><div><div><div>Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose. Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege.</div></div><div><div><h2 class="jobSectionHeader"><b>
About the role</b></h2>
</div><div><p>
We are looking for a <b>Commercial &amp; EMO Quality Manager</b> to lead end-to-end quality governance across Egypt &amp; North Africa. This role is responsible for ensuring product compliance, protecting consumers, and driving quality excellence across commercial operations and external manufacturing partners (EMOs), in line with global standards.</p>
<p>
You will act as the key Quality partner to the local leadership team, ensuring robust Quality Management Systems (QMS), strong supplier performance, and continuous improvement across the value chain.</p></div></div><div><div><h2 class="jobSectionHeader"><b>
Your responsibilities</b></h2>
</div><div><p><b>
Quality Leadership &amp; Governance</b></p>
<ul>
<li>Lead and maintain a compliant and effective Quality Management System (QMS)</li>
<li>Ensure ongoing inspection readiness and compliance with global and local regulations</li>
<li>Partner with the local Management Team as the Quality representative</li>
</ul>
<p><b>EMO &amp; Supplier Quality</b></p>
<ul>
<li>Approve, monitor, and audit external manufacturers and suppliers</li>
<li>Drive supplier performance, risk management, and continuous improvement</li>
<li>Ensure robust technical agreements and adherence to Reckitt quality standards</li>
</ul>
<p><b>Compliance &amp; Risk Management</b></p>
<ul>
<li>Ensure full compliance with regulatory, internal, and safety requirements</li>
<li>Lead quality risk assessments (e.g., product stability, packaging integrity, supply chain risks)</li>
<li>Own investigation and resolution of quality issues, including CAPA implementation</li>
</ul>
<p><b>Consumer &amp; Product Quality</b></p>
<ul>
<li>Ensure safety, quality, and performance of all products in the market</li>
<li>Lead complaint handling, product recall readiness, and incident management</li>
</ul>
<p><b>Continuous Improvement</b></p>
<ul>
<li>Identify and implement improvements across processes, products, and suppliers</li>
<li>Use data and KPIs to drive performance and decision-making</li>
</ul>
<p></p><p><b>Key Performance Indicators</b></p>
<ul>
<li>Product compliance and audit outcomes</li>
<li>Supplier quality performance</li>
<li>CAPA effectiveness and closure rate</li>
<li>Consumer complaints and quality incidents</li>
<li>QMS compliance and inspection readiness</li>
</ul></div></div><div><div><h2 class="jobSectionHeader"><b>The experience we're looking for</b></h2>
</div><div><ul><li>Degree in Life Sciences or related field</li>
<li>Strong experience in Quality Management within FMCG / manufacturing</li>
<li>Proven expertise in supplier quality and external manufacturing (EMO)</li>
<li>Solid knowledge of QMS, GMP/GDP, and regulatory frameworks</li>
<li>Experience in risk management tools (e.g., FMEA, root cause analysis)</li>
<li>Strong auditing background (Lead Auditor is a plus)</li>
<li>Excellent stakeholder management and influencing skills</li>
</ul></div></div><div><div><h2 class="jobSectionHeader"><b>The skills for success</b></h2>
</div><div>#N/A</div></div><div><div><h2 class="jobSectionHeader"><b>
What we offer</b></h2>
</div><div>With inclusion at the heart of everything we do, working alongside our four global Employee Resource Groups, we support our people at every step of their career journey, helping them to succeed in their own individual way. We invest in the wellbeing of our people through parental benefits, an Employee Assistance Program to promote mental health, and life insurance for all employees globally. We have a range of other benefits in line with the local market. Through our global share plans we offer the opportunity to save and share in Reckitt's potential future successes. For eligible roles, we also offer short-term incentives to recognise, appreciate and reward your work for delivering outstanding results. You will be rewarded in line with Reckitt's pay for performance philosophy.</div></div><div><div><h2 class="jobSectionHeader"><b>
Equality</b></h2>
</div><div>We recognise that in real life, great people don't always 'tick all the boxes'. That's why we hire for potential as well as experience. Even if you don't meet every point on the job description, if this role and our company feels like a good fit for you, we still want to hear from you. All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion, faith; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law.</div></div></div></div>

Commercial and EMO Quality Manager, Egypt & North Africa

Henkel

<div>
 <strong>
  About this Position
 </strong>
 Responsible for optimizing and managing the Contract Manufacturing network by qualifying and auditing suppliers, analyzing and digitalizing the CM footprint, overseeing inventory efficiency, and evaluating supplier performance to support innovation, compliance, and cost-effective growth.
 <br/>
 <br/>
 <strong>
  What You&acute;ll Do
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Optimizing the Contract Manufacturing (CM) qualification process, coordinate and execute qualification audits to validate CM readiness and adherence to standards for supporting innovation initiatives.
  </li>
  <li>
   Creating yearly Inventory support /consolidation (FG, Material and Assets) while overseeing &amp; supporting end to end inventory operations to sustain accurate tracking, support product needs and drive cost-effective stock management.
  </li>
  <li>
   Analyzing CM Footprint &amp; Power BI updates (Digitalized footprint), assessing and optimizing the CM network to ensure balanced coverage, minimize risk and support future growth needs.
  </li>
  <li>
   Segmenting CMs on Classification / Strategy based on our Score card system, capability and strategic relevance to enable tailored management and aligning with business goals.
  </li>
  <li>
   Regular evaluate supplier performance using defined KPIs to support data driven decisions and enable continuous improvement and evaluate whether new CMs can be added to help with innovation projects.
  </li>
  <li>
   Supporting respective teams with Market Screening &amp; Scouting proactively to strengthen Henkel&rsquo;s supplier base by screening the market for new potential partners and scouting innovative technologies or capabilities.
  </li>
  <li>
   Co-leading supplier Audits and supporting the SHEQ team throughout the audit process by providing the necessary data, documentation, and cross functional inputs to ensure a comprehensive evaluation.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  What makes you a good fit
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor&rsquo;s degree in Engineering, Supply Chain, Operations, or related field
  </li>
  <li>
   1-3 years of experience in manufacturing, supply chain, or contract manufacturing management
  </li>
  <li>
   Strong understanding of SHEQ, GMP, and industrial operations
  </li>
  <li>
   Proven experience in cross-functional stakeholder management
  </li>
  <li>
   Solid financial and analytical skills (cost models, savings, KPIs)
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Some perks of joining Henkel
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Flexible work scheme with flexible hours, hybrid work model, and work from anywhere policy for up to 30 days per year
  </li>
  <li>
   Diverse national and international growth opportunities
  </li>
  <li>
   Global wellbeing standards with health and preventive care programs
  </li>
  <li>
   Gender-neutral parental leave for a minimum of 8 weeks
  </li>
  <li>
   Employee Share Plan with voluntary investment and Henkel matching shares
  </li>
  <li>
   Comprehensive Health Insurance for employee + dependents
  </li>
  <li>
   Employee Assistance Programme provides a wide range of mental health and wellbeing benefits
   <br/>
   <br/>
  </li>
 </ul>
 At Henkel, we come from a broad range of backgrounds, perspectives, and life experiences. We believe the uniqueness of all our employees is the power in us. Become part of the team and bring your uniqueness to us! We look for a diverse team of individuals who possess different backgrounds, experiences, personalities and mindsets.
</div>


Contract Manufacturing KAM

Oshkosh Defense

<div><p><b>About Oshkosh Defense, an Oshkosh company</b></p><p></p><p><b>
Oshkosh Defense stands behind those who dedicate their lives to protecting others. As an industry-leading tactical vehicle manufacturer, every day we strive to meet or exceed our customers' ever-changing needs with next generation defense technologies and advanced systems. We operate with unparalleled commitment to those who depend on our products and services worldwide to perform their missions.</b></p><p></p><p><b>
YOUR IMPACT</b></p><p>
We are looking for a dynamic Supplier Quality Engineer to launch new suppliers and support the facility into production. As a Supplier Quality Engineer, your mission is to continuously improve safety, quality, business, and manufacturing processes with an emphasis on eliminating process waste. The use of structured quality improvement tools is required through validation of the production processes. You will design new processes and re-engineer existing processes to produce outcomes that meet safety, quality, and business expectations.</p><ul><li><p>
Validate production processes to ensure potential failure risks are considered and mitigated on the suppliers FMEA and Process Control Plans</p></li><li><p>
Promote SPC and error proofing internally and externally with suppliers where there is risk of common mistakes and/or significant failure</p></li><li><p>
Provide support as needed and work with suppliers to prioritize defects using tools such as Pareto charts and trend charts. Apply structured problem-solving methods to identify true root causes and implement effective corrective actions, including fishbone diagrams, 5 Why analysis, histograms, SPC, FMEA, benchmarking, brainstorming, 5S, correlation analysis, error proofing, Cpk, Ppk, corrective action matrices, and continual improvement control plans.</p></li><li><p>
Revise procedures to drive process improvement.</p></li><li><p>
Investigate/analyze and benchmark industry practices for process validation assessments.</p></li><li><p>
Implement effective corrective and preventative actions utilizing structured planning methods.
</p></li><li><p>Coordinate and work cross-functionally with Employee Teams, Quality, Engineering, Contracts, Sales and Manufacturing to improve processes. Accurately maintain company records and documents in accordance with policies and procedures.
</p></li><li><p>Minimal travel as required. (Once per month on average for a duration of 1-3 days.)</p></li><li><p>
Accurately maintain company records and documents in accordance with policies and procedures.</p></li></ul><p></p><p><b>
MINIMUM QUALIFICATIONS
</b></p><ul><li><p>Bachelor's Degree in a related field</p></li><li><p>
1-3 plus years related work experience</p></li><li><p>
Must interpret basic technical drawings including characteristics such as views, title blocks, dimensioning, GD&amp;T symbols, etc. Interpret specification requirements in relation to product and process characteristics</p></li><li><p>
Training/experience in the use of statistical techniques and process improvement methods</p></li></ul><p></p><p><b>
STANDOUT QUALIFICATIONS
</b></p><ul><li><p>Hold a Six Sigma Green Belt or Black Belt or must acquire within eight months of filling this position</p></li><li><p>
ASQ Certified Quality Engineer certification (or equivalent) required within eight (8) months of filling this position</p></li><li><p>
Advanced training/experience in the use of statistical techniques and process improvement methods</p></li><li><p>
Must interpret basic technical drawings including characteristics such as views, title blocks, dimensioning, tolerancing, GD&amp;T symbols, etc. Interpret specification requirements in relation to product and process characteristics</p></li><li><p>
Must have experience with and be able to exhibit the use of structured problem-solving techniques utilizing computer applications</p></li><li><p>
MS Windows, Microsoft Word, Microsoft Excel, Microsoft Project, Lotus Notes e-mail, Visio, Statistical software, and JDE experience is recommended and will be mandatory within three (3) months in this position</p></li></ul><p></p><p><b>
Pay Range:</b></p>
$64,500.00 - $103,500.00<p></p><div><div><div><div><div><div><div><div><p>
The above pay range reflects the minimum and maximum target pay for the position across all U.S. locations. Within this range, individual pay is determined by various factors, including the scope and responsibilities of the role, the candidate's experience, education and skills, as well as the equity of pay among team members in similar positions. Beyond offering a competitive total rewards package, we prioritize a people-first culture and offer various opportunities to support team member growth and success.</p></div></div></div></div></div></div></div></div><p></p><p>
Oshkosh is committed to working with and offering reasonable accommodation to job applicants with disabilities. If you need assistance or an accommodation due to disability for any part of the employment process, please contact us at corporatetalentacquisition@oshkoshcorp.com.</p><p></p><p>
Oshkosh Corporation is a merit-based Equal Opportunity Employer. Job opportunities are open for application to all qualified individuals and selection decisions are made without regard to race, color, religion, sex, national origin, age, disability, veteran status, or other protected characteristic. To the extent that information is provided or collected regarding categories as provided by law it will in no way affect the decision regarding an employment application.</p><p></p><p>
Oshkosh Corporation will not discharge or in any manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with Oshkosh Corporation's legal duty to furnish information.</p><p></p><p>
Certain positions with Oshkosh Corporation require access to controlled goods and technologies subject to the International Traffic in Arms Regulations or the Export Administration Regulations. Applicants for these positions may need to be &quot;U.S. Persons,&quot; as defined in these regulations. Generally, a &quot;U.S. Person&quot; is a U.S. citizen, lawful permanent resident, or an individual who has been admitted as a refugee or granted asylum.</p></div>

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