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Quality Control Co-ordinator | Littleborough – Office Based | Full Time (39.5 hours per week) | £30,000 – £2,000 per annum

For almost 30 years, our client has been a specialist supplier of cable looms, electrical assemblies, and components to the automotive industry — particularly trailer manufacturers and vehicle converters.

They are now looking for an experienced and motivated Quality Control Co-ordinator to join their growing team in Littleborough. This is a fantastic opportunity for someone who is looking for a long-term position within a stable, well-established company where you can truly make an impact and grow with the business.

Are you the right person for the job?

You will ideally have:

• 2–3 years’ experience in a manufacturing environment (electrical or automotive preferred)
• Hands-on experience supervising or leading in Quality Control (QC)
• Working knowledge of 5S methodology, ISO 9001, and ideally TS/IATF 16949 QMS standards
• Strong skills in Microsoft Office (Excel, Word, Outlook) and the ability to produce clear internal and external documentation
• Experience using MRP/Planning tools such as SAP or Progress Plus for data extraction and analysis
• Excellent communication and teamwork skills across all levels of the organisation
• A methodical, organised approach and the ability to manage multiple tasks effectively
• Initiative and drive to promote QC principles and continuous improvement
• Experience implementing a Quality Management System is desirable
• Immediate availability (desirable)

What will your role look like?

• Manage and resolve quality issues raised by customers, suppliers, and internal teams —identifying root causes and driving solutions to completion
• Design and implement Quality Control processes and procedures in line with ISO 9001 standards, with the goal of regaining certification
• Establish and document QC checks across manufacturing operations, including visual displays and process tracking
• Monitor key performance indicators (KPIs) and address production pinch points
• Train and support staff, collaborating closely with the Production Manager to embed a strong QC culture within a 5S environment
• Continuously review and improve processes to ensure consistent quality and operational efficiency

What can you expect in return?

• Competitive salary of £30,000– 2,000 per year (depending on experience)
• Flexible start and finish times
• Company bonus scheme
• Pension scheme
• Supportive and friendly work environment

What’s next? It’s easy! Click “APPLY” now! We can’t wait to hear from you!

Your data will be handled in line with GDPR

• Develop, implement, and manage the company's Quality Management System (QMS).
• Establish and maintain quality control procedures and standards throughout the manufacturing process.
• Lead and mentor the Quality Control team, including inspectors, technicians, and auditors.
• Conduct regular quality audits of internal processes and supplier performance.
• Analyze quality data, identify trends, and implement corrective and preventive actions (CAPA).
• Ensure compliance with relevant industry standards and certifications (e.g., ISO 9001).
• Manage the inspection and testing of raw materials, in-process materials, and finished goods.
• Investigate customer complaints and non-conformances, and implement solutions to prevent recurrence.
• Collaborate with Production, Engineering, and R&D departments to improve product quality and reduce defects.
• Oversee the calibration and maintenance of testing equipment.
• Prepare quality reports for senior management, highlighting key metrics and areas for improvement.
• Promote a quality-first mindset throughout the organization.

• Bachelor's degree in Engineering, Science, or a related technical field.
• Minimum of 8 years of progressive experience in Quality Control or Quality Assurance within a manufacturing environment.
• Proven experience in managing and leading a QC/QA team.
• In-depth knowledge of Quality Management Systems (QMS) and relevant standards (e.g., ISO 9001).
• Strong understanding of statistical quality control (SQC) and Six Sigma methodologies.
• Experience with various inspection and testing techniques.
• Excellent analytical, problem-solving, and decision-making skills.
• Proficient in using quality management software and data analysis tools.
• Strong leadership, communication, and interpersonal skills.
• Ability to effectively implement change and drive continuous improvement.
• Familiarity with regulatory requirements specific to the manufacturing sector is essential.

• Oversee and perform a wide range of quality control tests on raw materials, in-process samples, and finished products using various analytical techniques.
• Develop, validate, and implement new testing methods and procedures according to regulatory guidelines (e.g., GMP, ICH).
• Train and mentor junior QC analysts, providing guidance on testing protocols, equipment usage, and data interpretation.
• Review and approve analytical test results, ensuring accuracy, completeness, and compliance with specifications.
• Manage and maintain laboratory equipment, including calibration, preventative maintenance, and troubleshooting.
• Investigate out-of-specification (OOS) results and deviations, determining root causes and implementing corrective and preventative actions (CAPAs).
• Participate in internal and external audits, ensuring the QC laboratory is inspection-ready.
• Maintain accurate and detailed laboratory records, including raw data, reports, and certificates of analysis.
• Contribute to the continuous improvement of QC processes and systems.
• Liaise with R&D, production, and regulatory affairs departments on quality-related matters.
• Ensure compliance with all health, safety, and environmental regulations within the laboratory.

• Bachelor's or Master's degree in Chemistry, Pharmacy, Biology, or a related scientific discipline.
• Minimum of 5 years of experience in a pharmaceutical Quality Control laboratory setting.
• Extensive hands-on experience with analytical techniques such as HPLC, GC, UV-Vis spectroscopy, FTIR, and dissolution testing.
• Thorough understanding of Good Manufacturing Practices (GMP), regulatory guidelines, and quality management systems.
• Proven ability to develop and validate analytical methods.
• Experience in investigating OOS results and deviations.
• Strong leadership, problem-solving, and decision-making skills.
• Excellent attention to detail and organizational abilities.
• Proficiency in using laboratory information management systems (LIMS) and standard laboratory software.
• Effective communication and interpersonal skills for team collaboration and interdepartmental liaison.

• Develop and implement comprehensive quality control procedures and standards.
• Oversee all aspects of the Quality Management System (QMS).
• Manage and mentor a team of quality control inspectors and technicians.
• Conduct regular inspections and testing of raw materials, in-process materials, and finished goods.
• Analyze production data to identify trends and areas for quality improvement.
• Lead quality improvement initiatives and projects.
• Ensure compliance with relevant industry standards and regulations (e.g., ISO 9001).
• Conduct internal audits and manage external audit processes.
• Investigate customer complaints and non-conformance issues, implementing corrective and preventive actions (CAPA).
• Prepare detailed quality reports for senior management.

• Bachelor's degree in Engineering, Manufacturing, Quality Management, or a related technical field.
• Minimum of 6 years of experience in quality control or quality assurance within a manufacturing environment.
• Proven experience in developing and implementing Quality Management Systems (QMS).
• Strong knowledge of ISO 9001 standards and other relevant industry regulations.
• Proficiency in Statistical Process Control (SPC) and Quality Tools (e.g., Six Sigma, Lean Manufacturing).
• Excellent leadership, team management, and motivational skills.
• Strong analytical, problem-solving, and decision-making abilities.
• Proficiency in quality control software and data analysis tools.
• Excellent written and verbal communication skills.
• Detail-oriented with a strong commitment to quality excellence.

Job Title: Quality Assurance/Quality Control Engineer
Job Type: Permanent
Start Date: ASAP - Subject to clearance
Salary: 45,000 per annum
Benefits Package: 25 annual days plus 8 bank holidays, pension scheme, cycle to work scheme
Location: Leeds
Fully Site Based or Hybrid/Remote: Fully site based
Hours of Work: 37 hours per week

Role & Responsibilities:
- Review supplier and sub-contractor quality procedures
- Review manufacturing quality plans
- Inspect manufactured and supplied items
- Ensure project quality requirements are met
- Develop and maintain manufacturing lifetime quality records
- Arrange 3rd party inspections where required

Qualifications/Experience Required:
- Full drivers license
- QA/QC experience in a Steelwork/Fabrication environment is essential
- Nationally recognised Quality Control certification
- Experience within medium to large steel fabrication
- Experience of working in a highly regulated industry
- Working knowledge of MQP and LTQR requirements
- Knowledge of relevant British Standards

UK National Security Vetting Status: Must be able to obtain SC clearance

Interested in this position? please click "apply now"
We try to respond to all applicants, but sometimes this is not possible due to high volumes of applications; if you have not heard from us within 14 days, regrettably it means you have been unsuccessful on this occasion.
This permanent vacancy is being advertised by Rullion Ltd
Since 1978, Rullion has been securing exceptional candidates for a range of clients; from large well-known brands, to SMEs and start-ups. As a family-owned business, Rullion's approach is credible and honest, focused on building long-lasting relationships with both clients and candidates.

Rullion is a forward-thinking recruitment company that specialises in providing a wide range of talent consultancy services to a diverse client base; from small start-ups to large household names.

Rullion celebrates and supports diversity and is committed to ensuring equal opportunities for both employees and applicants.

• Manage and lead a remote team of Quality Control analysts.
• Oversee the development, validation, and execution of analytical test methods.
• Ensure compliance with GMP, ICH, and other regulatory guidelines.
• Review and approve QC data, batch records, and documentation.
• Lead investigations into out-of-specification (OOS) results and deviations.
• Author and maintain quality control procedures and reports.
• Manage the stability testing program.
• Collaborate with other departments (e.g., R&D, Manufacturing, Regulatory Affairs).
• Contribute to the improvement of the Quality Management System.

• PhD or MSc in Pharmaceutical Sciences, Chemistry, or related discipline.
• Significant experience in pharmaceutical Quality Control (QC) and Quality Assurance (QA).
• Extensive knowledge of analytical techniques (HPLC, GC, spectroscopy, etc.).
• In-depth understanding of GMP, ICH guidelines, and regulatory requirements.
• Proven experience in managing QC teams, preferably in a remote setting.
• Excellent leadership, communication, and problem-solving skills.
• Proficiency in electronic QMS and data analysis software.

• Perform analytical testing on raw materials, in-process samples, and finished pharmaceutical products using various laboratory techniques and instrumentation (e.g., HPLC, GC, UV-Vis, Karl Fischer).
• Accurately document all testing procedures, results, and observations in compliance with Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP).
• Prepare reagents, standards, and solutions as required for testing.
• Maintain laboratory equipment, ensuring calibration and proper functioning.
• Investigate deviations, out-of-specification (OOS) results, and customer complaints, identifying root causes and recommending corrective actions.
• Participate in method validation and transfer activities.
• Review and approve testing data and associated documentation.
• Ensure adherence to all company SOPs, regulatory guidelines (e.g., FDA, EMA), and safety protocols.
• Contribute to the continuous improvement of quality control processes and systems.
• Collaborate with other departments, including R&D, Production, and Regulatory Affairs, to resolve quality-related issues.
• Maintain a clean and organized remote laboratory workspace.

• Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, Biotechnology, or a related scientific discipline.
• Minimum of 3-5 years of experience in pharmaceutical quality control or a related analytical laboratory setting.
• Proficiency with common analytical techniques and instrumentation (HPLC, GC are essential).
• Strong understanding of GMP, GLP, and relevant regulatory guidelines.
• Excellent documentation skills and attention to detail.
• Proficiency in data analysis and interpretation.
• Strong problem-solving and critical thinking abilities.
• Ability to work independently and manage time effectively in a remote environment.
• Excellent written and verbal communication skills.
• Familiarity with laboratory information management systems (LIMS) is a plus.

• Perform analytical testing of raw materials, in-process samples, and finished products using various laboratory techniques (e.g., HPLC, GC, UV-Vis, dissolution).
• Validate analytical methods and equipment according to regulatory guidelines.
• Troubleshoot and maintain laboratory instruments, ensuring they are calibrated and functioning correctly.
• Interpret test results, document findings accurately, and prepare detailed analytical reports.
• Ensure all laboratory activities comply with Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and other relevant regulatory requirements.
• Review and approve test data generated by junior analysts.
• Participate in investigations of out-of-specification (OOS) results and implement corrective actions.
• Contribute to the continuous improvement of laboratory processes and procedures.
• Maintain accurate and organized laboratory records.
• Assist in training and mentoring junior QC analysts.
• Liaise with other departments, such as production and R&D, regarding quality control matters.

• 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 a related analytical laboratory role.
• Strong practical experience with analytical instrumentation (HPLC, GC, spectrophotometry, etc.).
• Thorough understanding of GLP, GMP, and relevant pharmaceutical regulatory guidelines (e.g., FDA, EMA).
• Excellent attention to detail and accuracy in data recording and analysis.
• Strong problem-solving and troubleshooting skills.
• Ability to work independently and manage multiple tasks effectively.
• Good written and verbal communication skills.
• Proficiency in using laboratory information management systems (LIMS) is a plus.
• Experience with method validation and transfer is highly desirable.

• Supervising and mentoring junior QC analysts, providing technical guidance and support.
• Developing, validating, and implementing analytical methods for raw materials, in-process samples, and finished products.
• Performing complex analytical testing using techniques such as HPLC, GC, UV-Vis, FTIR, and KF titration.
• Reviewing and approving analytical data, ensuring accuracy and compliance with specifications.
• Investigating out-of-specification (OOS) results and implementing corrective and preventive actions (CAPAs).
• Maintaining laboratory equipment, ensuring calibration and qualification are up to date.
• Preparing and reviewing QC-related documentation, including SOPs, validation reports, and stability protocols.
• Ensuring all activities are conducted in compliance with Good Manufacturing Practices (GMP) and relevant regulatory guidelines (e.g., MHRA, FDA).
• Participating in internal and external audits.
• Contributing to process improvement projects to enhance efficiency and quality.