CNH Industrial

<div>Job ID: 2864<br>
Location: Fully On-Site, Noida, Uttar Pradesh, IN<br>
Job Family: Quality<br>
Job Type: Permanent<br>
Employment Type: Full Time</div>
<br><div><div><div><div><div><b>About Us</b></div>
</div><div><p>Innovation. Sustainability. Productivity. This is how we are Breaking New Ground in our mission to sustainably advance the noble work of farmers and builders everywhere. With a growing global population and increased demands on resources, our products are instrumental to feeding and sheltering the world.</p>
<p>From developing products that run on alternative power to productivity-enhancing precision tech, we are delivering solutions that benefit people &ndash; and they are possible thanks to people like you. If the opportunity to build your skills as part of a collaborative, global team excites you, you&rsquo;re in the right place.</p>
<p><b>Grow a Career. Build a Future!</b></p>
<p>Be part of this company at the forefront of agriculture and construction, that passionately innovates to drive customer efficiency and success. And we know innovation can&rsquo;t happen without collaboration. So, everything we do at CNH Industrial is about reaching new heights as one team, always delivering for the good of our customers.</p>
</div></div><div><div><div><b>Job Purpose</b></div>
</div><div><p>The Supplier Quality Specialist ensures the quality and reliability of materials, components, and services provided by suppliers. This role focuses on evaluating supplier performance, conducting audits, and driving continuous improvement initiatives to meet quality standards and support production needs.</p>
</div></div><div><div><div><b>Key Responsibilities</b></div>
</div><div><ul><li>Assess and monitor supplier performance to ensure compliance with quality standards and specifications.</li>
<li>Conduct supplier audits and inspections to identify areas for improvement and ensure adherence to requirements.</li>
<li>Investigate and resolve supplier-related quality issues, including root cause analysis and corrective actions.</li>
<li>Collaborate with suppliers and internal teams to implement quality improvement initiatives.</li>
<li>Maintain and update supplier quality documentation and reports.</li>
<li>Support the qualification and onboarding of new suppliers through evaluations and approvals.</li>
</ul></div></div><div><div><div><b>Experience Required</b></div>
</div><div><ul><li>BE / B.Tech in Electrical &amp; Electronics</li>
<li>10 years experience in handling SQA / SQE in an automotive organization handling Electrical &amp; Electronics parts development</li>
</ul></div></div><div><div><div><b>Preferred Qualifications</b></div>
</div></div><div></div><div><div><div><b>What We Offer</b></div>
</div><div><p>We offer dynamic career opportunities across an international landscape. As an equal opportunity employer, we are committed to delivering value for all our employees and fostering a culture of respect.</p>
<p>At CNH, we understand that the best solutions come from the diverse experiences and skills of our people. Here, you will be empowered to grow your career, to follow your passion, and help build a better future. To support our employees, we offer regional comprehensive benefits, including:</p>
<ul><li><i>Flexible work arrangements</i></li>
<li><i>Savings &amp; Retirement benefits</i></li>
<li><i>Tuition reimbursement</i></li>
<li><i>Parental leave</i></li>
<li><i>Adoption assistance</i></li>
<li><i>Fertility &amp; Family building support</i></li>
<li><i>Employee Assistance Programs</i></li>
<li><i>Charitable contribution matching and Volunteer Time Off</i></li></ul></div></div></div></div>

PPAP - SQE

<div><div><div><div><div>Requisition ID: 23261
</div></div></div></div><div><div><div><div>Job Category: Engineering &amp; Technology
</div></div></div></div><div><div><div><div>Career level: Specialist
</div></div></div></div><div><div><div><div>Contract type: Permanent
</div></div></div></div><div><div><div><div>Location:
Pune, IN
</div></div></div></div><h1 class="jobSectionHeader"><b>About SKF</b></h1>
<p>
SKF started its operations in India in 1923. Today, SKF provides industry leading automotive and industrial engineered solutions through its five technology-centric platforms: bearings and units, seals, mechatronics, lubrication solutions and services. Over the years the company has evolved from being a pioneer ball bearing manufacturing company to a knowledge-driven engineering company helping customers achieve sustainable and competitive business excellence.</p><br>
<p></p>
<div>
SKF's solutions provide sustainable ways for companies across the automotive and industrial sectors to achieve breakthroughs in friction reduction, energy efficiency, and equipment longevity and reliability. With a strong commitment to research-based innovation, SKF India offers customized value-added solutions that integrate all its five technology platforms.</div>
<div>
To know more, please visit: <i>www.skf.com</i><i>/in</i></div><br>
<p></p>
<h1 class="jobSectionHeader"><b>
SKF Purpose Statement</b></h1>
<p>
Together, we re-imagine rotation for a better tomorrow.</p>
<p>
By creating intelligent and clean solutions for people and the planet</p><br>
<p></p>
<div><b>
JOB </b><b>DESCRIPTION</b></div><br>
<p></p>
<div><b>
Position Title: </b>Solution Owner SQE</div>
<p><b>
Reports To: </b>Manager Digitalization</p>
<p><b>
Role Type: </b>Individual Contributor</p>
<p><b>
Location:</b><b> </b>Pune</p><br>
<p></p>
<h1 class="jobSectionHeader"><b>
Purpose of the role</b></h1><br>
<div></div>
<div>
We are seeking a dynamic and organized individual to join our SQE Digital team within the Center of Excellence. In this role, you will play a key part in coordinating and supporting the implementation of innovative digital solutions for Sustainability, Quality, and EHS (Environment, Health &amp; Safety).</div>
<div>
As a core team member, you will contribute to various projects and deployment initiatives, working across diverse functions within SKF&mdash;from Design &amp; Engineering and Sales to Demand Chain &amp; Logistics, Manufacturing, and Purchasing. Developing a solid cross-domain understanding of these business areas will be essential to your success.</div>
<div>
You will support global SKF teams in both current operations and the evolution of future digital processes and IT systems, ensuring alignment with strategic objectives across the organization.</div><div></div><p><br>
As a valued member of the SQE Digital Solutions team, you will:</p>
<p><b>
K</b><b>ey Responsibilities</b></p>
<ul>
<li>Provide specialist technical advice and support on all aspects of Tool assembly, change over, spare management, design, manufacturing and estimating.
</li></ul><ul><li><b>Manage Ideas and Demand:</b> Capture, screen, and prioritize incoming ideas and solution demands to support strategic decision-making.</li>
<li><b>Administer User Access:</b> Oversee user access and permissions for key systems such as Intelex, Relyence, and Any4M via ServiceNow Access Management.</li>
<li><b>Coordinate System Releases:</b> Plan and manage release cycles for digital solutions, ensuring smooth implementation and minimal disruption.</li>
<li><b>Maintain System Administration:</b> Handle configuration of user groups and maintain master data to ensure integrity and consistency across platforms.</li>
<li><b>Oversee Reports and Dashboards:</b> Develop, maintain, and optimize dashboards and reports to provide actionable insights for business stakeholders.</li>
<li><b>Manage Archived Systems:</b> Ensure the continued accessibility and governance of archived digital systems.</li>
<li><b>Provide Support:</b> Act as a second-line support contact for SKF users, managing escalations that go beyond standard ServiceNow assistance and liaising directly with IT vendors when needed.</li>
</ul>
<div><b>High interest in developing following knowledge</b></div><br>
<div></div>
<p>
We&rsquo;re looking for someone with a strong curiosity and drive to deepen their knowledge in the following areas:</p>
<ul>
<li><b>Understanding Business Processes:</b> Gain insights into functional business requirements and operational workflows across diverse domains.</li>
<li><b>Platform Configuration &amp; Implementation:</b> Learn how to design and implement new processes within global digital platforms like Intelex.</li>
<li><b>Technical Foundations:</b> Build a solid background in digital concepts such as master data structures and workflow automation.</li>
<li><b>Process Modeling &amp; Documentation:</b> Explore methods for visualizing, managing, and documenting business processes.</li>
<li><b>Data Handling:</b> Strengthen skills in data modeling, management, import/export processes, and data transformation.</li>
<li><b>ETL &amp; MDM Practices:</b> Develop knowledge of Extract-Transform-Load strategies and Master Data Management frameworks.</li>
<li><b>Systems Integration:</b> Understand API functionality and other data connection mechanisms to support seamless system interactions.</li></ul><br>
<p></p>
<p><b>
Preferred Experience</b></p>
<p>
Candidates with familiarity in the following SKF processes and systems will be at an advantage:</p>
<ul>
<li><b>Business Process Understanding:</b></li>
<li><ul><li>Solid grasp of business requirements and operational workflows across multiple domains (Design, Engineering, Sales, Logistics, Manufacturing, Purchasing).</li>
<li>Skills in visualizing, managing, and documenting business processes.</li>
<li>Examples of key Business processes in SQE domains: Audits Management, Incident Management (EHS), Customer Complaints, Vendor Complaints, Problem Solving and Corrective &amp; Preventive Actions, PPAP, Risk Management &amp; Core Documents, Change Management (ECM).</li>
</ul></li><li><b>Intelex Platform Experience</b>: Hands-on experience configuring or using Intelex modules, especially for Sustainability, Quality, and EHS.</li>
<li><b>Lotus Notes Databases</b>: Especially legacy databases related to Quality and Environment, Health &amp; Safety.</li>
<li><b>Microsoft 365 Tools including</b>:</li>
<li><ul><li>SharePoint for document management and collaboration</li>
<li>Power BI for data analysis and interactive reporting</li>
<li>Teams for team communication and meetings</li>
<li>Word &amp; Excel &amp; PowerPoint for documentation and data processing tasks.</li></ul></li></ul><br>
<p>
</p><p>If you are interested and meet the above requirements, you can also submit your application by sending your latest resumes to Senior Recruiter - Sharath (Sharath.kumar.d@Skf.com)</p></div>

Solution Analyst SQE

Anika Therapeutics

<div><p><b>Position Scope:</b></p><p>
The Supplier Quality Engineer (SQE) is responsible for the establishment/maintenance of a supplier quality program that enables realization of a zero-defect philosophy to our patients/customers for supplied material/services.</p><p><b>
Strategic Focus Areas:</b></p><p>
The SQE will be responsible for the development and control of suppliers and contract manufacturers (CM). The SQE has direct accountability to ensure that all material/services used in the fabrication and release of Anika products meets specification. The SQE will drive continuous improvement for supplier quality processes to increase compliance and efficiency. Additionally, they will collaborate with all functions to understand business/project requirements to execute improvement strategies for supplier quality performance.</p><p><b>
Specific Tactical Responsibilities:</b></p><ul><li>
Develop and implement product and/or process controls required to ensure supplied material/service meets all design output requirements and drive business efficiency.</li><li>
Provide input to incoming inspection requirements based on supplier assessments and product process controls for controlling risk.</li><li>
Actively drive the assessment and improvement of quality system processes associated with supplier development/quality.</li><li>
Full engagement and ownership in resolving supplier quality issues.</li><li>
Process requests for the onboarding of new suppliers.</li><li>
Track, analyze, and report on supplier performance metrics to stakeholders along with recommendations for tactical and strategic improvements.</li><li>
Perform/coordinate Supplier audits (Quality System and/or Product Quality based) and follow up on their results.</li><li>
Other duties as assigned.</li></ul><p><b>
Job Complexity:</b></p><p>
The Supplier Quality Engineer works on complex issues requiring analysis and use in-depth evaluation of factors.</p><p><b>
Supervisory Responsibilities:</b></p><p>
None</p><p><b>
Required Qualifications:</b></p><ul><li>
Bachelor&rsquo;s degree in Engineering or related field or equivalent experience.</li><li>
Minimum of 3-5 years of related experience in the medical device, biotech, or pharmaceutical industry.</li><li>
Strong understanding of medical device regulations and standards, including QSR (21 CFR Part 820), Quality Management Systems (ISO 13485), and EU MDR (2017/745).</li><li>
Lead Auditor Certification preferred. Preferably ISO 13485.</li><li>
Versed in application of ISO 14971 with regards to FMEAs, Verification/Validation, and Risk Management.</li><li>
Knowledge of statistical techniques with regards to product development, production processes, and inspection plans.</li><li>
Problem solving ability, strong analytical skills, and diplomacy required.</li><li>
Strong oral and written communication skills.</li><li>
Self-motivated and ability to manage time working on multiple projects simultaneously.</li><li>
Must be able to communicate appropriately and adequately to all levels of the organization in both individual and group settings.</li><li>
Competency in MS office applications.</li></ul><p><b>
Desired Experience, Knowledge, and Skills:</b></p><ul><li>
Experience with SAP preferred.</li><li>
Experience with MasterControl preferred.</li><li>
Project Management (conducting status meetings, project reporting, etc) is a plus.</li></ul><p><b>
Travel:</b></p><p>
May include up to 20% travel (including US and OUS).</p><p></p><p><i><br>
The salary range provided is based on the Company&rsquo;s reasonable estimate of the base salary pay range for this position at the time of posting. Actual base pay is determined by several factors relevant to the position, including skills, competencies, experience, education, and geographic location. Anika also offers a discretionary bonus program for all full-time employees, comprehensive healthcare benefits, health savings account, 401(k) plan with up to 5% company match which includes immediate vesting, employee stock purchase plan at a 15% discount, accrued paid time off, additional long-term incentives including stock awards, and much more. At Anika, we take pride in offering robust Total Rewards, inclusive of market-leading benefits to meet our employees where they are in their career and in life.</i></p><p><i>
The compensation and benefits information is provided as of the date of this posting. Anika reserves the right to modify compensation and benefits at any time, subject to applicable law.</i></p></div>

Senior Supplier Quality Engineer

Shively Diversified Management Services

<div><p>The Supplier Quality Engineer (SQE) manages supplier quality and component/service integrity through assessment of: capabilities, compliance to processes and automotive standards, performance scorecards, continuous improvement efforts, and corrective actions.</p><p></p><p><b>
ESSENTIAL FUNCTIONS:</b></p><p></p><ul><li>Evaluate supplier viability through feasibility studies, audits, capacity (run@rate) and record of performance.</li><li>Provide recommendations and develop action plans to close gaps and improve quality/delivery performance; monitor performance and follow-up to ensure full implementation of control plan objectives.</li><li>Perform engineering studies and analyses to root cause issues and develop effective resolutions.</li><li>Facilitate/lead Relyans Max supplier quality meetings, problem solving, reject/defect investigation related to supplier products and services.</li><li>Manage supplier scorecards; initiate appropriate action based on trends and performance.</li><li>Coordinate incoming material inspection processes with Materials, Quality and Engineering.</li><li>Manage purchased part quality issues including: initial supplier contact, containment for quality issues, and the permanent corrective action cycle.</li><li>Travel to supplier locations for verification.</li><li>Participate in Relyans Max global supplier quality strategies and initiatives.</li><li>Monitor and ensure timely implementation of Engineering Change Requests (supplier or customer initiated), including PPAP approval.</li><li>Manage IATF 16949 internal and external audit process for supplier activities.</li><li>Support cross-functional problem-solving and corrective actions for quality-related material shortages.</li><li>Develop and implement statistically valid sampling plans, designed experiments, capability studies, SPC, and trend analysis in support of products and service improvements.</li><li>Identify internal improvement opportunities and coordinate corrective actions within both Relyans Max and supplier manufacturing processes.</li><li>Manage the physical and electronic quarantine of suspect or defective product, both in-process and in the warehouse.</li><li>Manage supplier RMA numbers to complete disposition on suspect material within Hold Cage or RMA area in a timely manner.</li><li>Support Purchasing with cost recovery and debits related to supplier issues.</li><li>Serve as a role model within Relyans Max and with suppliers for creating a culture of quality through general awareness, training, and education of quality policies and practices; drive a zero-defect and continuous improvement mindset.</li><li>Review supplier quality manuals and recommend / implement improvements in coordination with Purchasing based on customer specific requirements and audit feedback.</li><li>Conduct training for suppliers in quality principles, effective corrective actions, and valid statistical techniques.</li><li>Support OEM Quality Management as assigned.</li><li>Perform other duties as identified in support of business objectives.</li></ul><p></p><p><b>
CORE COMPETENCIES REQUIRED:</b></p><p></p><ul><li>Intermediate or higher level knowledge of general statistical analysis, PFMEA, Control Plans, Containment Plans, MSA, GD&amp;T, Gage Methodology, Gage R&amp;R, APQP, PPAP, Run@Rate, Capacity and Feasibility analysis.</li><li>High level knowledge of product reliability and testing methods.</li><li>High level root cause and problem-solving skills.</li><li>High level presentation, facilitation and conflict resolution skills.</li><li>Able to draft effective policies, plans, and supplier communications.</li><li>Comprehensive understanding and successful application of ASTM, ISO:9001 / IATF16949, ISO:14001, ISO/IEC:17025:VDA 6.3 standards.</li><li>Comprehensive knowledge of preparing &amp; executing audits and assessments and following up on corrective actions.</li><li>Proficient in the use of Microsoft Office, SAP and Document Management Systems.</li><li>Team-orientation to participate in and frequently lead cross-functional teams.</li></ul><p></p><p><b>
Requirements</b></p><p><b>
JOB QUALIFICATIONS:</b></p><p></p><ul><li>Bachelor&rsquo;s degree in a technical field and/or 5+ years of combined Manufacturing/Quality Engineering and/or Quality Systems experience.</li><li>5+ years of experience working in an ISO / IATF certified environment preferred.</li><li>1+ year of working in the fastener industry highly preferred.</li><li>ASQ certification (CQI, CQA, CQT, CQE etc...) and / or PMP certifications a plus.</li><li>Ability to travel up to 25% of the work week with little advanced notice.</li></ul><p></p><p><b>
ENVIRONMENTAL EXPOSURES:</b></p><p></p><ul><li>Noise &ndash; heavy machinery if in plant.</li><li>Noise &ndash; vibratory bowls and air feed systems &ndash; if in plant.</li><li>Chemicals, oils, acids, sprays, coolants and solvents.</li><li>Responsible for complying with regulations and standards covered under MISOSHA.</li></ul></div>

Supplier Quality Engineer

GE HealthCare

<div>
 <strong>
  Job Description Summary
  <br/>
  <br/>
 </strong>
 Engineering associated with the manufacturing process. Impacts departmental operations and responsible for planning/execution. The role has some autonomy but is focused on execution of activities within an operating discipline covered by standard functional practices and procedures. Some judgment may be required but this is typically with guidance.
 <br/>
 <br/>
 <strong>
  Job Description
  <br/>
  <br/>
 </strong>
 <strong>
  This Job is responsible for:
  <br/>
  <br/>
 </strong>
 <strong>
  Design Transfer
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Lead the design transfer activities of product specifications to manufacturing by working with global design owners and local partners.
  </li>
  <li>
   Review the design specifications feasibility in terms of assembly and test, make sure that production constrains are respected.
  </li>
  <li>
   Define and validate production and test processes including production instructions and reports.
  </li>
  <li>
   Coordination of manufacturing releases
  </li>
  <li>
   Lead the manufacturing documentation development and release
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Manufacturing Process Set Up, Validation And Continuous Improvement
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Drive improved product quality by identifying manufacturing issues, developing cost-effective solutions, and overseeing successful implementation into production.
  </li>
  <li>
   Work with contract manufacturing supplier&rsquo;s production associates to resolve manufacturing and quality problems related to methods, processes, tooling, equipment and product design.
  </li>
  <li>
   Monitor and optimize contract manufacturing supplier&rsquo;s workstations designs and manufacturing cycle time
  </li>
  <li>
   Actively support lean, continuous improvement and design for manufacturing initiatives.
  </li>
  <li>
   Monitor and improve productivity, while ensuring all customer commitments are met in a timely, quality and cost-conscious manner
  </li>
  <li>
   Maintain (calibration and verification support) and troubleshoot production equipment
  </li>
  <li>
   Define, validate and control production process including tooling and equipment. Work with local and global suppliers to purchase and maintain them.
  </li>
  <li>
   Validate design specifications and shop floor application of new product, tools, or equipment.
  </li>
  <li>
   Specify and expedite planned maintenance routines on all production equipment and systems.
  </li>
  <li>
   Work closely with regulatory affairs department to support the compliance with all local regulations.
  </li>
  <li>
   Define and support local parts purchases and validation process according to GE HealthCare quality procedures.
  </li>
  <li>
   Design the production layout and assure the conformity to EHS policy and to local regulations.
  </li>
  <li>
   Act as a materials change coordinator or/and manufacturing process leader: be the contact point for design or process change communications and lead the implementation of changes in cooperation with supplier quality engineer (SQE)
  </li>
  <li>
   Provide guidance and expertise to manufacturing engineer
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Quality Control
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Responsible for determining processes requiring validation, development of plans and analysis criteria, execution and final analysis.
  </li>
  <li>
   Ensuring regulatory compliance through Validation &amp; Verification.
  </li>
  <li>
   Lead quality metrics follow up and control in production and drives process quality improvements and simplification
  </li>
  <li>
   Assure that corrective action is taken to resolve observed safety concerns in all areas.
  </li>
  <li>
   Support and follow up contract manufacturing supplier&rsquo;s CAPA cases management.
  </li>
  <li>
   Support SQE &amp; follow up for contract manufacturing supplier&rsquo;s SCAR&rsquo;s
  </li>
  <li>
   Ensure compliance to GE HealthCare quality procedures and local regulations.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Minimum Requirements
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   B.S. Degree in Mechanical, Electrical, Industrial Engineering or related technical degree
  </li>
  <li>
   7 years of experience in production, engineering
  </li>
  <li>
   Good analytical and planning skills
  </li>
  <li>
   Excellent English (Writing &amp; Communicating)
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  <strong>
   <strong>
    Additional Information
    <br/>
    <br/>
   </strong>
  </strong>
 </strong>
 <strong>
  Relocation Assistance Provided:
 </strong>
 Yes
 <br/>
 <br/>
</div>


Manufacturing Engineer

<div><h1 class="jobSectionHeader"><b>Job Description Summary</b></h1>
Engineering associated with the manufacturing process. Impacts departmental operations and responsible for planning/execution. The role has some autonomy but is focused on execution of activities within an operating discipline covered by standard functional practices and procedures. Some judgment may be required but this is typically with guidance.<p></p><h1 class="jobSectionHeader"><b>
Job Description</b></h1><p><b>
This Job is responsible for:</b></p><p><b>
Design transfer</b><b>:</b></p><ul><li><p>
Lead the design transfer activities of product specifications to manufacturing by working with global design owners and local partners.</p></li><li><p>
Review the design specifications feasibility in terms of assembly and test, make sure that production constrains are respected.</p></li><li><p>
Define and validate production and test processes including production instructions and reports.</p></li><li><p>
Coordination of manufacturing releases</p></li><li><p>
Lead the manufacturing documentation development and release</p></li></ul><p><b>
Manufacturing process set up, validation and continuous improvement:</b></p><ul><li><p>
Drive improved product quality by identifying manufacturing issues, developing cost-effective solutions, and overseeing successful implementation into production.</p></li><li><p>
Work with contract manufacturing supplier&rsquo;s production associates to resolve manufacturing and quality problems related to methods, processes, tooling, equipment and product design.</p></li><li><p>
Monitor and optimize contract manufacturing supplier&rsquo;s workstations designs and manufacturing cycle time</p></li><li><p>
Actively support lean, continuous improvement and design for manufacturing initiatives.</p></li><li><p>
Monitor and improve productivity, while ensuring all customer commitments are met in a timely, quality and cost-conscious manner</p></li><li><p>
Maintain (calibration and verification support) and troubleshoot production equipment</p></li><li><p>
Define, validate and control production process including tooling and equipment. Work with local and global suppliers to purchase and maintain them.</p></li><li><p>
Validate design specifications and shop floor application of new product, tools, or equipment.</p></li><li><p>
Specify and expedite planned maintenance routines on all production equipment and systems.</p></li><li><p>
Work closely with regulatory affairs department to support the compliance with all local regulations.</p></li><li><p>
Define and support local parts purchases and validation process according to GE HealthCare quality procedures.</p></li><li><p>
Design the production layout and assure the conformity to EHS policy and to local regulations.</p></li><li><p>
Act as a materials change coordinator or/and manufacturing process leader: be the contact point for design or process change communications and lead the implementation of changes in cooperation with supplier quality engineer (SQE)</p></li><li><p>
Provide guidance and expertise to manufacturing engineer</p></li></ul><p></p><p><b>
Quality control:</b></p><ul><li><p>
Responsible for determining processes requiring validation, development of plans and analysis criteria, execution and final analysis.</p></li><li><p>
Ensuring regulatory compliance through Validation &amp; Verification.</p></li><li><p>
Lead quality metrics follow up and control in production and drives process quality improvements and simplification</p></li><li><p>
Assure that corrective action is taken to resolve observed safety concerns in all areas.</p></li><li><p>
Support and follow up contract manufacturing supplier&rsquo;s CAPA cases management.</p></li><li><p>
Support SQE &amp; follow up for contract manufacturing supplier&rsquo;s SCAR&rsquo;s</p></li><li><p>
Ensure compliance to GE HealthCare quality procedures and local regulations.</p></li></ul><p></p><p><b>
Minimum Requirements:</b></p><ul><li><p>
B.S. Degree in Mechanical, Electrical, Industrial Engineering or related technical degree</p></li><li><p>
7 years of experience in production, engineering</p></li><li><p>
Good analytical and planning skills</p></li><li><p>
Excellent English (Writing &amp; Communicating)</p></li></ul><p></p><p>
#LI-AO</p><p>
#LI-HYBRID</p><p></p><h1 class="jobSectionHeader"><b>
Additional Information</b></h1><div><div><div><div><div><div><div><p><b>
Relocation Assistance Provided: </b>Yes</p></div></div></div></div></div></div></div></div><p></p>

targetjobs UK

<p>White & Case is a global law firm with more than 2,500 lawyers worldwide. We've built an unrivalled network of 43 offices in 29 countries, an investment that is the foundation for our client work in more than 200 countries today.</p><p>Our innovative approaches and nuanced local market knowledge create unique solutions to our clients' most complex domestic and multijurisdictional deals and disputes. We anticipate what they want, provide what they need and build lasting relationships. Our culture comes to life through our three core values: Pioneering, United and Human.</p><p>The training contract consists of four six-month seats, one of which is <b>guaranteed to be spent in one of our overseas offices</b>: Abu Dhabi, Doha, Dubai, Riyadh, Geneva, Helsinki, Madrid, New York, Paris, Singapore, Stockholm, Tokyo and Washington, DC.</p><p>Discover White & Case through the eyes of our people. Read more about our work, our people and our offer.</p><p><b>Who we're looking for</b></p><p>There's no such thing as a typical White & Case lawyer. We recruit ambitious trainees who have a desire to gain hands-on practical experience from day one and a willingness to take charge of their own career. We value globally minded people who are eager to work across borders and cultures, are intrigued by solving problems within multiple legal systems and have an understanding of international commercial issues</p><p>We recruit both law and non-law students and, owing to the nature of our work, language skills are highly valued. Applicants will be welcomed for their individuality, their enthusiasm for the cutting-edge work we do and having a positive, proactive mindset that puts our clients first.</p> GCC English Law Trainee Program <p>White & Case consistently ranks as one of the premier law firms operating in the Middle East. We have advised on some of the country's most significant energy and infrastructure projects, and high-profile capital markets and corporate M&A deals, working alongside leading government-owned enterprises and international clients.</p><p>Be part of our growth story in the Middle East. Join us as a trainee in Abu Dhabi, Dubai or Riyadh and you'll work on some of the highest-profile matters for the most prominent clients in the region. Benefit from being part of a supportive and friendly team, with deep local roots, as well as the strength of a top-ranked global law firm.</p><p>It's an exciting time to start your career here. We have been advising clients in the Middle East for almost 40 years, often on their most complex global and local legal challenges. We're committed to building our business in this exciting part of the world, and you'll benefit from the chance to take on real responsibility and accelerate your own career.</p><p>Build the friendships and personal connections that will last a lifetime, and get the training and experience to become a top lawyer in one of the most exciting and rapidly evolving parts of the world. A lot can happen in two years.</p><ul><li>Law graduates start their SQE in September 2026 or September 2027 (or PGDL for non-law graduates)</li><li>Trainees start in Abu Dhabi, Dubai or Riyadh in September 2027, March/September 2028</li><li>All PGDL/SQE fees covered and a maintenance grant provided</li></ul><p>For more information and to apply please visit our website.</p><p><b>How to apply & deadlines</b></p><p>Apply online by <b>12 January 2026</b>. If you require any additional support throughout the recruitment process, please contact our Disability & Support Champions to discuss in confidence.</p><img src="https://www.jobg8.com/Tracking.aspx?FXIqvVuqFNgR16HfJ6nrEC2K5OaxzrKnf" width="0" height="0" />

GCC English Law Trainee Program

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GCC English Law Trainee Program