151 Supplier Quality Engineer jobs in London
Supplier Quality Engineer
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Position: Supplier Quality Engineer
Location: Camden, NJ; KPS Technology Center
Holtec International seeks applicants for its quality department based at the company's KPS Technology Campus in Camden, NJ. This department is responsible for assuring compliance with all regulations, codes, standards and customer specifications. At Holtec, we recognize that our employees are our most valuable asset, and we seek to identify, attract and recruit the most qualified talent while recognizing and encouraging the value of in the global workplace.
Minimum Technical Requirements:
- A bachelor’s degree in an Engineering discipline or equivalent is required.
- Proficient in MS Office software including Word, Excel, Outlook, and PowerPoint.
- NQA-1 Certified Auditor certification is desirable.
- Working knowledge and application with US NRC Regulations and European Standards such as 10CFR50 Appendix B and 10CFR21; and consensus standards of quality assurance, such as ASME B&PV Code, CSA N.299, CSA N.285, ISO, ANSI ASME NQA-1 ESPN, RCC-M, RCC-E, ISO 19443, ISO 17025, ISO 9001, ISO 9712, and Appendices, ANSI N45.2 and the daughter standards, IEEE Standards.
- Familiarity with NDE techniques and applicable practices such as SNT-TC-1A, ESPN / RCC.
- Familiarity with Commercial Grade Dedication.
The Quality Engineer will work in a variety of quality assurance duties to ensure products meet the quality and technical requirements defined by Holtec. Within this role, the primary focus will be to work on a variety of quality assurance duties to ensure externally sourced products meet the quality and technical requirements defined by Holtec. This includes working across functional teams in the development and execution of complex plans for supplier audits, oversight, quality verification activities, and the certification documents for externally provided items. Domestic and International travel is required, with the ability to possess a passport and any needed Visa’s.
The candidate's principal activities will consist of the planning, development, implementation, communication and maintenance of the qualification and requalification of Holtec suppliers in accordance with regulations, codes, standards, and customer specifications. In this role, you will be responsible for ensuring the safety and quality of our products and procedures through rigorous audits, surveillances, inspections, implementation of quality control measures, and identification of areas for improvement. You will collaborate with cross-functional teams to address quality issues, drive continuous improvement, and contribute to building high-quality products that exceed customer expectations.
The ideal candidate will possess a strong background in engineering or quality assurance, exceptional attention to detail, a proactive mindset, and shall perform the following day-to-day activities in this position:
- Help in the development of less senior oversight personnel with the execution of verification activities, supplier oversight, and resolution of supplier quality issues.
- Support cross-disciplined teams in the execution of supplier oversight activities to verify Holtec suppliers have implemented a Quality Assurance Program commensurate with the items/services being provided.
- Develop and implement supplier surveillance and oversight plans for complex and first of a kind procurement to ensure compliance with quality and technical standards.
- Work with cross-functional teams in the resolution of complex supplier quality issues which adversely impact product quality.
- Perform verification and acceptance activities to confirm items and/or services being provided by suppliers conform to Holtec purchase order requirements.
- Generate robust certification documents, which identify the specific procurement requirements met by the purchased material or equipment, such as codes, standards, and other specifications imposed by Holtec and/or Customers, for major equipment and components.
- Participate in assessments and/or QSL maintenance of the global supply base to ensure compliance with applicable regulations, codes and standards.
- Evaluate supplier quality plans, procedures, and processes to verify compliance with quality and technical requirements defined by Holtec Engineering.
- Perform reviews of procurement documents to verify technical and quality requirements have been correctly translated from Holtec design documents and Customer contracts.
- Follow-up on supplier corrective action, evaluate responses and ensure objective evidence substantiates adequate closure.
- Apply quality control techniques and statistical methods for collection of deficiency information to identify failure causes and trends, rate performance and measure effectiveness of supplier QA programs, and internal processes.
- Provide input to business development, procurement, and other departments throughout Holtec concerning supplier qualification and development.
- Write detailed segments of QA plans/programs according to current U.S. Nuclear Regulatory Commission (NRC), Holtec and customer QA standards for nuclear and non-nuclear facilities.
- Investigate and report on compliance with technical specifications and verify accuracy of procedures, tests, and records. Review inspection and non-destructive examination procedures to ensure compliance with drawings and specifications.
The Company uses Kinetics ERP software and customized software for manufacturing, project management, supplier, and quality management activities in which the candidate will receive the necessary training. The Company’s business management is completely paperless and web-based. It is expected that the Candidate's work will involve frequent remote video contact with their counterparts at other HOLTEC operation centers and occasional travel.
As a technology trailblazer and a prominent innovator in clean energy (nuclear and solar) industry, Holtec strives to foster a meritocratic work environment conducive to continuous learning and professional growth of its associates. Holtec is an equal opportunity employer with a long-standing commitment to social equity and environmental justice. The company gives special preference to disabled veterans as a part of its recruitment policy. Detailed information on the Company can be obtained by consulting the website: holtecinternational.com . Candidates interested in considering a career at the Company should submit their resume along with at least three references.
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Senior Supplier Quality Engineer - Injection Moulding
Posted 18 days ago
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Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in Advanced Wound Care, Ostomy Care, Continence Care, and Infusion Care. With more than 10,000 colleagues, we provide our products and services in around 90 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at-risk skin, to improved patient outcomes and reduced care costs. Convatec's revenues in 2024 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more please visit the role:**
The Senior Supplier Quality Engineer - Injection Moulding, identifies, leads and executes large scale complex and strategic projects and improvements with regards to Injection moulding. Furthermore, the Senior Supplier Quality Engineer -Injection Moulding is the recognized subject matter expert in the management and auditing of injection molding and resin suppliers to ConvaTec.
The role is focused on being the Global Supplier Quality point of contact for projects and management of activities relating to injection molding for Convatec's Infusion Care business unit, driving forward improvement.
The job holder will not only demonstrate, but also support establishing the highest Quality standards and will embrace/drive Convatec core mission, values, and priorities.
**Your key duties and responsibilities:**
+ Provides leadership as subject matter expert in Injection Molding, Statistical Sampling, Quality Sampling, CTQ Characterization, Risk Management activities, mold maintenance and statistical process controls at supplier sites including mould maintenance.
+ Lead and provide input into global quality standards and polices regarding supplier quality performance and supplier selection process, ensuring compliance to industry and regulatory standards.
+ Conduct Supplier audits related to injection molding, mold or resin suppliers during the onboarding process and lifecycle of supplier relationships as per the Global Supplier Quality Schedule.
+ Drives significant change requests through to closure for our CCR process.
+ Works with R&D on improving CTQ requirements for the current product portfolio and NPD projects relating to injection molding.
+ Support maintaining and develops a robust incoming inspection process related to injection molded parts.
+ Collates and shares information/data through reports and follows up on identified improvement opportunities related to injection molding?
+ Actively participates and/or drives Quality System improvements as required.
+ Manages complex supplier manufacturing Investigations relating to suppliers' issues through the SCAR and CAPA process.
+ Demonstrates high commitment to quality and customer service based on customer needs.
+ Build strong relationships with customers, suppliers, senior stakeholders, and support groups worldwide to meet the demands of a changing business environment.
+ Coaches, reviews, and appropriately delegates work with lower-level professionals.
+ Demonstrates strong technical knowledge and principles in relation to injection molding medical devices in line with ISO13485 ISO9001 GMP Parts 201 and 211, EU MDR
+ In collaboration with procurement and R&D, identify, manage, and develop injection molding, resin and mold suppliers according to established organization quality standards and policies.
+ Represent CovaTec as a subject matter expert for injection molding, resins and molds for Global Supplier Quality in general and during internal and external body audits.
+ Support the maintenance of ConvaTec's Global Supplier Quality program, whilst driving opportunities for improvement.
+ Leads, identifies, and establishes processes and measures for maintaining, and improving supplier performance metrics, policies, and procedures in administering quality relationships with suppliers.
+ Actively resolves Supplier related issues associated with quality or poor performance to supplier performance metrics.
+ Work autonomously in alignment with defined process and ways of working
+ Collaborates with the procurement and R&D teams to identify and certify new and/or alternative suppliers/manufacturers to mitigate supply risks or support new product launches.
+ Use and promote the benefits of structured and standardized Lean / Six Sigma / KT methodology for process improvement and development.
+ Leads and manages large-scale projects or processes relating to injection molding, resins and molds on behalf of Global Supplier Quality.
+ Raise appropriate questions or concerns regarding regulatory compliance to appropriate authorities regarding Purchasing Control activities.
+ Quality Subject Matter Expert support with R&D and to complete trials, Technical & Statistical studies such as MSA, VSM, and Gage R-R at suppliers, including introduction of new resins and injection molds.
**Skills & Experience:**
+ Minimum of 5 years' experience in injection moulding
+ An end-to-end perspective in creating high quality molds.
+ Experience in defining CTQ requirements and incoming inspection requirements.
+ Experience using and reviewing 3D CAD system and technical drawings
+ Preferably minimum 2 years of experience in the medical device industry
+ Minimum 3 years of experience in Supplier Quality Control
+ Experience in internal and supplier related CAPA/ NC/ SCAR initiation.
+ Knowledge of ISO 9001, and preferably ISO13845 and FDA medical requirements.
+ Strong statistical, analytical and problem-solving skills.
+ Proficiency in quality tools and methodologies, such as Six Sigma, FMEA and SPC
+ Strong prioritization and coordination skills.
+ Ability to work with electronic databases (i.e. Documentum, Trackwise, SAP).
+ Advanced computer management skills including Microsoft Word, Excel and Visio.
+ Proactivity and flexibility to meet priorities and achieve deliverables
+ Ability to operate autonomously, negotiate and partner with internal and external customers to enhance operational effectiveness.
**Qualifications/Education:**
+ BS or higher degree qualified in Science or Mechanical Engineering or Plastics Technology.
+ Quality Auditor or Lead Auditor certification in ISO9001 or ISO13485.
+ Lean Six Sigma Greenbelt is preferable.
**Travel Requirements:**
+ The position may involve travel up to 25% of the time to Convatec sites and supplier locations globally.
**Working Conditions:**
+ **Fixed-term contract for a duration of 2 years with remote work setting** , presence at the local or global offices may be required based on in-country legal requirements and for specific meeting, projects, and events.
**Ready to join us?**
At Convatec, we're pioneering trusted medical solutions to improve the lives we touch. If you're ready to make a real impact, apply today and help us bring our Forever Caring promise to life.
#LI-CC1
#LI-Remote
**Beware of scams online or from individuals claiming to represent Convatec**
A formal recruitment process is required for all our opportunities prior to any offer of employment. This will include an interview confirmed by an official Convatec email address.
If you receive a suspicious approach over social media, text message, email or phone call about recruitment at Convatec, do not disclose any personal information or pay any fees whatsoever. If you're unsure, please contact us at .
**Equal opportunities**
Convatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law.
**Notice to Agency and Search Firm Representatives**
Convatec is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Convatec employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of Convatec. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
**Already a Convatec employee?**
**If you are an active employee at Convatec, please do not apply here. Go to the Career Worklet on your Workday home page and View "Convatec Internal Career Site - Find Jobs". Thank you!**
Supplier Quality Assurance Specialist
Posted today
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Supplier Quality Assurance Specialist
Hertfordshire
£35k - £40k
Drive supplier compliance and quality with these products that millions love. Join as a Supplier Assurance Specialist and make an impact.
There’s a unique kind of rigour in food manufacturing. The pace. The precision. The pressure. And if you’re already working in FMCG, you know exactly what that means. From the first link in the supply chain to the final pack on the shelf, quality isn’t just a box to tick – it’s the foundation.
This is your opportunity to play a critical role in one of the industry’s most performance-driven environments – where operational integrity, supplier compliance, and audit readiness are business-critical. If you understand the technical nuance behind raw material assurance, third-party standards, and supplier risk management, this isn’t just another technical role. It’s a strategic one.
About the Role
As Supplier Assurance Specialist , you’ll be the technical gatekeeper of supplier integrity across a diverse and dynamic FMCG portfolio. You’ll ensure our supplier base – from primary ingredients to indirect materials – not only meets but exceeds internal standards and external regulations. From onboarding and auditing to documentation and performance monitoring, you’ll bring structure to complexity and rigour to compliance.
Reporting into Quality or Technical leadership (depending on the business structure), you’ll be a driving force behind continuous supplier improvement. Think root cause analysis, specification compliance, and collaborative corrective action – not endless box-ticking.
Candidate Profile
You’re already in a supplier assurance, quality, or technical compliance role within food production or FMCG – possibly from a background in raw materials, packaging, or co-manufacturing. You understand BRCGS, HACCP, VACCP, TACCP and supplier risk assessments like the back of your hand.
You’ll likely have a food science, technical or quality qualification, and you’re no stranger to working cross-functionally with procurement, NPD, or regulatory teams. Above all, you combine technical fluency with commercial awareness – balancing compliance with operational pace.
What’s on Offer
Exposure to a fast-paced, commercially ambitious FMCG environment
Influence over a critical area of the supply chain with measurable business impact
A business genuinely invested in ethical sourcing, sustainability, and quality
Ready to Take Ownership?
If you’re driven by purpose, precision, and the challenge of maintaining world-class standards across a complex supplier network, this is your next move. Apply now and take control of the standards that define industry-leading FMCG.
Ref DAC55941
Associate, Quality Control
Posted 18 days ago
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Job Description
Discover your opportunity with Mitsubishi UFJ Financial Group (MUFG), one of the world's leading financial groups. Across the globe, we're 120,000 colleagues, striving to make a difference for every client, organization, and community we serve. We stand for our values, building long-term relationships, serving society, and fostering shared and sustainable growth for a better world.
With a vision to be the world's most trusted financial group, it's part of our culture to put people first, listen to new and diverse ideas and collaborate toward greater innovation, speed and agility. This means investing in talent, technologies, and tools that empower you to own your career.
Join MUFG, where being inspired is expected and making a meaningful impact is rewarded.
Mitsubishi UFJ Financial Group, Inc. (MUFG) is one of the world's leading financial groups. Headquartered in Tokyo and with over 360 years of history, MUFG has a global network with around 3,000 offices in more than 50 markets. The Group has over 180,000 employees, and offers services including commercial banking, trust banking, securities, credit cards, consumer finance, asset management, and leasing.
As one of the top financial groups globally with a vision to be the world's most trusted, we want to attract, nurture and retain the most talented individuals in the market. The size and range of MUFG's global business creates opportunities for our employees to stretch themselves and reap the rewards, whilst our common values, to behave with integrity and responsibility, and to build a culture which is fair, transparent, and honest, underpin everything that we do. We aim to be the financial partner of choice for our clients, whatever their requirements, building long-term relationships, serving society, and fostering shared and sustainable growth for a better world.
Please visit our website for more information - mufgemea.com.
The Client On-Boarding team is part of the Client Management Services, which is situated within the Corporate and Investment Banking Division of MUFG Bank. However, this function acts as a centralized 1st line support team, providing support to Investment Banking and Corporate Banking in EMEA, Capital Markets and MUFG Securities both in London and in Amsterdam.
**MAIN PURPOSE OF THE ROLE**
This individual will be responsible for conducting Quality Control (QC) assessments across new on-boarding, Periodic Reviews and Event Driven Reviews - including KYC and Regulatory Classifications. The Client On-Boarding Team covers a highly varied portfolio of Circa. 6,000 entities - ranging from simple listed customers, to much more complex structures, entities and product offerings, as such it will be key for this individual to fully understand all customers and to assist the lead to design effective Quality Control program - identifying and escalating risks appropriately.
This function is critical during both on-boarding and other reviews to ensure that the KYC process effectively mitigates the risks of Money Laundering, Bribery and Corruption, reputational and any other associate risks. With this in mind, the successful individual needs to have good experience within KYC, and a demonstrable strong knowledge of the AML/KYC environment.
Key stakeholders in this role are; Operational KYC counterparts, QA Counterparts, Financial Crime (2nd line of Defence), Front Office RM/Trader/Account Officers and Audit. Working closely with stakeholders to both standardize and clarify requirements and proactively identify future issues with procedures/process. Driving forward and influencing change is therefore essential in this role.
This function will also assist the lead in the development and roll out of a suite of training (related to requirements / roles and responsibilities) for new and existing individuals within the team and for those within the various front office functions, where required. Working closely with individuals to improve the understanding of both the process and the underlying rationale for requirements.
**KEY RESPONSIBILITIES**
In this role, you will be responsible for KYC across MUFG's banking arm and securities business under a dual-hat arrangement. Under this arrangement, you will act and make decisions on behalf of both the bank and the securities business, subject to the same remit and level of authority and irrespective of the entity which employs you.
+ Ensure that thorough and effective Customer Due Diligence is completed, by conducting Quality Control Assessments on entities/structures across all business lines (predominantly the complex structure/entities/product offerings) - including New Business, Periodic Reviews and Event Driven Reviews. Raising issues and ensuring appropriate actions are undertaken before KYC approval.
+ Identifying thematic issues within the On-Boarding process, highlighting to management and recommending appropriate actions.
+ Liaising with Quality Assurance on any issues identified within the QA process, to consider impact and where needed make relevant changes to the QC process. In addition, where remedial action is required - liaising and notifying the operational leads accordingly.
+ Liaising with Financial Crime KYC team on any issues identified within the 2nd line checks / testing, to consider impact and where needed make relevant changes to the QC process. In addition, where remedial action is required - liaising and notifying the operational leads accordingly.
+ Supporting the lead to understand, challenge and implement any changes to procedures.
+ Assist in the development of a suite of Training for New & Existing Team members on all KYC/On-Boarding procedural related aspects.
+ Deliver training, where required, to front office representatives on KYC/On-Boarding procedural related aspects.
+ Deliver and support lean processes, to deliver effective and efficient KYC process.
+ Training and Development of more junior members of the team
+ Act as a Subject Matter Expert in relation to all AML On-Boarding aspects, assisting on ad-hoc queries where required.
+ Support the QC Lead, producing relevant reports to key counterparties, identifying and resolving Anti Money Laundering issues, and providing support/guidance to more junior members of the team.
+ Keep abreast of developments in current trends and progress on money laundering, bribery and corruption and it prevention.
**WORK EXPERIENCE**
Essential:
+ At least 3 years' experience in Anti Money Laundering, fraud and bribery or Financial Crime roles (ESSENTIAL)
+ Experience with Investment Banking & the On-Boarding of Corporate entities (Inc. Private Companies and SPVs) (ESSENTIAL)
+ Experience of managing a KYC team or function. (BENEFICIAL)
**SKILLS AND EXPERIENCE**
**Functional / Technical Competencies:**
+ Awareness of UK & European Anti-Money Laundering regulations (ESSENTIAL)
+ Knowledge of various corporate structures (ESSENTIAL)
+ Able to communicate effectively to key stakeholders at all levels. (ESSENTIAL)
+ Attention to detail is essential (ESSENTIAL)
+ Ability to effectively utilize Microsoft Office (particularly word & excel). (ESSENTIAL)
**Education / Qualifications:**
+ Degree Level or relevant industry experience (ESSENTIAL)
+ Relevant qualifications in Anti Money Laundering, fraud and bribery or Financial Crime roles. (BENEFICIAL)
**PERSONAL REQUIREMENTS**
+ Excellent communication skills
+ Results driven, with a strong sense of accountability
+ A proactive, motivated approach.
+ The ability to operate with urgency and prioritise work accordingly
+ Strong decision making skills, the ability to demonstrate sound judgement
+ A structured and logical approach to work
+ Strong problem solving skills
+ A creative and innovative approach to work
+ Excellent interpersonal skills
+ The ability to manage large workloads and tight deadlines
+ Excellent attention to detail and accuracy
+ A calm approach, with the ability to perform well in a pressurised environment
+ Strong numerical skills
+ Excellent Microsoft Office skills
+ A confident approach, with the ability to provide clear direction to more junior members of the team
+ A strategic approach, with the ability to lead and motivate more junior members of the team
We are open to considering flexible working requests in line with organisational requirements.
MUFG is committed to embracing diversity and building an inclusive culture where all employees are valued, respected and their opinions count. We support the principles of equality, diversity and inclusion in recruitment and employment, and oppose all forms of discrimination on the grounds of age, sex, gender, sexual orientation, disability, pregnancy and maternity, race, gender reassignment, religion or belief and marriage or civil partnership.
We make our recruitment decisions in a non-discriminatory manner in accordance with our commitment to identifying the right skills for the right role and our obligations under the law.
At MUFG, our colleagues are our greatest assets. Our Culture Principles provide a roadmap for how each of our colleagues must think and act to become more client-obsessed, inclusive and innovative. They reflect who we are, who we want to be and what we expect from one another. We are excited to see you take the next step in exploring a career with us and encourage you to spend more time reviewing them!
**Our Culture Principles**
+ Client Centric
+ People Focused
+ Listen Up. Speak Up.
+ Innovate & Simplify
+ Own & Execute
Quality Control Inspector
Posted 28 days ago
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Job Description
About the opportunity:
We are the internal recruitment partner for our client, a global organisation offering excellence in manufacturing solutions for the aerospace market.
Are you passionate about precision, quality, and aerospace engineering? Do you thrive in a dynamic manufacturing environment where attention to detail is everything?
We’re on a mission to deliver excellence and we need a dedicated Quality Control Inspector to help us ensure our products meet the highest standards.
Responsibilities:
- Verifying the conformity of aerospace parts, assemblies, and sub-assemblies to engineering drawings and customer requirements
- Completing detailed and traceable inspection records
- Supporting production teams with batch verifications and first-off inspections
- Compiling First Article Inspection Reports (FAIRs)
- Performing inspections throughout the manufacturing and supply chain process
- Reporting and escalating non-conformances, and supporting root cause investigations
- Actively participating in Continuous Improvement and New Product Introduction meetings
Requirements
The successful candidate will be able to demonstrate the following:
- Ability to read and interpret technical drawings and specifications
- Solid experience in inspecting precision components
- Familiarity with inspection tools, CMM equipment, and industry measurement techniques
- Experience in aerospace or pharmaceutical environments preferred
- Strong communication and organisational skills
- Confidence to challenge and escalate quality issues
- HND or equivalent qualification, with a good grasp of imperial and metric systems would be desirable.
Benefits
In return we are offering:
- A competitive salary of £35,000 - £45,000 dependent on skills knowledge and experience.
- Flexible working hours with an early finish every Friday.
- 23 days holiday increasing to 26 days after 5 years’ service, plus bank holidays.
- Life assurance scheme.
- Auto enrolment pension scheme.
- Employee Assistance Programme.
- Employee Referral Scheme.
- Employee Recognition Scheme.
- Long Service Awards.
Interested? Then APPLY now for immediate consideration.
Remediation Quality Control Inspector
Posted 8 days ago
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Job Description
In a Nutshell
We have a new opportunity for a Remediation Quality Control Inspector to join our team within Vistry Services, covering various locations around London. As our Remediation Quality Control Inspector, you will be responsible for visiting various sites / offices carrying out the duty of a Site Manager / Quality Control Manager. You will carry out inspections of the works being carried ou.
WHJS1_UKTJ
Remediation Quality Control Inspector - London
Posted 12 days ago
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Job Description
We have a new opportunity for a Remediation Quality Control Inspector to join our team within Vistry Services, covering various locations around London. As our Remediation Quality Control Inspector, you will be responsible for visiting various sites / offices carrying out the duty of a Site Manager / Quality Control Manager. You will carry out inspections of the works being carried out at various stages of the construction process and manage the QA process. you will also carry out inspections of the sites ensuring that all processes and procedures are being carried out correctly and reporting on any issues that you raise and how you have closed them out.
We value in-person collaboration and team culture, but we’re also committed to supporting flexible working where possible. We encourage you to raise any specific requirements during the interview process so we can explore how this could be accommodated.
Let’s cut to the chase, what’s in it for you…- Competitive basic salary and annual bonus
- Company car, car allowance or travel allowance
- Salary sacrifice car scheme available to all employees
- Up to 33 days annual leave plus bank holidays increasing to up to 39 days with service
- 2 Volunteering days per annum
- Private medical insurance, with employee paid cover
- Enhanced maternity, paternity and adoption leave
- Competitive pension scheme through salary sacrifice
- Life assurance at 4 x your annual salary
- Share save and share incentive schemes
- Employee rewards portal with many more benefits…
- Behave in line with our company values – Integrity, Caring and Quality
- Educated to GSCE/GCE standard in Math’s and English, and/or
- BTEC diploma in Building Construction or an NVQ Level 2 or similar, or City and Guilds in relevant trade
- Valid CSCS card
- Previous experience working as a Customer Care Technician or Site Manager.
- Detailed understanding of NHBC customer handover requirements.
- Building Experience
- Onsite inspection experience
- Housing Developer or Main Contractor background
- Client facing exposure
- Good understanding of Microsoft office, excel, outlook.
- Ability to handle complaints and difficult situations.
- Solid understanding of building regulations and legal obligations.
- Excellent planning and organisation skills
- Capable of strategi vision
- Decision making/problem solving/multi-tasking.
- A polite, tactful and assertive attitude
- Patience and calmness under pressure
- Excellent communication skills
- Good team working skills.
- Willing to work extra to meet deadlines as and when the business needs require it.
Desirable –
- NVQ levels 3 & 4 in customer services.
- Be working towards or completed an ONC/HND in Construction.
- The candidate must have gained relevant experience within the construction industry or hold relevant qualifications.
- Record non-conformances, assess and implement both corrections and corrective action.
- Identify and record items/processes that lead to non-conformances.
- Assist in the development of the team’s ‘Defect Free’ culture and carry out training where required, in particular mentoring team members.
- The postholder must at all times carry out their duties and responsibilities to comply with Vistry Partnerships policies/procedures.
- Comply with programmes/deadlines etc.
- Conduct site inspections to ensure compliance with contract drawings, specifications and quality and notify their manager of any problems, errors, discrepancies or divergences and non-confirming work.
- To assess the safety of works on site and compliance with current regulations and project requirements and advise of any infringements to the Project Manager/Project Director/Operations Manager and contractor.
- Provide periodic reports as specified, maintain a diary of events, and comply with all procedures and administration identified within the department’s quality assurance policy. Record any delays and reasons for them.
- Arrange and witness as necessary any tests required by the contract or instructed by their manager.
- Attend site meetings.
- Take site photographs regularly and systematically, ensuring they are date endorsed.
- Carry out pre practical completion and end of defects inspections, including preparation of ‘snagging’ lists and ‘back-snagging’ inspections if necessary.
- To effectively manage all customer expectations and deliver excellent customer service, ensuring defects are dealt with promptly, efficiently and to the satisfaction of the customer and company.
- Instruct clients/tenants in workings/use of any technical appliance/equipment installed.
- Attend weekly meetings reporting to the Line Manager on status of all issues within the projects.
- Carry out formal inspections of the works, and attend any benchmark works.
- Ensure that the QA process is followed and is accurate up to date and signed off. Advise changes to procedures as required. Ensure any issues raised are closed out.
- Review, investigate and execute issues arising from customer contact, maintaining proper records and communication to all stakeholders within an agreed timescale.
We build more than homes, we’re making Vistry. Being a responsible developer and award-winning employer means we live each day through our ethos - doing the right thing. Our behaviours reflect this, as well as our values of integrity, caring and quality. Shaping all we do; they empower us to develop sustainable communities across affordable and private housing. We work in a partnership-led way, and you’ll recognise our renowned brands Bovis Homes, Linden Homes and Countryside Homes. Together with Vistry Works, our manufacturing operation, and the functional support of Vistry Services, we’re a proud UK Green Building Council member, UK top five housebuilder with a five-star House Builders Federation (HBF) customer satisfaction rating, and winner of many awards including Top Employer, Global Top Inspiring Workplaces, and Best for Talent Attraction and Outreach.
Join us in making Vistry.
#LI-WS1
Quality Control Supervisor (External Wall Insultation)
Posted 9 days ago
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Job Description
PLEASE NOTE, we will only consider candidates with specific External Wall Insulation experience.
We are currently looking for a Supervisor with a background in External Wall Insulation Quality Control/Quality Assurance for a project in London. This is a temp to perm opportunity so a full time position will be available after the temporary contract has been completed.
The ideal candidate will need to demonstrate their previous experience by providing two minimum references.
Job Description:
QAQC
Knowledge of External Wall Insulation (EWI) Systems
Detailed knowledge of the QA/QC role
Experience in using cloud-based systems to store information, produce reports, snagging etc.
Perform routine inspections of the quality of installations and upload to digital platform
All other reasonable tasks assigned to you from time to time from your manager
Valid CSCS
Communication Skills
IT Skills
If interested apply online or call (phone number removed)
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Quality Control Laboratory Analyst GMP / GLP
Posted 9 days ago
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Quality Control Laboratory Analyst GMP / GLP – Kent
Opportunity:
Are you currently working in analytical quality control? Does your experience include hands on particle size analysis, analytical testing of Raw Materials, In-process, Release and Stability checks of drug products? Want to work for a large pharmaceutical company? Yes then this is the role for you!
Your role as a Quality Control Analytical Laboratory Analyst GMP/GLP based in Kent will involve testing raw materials, finished products, in process controls and composite samples to GMP / GLP standards.
Testing techniques may include, but is not limited to, routine particle size analysis (Malvern Mastersizers, Sympatec), cleaning verification (HPLC), identification testing (FTIR and Raman), method development and validation (including particle size and cleanability assessments), DSC, Light microscopy, SEM, Moisture content (Karl Fisher), method optimisation and trouble-shooting, technology transfer and pharmacopoeia analyses.
You will also get involved in CAPA’s, deviations and document control.
The hours of work are:
- Early shift 6am - 2pm Monday-Friday – for 3 weeks then it changes to li>Late shift 1.30pm - 10pm Monday-Thursday, 1.30pm - 7pm Friday for 3 weeks then it changes to
- Night shift 9pm - 7am Monday - Thursday for 3 weeks then back to the early shift.
This is a 6 months contract which will be reviewed for a possible extension or go permanent but this is all dependent on the candidate and business performance. The PAYE rate is £17.18 per hour.
Skills:
To apply for the Quality Control Analytical Laboratory Analyst GMP / GLP role you will have the following skills:
- Experience in wet chemistry / analytical techniques ideally within the pharmaceutical or related industry.
How to Apply:
To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy which can be found on the Quality Start website.
If this sounds like the role for you or a colleague then please don’t hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information.
For a list of our current vacancies, please visit the Quality Start website.
If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role.
Quality Start are acting as a specialist recruitment consultancy for this role.
Quality Control Laboratory Analyst GMP / GLP
Posted 12 days ago
Job Viewed
Job Description
Quality Control Laboratory Analyst GMP / GLP – Kent
Opportunity:
Are you currently working in analytical quality control? Does your experience include hands on particle size analysis, analytical testing of Raw Materials, In-process, Release and Stability checks of drug products? Want to work for a large pharmaceutical company? Yes then this is the role for you!
Your role as a Quality Control Analytical Laboratory Analyst GMP/GLP based in Kent will involve testing raw materials, finished products, in process controls and composite samples to GMP / GLP standards.
Testing techniques may include, but is not limited to, routine particle size analysis (Malvern Mastersizers, Sympatec), cleaning verification (HPLC), identification testing (FTIR and Raman), method development and validation (including particle size and cleanability assessments), DSC, Light microscopy, SEM, Moisture content (Karl Fisher), method optimisation and trouble-shooting, technology transfer and pharmacopoeia analyses.
You will also get involved in CAPA’s, deviations and document control.
The hours of work are:
- Early shift 6am - 2pm Monday-Friday – for 3 weeks then it changes to li>Late shift 1.30pm - 10pm Monday-Thursday, 1.30pm - 7pm Friday for 3 weeks then it changes to
- Night shift 9pm - 7am Monday - Thursday for 3 weeks then back to the early shift.
This is a 6 months contract which will be reviewed for a possible extension or go permanent but this is all dependent on the candidate and business performance. The PAYE rate is £17.18 per hour.
Skills:
To apply for the Quality Control Analytical Laboratory Analyst GMP / GLP role you will have the following skills:
- Experience in wet chemistry / analytical techniques ideally within the pharmaceutical or related industry.
How to Apply:
To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy which can be found on the Quality Start website.
If this sounds like the role for you or a colleague then please don’t hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information.
For a list of our current vacancies, please visit the Quality Start website.
If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role.
Quality Start are acting as a specialist recruitment consultancy for this role.
Quality Control Supervisor (External Wall Insultation)
Posted 12 days ago
Job Viewed
Job Description
PLEASE NOTE, we will only consider candidates with specific External Wall Insulation experience.
We are currently looking for a Supervisor with a background in External Wall Insulation Quality Control/Quality Assurance for a project in London. This is a temp to perm opportunity so a full time position will be available after the temporary contract has been completed.
The ideal candidate will need to demonstrate their previous experience by providing two minimum references.
Job Description:
QAQC
Knowledge of External Wall Insulation (EWI) Systems
Detailed knowledge of the QA/QC role
Experience in using cloud-based systems to store information, produce reports, snagging etc.
Perform routine inspections of the quality of installations and upload to digital platform
All other reasonable tasks assigned to you from time to time from your manager
Valid CSCS
Communication Skills
IT Skills
If interested apply online or call (phone number removed)