Quality Control

Derbyshire, East Midlands Gi Group

Posted today

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Job Description

temporary

Quality Control

Our client based in Ashbourne is looking for an experienced Quality Control person to work temporarily.

Monday, Tuesday, and Wednesday on a rotating 9-hour shift.

Hours for each week will be either 6am - 3pm, 8am - 5pm or 9am - 6pm.

12.69 per hour

The main duties for Quality Control:

* Inspecting and booking in of raw material deliveries
* Collection, Inspection and filing of finished product samples
* Processing customer returns
* In the mill/ office 50/50
* Need to have some basic IT skills
* Quality or feed experience would be fab but not essential

If you are interested for more information regarding this role, call Gi Group Derby or send your CV

Should you require any support or assistance, please contact your local Gi Group office.

Gi Group Holdings Recruitment Limited are proud founding members of Menopause in business, pledge members for Neurodiversity in business, Disability committed members, Silver status pledge members for the Armed Forces Covenant, and Bronze trail blazers for Racial Equality matters.

Gi Group Holdings Recruitment Limited group of companies includes Gi Recruitment Limited, Draefern Limited, Gi Group Recruitment Ltd, INTOO (UK) Limited, Marks Sattin (UK) Limited, TACK TMI UK Limited, Grafton Professional Staffing Limited, Encore Personnel Services, Gi Group Ireland Limited and Kelly Services (UK) Ltd. Gi Group Ireland Limited are acting as an Employment Agency in relation to this role.

We are committed to protecting the privacy of all our candidates and clients. If you choose to apply, your information will be processed in accordance with the Gi Group Privacy Statement. To view a copy and to help you understand how we collect, use and process your personal data please visit the Privacy page on our Gi Group website.

This advertiser has chosen not to accept applicants from your region.

Quality Control

Derbyshire, East Midlands £12 - £13 Hourly Gi Group

Posted today

Job Viewed

Tap Again To Close

Job Description

temporary

Quality Control

Our client based in Ashbourne is looking for an experienced Quality Control person to work temporarily.

Monday, Tuesday, and Wednesday on a rotating 9-hour shift.

Hours for each week will be either 6am - 3pm, 8am - 5pm or 9am - 6pm.

12.69 per hour

The main duties for Quality Control:

* Inspecting and booking in of raw material deliveries
* Collection, Inspection and filing of finished product samples
* Processing customer returns
* In the mill/ office 50/50
* Need to have some basic IT skills
* Quality or feed experience would be fab but not essential

If you are interested for more information regarding this role, call Gi Group Derby or send your CV

Should you require any support or assistance, please contact your local Gi Group office.

Gi Group Holdings Recruitment Limited are proud founding members of Menopause in business, pledge members for Neurodiversity in business, Disability committed members, Silver status pledge members for the Armed Forces Covenant, and Bronze trail blazers for Racial Equality matters.

Gi Group Holdings Recruitment Limited group of companies includes Gi Recruitment Limited, Draefern Limited, Gi Group Recruitment Ltd, INTOO (UK) Limited, Marks Sattin (UK) Limited, TACK TMI UK Limited, Grafton Professional Staffing Limited, Encore Personnel Services, Gi Group Ireland Limited and Kelly Services (UK) Ltd. Gi Group Ireland Limited are acting as an Employment Agency in relation to this role.

We are committed to protecting the privacy of all our candidates and clients. If you choose to apply, your information will be processed in accordance with the Gi Group Privacy Statement. To view a copy and to help you understand how we collect, use and process your personal data please visit the Privacy page on our Gi Group website.

This advertiser has chosen not to accept applicants from your region.

Quality Control Manager

S1 Sheffield, Yorkshire and the Humber Adecco

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Job Description

full time

Adecco is excited to be partnering with a dynamic and forward-thinking organisation based in South Yorkshire, renowned for delivering reliable and innovative solutions across a diverse range of industries. We are currently seeking a driven and experienced Quality Control Manager to join their global team.

In this pivotal role, you'll lead the charge in enhancing the Quality Control function-boosting capability, increasing efficiency, and strengthening capacity, particularly within the AQL system and quarantine disposition processes.

You'll be a key player in ensuring products meet rigorous quality specifications and maintain the highest standards across the board.



Key Responsibilities:

  • Oversee and continuously improve quality control policies and procedures

  • Manage and develop a team of quality control professionals

  • Lead training in measurement and assessment techniques, including calibration equipment

  • Make decisions on non-conforming product disposition

  • Ensure production quality is consistently aligned with specifications

  • Drive innovation in quality control through the adoption of new technologies and techniques

  • Foster a strong customer-focused approach within quality processes



What We're Looking For:

  • Proven experience as a quality control professional

  • Strong background in managing and mentoring quality control teams

  • Advanced metrology skills, including CMM machine programming

  • Solid understanding of geometric tolerancing and calibration

  • A degree in Engineering or a related field is preferred



Key Personal Attributes:

  • Excellent communication and active listening skills

  • Self-motivated with a positive, "can-do" attitude

  • High levels of integrity, fairness, and discretion

  • A collaborative team player who leads with authenticity and transparency

  • Detail-oriented, process-driven, and proactive in suggesting improvements

Working Hours:

  • Monday to Thursday: 9:00 AM - 5:00 PM

  • Friday: 9:00 AM - 4:30 PM

If you're ready to bring your expertise to a company that values innovation, integrity, and continuous improvement, we'd love to hear from you.

Adecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer.

By applying for this role your details will be submitted to Adecco. Our Candidate Privacy Information Statement explaining how we will use your information is available on our website.

This advertiser has chosen not to accept applicants from your region.

Quality Control Manager

South Yorkshire, Yorkshire and the Humber £45000 Annually Adecco

Posted today

Job Viewed

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Job Description

permanent

Adecco is excited to be partnering with a dynamic and forward-thinking organisation based in South Yorkshire, renowned for delivering reliable and innovative solutions across a diverse range of industries. We are currently seeking a driven and experienced Quality Control Manager to join their global team.

In this pivotal role, you'll lead the charge in enhancing the Quality Control function-boosting capability, increasing efficiency, and strengthening capacity, particularly within the AQL system and quarantine disposition processes.

You'll be a key player in ensuring products meet rigorous quality specifications and maintain the highest standards across the board.



Key Responsibilities:

  • Oversee and continuously improve quality control policies and procedures

  • Manage and develop a team of quality control professionals

  • Lead training in measurement and assessment techniques, including calibration equipment

  • Make decisions on non-conforming product disposition

  • Ensure production quality is consistently aligned with specifications

  • Drive innovation in quality control through the adoption of new technologies and techniques

  • Foster a strong customer-focused approach within quality processes



What We're Looking For:

  • Proven experience as a quality control professional

  • Strong background in managing and mentoring quality control teams

  • Advanced metrology skills, including CMM machine programming

  • Solid understanding of geometric tolerancing and calibration

  • A degree in Engineering or a related field is preferred



Key Personal Attributes:

  • Excellent communication and active listening skills

  • Self-motivated with a positive, "can-do" attitude

  • High levels of integrity, fairness, and discretion

  • A collaborative team player who leads with authenticity and transparency

  • Detail-oriented, process-driven, and proactive in suggesting improvements

Working Hours:

  • Monday to Thursday: 9:00 AM - 5:00 PM

  • Friday: 9:00 AM - 4:30 PM

If you're ready to bring your expertise to a company that values innovation, integrity, and continuous improvement, we'd love to hear from you.

Adecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer.

By applying for this role your details will be submitted to Adecco. Our Candidate Privacy Information Statement explaining how we will use your information is available on our website.

This advertiser has chosen not to accept applicants from your region.

Quality Control Inspector

S1 2AU Sheffield, Yorkshire and the Humber £28000 Annually WhatJobs

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Job Description

full-time
Our client , a leading manufacturing company in **Sheffield, South Yorkshire, UK**, is seeking a diligent and meticulous Quality Control Inspector to join their team. This role is crucial for ensuring that all manufactured products meet the highest standards of quality and compliance. While the core of the work involves inspecting products on the manufacturing floor, this role offers flexibility with a significant portion of the reporting, data analysis, and documentation processes being executable remotely. You will be responsible for conducting thorough inspections of raw materials, in-process components, and finished goods, identifying defects, and reporting non-conformances. The ideal candidate will possess a keen eye for detail, a strong understanding of quality control principles, and a commitment to maintaining product integrity. This role provides an excellent opportunity to contribute to a company renowned for its commitment to excellence.

Key responsibilities include:
  • Performing detailed inspections of incoming raw materials, components, and finished products against established specifications and standards.
  • Utilizing various measurement tools and testing equipment (e.g., calipers, micrometers, gauges) to verify dimensions and material properties.
  • Identifying, documenting, and reporting product defects, non-conformances, and quality issues.
  • Collaborating with production and engineering teams to address quality concerns and implement corrective actions.
  • Maintaining accurate records of inspection results, test data, and quality reports.
  • Participating in the development and implementation of quality control procedures and standards.
  • Conducting internal audits to ensure compliance with quality management systems (e.g., ISO 9001).
  • Assisting with the calibration and maintenance of inspection and testing equipment.
  • Reviewing production documentation for adherence to quality requirements.
  • Contributing to continuous improvement initiatives aimed at enhancing product quality and reducing defects.

The ideal candidate will have a minimum of 2 years of experience in a Quality Control or Quality Assurance role within a manufacturing environment. Experience with various inspection techniques and the use of precision measuring instruments is essential. A strong understanding of quality management systems and relevant industry standards (e.g., ISO) is highly desirable. Excellent attention to detail, analytical skills, and problem-solving abilities are critical. Good written and verbal communication skills are needed for accurate documentation and reporting. The ability to interpret technical drawings and specifications is required. This hybrid role offers the flexibility of remote work for reporting and analysis, alongside essential on-site duties in **Sheffield, South Yorkshire, UK**.
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Quality Control Assistant Manufacturing

DN6 7BD Doncaster, Yorkshire and the Humber DFS Furniture Ltd

Posted today

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Job Description

permanent

Location: Bentley Moor Ln, Adwick le Street, Doncaster DN6 7BD

Hours: Full Time. 40 hours per week.

Shifts: Alternate shift Pattern

Week 1 - 5:30 - 13:50 Monday - Friday

Week 2 - 14:00 till 00:30 Monday to Wednesday and 14:00 - 00:05 on Thursday (4 days working week.)


Salary: £25,485 + Company Benefits

About DFS

It takes a whole lot of passion to be at the centre of what makes a house feel like home and .






WHJS1_UKTJ

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Quality Control Inspector - Electrical

Retford, East Midlands 1st Select Ltd

Posted 26 days ago

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Job Description

permanent

Job Title: Quality Control Inspector Electrical
Reports To: Quality and Performance Officer

Role Overview:

As the Quality Control Inspector Electrical, you will be responsible for ensuring the highest standards of quality across all building-related projects. This includes responsive and cyclical maintenance, capital investment works, refurbishments, modernisation projects, and new-build developments.











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Remote Pharmaceutical Quality Control Analyst

S1 1AD Sheffield, Yorkshire and the Humber £40000 Annually WhatJobs

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full-time
Our client is seeking a highly skilled and detail-oriented Remote Pharmaceutical Quality Control Analyst to join their dynamic team. This fully remote position is ideal for an experienced analyst who is proficient in pharmaceutical testing methodologies and adheres strictly to Good Manufacturing Practices (GMP). You will be responsible for performing a variety of analytical tests on raw materials, in-process samples, and finished pharmaceutical products to ensure they meet established quality standards and regulatory requirements. Key duties include operating and maintaining analytical instruments such as HPLC, GC, UV-Vis spectrophotometers, and Karl Fischer titrators; preparing reagents and standards; executing test methods according to compendial (USP, EP, BP) and in-house procedures; and meticulously documenting all test results, observations, and deviations. The ideal candidate will possess a strong background in analytical chemistry, a thorough understanding of pharmaceutical quality systems, and excellent data interpretation and reporting skills. You must be able to work autonomously from a home-based laboratory or designated workspace, maintaining a high level of accuracy and compliance. Collaboration with internal teams, including Quality Assurance and Manufacturing, is crucial, requiring effective remote communication skills. This role demands a proactive approach to identifying and troubleshooting analytical issues, ensuring the integrity of test data, and contributing to the overall quality and safety of pharmaceutical products. A commitment to continuous learning and staying abreast of regulatory updates is essential. This is an exceptional opportunity for a qualified analyst to advance their career in the pharmaceutical industry with the flexibility of remote work.

Responsibilities:
  • Perform analytical testing on raw materials, intermediates, and finished pharmaceutical products.
  • Operate and maintain analytical instrumentation (HPLC, GC, UV-Vis, KF, etc.).
  • Prepare reagents, standards, and sample solutions according to SOPs.
  • Execute test methods accurately following USP, EP, BP, and internal specifications.
  • Document all laboratory activities, results, and deviations meticulously in compliance with GMP.
  • Analyze test data, interpret results, and report findings to Quality Assurance.
  • Troubleshoot analytical methods and instrumentation issues.
  • Ensure compliance with all relevant regulatory guidelines and quality standards.
  • Participate in method validation and
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Senior Pharmaceutical Quality Control Analyst

S1 2GT Sheffield, Yorkshire and the Humber £40000 Annually WhatJobs

Posted 3 days ago

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full-time
We are recruiting a Senior Pharmaceutical Quality Control Analyst for a leading pharmaceutical company with operations in Sheffield, South Yorkshire, UK . This role is integral to ensuring the quality, safety, and efficacy of pharmaceutical products through rigorous testing and analysis. You will be responsible for performing analytical testing on raw materials, in-process samples, and finished products using a range of sophisticated laboratory equipment, including HPLC, GC, and UV-Vis spectrophotometry. Key duties include developing and validating analytical methods, documenting all procedures and results meticulously in compliance with GMP guidelines, investigating deviations and out-of-specification results, and contributing to the continuous improvement of quality control processes. The ideal candidate will hold a degree in Chemistry, Pharmacy, or a related life science discipline, coupled with significant experience in a pharmaceutical QC laboratory. A thorough understanding of pharmaceutical quality systems, regulatory requirements (e.g., MHRA, FDA), and analytical techniques is crucial. Excellent attention to detail, problem-solving abilities, and strong communication skills are essential. This hybrid role offers a mix of laboratory-based work and remote data analysis and documentation. Join our client's dedicated team and contribute to the production of life-saving medicines.
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Senior Pharmaceutical Quality Control Analyst

S1 2AE Sheffield, Yorkshire and the Humber £38000 Annually WhatJobs

Posted 8 days ago

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Job Description

full-time
Our client is seeking a meticulous and highly skilled Senior Pharmaceutical Quality Control Analyst to join their state-of-the-art facility in Sheffield, South Yorkshire, UK . This is a critical on-site role focused on ensuring the highest standards of quality for pharmaceutical products. You will be responsible for performing a wide range of analytical tests on raw materials, in-process samples, and finished products using various sophisticated analytical techniques. This includes HPLC, GC, UV-Vis spectroscopy, titration, and other relevant methodologies. Key duties involve method development and validation, stability testing, equipment calibration, and troubleshooting analytical instrumentation. You will also be involved in data review and reporting, ensuring all activities are meticulously documented in compliance with GMP, ICH guidelines, and regulatory requirements. The ideal candidate will have a strong background in analytical chemistry, specifically within the pharmaceutical industry. Proven experience with QC laboratory operations and a thorough understanding of regulatory compliance are essential. You should possess excellent technical skills, attention to detail, and the ability to work independently as well as part of a team. This role also involves mentoring and training junior analysts, contributing to the overall efficiency and expertise of the QC department. A Bachelor's or Master's degree in Chemistry, Pharmaceutical Science, or a related field is required, along with substantial hands-on experience in a pharmaceutical QC environment. This is a fantastic opportunity to advance your career within a leading pharmaceutical company, contributing to the development and manufacturing of life-saving medicines.
Responsibilities:
  • Perform analytical testing on raw materials, intermediates, and finished products.
  • Utilize HPLC, GC, spectroscopy, and other analytical techniques.
  • Conduct method validation and development according to regulatory guidelines.
  • Execute stability studies and monitor product shelf-life.
  • Calibrate and maintain laboratory instrumentation.
  • Review and interpret analytical data, ensuring accuracy and compliance.
  • Document all laboratory activities following GMP and ICH standards.
  • Train and mentor junior QC analysts.
Qualifications:
  • BSc/MSc in Chemistry, Pharmaceutical Science, or a related field.
  • Significant experience in a pharmaceutical Quality Control laboratory.
  • Proficiency with analytical instrumentation (HPLC, GC, UV-Vis).
  • Knowledge of GMP, ICH guidelines, and regulatory requirements.
  • Strong attention to detail and analytical problem-solving skills.
  • Excellent documentation and communication abilities.
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