What Jobs are available for Manufacturing Companies in Tunstall?

Job Title: Quality Control Engineer

Location: Newcastle

Salary : Competitive

Our client is seeking a Quality Control Engineer to ensure that all products and services meet customer specifications, internal standards, and legal requirements. The role involves reviewing and creating work instructions, conducting thorough inspections throughout the production process, and driving the investigation and resolution of quality issues. This position plays a key role in maintaining the company's quality management and calibration systems, while liaising with customers, suppliers, and external inspectors to uphold the highest standards.

Key Responsibilities

• Conduct and record comprehensive inspections on incoming materials, in-process work, and final products.
• Perform internal QMS and product-specific audits, coordinating inspections with external parties where required.
• Halt any process or delivery if quality compliance is at risk, immediately informing the Production Manager.
• Review and issue clear work instructions for contracts to meet customer and internal standards.
• Raise, review, and manage Non-Conformance Reports (NCRs), concession reports, and material certifications.
• Initiate and participate in investigations into warranty claims and quality problems, utilising Root Cause Analysis (RCA).
• Assess claims and coordinate corrective actions, driving continuous improvement to enhance processes and reduce waste.
• Maintain the company's Quality Management System (QMS) and monitor its effectiveness.
• Manage the equipment calibration system, performing internal calibrations and coordinating external ones.
• Liaise with customer representatives and suppliers to ensure adherence to all quality requirements.
• Collate data dossiers and support the Operations Manager in compiling and publishing KPIs.
• Advise staff on health and safety hazards and stop any unsafe actions observed.

Skills & Experience

• CSWIP 3.0 or higher is required.
• PCN Level II for MPI and DPI, or an equivalent qualification.
• Apprenticeship certificate in a relevant engineering discipline is preferred.
• Extensive knowledge and understanding of reading and interpreting engineering drawings.
• Experience within a manufacturing environment is essential.
• Proven experience dealing directly with external suppliers and customers.
• Familiarity with Quality Standards such as ISO 9001 and industry standards like ASME.
• Proficient in Microsoft Office (Word, Excel, PowerPoint).
• Enthusiastic, conscientious, results-orientated, self-motivated, with a "can-do" attitude.
• Able to develop strong working relationships with the team and customers.
• Excellent communicator at all levels, both internally and externally.
• Ability to work effectively under pressure in a demanding environment.
• Strong planning and organisational skills.
• Willingness to learn and apply company principles and tools, including operational control concepts (OCCs).

• Conducting visual inspections and functional tests on raw materials, in-process components, and finished goods.
• Utilising measuring instruments and testing equipment to verify product dimensions, tolerances, and performance characteristics against specifications.
• Documenting inspection results accurately and thoroughly in quality control logs and databases.
• Identifying non-conforming products and initiating the non-conformance reporting process.
• Working closely with production and engineering teams to address quality issues and implement corrective actions.
• Participating in internal quality audits and supporting external audits.
• Maintaining a clean and organised inspection area, ensuring all equipment is calibrated and in good working order.
• Adhering to all company quality policies, procedures, and health and safety regulations.
• Contributing to continuous improvement initiatives aimed at enhancing product quality and reducing waste.
• Providing feedback to production teams regarding quality trends and areas for improvement.

Great opportunity to work as a Quality Control Laboratory Technician for our client, which processes and manufactures yogurts and desserts, supplying the UK market as one of the most efficient yogurt processors in the world.

Staffline is recruiting Quality Control Laboratory Technicians in Market Drayton.

The rate of pay is £14.23 per hour.

Hours of Work, Shift, and Work Pattern Schedule:
- 12-hour shifts with a 45-minute paid break
- Average of 42 hours per week
- 4 on 4 off, days only - 7am to 7pm

Your Time at Work

As a Quality Control Laboratory Technician your duties include:

- General laboratory duties, including cleaning, preparing reagents, and cleaning glassware
- Taking samples from process, production, and warehouse, and adding results to databases ready for testing
- Rotate stock in the control temperature room
- Ensure external laboratory samples are collected and booked according to the schedule
- Assuring accurate and complete records of work done, and all other appropriate laboratory information and results are maintained.
- Adhere to all legal and company standards & procedures with reference to health & safety at work
- Report records, hazards, accidents and potential accidents

Our Perfect Worker

Our perfect worker will have good communication and timekeeping skills. You will work efficiently and cleanly.

Applicants will hold a Level 2/basic Food Safety qualification and a Level 2/basic Working Safely certificate.

Experience in a similar role is required.

Key Information and Benefits

- Earn £14.23 per hour
- 7am to 7pm
- On-site support from Staffline
- Canteen on site
- Free car parking on site
- Free hot drinks
- Full training provided

Job Ref: 1MUD

About Staffline

Staffline is the UK's leading provider of flexible, temporary and permanent workforce solutions, enabling over 28,000 people into good work every day. We operate at more than 350 customer sites across England, Scotland and Wales.

Please note that our job adverts are correct at the time of publication, but some details and job responsibilities are subject to change.

This job advert may not be copied, imitated or used, in whole or in part, by third-party websites, without prior written consent from Staffline.

Great opportunity to work as a Quality Control Laboratory Technician for our client, which processes and manufactures yogurts and desserts, supplying the UK market as one of the most efficient yogurt processors in the world.

Staffline is recruiting Quality Control Laboratory Technicians in Market Drayton.

The rate of pay is £14.23 per hour.

Hours of Work, Shift, and Work Pattern Schedule:
- 12-hour shifts with a 45-minute paid break
- Average of 42 hours per week
- 4 on 4 off, days only - 7am to 7pm

Your Time at Work

As a Quality Control Laboratory Technician your duties include:

- General laboratory duties, including cleaning, preparing reagents, and cleaning glassware
- Taking samples from process, production, and warehouse, and adding results to databases ready for testing
- Rotate stock in the control temperature room
- Ensure external laboratory samples are collected and booked according to the schedule
- Assuring accurate and complete records of work done, and all other appropriate laboratory information and results are maintained.
- Adhere to all legal and company standards & procedures with reference to health & safety at work
- Report records, hazards, accidents and potential accidents

Our Perfect Worker

Our perfect worker will have good communication and timekeeping skills. You will work efficiently and cleanly.

Applicants will hold a Level 2/basic Food Safety qualification and a Level 2/basic Working Safely certificate.

Experience in a similar role is required.

Key Information and Benefits

- Earn £14.23 per hour
- 7am to 7pm
- On-site support from Staffline
- Canteen on site
- Free car parking on site
- Free hot drinks
- Full training provided

Job Ref: 1MUD

About Staffline

Staffline is the UK's leading provider of flexible, temporary and permanent workforce solutions, enabling over 28,000 people into good work every day. We operate at more than 350 customer sites across England, Scotland and Wales.

Please note that our job adverts are correct at the time of publication, but some details and job responsibilities are subject to change.

This job advert may not be copied, imitated or used, in whole or in part, by third-party websites, without prior written consent from Staffline.

• Perform analytical testing on raw materials, intermediates, and finished products.
• Operate and maintain analytical instruments (e.g., HPLC, GC, UV-Vis).
• Develop, validate, and transfer analytical methods.
• Accurately record, analyse, and report test results.
• Investigate out-of-specification (OOS) results and deviations.
• Troubleshoot analytical equipment and methodologies.
• Ensure compliance with GMP, pharmacopoeial standards, and SOPs.
• Participate in stability testing programs.
• Maintain laboratory records and documentation to the highest standard.
• Collaborate with other departments as needed.
• Contribute to process improvement initiatives within the QC laboratory.
• Ensure a safe working environment within the remote laboratory setup.

• Bachelor's or Master's degree in Chemistry, Pharmaceutical Science, or a related discipline.
• Significant hands-on experience in a pharmaceutical Quality Control laboratory.
• Proficiency with a range of analytical techniques, particularly HPLC and GC.
• In-depth understanding of GMP and relevant regulatory guidelines.
• Excellent analytical, problem-solving, and critical thinking skills.
• Meticulous attention to detail and strong documentation practices.
• Ability to work independently and manage time effectively in a remote setting.
• Proficiency in LIMS and MS Office Suite.

• Perform analytical testing of raw materials, intermediates, and finished pharmaceutical products.
• Operate and maintain laboratory equipment such as HPLC, GC, UV-Vis spectrophotometers, and dissolution apparatus.
• Conduct method validation and transfer activities.
• Interpret analytical data and generate accurate reports.
• Investigate out-of-specification (OOS) results and deviations.
• Ensure compliance with GMP, FDA, and other regulatory standards.
• Participate in internal and external audits.
• Contribute to the development and optimization of analytical methods.
• Maintain laboratory records and documentation in accordance with regulatory requirements.
• Collaborate with R&D, Production, and QA teams.

• Bachelor's or Master's degree in Chemistry, Pharmacy, or a related life science discipline.
• Minimum of 5 years of experience in pharmaceutical quality control.
• Hands-on experience with analytical techniques like HPLC, GC, and spectroscopy.
• In-depth knowledge of GMP and regulatory requirements in the pharmaceutical industry.
• Strong understanding of analytical method validation.
• Excellent laboratory skills and meticulous attention to detail.
• Proficiency in data analysis and report writing.
• Good communication and teamwork skills.
• Experience with laboratory information management systems (LIMS) is a plus.

• Prepare chemical samples for analysis according to standard operating procedures.
• Perform routine laboratory tests and analyses using appropriate equipment.
• Record experimental data accurately and maintain detailed laboratory notebooks.
• Assist in the calibration and maintenance of laboratory instruments.
• Learn and apply various analytical techniques.
• Ensure compliance with health, safety, and environmental regulations within the laboratory.
• Support the quality control team in ensuring product consistency and integrity.
• Participate in training sessions and contribute to continuous improvement initiatives.
• Manage laboratory consumables and maintain stock levels.

• Minimum of 4 GCSEs (or equivalent) at grade C/4 or above, including science subjects, Maths, and English.
• A keen interest in chemistry, science, and laboratory work.
• Strong attention to detail and accuracy.
• Good numeracy and literacy skills.
• Ability to follow instructions precisely and work systematically.
• Willingness to learn and adapt to new techniques.
• Team-oriented attitude with good communication skills.
• Commitment to completing the full apprenticeship program.

• Develop, implement, and maintain the company's Quality Management System (QMS) in accordance with IATF 16949 standards.
• Lead and manage the quality control team, including inspectors and technicians.
• Establish quality control standards and procedures for all manufacturing processes and finished products.
• Conduct internal and external audits to ensure compliance with quality standards and regulations.
• Analyze quality data, identify trends, and implement corrective and preventive actions (CAPA).
• Oversee product inspection, testing, and validation processes.
• Manage non-conformance reporting and resolution processes.
• Collaborate with engineering and production teams to address quality issues and implement improvements.
• Ensure supplier quality through audits and performance monitoring.
• Develop and deliver quality training programs for employees.
• Monitor key quality metrics and report on performance to senior management.
• Drive continuous improvement initiatives to enhance product quality and process efficiency.
• Stay up-to-date with automotive industry quality standards and best practices.

• Bachelor's degree in Engineering, Quality Management, or a related field. Master's degree preferred.
• Minimum of 7 years of experience in quality control or quality assurance, with a significant portion in the automotive industry.
• Proven experience in developing and implementing IATF 16949 compliant QMS.
• Strong knowledge of quality control tools and methodologies (e.g., SPC, FMEA, APQP, PPAP).
• Experience leading and managing a quality team.
• Excellent analytical, problem-solving, and decision-making skills.
• Strong understanding of manufacturing processes, particularly in automotive component production.
• Proficiency in quality management software and data analysis tools.
• Excellent communication, leadership, and interpersonal skills.
• Ability to work effectively and autonomously in a remote environment.
• Auditor certification (e.g., IATF 16949 Lead Auditor) is highly desirable.

• Perform analytical testing of raw materials, intermediates, and finished pharmaceutical products according to established SOPs and pharmacopoeial methods.
• Operate and maintain laboratory equipment such as HPLC, GC, UV-Vis, FTIR, and dissolution testers.
• Interpret test results, analyze data, and document all laboratory activities accurately in compliance with GMP guidelines.
• Investigate Out-of-Specification (OOS) results and deviations, implementing corrective and preventative actions (CAPAs).
• Participate in method validation and transfer activities.
• Ensure laboratory areas are maintained in a clean and orderly condition, adhering to safety protocols.
• Prepare and review analytical reports, certificates of analysis, and other quality documentation.
• Collaborate with other departments, including Production, R&D, and Regulatory Affairs, to resolve quality issues.
• Stay current with relevant regulatory guidelines (e.g., FDA, EMA) and industry best practices.
• Train and mentor junior QC analysts as needed.

• A degree in Chemistry, Pharmaceutical Science, or a related scientific discipline.
• Minimum of 5 years of experience in pharmaceutical quality control or a related analytical laboratory environment.
• Proven hands-on experience with analytical techniques such as HPLC, GC, spectroscopy, and wet chemistry.
• Strong understanding of Good Manufacturing Practices (GMP) and regulatory requirements.
• Excellent data analysis, interpretation, and problem-solving skills.
• Meticulous attention to detail and strong documentation skills.
• Ability to work effectively both independently and as part of a team.
• Good communication and interpersonal skills.
• Proficiency in using laboratory information management systems (LIMS) is an advantage.
• Commitment to quality and safety in a pharmaceutical setting.