Inspection Quality Engineer Job at SYNTECH RECRUITMENT LTD (Uxbridge)

Senior Quality Engineer (Bulk Inspection)

We are seeking an experienced Senior Quality Engineer to support supplier manufa...

Location

United Kingdom , Bradford

Salary:

Not provided

ASSYSTEM

Expiration Date

Until further notice

Requirements

Qualification in an Engineering discipline (ONC / HNC / HND / Degree or equivalent experience)
Experience in a quality inspection or supplier quality role within engineering or manufacturing
Significant experience in quality inspection or quality engineering within a manufacturing environment
Experience overseeing supplier manufacturing and inspection activities
Strong understanding of engineering drawings, specifications and inspection requirements
Experience working to UK and international engineering standards and codes
Ability to identify, document and manage non-conformances and corrective actions
Experience supporting quality surveillance programmes and supplier oversight

Job Responsibility

Perform supplier inspections and witnessing activities in line with Inspection & Test Plans (ITPs)
Verify that manufactured equipment and components meet contract specifications, drawings and applicable standards
Review supplier quality documentation and manufacturing records prior to product release
Identify, raise and track non-conformances, ensuring appropriate corrective actions are implemented
Accept or reject manufactured items based on inspection outcomes
Work closely with suppliers to ensure quality requirements are fully understood and implemented
Support the development and delivery of the supplier surveillance and inspection programme
Produce inspection reports and summary updates highlighting quality performance and key issues
Ensure compliance with relevant national and international engineering standards
Collaborate with project quality leads to ensure effective quality oversight across the supply chain

What we offer

Hybrid Working – Flexibility to work from home and the office
25 Days Annual Leave + Bank Holidays
Buy & Sell Holiday – Make your time off work for you
8% Company Pension Contributions
Income Protection & 3x Salary Death-in-Service Cover
Competitive Sick Pay – Support when you need it
Healthcare Cash Plan – Claim back on dental, optical & more
Free Digital Gym Access – Expert-led fitness classes
Exclusive Discounts – Restaurants, days out & top brands
24/7 Employee Support Line – Mental health, financial & legal help

Fulltime

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

New

Optical Quality Engineer, Meta Reality Lab

In this role, you will ensure the component quality sourced from suppliers can m...

Location

United States , Sunnyvale

Salary:

173000.00 - 245000.00 USD / Year

New

Sr Staff MFG Quality Engineer

The NPI-focused Manufacturing Quality Engineer provides oversight and guidance i...

Location

United States , Secaucus

Salary:

116250.00 - 155000.00 USD / Year

Sanmina

Expiration Date

Until further notice

Requirements

Excellent verbal and written communication skills
Experience managing projects using six sigma tools and techniques
Experience in Quality auditing for ISO 9001 or equivalent standards
Demonstrated experience in analyzing and solving complex problems
Experience in coaching engineers and technicians in problem solving
Rigorous engineering and leadership skills
Experience in effectively working with cross functional teams and executive management to get measurable results
Proficiency with Microsoft office applications (Outlook, Excel, Power Point, Visio, Word)
Familiarity with data visualization tools (Tableau, Power BI) and data analysis software (Minitab)
Proven ability to perform effectively in a demanding environment with changing workload and deadlines

Job Responsibility

Support System Test teams and assembly teams in quality issue investigation and solutions development for NPI builds
Investigate and document causes of non-conformance issues in the Quality Incident Report Database and drive/implement corrective actions with supplier quality engineering
Create quality and process alerts to drive corrective actions and train employees
Lead pilot build audits for new SKUs to identify risks and drive improvement actions with New Product Introduction (NPI) and Manufacturing Engineering teams
Develop, implement, and maintain quality Control Plans and inspection strategies for new SKUs, ensuring effective in-process and final inspection requirements
Create inspection SOPs with checkpoints based on critical-to-quality requirements
Participate in DFM (Design for Manufacturing) and PFMEA reviews for NPI SKUs
Drive improvements in assembly processes to reduce workmanship errors through established Root Cause Corrective Action methodologies
Monitor Quality KPIs for test and assembly process areas and ensure that processes remain in control
Participate in LEAN initiative, and engage Six Sigma tools for process improvements

What we offer

Competitive base salary
Performance-based annual bonus eligibility
401(k) retirement savings plan
Tuition reimbursement for eligible education programs
Comprehensive medical, dental, and vision coverage with access to leading providers
Mental health resources and employee wellness support programs
Company-paid life and disability insurance
Paid time off (PTO) and company-paid holidays
Parental leave and family care support programs
Structured training programs and on-the-job learning opportunities

Fulltime

Senior Supplier Quality Engineer

As a global medtech company, we are driven by our Vision of changing the traject...

Location

United States , Clear Lake

Salary:

110000.00 - 120000.00 USD / Year

LivaNova

Expiration Date

Until further notice

Requirements

A Bachelor's Degree in Engineering is required
8+ Years of Quality or Manufacturing Engineering
Experience working in a regulated environment industry such as a FDA medical device manufacturer preferred
Understanding of basic quality engineering principles including, but not limited to: quality leadership, implementation, acceptance sampling, statistical process control, lean business systems and other continuous improvement techniques, and risk management
Pragmatic and result-oriented: capable to prioritize and plan activities with specific attention to understand expectations of internal personnel and external stakeholders
Good team player: open and honest when communicating among peers and management
Resolves most issues with peers, but understands what issues are important to escalate to management
Project management skills including the ability to drive cross-functional internal and external teams to completion of projects within planned timeframes
Strong interpersonal skills
Sustained record of performance during tenure in previous position as shown through consistency with which metrics in their areas of responsibility meet performance objectives as established in Management Review and a track record of implementing improvements

Job Responsibility

Leads the supplier selection, evaluation and approval process by assessing manufacturing/ technology capabilities, supplier risk levels, Quality Management System compliance, etc.
Serves as a core team member on component development teams by providing technical leadership and direction
Responsible for supplier process qualification, verification and validation activities
Reviews supplier process changes for completeness, accuracy, and safety/effectiveness including the identification of all impacts and timely management of these changes with to ensure continued supply of parts
Acts as business process owner for all supplier related nonconformance report (NCR) management system, including material review board (MRB) activities, monitoring the timeliness and effectiveness of the system and activities
Carries out supplier Quality Management System (QMS) and process audits
Collaborates with suppliers on process manufacturing process improvement, process validation (TMV, IQ, OQ and PQ) and value enhancement opportunities
Ensures ongoing compliance per ISO 13485 and MDSAP requirements
Collaborates with Purchasing and procurement functions to support business strategy initiatives including cost saving efforts, alternate sourcing, outsourced processes etc.
Provides quality criteria (risk assessment, acceptance criteria, sample size, parameter definition) for receiving inspection activities

What we offer

Health benefits – Medical, Dental, Vision
Personal and Vacation Time
Retirement & Savings Plan (401K)
Employee Stock Purchase Plan
Training & Education Assistance
Bonus Referral Program
Service Awards
Employee Recognition Program
Flexible Work Schedules
discretionary annual bonus

Fulltime

Quality Engineer

In the role you will be responsible for and has the authority for product/proces...

Location

Ireland , Clara

Salary:

Not provided

Nelipak

Expiration Date

Until further notice

Requirements

Third level qualification in science/ engineering
Demonstrable Lean/ Six Sigma certification is an advantage
Training and/or experience in working in a ISO13485:2016 certified manufacturing environment
Ability to work independently and collaboratively with limited supervision
Good interpersonal skills and enjoys being part of a team
Ability to work on own initiative

Job Responsibility

Ensure that safe working practices are always adhered to, including wearing PPE as appropriate
Acquire knowledge of Health & Safety procedures, work instructions, and associated documentation
Comply with all Health & Safety Policies and instructions and actively contribute to Company efforts to promote safe behaviour and safe systems of work
Lead quality improvement programmes using recognised problem-solving and project management techniques
Participate in cross-functional teams to ensure that we achieve our Quality Policy and Quality Objectives
Evaluate quality trends and reasons for product or process failures relating to customer complaints and lead corrective action plans
Evaluate quality costs and determine critical causes
Prepare and approve quality assurance specifications and assist in the formulation of written policy/procedures
Align and integrate company test procedures with International Standards requirements
Assist in determining inspection frequencies and sampling plans using significance testing, capability studies and through collation and analysis of data

What we offer

EAP (Employee Assistance Programme)
Work/Life Balance
Wellness Programs
Employee Recognition
Free onsite parking
Learning and development opportunities
Cycle to Work Scheme
E-Learning and Development opportunities

Fulltime

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

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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Inspection Quality Engineer

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