Engineer - Quality Job at BorgWarner (Kakkalur)

Principal Quality Engineer (Quality Management Lead)

We are recruiting Principal Quality Engineers (PQEs) to support the Sizewell C (...

Location

United Kingdom , London; Bristol; Suffolk (Sizewell C site); Manchester

Salary:

Not provided

ASSYSTEM

Expiration Date

Until further notice

Requirements

Background in large, complex and highly regulated environments—ideally in nuclear or similarly regulated sectors—with strong focus on project quality and expertise in a relevant engineering discipline (mechanical, electrical, I&C, fabrication)
Strong understanding of Quality Assurance and Quality Control across engineering, procurement, manufacturing, construction and commissioning
Knowledge of the nuclear sector (preferably new build) and familiarity with Licence Conditions LC6, LC17 and ONR TAG 077 is desirable
Clear understanding of quality management best practice for deployment in large, complex, contract-led organisations
Confident communicator with strong presentation skills, comfortable engaging with individuals, small groups and large audiences
Experience ensuring compliance with national and international standards such as GS‑R‑3, ISO 9001, ISO 19443, ISO 3834 and EN10204
Proven ability to plan and conduct internal and supplier audits
Able to carry out unsupervised inspections to appropriate standards (e.g., pressurised systems)
Experienced in reviewing quality records (e.g., material certification, CFSI) and analysing quality data across an organisation
Experience managing people or leading teams

Job Responsibility

Support development and implementation of QA/QC arrangements across SZC
Identify and conduct supplier audits, and close out findings
Manage quality execution and support supplier technical assessments
Oversee manufacturing and construction surveillance
Manage non-conformances and Quality Release Certificate processes
Drive improvements in quality implementation across the project
Review, accept and monitor Contractors’ Quality Assurance Plans (CQAPs)
Produce and implement Project Quality Control Plans
Ensure deployment of key contractual quality arrangements (GQAS, LTQRs, ITP specifications)
Guide contractors on quality requirements and project-specific arrangements

What we offer

Hybrid Working Opportunity
Flexible working hours – 2/3 days per week in the Bristol office
Market Leading Pension scheme (8% company contribution / 4% personal contribution)
25 days’ paid annual leave + bank holidays + option to buy or sell days
Professional fees reimbursed
Employee referral scheme
Competitive Sick Pay – Support when you need it
Income Protection & 3x Salary Death-in-Service Cover
Free Digital Gym Access – Expert-led fitness classes
24/7 Employee Support Line – Mental health, financial & legal help

Fulltime

Senior Quality Supplier Engineer / Quality Supplier Manager

As Quality Supplier Manager / Senior Quality Engineer (QSM), you are responsible...

Location

Malaysia , Kulim, Penang

Salary:

Not provided

ASML

Expiration Date

Until further notice

Requirements

Bachelor or Master degree in Engineering, Electrical Engineering, Mechanical Engineering, other technical field
5 – 15 years relevant work experience in a similar role
Experience with supply chain processes in production environment, eg. Six sigma, lean, etc.
Experience in improvement projects in supply chain, preferably in High-tech industry
Experience in relationships with suppliers
Excellent communication skills
Convincing/negotiation skills
Relationship builder (internal and external)
Pro-active attitude
Strong analytical skills

Job Responsibility

Responsible for the entire Quality and Technical process performance for suppliers and their n-tier suppliers
Monitor, review and drive supplier quality performance from incidents to structural improvement
Contribute to supplier development (e.g. implementing SPC, lean, FMEA, operational excellence at suppliers or n-tier suppliers)
Optimize manufacturing processes at suppliers by improving quality, testing and qualification infrastructure
Drive yield improvements and process improvements at suppliers
Actively participate in improvement project at suppliers (cycle time reduction, cost of goods reduction)
Carry-out analysis of quality issues and drive technical solutions needed during material availability escalations
Support implementation of hardware changes at suppliers
Build-up and develop technical competences within ASML (SPC, lean manufacturing, FMEA, operational excellence) to drive and support operational excellence at suppliers

Fulltime

Lead Quality Assurance Engineer, Supplier Quality

The Lead Quality Assurance Engineer, Supplier Quality will provide supplier rela...

Location

United States , Madison

Salary:

112000.00 - 190000.00 USD / Year

Exact Sciences

Expiration Date

Until further notice

Requirements

Bachelor’s degree in a Science or technical field
or Associate’s degree in Science or technical field and 2 years of relevant experience as outlined in the essential duties in lieu of a Bachelor’s degree
5+ years of experience in quality principles and practice including experience in assigned area (Design Control, Supplier Management, Risk Management, etc.)
Product Development assignments require 8+ years of experience in product development in the medical device industry with experience in complex systems including software
Design Transfer assignments require 8+ years of experience in process validation principles and practice
Manufacturing Support assignments require 8+ years of experience in a manufacturing operation environment
Demonstrated ability to successfully work within an CFR 820, ISO 13485, ISO 9001, and/or cGMP structured environment
Applicants must be currently authorized to work in country where work will be performed on a full or part-time basis
Demonstrated ability to perform the Essential Duties of the position with or without accommodation

Job Responsibility

Represent Quality on a variety of projects as assigned
Communicate and collaborate with business partners to ensure robust materials, products, processes, and systems and compliance to procedures and specifications
Create documentation and records in the Electronic Quality Management System (EQMS)
Perform risk assessments and provide risk mitigation strategies
Implement processes to monitor product and process performance, compliance, and reliability
Implement, conduct, and report on process quality programs using statistical data analysis
Review and approve documentation related to Exact Sciences products
Conduct periodic reviews of Quality System documentation
Generate and distribute Quality metrics as assigned
Generate, prepare, and issue data for assigned quality plans

What we offer

Paid time off (including days for vacation, holidays, volunteering, and personal time)
Paid leave for parents and caregivers
A retirement savings plan
Wellness support
Health benefits including medical, prescription drug, dental, and vision coverage
Bonus eligibility

Fulltime

Engineer/ Senior Supplier Quality Engineer

Location

Singapore , Singapore

Salary:

Not provided

BorgWarner

Expiration Date

Until further notice

Requirements

Degree in Engineering (Electrical)
Minimum 5 years’- 15 years' experience is preferable

Job Responsibility

Assess purchase productive part suppliers to determine whether the suppliers' quality system is acceptable with final approval sourcing decisions from a quality perspective
Approve sourcing decisions from a quality perspective
Serve as the primary Purchasing Supplier quality liaison between Operation and the Supplier
Ensure purchased productive parks are approved and production ready
Work with buyers to assess and select new and capable Electrical suppliers
Serve as technical resource to Engineering and SQE
Support Asia Pacific PML purchased productive supplier quality issue after Product SOP
Monitor and evaluate suppliers quality performance to ensure Continuous Improvement of purchased productive Electrical parts quality
Provide technical resource and conduct quality workshops with suppliers

Fulltime

Quality Assurance Quality Control Engineer

Location

Germany , Dresden

Salary:

Not provided

ASafe Global

Expiration Date

Until further notice

Requirements

Degree or diploma in Civil, Mechanical, Electrical Engineering or a related field
5+ years of relevant QA/QC experience, preferably in semiconductor, cleanroom, or high-tech industrial construction
Solid understanding of ISO standards, quality control processes, and construction QA/QC documentation
Strong experience with inspection test plans (ITPs), material verification, and construction methodology
Familiarity with EU and German quality standards and construction regulations
Excellent communication skills and ability to liaise with multidisciplinary teams
Fluent in English
Ability to work on-site in Dresden, Germany for the duration of the project
A valid Visa/Work permit for the specific job location is essential

Job Responsibility

Oversee and implement the quality control procedures for the construction project, ensuring compliance with all codes, standards, and client specifications
Conduct inspections, audits, and testing across all stages of construction activities
Review and approve material submittals, method statements, and test plans in coordination with engineering and project teams
Track and document all QA/QC activities and maintain inspection test records
Identify non-conformances, ensure timely corrective actions, and lead root cause analyses
Coordinate with subcontractors and vendors to verify quality compliance throughout the supply and installation phases
Participate in progress meetings and provide regular reporting on QA/QC metrics to the management team
Support project close-out through the preparation of handover documentation and as-built records

What we offer

Valuing Our Team: At ASafe Global, we recognize that our employees are our greatest asset, and we are dedicated to fostering a supportive and rewarding work environment
Competitive Compensation: We provide a competitive compensation package, ensuring that our employees are fairly rewarded for their contributions
Growth Opportunities: ASafe Global offers a range of professional development opportunities to support the continuous growth and advancement of our team members
Employee Success: We believe in the interconnectedness of our company’s success and the well-being of our employees, emphasizing a mutually beneficial relationship
Meaningful Impact: Play a key role in shaping the future of construction and innovation
Inclusive Workplace: Join a diverse and supportive team committed to forward-thinking solutions

New

Nxe Factory Quality Engineer

The JG7 Factory Quality Engineer is an independent contributor who owns module-l...

Location

United States , Wilton

Salary:

Not provided

ASML

Expiration Date

Until further notice

Requirements

Bachelors or Masters of Science degree in technical domain (e.g. mechanical/electrical/optical/chemical/industrial engineering, mechatronics, physics, or related field) with 2+ years (BS) or a (MS) of relevant work experience in in a technical environment such as quality, manufacturing engineering, or related fields
Hands-on technical experience related to manufacturing quality preferred
Ability to independently lead RCA/CAPA activities
Strong statistical and analytical capabilities
Proficiency in SAP/QMS tools, SPC, FMEA, and structured problem solving
Six Sigma Green Belt preferred (or willingness to achieve)
Ability to influence cross functional teams and drive actions to closure
Legally authorized to access controlled technology as defined in United States Export Administration Regulations

Job Responsibility

Lead DRB / MRB sessions for assigned areas which are directly tied to Quality, ensure rigorous root cause validation, and drive structural implementation of corrective actions
Own SPC performance reviews, including control limit adjustments, capability analysis, and communication of required process improvements
Leads factory in discussions for assigning CTD/CTQ/CTC Definitions
Lead pFMEA updates in response to systemic issues, new learnings, or high-impact events
Own execution and analysis of MSA / Gage R&R studies, driving cross-functional improvements where measurement systems underperform
Actively represent assigned work centers during QMM / 6P Quality Assessments, ensuring evidence of readiness, process compliance, and gap closure
Analyze First Pass Yield Data to understand and drive process stability
Develops dashboards and tracking methodologies related to quality activities
Drive adoption and enforcement of Quality Gates across upstream/downstream partners, ensuring handshakes occur with complete, accurate inputs
Participates, facilitates, or co-lead 4-Eye reviews / Quality Circles to strengthen discipline in quality fundamentals and prevent recurrence of known issues

Fulltime

New

Quality Engineer Associate III

This is where you make a difference in our patients’ safety. As a member of the ...

Location

United States , Round Lake

Salary:

96000.00 - 132000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Bachelor's degree in Science or Engineering required
5 or more years experience in IT, Engineering, Science or related field
Working knowledge of FDA Regulations, Application of Good Laboratory Practices, and Application of Good Manufacturing Practices
Strong technical writing skills
Strong technical, analytical and problem solving skills
Good interpersonal, communication, influencing, negotiation skills
Understand scientific strategies and be able to invent new methods or new avenues of investigation
Good project management skills

Job Responsibility

Lead ongoing daily departmental activities for areas of direct responsibility and assist other Quality areas in the successful performance of these activities
Drive root cause problem solving for non-conformances in area of responsibility, and champion problems solving on the manufacturing floor
Lead multiple process/product improvement projects, design of experiments, validations, development of new methodologies and improving existing methodologies, data generation, report development and presentation
Manage activities in achieving defined quality goals in an efficient, accurate and timely manner
Ensure business needs and timeliness requirements of the department are met or exceeded
Write, review, analyze and revise written Procedures and submit procedural changes as needed to meet Corporate, Divisional, Plant, Regulatory Requirements, etc.
Partners with other functions, facilities, divisions, and regions to ensure successful implementation and compliance to procedures / regulations
Lead audit ready status efforts for assigned areas and assist other areas within the facility in understanding FDA, ISO and Baxter quality requirements
Demonstrate leadership ability and be recognized by all levels of the facility as a subject matter expert in their area
Assists and writes validations, audits and assessments

What we offer

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

Fulltime

New

Quality Engineer Associate III

The Quality Associate III (Quality Engineer) is a key individual contributor res...

Location

United States , Round Lake

Salary:

96000.00 - 132000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Science or Engineering required
5 or more years experience in IT, Engineering, Science or related field
Working knowledge of FDA Regulations, Application of Good Laboratory Practices, and Application of Good Manufacturing Practices
Strong technical writing skills
Must be able to clearly document audit findings within audit reports
Strong technical, analytical and problem solving skills
Good interpersonal, communication, influencing, negotiation skills
Understand scientific strategies and be able to invent new methods or new avenues of investigation
Good interpersonal/communication/influencing/negation skills
Good project management skills

Job Responsibility

Lead ongoing daily departmental activities for areas of direct responsibility and assist other Quality areas in the successful performance of these activities
Drive root cause problem solving for non-conformances in area of responsibility, and champion problems solving on the manufacturing floor
Lead multiple process/product improvement projects, design of experiments, validations, development of new methodologies and improving existing methodologies, data generation, report development and presentation
Manage activities in achieving defined quality goals in an efficient, accurate and timely manner
Ensure business needs and timeliness requirements of the department are met or exceeded
Write, review, analyze and revise written Procedures and submit procedural changes as needed to meet Corporate, Divisional, Plant, Regulatory Requirements, etc
Partners with other functions, facilities, divisions, and regions to ensure successful implementation and compliance to procedures / regulations
Lead audit ready status efforts for assigned areas and assist other areas within the facility in understanding FDA, ISO and Baxter quality requirements
Maintain a high level of expertise in current regulatory requirements
Demonstrate leadership ability and be recognized by all levels of the facility as a subject matter expert in their area

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
medical and dental coverage that start on day one
insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount
401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
Flexible Spending Accounts

Fulltime

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Engineer - Quality

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