Quality Control Assistant

West Yorkshire, Yorkshire and the Humber £28000 - £30000 Annually SRG

Posted 4 days ago

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Job Description

permanent

Title: QC Assistant
Location: West Yorkshire
Salary: 28,000-30,000
Term: Permanent

SRG is working with an independent contract manufacturer of personal care / skincare products, based in West Yorkshire. They are now looking for a quality control assistant to join the team. You would be responsible for wet chemistry / bench chemistry testing and techniques. Ensure products meet specifications, as well as some small-scale formulation projects. This position would be an excellent opportunity for someone with experience in Quality Control or lab-based testing to join a supportive, friendly, family-owned company.

Working Hours: Monday to Friday 7:30am to 4:15pm (Mon-Fri), 45-minute lunch break

Role / Description

  • QC testing of raw materials, in-process samples and finished product to check batches meet specifications
  • Development and implementation of SOP's and QC procedures
  • Lab techniques include PH testing, viscosity, stability testing and packaging compatibility testing
  • Conduct routine microbiological and physical testing on products to ensure batches are compliant against industry regulations
  • Work in harmony with Production and QA to achieve production delivery plans and resolve any quality issues
  • Collaborate with stakeholders to ensure R&D, production and packaging compliance and resolve any inconsistencies to ensure batch consistency
  • Formulation and development of batches to help improve new and existing batches

Requirements

  • 2+ years recent experience in QC testing / wet chemistry within the personal care / skincare industry
  • Willing and able to work stood up in a Fast-paced manufacturing environment
  • Experience of working to cosmetic regulations such as EU Cosmetics Regulation, UK REACH, FDA etc.
  • Strong communication skills and can relay information accurately
  • Full right to work in the UK - there is no sponsorship available for this role


SRG is the UK's number one recruitment company specialising in the scientific, engineering, clinical, pharmaceutical, food/FMCG, energy & renewables, biotech, chemical and medical device sectors.

As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients.

If you would like to apply for this position, please use the link provided. Alternatively, please email a copy of your CV For more information regarding this position or any others, please call Rhi on (phone number removed).

If you have a scientific background and this position is not relevant / suitable for you, please feel free to get in touch or visit (url removed) to view our other vacancies.

Keywords: formulation, NPD, new product development, new product innovation, packaging development, sustainable packaging, packaging trends, packaging innovation, supplier management, green chemistry, beauty, cosmetics, skincare, personal care, haircare, packaging innovation, soap, quality, quality control, quality assurance, sop's, haccap, ISO22716, Six Sigma, EU Cosmetics Regulation, UK REACH, FDA, manufacturing, ingredient safety

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

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

Quality Control Manager

South Yorkshire, Yorkshire and the Humber £45000 Annually Adecco

Posted 4 days ago

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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 Manager

S1 Sheffield, Yorkshire and the Humber Adecco

Posted 1 day ago

Job Viewed

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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 Assistant

HD6 Brighouse, Yorkshire and the Humber SRG

Posted 1 day ago

Job Viewed

Tap Again To Close

Job Description

full time

Title: QC Assistant
Location: West Yorkshire
Salary: 28,000-30,000
Term: Permanent

SRG is working with an independent contract manufacturer of personal care / skincare products, based in West Yorkshire. They are now looking for a quality control assistant to join the team. You would be responsible for wet chemistry / bench chemistry testing and techniques. Ensure products meet specifications, as well as some small-scale formulation projects. This position would be an excellent opportunity for someone with experience in Quality Control or lab-based testing to join a supportive, friendly, family-owned company.

Working Hours: Monday to Friday 7:30am to 4:15pm (Mon-Fri), 45-minute lunch break

Role / Description

  • QC testing of raw materials, in-process samples and finished product to check batches meet specifications
  • Development and implementation of SOP's and QC procedures
  • Lab techniques include PH testing, viscosity, stability testing and packaging compatibility testing
  • Conduct routine microbiological and physical testing on products to ensure batches are compliant against industry regulations
  • Work in harmony with Production and QA to achieve production delivery plans and resolve any quality issues
  • Collaborate with stakeholders to ensure R&D, production and packaging compliance and resolve any inconsistencies to ensure batch consistency
  • Formulation and development of batches to help improve new and existing batches

Requirements

  • 2+ years recent experience in QC testing / wet chemistry within the personal care / skincare industry
  • Willing and able to work stood up in a Fast-paced manufacturing environment
  • Experience of working to cosmetic regulations such as EU Cosmetics Regulation, UK REACH, FDA etc.
  • Strong communication skills and can relay information accurately
  • Full right to work in the UK - there is no sponsorship available for this role


SRG is the UK's number one recruitment company specialising in the scientific, engineering, clinical, pharmaceutical, food/FMCG, energy & renewables, biotech, chemical and medical device sectors.

As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients.

If you would like to apply for this position, please use the link provided. Alternatively, please email a copy of your CV For more information regarding this position or any others, please call Rhi on (phone number removed).

If you have a scientific background and this position is not relevant / suitable for you, please feel free to get in touch or visit (url removed) to view our other vacancies.

Keywords: formulation, NPD, new product development, new product innovation, packaging development, sustainable packaging, packaging trends, packaging innovation, supplier management, green chemistry, beauty, cosmetics, skincare, personal care, haircare, packaging innovation, soap, quality, quality control, quality assurance, sop's, haccap, ISO22716, Six Sigma, EU Cosmetics Regulation, UK REACH, FDA, manufacturing, ingredient safety

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

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

Quality Control Lead

Wales, Yorkshire and the Humber SRG

Posted today

Job Viewed

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Job Description

QC Section Lead

North-Wales


SRG are recruiting for a QC Section Leader to manage a GMP QC team testing pharmaceutical products. Based in North Wales, this position will be based with a one of the UKs leading pharmaceutical manufacturers and will be responsible for ensuring the highest standards of quality are maintained and be a key figure in driving continuous improvement.


The Role:


Leading a team of analysts, you will manage day to day activities of the team and ensure key metrics and quality standards are maintained. Key responsibilities will include:


  • Managing the workload of the QC team, planning daily & weekly schedules.
  • Motivating, Mentoring & Developing an effective QC team.
  • Leading OOS/OOT investigations.
  • Leading method transfer, verification & validation activities
  • Representing the QC group at internal & client meetings as well as audits.


Benefits:

  • Generous pension scheme & annual holiday allowance
  • Subsidised on-site canteen
  • Social & sporting clubs
  • Free on-site parking



Requirements:


  • A degree or similar qualification in Chemistry or similar relevant qualification
  • Proven experience in a pharmaceutical laboratory or similar GMP environment.
  • Previous experience of leading, supervising or managing a team.
  • Solid knowledge of pharmaceutical testing methods and experience of method transfer, verification & validation.
This advertiser has chosen not to accept applicants from your region.

Quality Control Assistant Manufacturing

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

Posted 1 day ago

Job Viewed

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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

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

Senior Pharmaceutical Quality Control Analyst

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

Posted 3 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.
This advertiser has chosen not to accept applicants from your region.
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Senior Pharmaceutical Quality Control Analyst

BD4 0AA Bradford, Yorkshire and the Humber £38000 Annually WhatJobs

Posted 4 days ago

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Job Description

full-time
Our client, a leading pharmaceutical company, is seeking a highly skilled and meticulous Senior Pharmaceutical Quality Control Analyst to join their expanding team in Bradford. This critical role ensures that all manufactured products meet stringent quality standards and regulatory requirements. 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. This includes method development and validation, data analysis, and interpretation to ensure product integrity and safety. You will also be involved in reviewing and approving analytical test results, preparing Certificates of Analysis, and maintaining accurate and detailed laboratory records in compliance with Good Manufacturing Practices (GMP) and other relevant regulations. The ideal candidate will possess a strong background in pharmaceutical quality control, with extensive experience in analytical techniques such as HPLC, GC, UV-Vis spectroscopy, and dissolution testing. A Bachelor's or Master's degree in a relevant scientific discipline (e.g., Chemistry, Pharmacy, or a related field) is required. You should have a thorough understanding of pharmaceutical manufacturing processes, quality systems, and regulatory guidelines (e.g., MHRA, FDA). Excellent attention to detail, strong problem-solving skills, and the ability to work independently and as part of a team are essential. You will contribute to internal audits and support external regulatory inspections. This hybrid role requires you to be present in our Bradford facility for essential laboratory work and team collaboration, with flexibility for remote data review and reporting. This is an excellent opportunity to advance your career in pharmaceutical quality assurance within a reputable organization.
This advertiser has chosen not to accept applicants from your region.

Remote Quality Control Engineer - Manufacturing Processes

BD1 1SX Bradford, Yorkshire and the Humber £40000 Annually WhatJobs

Posted today

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Job Description

full-time
Our client, a leading manufacturer, is seeking a highly skilled and diligent Remote Quality Control Engineer to oversee and improve their manufacturing processes. This fully remote position allows you to apply your expertise in quality assurance and process improvement from your home office. You will be responsible for developing, implementing, and maintaining comprehensive quality control systems to ensure products consistently meet established standards and customer requirements. Your duties will include designing and executing quality inspection procedures, analyzing production data to identify trends and root causes of defects, and recommending corrective and preventive actions (CAPA). You will also be involved in supplier quality management, assessing incoming materials and components. The successful candidate will have a strong understanding of statistical process control (SPC), Six Sigma, and Lean Manufacturing principles. Experience with various quality management systems (e.g., ISO 9001) is essential. You will be tasked with conducting internal audits, generating quality reports, and collaborating with production and engineering teams to implement quality improvements. This role requires excellent analytical skills, attention to detail, and the ability to interpret technical specifications and quality standards. You will need to be proficient in using quality control software and tools. This is a critical role that ensures the integrity and reliability of our client's products, contributing directly to customer satisfaction and the company's reputation. The ability to work independently, manage tasks efficiently, and communicate effectively across remote teams and departments is vital. Join a forward-thinking company that values quality and offers a flexible working arrangement.

Key Responsibilities:
  • Develop and implement quality control plans and procedures.
  • Monitor manufacturing processes to ensure compliance with quality standards.
  • Analyze production data, identify defects, and determine root causes.
  • Implement corrective and preventive actions (CAPA).
  • Conduct internal quality audits and assessments.
  • Manage supplier quality and incoming material inspections.
  • Utilize statistical process control (SPC) techniques.
  • Prepare quality reports and document findings.
  • Collaborate with production and engineering teams on quality initiatives.
  • Ensure adherence to relevant quality management systems (e.g., ISO 9001).
Qualifications:
  • Bachelor's degree in Engineering (Mechanical, Manufacturing, or related) or equivalent experience.
  • Minimum of 5 years of experience in quality control or quality assurance within a manufacturing environment.
  • Strong knowledge of quality management systems (ISO 9001) and methodologies (SPC, Six Sigma, Lean).
  • Proficiency in data analysis and interpretation.
  • Excellent problem-solving and analytical skills.
  • Strong written and verbal communication skills.
  • Ability to work independently and manage time effectively in a remote setting.
  • Experience with quality control tools and software.
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