618 matching jobs for “Sourcing Engineer”

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Allstate

Software Engineer Manager

Ind – Blr Sez 1 (3Rd, 6Th & 7Th Floor) +1 location

Full time
Regular

The Software Engineer Manager architects and designs their digital products using modern tools, technologies, frameworks, and …

Added Oct 30, 2026

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Thermo Fisher Scientific

… autonomy, resources and tools they need to take science a step beyond. Role Purpose Summary: The Hardware Engineer III is a professional level member of a global R&D Team. The role is of a hands-on Electrical/Electronic …

Added Oct 16, 2026

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Medline

Advanced Engineer DQA

Shanghai 上海 +2 locations 2 postings

The Division Quality Assurance Engineer plays a critical leadership role within Medline product divisions, ensuring that robust quality standards …

Added Nov 3, 2026

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Carrier Global

Advanced Supplier Quality Engineer

PRT5208: Rua Rua Santos Dias No. 1121, Matosinhos, 4465-255, Portugal

Role: Advanced Supplier Quality Engineer Location: Porto, Portugal Type of contract: permanent, full-time Carrier is the leading worldwide provider …

Added Oct 27, 2026

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Fidelity National Information Services

Software Engineer Lead

US GA ATL 201 STE 900 +1 location

… All reasonable accommodation requests will be reviewed and evaluated on a case-by-case basis. Sourcing Model Recruitment at FIS works primarily on a direct sourcing model; a relatively small portion of our …

Added Nov 3, 2026

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Carrier Global

Senior Sales Engineer

Jeddah, Mecca Region, Saudi Arabia

… recruitment process for everyone. If selected, you will follow the next stages: Initial call with our sourcing/recruitment team Interview with the Manager Our commitment to you As an employer of choice, our greatest …

Added Oct 27, 2026

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Xylem

Sr. Engineer Application

Vadodara Plot 731

In person
Full time
Regular

… Veteran’s, People of Color and Allies, Emerging Leaders, and Working Parents Networks. The role – Senior Engineer Application Engineer at Xylem Vadodara Plant location. Responsible for evaluating customer requirements and …

Added Oct 27, 2026

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GE Vernova

Lead Project Engineer

Chennai, Tamil Nadu, India 2 postings

… of projects, responsibilities also include activities such as schedule development and updates, supporting sourcing initiatives, planning and tracking project design reviews, quality control/quality assurance, and …

Added Oct 27, 2026

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Capital One Financial

Senior iOS Engineer

Nottingham, England, United Kingdom

… continuous integration and delivery pipelines And meet most of the following: You are a capable senior engineer, passionate about guiding and growing junior engineers towards appropriate target architectures You have …

Added Oct 27, 2026

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GE Vernova

Power Electronics Engineer

Imperial, California, United States

Pay posted by employer$89,300–$148,700

Summary As the Power Electronics Engineer you will be responsible for leading and performing Low Voltage and Medium Voltage power electronics and …

Added Oct 27, 2026

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GE Vernova

Lead P&C Engineer

Remote

Pay posted by employer$98,400–$164,000

Summary The Lead Protection & Control Engineer works on T&D substations for AC, HVDC and FACTS projects with designers, peer engineers & leaders. The …

Added Oct 27, 2026

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Fidelity National Information Services

Lead Network Engineer - Telecommunications

US FL JAX 347

… like to know: Are you FIS? About the Role: The FIS Telecommunications Team is hiring a Senior Lead Network Engineer who is responsible for developing Telecom strategy, including Global backbone and network aggregation …

Added Nov 3, 2026

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GE Vernova

Lead Engineer (Gas Turbine)

Greenville +2 locations

Pay posted by employer$98,400–$164,000

… on today and building the energy technologies of the future. What impact you’ll make? The Agile ITR Lead Engineer for Conversions, Modifications, and Uprates (CM&Us) Services projects plays a pivotal role in the Americas …

Added Oct 27, 2026

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Thermo Fisher Scientific

Staff Engineer Systems design

Hyderabad, Telangana, India

… sure our food is safe or helping find cures for cancer. Position Summary We are seeking a Staff Systems Engineer to join a growing R&D team in Hyderabad supporting sustaining engineering, VAVE, and lifecycle management …

Added Oct 16, 2026

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AES

Principal Engineer, Utility

Louisville, Colorado, United States +5 locations

Pay posted by employer$145,000–$181,050 per year

include engineer management , design reviews , contract document development and negotiation, procurement specification …

Added Nov 3, 2026

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KLA

Supply Chain Engineer

Singapore, Singapore

Full time
Regular

… require solid technical, business, interpersonal, and negotiation skills. Ability to develop and execute sourcing strategies that map to and support overall business strategies. Ability to lead complex supplier …

Added Oct 15, 2026

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KLA

Supply Chain Engineer

Singapore, Singapore

Full time
Regular

… priorities by delivering high-impact work across your area of expertise. 1. Responsible for technical sourcing, contracting and contract management, supplier relationship management, and program management of technical …

Added Oct 15, 2026

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GE HealthCare Technologies

Senior Mechanical Engineer

WuXi 2 postings

Summary The Senior Mechanical Engineer is responsible for the mechanical design, development, verification, and lifecycle support of diagnostic …

Added Oct 30, 2026

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GE Vernova

Senior Engineer- System Engineering

Chennai, Tamil Nadu, India

Added Oct 27, 2026

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BorgWarner

Engenheiro de Compras | Purchasing Engineer

Piracicaba - Brazil

Full time
Regular

… um(a) Engenheiro(a) de Compras motivado(a) e orientado(a) para resultados para apoiar atividades de sourcing estratégico e desenvolvimento de fornecedores para produtos automotivos. Esta posição é responsável por …

Added Nov 3, 2026

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Medline

Advanced Engineer DQA

Shanghai 上海 +2 more

Same role posted 2 times, once per location

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About this opportunity

Original employer description

Job Summary

The Division Quality Assurance Engineer plays a critical leadership role within Medline product divisions, ensuring that robust quality standards are defined, implemented, and continuously improved across the full product lifecycle—from development through mass production
Key responsibilities include:
1. Lead projects effectively, establish robust quality standards and manage mass production, with final approval authority over product samples, process validation reports, testing results, DMR, NCMR, complaint and change control.
2. Drive the implementation of effective corrective and preventive actions (CAPA) to address customer complaints and adverse quarterly quality trends.
3. Demonstrate strong leadership and communication skills to drive cross-functional collaboration, particularly with US R&D, US PM, US RA, Sourcing, SQE, suppliers, and regional teams across Asia.
4. Ensure full compliance with applicable domestic and international regulations governing product lines and manufacturing processes.

Job Description

CORE JOB RESPONSIBILITIES:

Take ownership of project management and product development, collaborating with cross-functional teams (R&D, PM) to define appropriate testing strategies and minimize product failures during new product introduction (NPI).

Develop, approve and implement standardized methods and procedures for process control, process validation, process improvement, testing, and inspection to ensure product quality and functionality.

Design and execute experimental testing and data analysis to maintain quality performance, minimize defects and failure rates, and drive data-driven decision-making using statistical quality tools.

Collaborate with suppliers and key stakeholders (US R&D, US PM, Sourcing, SQE, QE, QC, etc.) to resolve customer complaints, ensure effective implementation of CAPA/SCAR, and drive continuous supplier quality improvement.

Ensuring quality decision making, compliance, and final release risk acceptance for both NCMR and Deviation processes.

Identify and drive product and process improvement opportunities with suppliers to enhance quality performance and achieve cost efficiencies.

Manage and oversee supplier-initiated change requests, ensuring changes are properly evaluated, validated, and implemented in compliance with quality and regulatory requirements

Establish and maintain compliant product documentation (e.g., Device Master Records, technical files) and collaborate with Regulatory Affairs and suppliers to support regulatory submissions (e.g., 510(k), Letter to File).

Provide expertise in product development, including Design Control, Risk Management, and compliance with applicable technical documentation requirements (e.g., CE Technical Files).

Conduct thorough quality reviews of design and development documentation to ensure compliance with internal standards, regulatory requirements, and supplier quality documentation.

Drive continuous communication and alignment with suppliers to ensure clear understanding and adherence to internal standards, regulatory requirements, and quality expectations.

Coordinate product testing activities with internal and external laboratories to ensure timely and accurate execution of qualification and validation testing.

BASIC QUALIFICATIONS:

Education

Bachelor’s degree in mechanical engineering, Materials Engineering, Industrial Engineering, Medical Devices, or a related engineering discipline

Relevant Work Experience

Minimum 5+ years of engineering experience, preferably with strong project management exposure.

Hands-on experience in process control and quality control is required.

Medical device quality background is preferred.

Additional

-Understanding of quality system requirements (ISO 13485 or ISO 9001).

-Proven ability to read and interpret product specifications, drawings, and technical documentation.

- Demonstrates a professional attitude and a heightened sense of urgency to complete tasks accurately and efficiently.

- Capable of identifying improvement opportunities in products, processes, and documentation, and driving implementation with suppliers and internal teams.

- Strong leadership, collaboration, and influencing skills across cross-functional and cross-regional teams.

- Proficient in engineering and office software tools, including MS Office (Word, Excel), and Adobe tools.

-Experienced in key quality methodologies and tools, such as FMEA, Control plan, MSA, PPAP.

- Willingness to travel frequently (≥30%) as required by project needs

- Fluent in English (spoken, written, and reading).

- Ability to manage special projects and assignments as directed by manager

PREFERRED QUALIFICATIONS:

Education

Master’s degree in mechanical engineering, Materials Engineering, Industrial Engineering, Medical Devices, or a related engineering discipline, CQE or PMP certification is preferred

Relevant Work Experience

Minimum of 5 years of industry experience in medical devices, pharmaceuticals, or other relevant fields directly related to this role

Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For a more comprehensive list of our benefits please click here. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp.

We’re dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Explore our Belonging page here.

Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws.

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