10 Tata Steel jobs in Corby

Quality Control Inspector

CV21 Rugby, West Midlands Hays Technology

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full time

Your new company: Our client is a world leader in Power Conversion & Storage and provides electrification systems that are critical to their global customers' power and energy needs. They work with the world's major energy, maritime, and industrial organisations, enabling their transition to energy efficiency and decarbonisation, including through their specialist motors, drives, and control technologies.
Having won major contracts in the UK defence sector, this company will work in partnership with 3 major global engineering organisations to deliver


Your new role:
Our client has an exciting opportunity for someone to join their team on a UK eyes-only project as a Quality Control Inspector working on challenging and exciting world-leading defence projects.
The Quality Control Inspector will ensure that all Quality standards are achieved for both manufactured and purchased component products.
You will provide the final point of inspection for the products, maintain reports and performance metrics and raise quality non-conformance reports (NCR), support the problem resolution process, including Containment, Root Cause Analysis, and Corrective and Preventative Actions.
The successful candidate must possess the ability to solve simple problems, provide operable solutions, and act with minimal direction on their own initiative.


Responsibilities:

  • Approves incoming materials by confirming specifications; conducting visual and measurement tests; rejecting and returning unacceptable materials.
  • Approves in-process production by confirming specifications; conducting visual and measurement tests; communicating required adjustments to production.
  • Approves finished products by confirming specifications; conducting visual and measurement tests; returning products for re-work; confirming re-work.
  • Documents inspection results by completing reports and logs; inputting data into a quality database (SAP).
  • Keeps measurement equipment operating and manages calibration systems.
  • Maintains a safe and healthy work environment by following standards and procedures, complying with legal regulations.
  • Auditing manufacturing processes where required.
  • Completing Non-Conforming Reports with root cause analysis.
  • To work closely with production personnel, carrying out first off, final, and random inspections using CMM and FARO Mechanical inspection equipment.

What you'll need to succeed: To be successful in the role, you will need proven experience as a quality inspector or in a relevant role with a keen eye for detail and a results-driven approach.
If you are a traditional Quality Control professional with experience in Quality Inspection, then you are highly encouraged to apply.You will need to have practical experience with CMM measuring equipment and be able to reverse-check CAD models.
Have familiarity with FARO laser measuring equipment on large heavy industrial components and a thorough knowledge of quality control standards and inspection methodologies for both electrical and mechanical systems.
The ability to obtain UK security clearance to SC level is essential for this role
What you get in return: Apart from an industry-leading benefits package that includes health insurance, income protection, life assurance, generous pension, hybrid working pattern and 26-day holidays plus bank holidays, you get the opportunity to deliver technology which will have a lasting national impact and get to work on projects that are cutting-edge and world-leading.
You will get the chance to work with end clients and partner organisations on schemes that will redefine engineering in the defence sector.
What you do now: Please get in touch with me directly for an informal conversation on

Hays Specialist Recruitment Limited acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers. By applying for this job you accept the T&C's, Privacy Policy and Disclaimers which can be found at (url removed)

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Quality Control Inspector

Rugby, West Midlands GE Vernova

Posted 17 days ago

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**Job Description Summary**
GE's Power Conversion & Storage business, part of GE Vernova, provides electrification systems that are critical to customers' power and energy needs for their high-performance applications. We work with some of the world's major energy, maritime and industrial organizations, helping to enable a transition to energy efficiency and decarbonization, including through our specialist motors, drives and control technologies.
**Job Description**
The Quality Control Inspector will ensure that all Quality standards are achieved for both manufactured and purchased products. Providing the final point of inspection for the products and maintaining reports and performance metrics. Raising quality non-conformance reports (NCR) and supporting the problem resolution process, including Containment, Root Cause Analysis, and Corrective and Preventative Actions.
The candidate must possess the ability to solve simple problems, provide operable solutions, act with minimal direction on their own initiative.
The candidate will work within the current quality team reporting directly to the UK Quality Leader
**Responsibilities:**
+ Approves incoming materials by confirming specifications; conducting visual and measurement tests; rejecting and returning unacceptable materials.
+ Approves in-process production by confirming specifications; conducting visual and measurement tests; communicating required adjustments to production.
+ Approves finished products by confirming specifications; conducting visual and measurement tests; returning products for re-work; confirming re-work.
+ Documents inspection results by completing reports and logs; inputting data into quality database (SAP).
+ Keeps measurement equipment operating and manages calibration systems.
+ Maintains safe and healthy work environment by following standards and procedures, complying with legal regulations.
+ Auditing manufacturing processes where required.
+ Completing Non-Conforming Reports with root cause analysis.
+ To work closely with production personnel carrying out first off, final, and random inspections using CMM and FARO Mechanical inspection equipment
+ Provide training and guidance to inspect using best practice.
**Qualifications and Experience Levels:**
+ Proven experience as quality inspector or relevant role.
+ A keen eye for detail and a results-driven approach.
+ Familiarity with quality measurement equipment - CMM, FARO -Laser and Arm
+ Thorough knowledge of quality control standards and inspection methodologies electrical and mechanical.
+ Working knowledge of MS Office.
+ Ability to obtain UK security clearance to SC level.
**You can expect from us**
+ Challenging and exciting projects
+ A work environment where we understand that not everyone has the same expectations about their jobs, careers and work-life balance and we are happy to discuss flexibility requirements.
+ Attractive compensation.
+ Flexible benefits so you can build a package that fits your personal needs. Some core benefits are: Employer pension contribution (not subject to individual contribution); Income protection; Private Health Insurance; Life Assurance
+ 26 days vacation + bank holidays
**Additional Information**
**Relocation Assistance Provided:** No
GE Vernova is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.
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Quality Control Inspector

Rugby, West Midlands Hays

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Job Description

permanent

Your new company: Our client is a world leader in Power Conversion & Storage and provides electrification systems that are critical to their global customers' power and energy needs. They work with the world's major energy, maritime, and industrial organisations, enabling their transition to energy efficiency and decarbonisation, including through their specialist motors, drives, and control techno.














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Lead Quality Control Engineer

LE2 7AD Leicester, East Midlands £45000 Annually WhatJobs

Posted 3 days ago

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full-time
Our client, a leading innovator in the manufacturing sector, is seeking a highly skilled and meticulous Lead Quality Control Engineer to join their expanding production facility in **Leicester, Leicestershire, UK**. This is a critical role responsible for ensuring the highest standards of product quality and process integrity throughout the manufacturing lifecycle. You will lead a team of quality inspectors and technicians, establishing and enforcing stringent quality control procedures, and driving continuous improvement initiatives. Key responsibilities include developing and implementing comprehensive quality management systems, conducting rigorous inspections and testing of raw materials, in-process components, and finished goods, and analysing defect data to identify root causes and implement corrective actions. The ideal candidate will possess a deep understanding of quality control methodologies, statistical process control (SPC), and relevant industry standards (e.g., ISO 9001). You should have a proven ability to lead and mentor a technical team, fostering a culture of quality excellence. Experience with various inspection techniques and equipment, such as CMMs, calipers, and micrometers, is essential. You will collaborate closely with engineering, production, and R&D teams to resolve quality issues and improve product design and manufacturability. Strong analytical, problem-solving, and communication skills are paramount. This role offers an excellent opportunity to significantly influence product quality and contribute to the company's reputation for excellence. If you are a dedicated quality professional with a passion for manufacturing and a commitment to upholding the highest standards, we invite you to apply.

Responsibilities:
  • Lead and manage the Quality Control department and its team members.
  • Develop, implement, and maintain the Quality Management System (QMS).
  • Establish and enforce quality standards for all production processes and products.
  • Conduct routine inspections and testing of materials, components, and finished products.
  • Analyse quality data, identify trends, and implement root cause analysis for defects.
  • Develop and implement corrective and preventive actions (CAPA).
  • Collaborate with engineering and production teams to resolve quality issues.
  • Ensure compliance with industry standards and regulatory requirements.
  • Train and mentor QC inspectors and technicians.
  • Manage calibration and maintenance of testing equipment.
Qualifications:
  • Bachelor's degree in Engineering, Manufacturing Technology, or a related field.
  • 5+ years of experience in quality control or quality assurance within a manufacturing environment.
  • Proven experience leading and managing a technical team.
  • Strong knowledge of quality management systems (e.g., ISO 9001).
  • Proficiency in statistical process control (SPC) and quality analysis tools.
  • Experience with various inspection techniques and measurement equipment.
  • Excellent problem-solving and analytical skills.
  • Strong understanding of manufacturing processes.
  • Effective communication and interpersonal skills.
  • Familiarity with Lean Manufacturing principles is a plus.
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Pharmaceutical Quality Control Analyst

LE1 5AA Leicester, East Midlands £30000 Annually WhatJobs

Posted 3 days ago

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full-time
Our client, a leading pharmaceutical company, is seeking a meticulous and dedicated Pharmaceutical Quality Control Analyst to join their team in **Leicester, Leicestershire, UK**. This role is critical in ensuring the quality, safety, and efficacy of pharmaceutical products through rigorous testing and analysis. You will perform a variety of laboratory tests on raw materials, in-process samples, and finished products using advanced analytical techniques and instrumentation. Your responsibilities will include adhering to strict Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP) guidelines, documenting all experimental procedures and results accurately, and troubleshooting any analytical issues that may arise. The ideal candidate will have a strong background in analytical chemistry or a related scientific discipline, with hands-on experience in techniques such as HPLC, GC, UV-Vis spectroscopy, and Karl Fischer titration. Familiarity with pharmacopoeial methods (e.g., BP, USP, EP) is essential. You will be responsible for maintaining laboratory equipment, ensuring its calibration and performance. A keen eye for detail, excellent organizational skills, and the ability to work effectively both independently and as part of a team are crucial. We are looking for a proactive individual who is committed to upholding the highest standards of quality in pharmaceutical manufacturing. This is an exciting opportunity to contribute to the development and release of life-saving medicines within a state-of-the-art facility. The role requires a scientific mind, a commitment to accuracy, and a passion for quality assurance.
Responsibilities:
  • Perform chemical and physical analysis on raw materials, intermediates, and finished pharmaceutical products.
  • Utilize various analytical techniques including HPLC, GC, FTIR, UV-Vis, and wet chemistry.
  • Ensure all testing is conducted in compliance with GMP, GLP, and relevant pharmacopoeial standards.
  • Accurately document all experimental data, observations, and results in laboratory notebooks and LIMS.
  • Calibrate, maintain, and troubleshoot laboratory equipment.
  • Investigate out-of-specification (OOS) results and deviations, participating in root cause analysis.
  • Prepare and standardize reagents and solutions.
  • Contribute to method validation and transfer activities.
  • Maintain a clean and organized laboratory environment.
  • Participate in internal and external audits.
Qualifications:
  • Bachelor's degree in Chemistry, Pharmaceutical Science, or a related field.
  • Proven experience in a pharmaceutical Quality Control laboratory setting.
  • Hands-on experience with HPLC, GC, and other relevant analytical instrumentation.
  • Knowledge of GMP and GLP regulations.
  • Familiarity with pharmacopoeial methods (BP, USP, EP).
  • Strong understanding of analytical chemistry principles.
  • Excellent documentation skills and attention to detail.
  • Ability to work independently and as part of a team.
  • Good problem-solving skills.
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Senior Quality Control Engineer

LE1 5AA Leicester, East Midlands £45000 Annually WhatJobs

Posted 3 days ago

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full-time
Our client, a leader in advanced manufacturing solutions, is seeking a highly skilled and motivated Senior Quality Control Engineer to join their dynamic team. This is a fully remote position, offering the flexibility to work from anywhere within the UK. You will play a critical role in ensuring the highest standards of product quality throughout the entire manufacturing process, from raw material inspection to final product release. Your expertise will be vital in developing and implementing robust quality assurance strategies, identifying potential defects, and driving continuous improvement initiatives. The role involves extensive collaboration with cross-functional teams, including R&D, production, and engineering, to resolve quality issues and implement corrective actions.

Responsibilities:
  • Develop, implement, and maintain comprehensive quality control plans and procedures.
  • Conduct regular audits of manufacturing processes to ensure compliance with quality standards and regulatory requirements.
  • Analyze production data to identify trends, root causes of defects, and areas for improvement.
  • Design and execute validation and verification protocols for new and existing products.
  • Lead investigations into non-conformances and implement effective corrective and preventive actions (CAPA).
  • Collaborate with suppliers to ensure the quality of incoming materials and components.
  • Train and mentor junior quality control personnel.
  • Stay abreast of industry best practices and emerging quality control technologies.
  • Maintain detailed records and documentation related to quality control activities.
  • Prepare regular reports on quality performance metrics for management review.
  • Contribute to the continuous improvement of quality management systems.
  • Uphold the company's commitment to excellence in product quality and customer satisfaction.
Qualifications:
  • Bachelor's degree in Engineering, Science, or a related field.
  • Minimum of 5 years of experience in a quality control or quality assurance role within a manufacturing environment.
  • Strong understanding of quality management systems (e.g., ISO 9001).
  • Proficiency in statistical process control (SPC) and other quality tools.
  • Excellent analytical, problem-solving, and decision-making skills.
  • Exceptional communication and interpersonal skills, with the ability to collaborate effectively across teams.
  • Proven experience in leading root cause analysis and CAPA implementation.
  • Experience with auditing and supplier quality management is highly desirable.
  • Familiarity with lean manufacturing principles.
  • Ability to work independently and manage multiple priorities in a remote setting.
This is an exciting opportunity to contribute to a forward-thinking company and shape the future of manufacturing quality. The ideal candidate will be passionate about quality and possess a proactive, detail-oriented approach. Join us and be part of a team dedicated to delivering exceptional products to our global customer base, all while enjoying the benefits of a remote-first work environment. The successful applicant will be based in or able to reliably work from **Leicester, Leicestershire, UK**, providing input to production processes impacting various industries.
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Quality Control Vehicle Inspector

PE28 Newtown, Eastern Cox Automotive

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*Quality Control Inspector *

*Wyton *

*£30,812 *

*40 hours a week (Monday – Friday) with optional overtime available as and when required. *

*Accelerate your career with a company that leads the way!

*

Manheim Vehicle Services, part of the Cox Automotive Group is a dynamic and fast-moving part of our business, delivering expert support across customer de-fleet programs, multiple remarketing channels, and full vehicle preparation — from wholesale through to retail-ready.

We pride ourselves on being agile and responsive, managing a wide range of customer needs with precision and care. Our team carries out detailed cosmetic inspections, oversees the authorisation process, and ensures every vehicle meets both contractual and customer-specific standards before hitting the market. It's all about getting vehicles sale-ready — and done right, every time.

*Why Join Us & What’s In It For You?

*

As a Cox Automotive team member, you’ll have access to a wide range of benefits, including exclusive discounts, cashback offers and our brilliant peer to peer recognition scheme.

And there’s even more to enjoy:

* Option to buy additional holiday daysn* Your birthday off every year - paidn* One annual Well-Being Day for you to relax and rechargen* One paid Charity Day to give back and support a cause that matters to youn* Opportunities for career progression across the Cox Automotive networkn* Competitive pension scheme

*About The Role *

As a Quality Control Inspector, you will be responsible for performing detailed quality control checks on all vehicles, ensuring they meet both our high internal standards and the specific requirements of each customer contract.

Working across three key quality control stages, you will play a vital role in maintaining the consistency, quality, and readiness of every vehicle as it moves through the refurbishment process.

*What You’ll Be Doing *

* Understand and correctly apply the standards for each customer contract.n* Meet daily targets for moving vehicles through the refurbishment process, identifying and escalating any delays.n* Spot and report any sub-standard repairs, maintaining the integrity of our processes.n* Make clear, confident decisions — recognising both when a repair meets standards and when it does not.

*What We’re Looking For *

* Experience working within strict regulations and procedures.n* Exceptional eye for detail and quality.n* Strong understanding of vehicle repairs and the desired outcomes.n* Knowledge of both car and commercial vehicle components.n* Excellent communication skills, both verbal and written.n* Ability to adapt to new and evolving technology.n* Proactive, flexible, and able to quickly react to change.n* Team player, committed to achieving departmental goals.n* Strong time management and organisational skills, with the ability to work under pressure and meet tight deadlines.

*We’re Committed to Inclusion

*

We are proud to be an inclusive and equal opportunity employer. We celebrate diversity in all its forms.

We are a place where you can be you.

*Ready To Join Our Team & Make A Difference?

*nApply now and drive your career forward with one of the automotive industry’s most trusted names.

*STRICTLY NO AGENCIES PLEASE

*nWe kindly ask that agencies do not contact us regarding this vacancy.

We work with a carefully selected and trusted group of recruitment partners.

We do not accept unsolicited CVs sent to the recruitment team or directly to a hiring manager. We will not be responsible for any fees related to unsolicited submissions.

Job Types: Full-time, Permanent

Pay: £30,812.00 per year

Benefits:n* Company pensionn* Free parkingn* On-site parkingn* Referral programme

Application question(s):n* Do you have the right to work in the UK?n* If you have a visa to work in the UK, what type of visa is it and when does it expire?n* Do you hold a full UK driving licence?n* Have you worked in the motor sector?

Work Location: In personn
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Senior Pharmaceutical Quality Control Scientist

LE1 6TY Leicester, East Midlands £45000 Annually WhatJobs

Posted 1 day ago

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full-time
Our client, a reputable pharmaceutical company, is seeking an experienced Senior Pharmaceutical Quality Control Scientist to join their vital Quality Assurance department in **Leicester, Leicestershire, UK**. This role is integral to ensuring the safety, efficacy, and quality of pharmaceutical products through rigorous testing and adherence to strict regulatory standards. You will be responsible for performing a wide range of analytical tests on raw materials, in-process samples, and finished products using various laboratory techniques and instrumentation. Key duties include method development and validation, data analysis and interpretation, accurate documentation of results, and troubleshooting laboratory issues. The ideal candidate will possess a strong background in pharmaceutical analysis, comprehensive knowledge of GMP (Good Manufacturing Practice), and proficiency with analytical instrumentation such as HPLC, GC, UV-Vis, and dissolution apparatus. Excellent attention to detail, strong scientific acumen, and the ability to work effectively within a regulated laboratory environment are essential. This on-site position requires your dedication within our **Leicester, Leicestershire, UK** facility.

Key Responsibilities:
  • Perform analytical testing on raw materials, intermediates, and finished pharmaceutical products.
  • Utilize various analytical techniques and instrumentation, including HPLC, GC, UV-Vis, IR, and dissolution testing.
  • Develop, validate, and transfer analytical methods according to regulatory guidelines.
  • Analyze and interpret test data, ensuring accuracy and compliance with specifications.
  • Document all laboratory activities, results, and deviations meticulously in accordance with GMP standards.
  • Troubleshoot analytical equipment and resolve laboratory issues promptly.
  • Prepare Certificates of Analysis (CoA) and technical reports.
  • Maintain laboratory equipment and ensure calibration and qualification are up-to-date.
  • Adhere strictly to all safety protocols and environmental health regulations.
  • Collaborate with R&D, production, and regulatory affairs teams to support product development and release.

Qualifications:
  • Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or a related scientific discipline.
  • Minimum of 5 years of experience in pharmaceutical quality control or analytical development.
  • In-depth knowledge of GMP, ICH guidelines, and regulatory requirements for pharmaceuticals.
  • Proven experience with HPLC, GC, and other common pharmaceutical analytical techniques.
  • Strong understanding of analytical method development and validation principles.
  • Excellent data analysis, interpretation, and report writing skills.
  • Proficiency in laboratory information management systems (LIMS) is a plus.
  • Strong attention to detail, organizational skills, and problem-solving abilities.
  • Ability to work independently and as part of a collaborative team in a fast-paced environment.
  • Must be eligible to work in the UK.
This is an on-site position located in **Leicester, Leicestershire, UK**. Join our dedicated team and contribute to delivering high-quality pharmaceutical products.
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Senior Pharmaceutical Quality Control Analyst

LE2 7FL Leicester, East Midlands £45000 Annually WhatJobs

Posted 3 days ago

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full-time
A leading pharmaceutical company located in Leicester, Leicestershire, UK is seeking a highly skilled and meticulous Senior Pharmaceutical Quality Control Analyst to join their expanding team. This is a critical role responsible for ensuring the quality and integrity of pharmaceutical products through rigorous testing and analysis. You will work in a state-of-the-art laboratory environment, employing a range of analytical techniques and instrumentation to meet stringent regulatory standards. As a Senior Analyst, you will play a key role in method development, validation, and troubleshooting, as well as providing mentorship to junior members of the QC team.

Your responsibilities will include performing a variety of analytical tests on raw materials, in-process samples, and finished products using techniques such as HPLC, GC, UV-Vis, and Karl Fischer titration. You will meticulously document all experimental procedures, results, and deviations in accordance with Good Manufacturing Practices (GMP) and other relevant regulatory guidelines. A significant part of your role will involve reviewing and approving analytical data, ensuring compliance with specifications and release criteria. You will actively participate in investigations of out-of-specification (OOS) or out-of-trend (OOT) results, identifying root causes and implementing corrective and preventive actions (CAPAs). Method validation and transfer activities will also be a key responsibility, ensuring that analytical methods are fit for purpose and reliably executed. Collaboration with other departments, including R&D, Production, and Regulatory Affairs, is essential to address quality issues and support product development. The ideal candidate will possess a strong scientific background, a comprehensive understanding of pharmaceutical quality systems, and proven experience in a QC laboratory setting.

Responsibilities:
  • Conduct routine and non-routine analytical testing of pharmaceutical products.
  • Perform method development, validation, and transfer.
  • Operate and maintain analytical instruments (e.g., HPLC, GC).
  • Review and approve analytical data and laboratory notebooks.
  • Investigate Out-of-Specification (OOS) results.
  • Ensure compliance with GMP and regulatory requirements.
  • Write and revise Standard Operating Procedures (SOPs).
  • Mentor and train junior QC analysts.
  • Liaise with other departments on quality-related matters.

Qualifications: Bachelor's or Master's degree in Chemistry, Pharmaceutical Science, or a related scientific discipline. Minimum of 5 years of experience in a Pharmaceutical Quality Control (QC) laboratory. Proven expertise in analytical techniques such as HPLC, GC, dissolution testing, and spectroscopy. Strong understanding of GMP, ICH guidelines, and regulatory requirements. Experience with method validation and transfer protocols. Excellent problem-solving, analytical, and critical thinking skills. Meticulous attention to detail and strong documentation practices. Ability to lead investigations and implement CAPAs. Good communication and interpersonal skills. Experience with LIMS systems is a plus. This position is based in Leicester, Leicestershire, UK .
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Senior Quality Control Inspector (Automotive)

LE3 0FL Leicester, East Midlands £35000 Annually WhatJobs

Posted 3 days ago

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full-time
Our client, a leading automotive manufacturing facility located in **Leicester, Leicestershire, UK**, is seeking a highly skilled and experienced Senior Quality Control Inspector to join their dedicated production team. This pivotal role involves ensuring that all manufactured products meet stringent quality standards and specifications. The ideal candidate will possess a meticulous eye for detail, a strong understanding of manufacturing processes, and the ability to lead and mentor junior inspection staff. You will be responsible for implementing and refining quality control procedures, conducting thorough inspections of raw materials, in-process components, and finished goods, and meticulously documenting all findings.

Key Responsibilities:
  • Perform comprehensive quality inspections on automotive parts and assemblies using various measurement tools and techniques.
  • Develop, implement, and maintain quality control plans and procedures.
  • Conduct root cause analysis for quality deviations and implement corrective and preventative actions.
  • Interpret technical drawings, blueprints, and specifications to ensure product compliance.
  • Calibrate and maintain inspection equipment to ensure accuracy.
  • Train and supervise junior quality inspectors, providing guidance and feedback.
  • Collaborate with production and engineering teams to resolve quality issues and improve processes.
  • Maintain accurate and detailed inspection records and reports.
  • Ensure compliance with relevant industry standards and certifications (e.g., ISO 9001, IATF 16949).
  • Participate in internal and external audits as required.
  • Proactively identify areas for quality improvement within the production environment.
  • Adhere strictly to health and safety regulations on the production floor.
Qualifications and Experience:
  • Proven experience as a Quality Control Inspector in a manufacturing environment, preferably automotive.
  • Demonstrable experience with quality control methodologies and tools (e.g., CMM, calipers, gauges).
  • Strong understanding of manufacturing processes and defect identification.
  • Ability to read and interpret technical documentation and engineering drawings.
  • Excellent analytical and problem-solving skills.
  • Leadership or supervisory experience is highly desirable.
  • Good communication and interpersonal skills for effective teamwork.
  • Proficiency in data recording and analysis.
  • Relevant certifications in quality control are a significant advantage.
  • A commitment to maintaining the highest standards of quality and efficiency.
This is an excellent opportunity for a dedicated professional to advance their career within a reputable manufacturing organization. The successful candidate will play a crucial role in upholding product integrity and contributing to the company's ongoing success.
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