What Jobs are available for Manufacturing Companies in Sandwell?

What you’ll be doing (Quality Engineer / Quality Control Technician responsibilities):

• Carrying out hands-on inspections of incoming parts and finished products. 
• Manually checking components (sometimes in the hundreds or thousands per month).
• Using Excel spreadsheets to record and analyse inspection data.
• Assisting with supplier quality issues, reporting non-conformances, and supporting investigations. 
• Manage and oversee the calibration of inspection equipment. 
• Supporting customer quality checks, PPAP submissions, and internal audits. 
• Compile ISIR’s for PPAP submissions and product approvals.

What we’re looking for:

• An engineering qualification (degree, HNC, or similar) or some hands-on manufacturing/engineering experience. 
• A sharp eye for detail and patience to carry out repetitive inspection work accurately. 
• Confident IT skills (particularly Excel). 
• This role is ideal for someone who enjoys hands-on and practical work, as it involves standing, bending, lifting up to 25 pounds, and occasionally working on their feet.
• An awareness of quality tools, such as PPAP, SPC, and FMEA, would be desirable. 

Why join?

• Global engineering business with strong career progression opportunities.
• Excellent training in quality tools and processes, build a long-term career in Quality Engineering.
• 25 days holiday + bank holidays.
• Pension, life insurance, and other benefits upon completion of the probationary period.

• 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.

• Develop, implement, and manage the company's Quality Management System (QMS) in accordance with industry standards (e.g., ISO 9001).
• Lead and mentor the quality control team, providing guidance and fostering professional development.
• Establish quality control procedures, including inspection, testing, and sampling protocols.
• Monitor production processes to identify potential quality issues and implement corrective actions.
• Conduct root cause analysis for quality deviations and implement preventive measures.
• Manage internal and external audits, ensuring compliance with quality standards and regulations.
• Collaborate with R&D and production teams on new product development to ensure quality is integrated from the outset.
• Oversee product release processes and documentation.
• Analyze quality data to identify trends, areas for improvement, and opportunities for efficiency gains.
• Champion a company-wide culture of quality and continuous improvement.

• Bachelor's degree in Engineering, Science, or a related technical field.
• Minimum of 7 years of experience in quality control or quality assurance, with at least 3 years in a management or supervisory role.
• Proven experience in developing and managing Quality Management Systems (QMS).
• Strong knowledge of quality control methodologies, statistical process control (SPC), and root cause analysis techniques.
• Experience with relevant industry standards and certifications (e.g., ISO 9001, Six Sigma).
• Excellent leadership, team management, and interpersonal skills.
• Strong analytical, problem-solving, and decision-making abilities.
• Proficiency in quality management software and MS Office Suite.
• Excellent communication and reporting skills.
• Experience in a high-volume manufacturing environment is essential.

• Conduct routine and non-routine analytical testing on raw materials, in-process samples, and finished products.
• Perform tests using various laboratory techniques, including HPLC, GC, UV-Vis spectroscopy, and titrations.
• Prepare reagents, standards, and samples for analysis.
• Operate and maintain analytical instruments, ensuring calibration and performance.
• Accurately record test results and maintain laboratory documentation in compliance with GMP.
• Investigate out-of-specification (OOS) results and participate in root cause analysis.
• Prepare certificates of analysis and analytical reports.
• Ensure laboratory safety procedures are followed at all times.
• Participate in method validation and transfer activities.
• Collaborate with production, quality assurance, and R&D teams.
• Stay updated with current Good Manufacturing Practices (GMP) and relevant pharmacopoeial standards.

• Bachelor's degree in Chemistry, Analytical Chemistry, Pharmacy, or a related science discipline.
• Minimum of 2-3 years of experience in a Quality Control laboratory, preferably within the pharmaceutical industry.
• Hands-on experience with HPLC and other common analytical techniques.
• Knowledge of GMP principles and regulatory requirements.
• Proficiency in laboratory data recording and documentation.
• Strong attention to detail and accuracy.
• Good organisational and time management skills.
• Ability to work effectively both independently and as part of a team.
• Excellent problem-solving skills.
• Good written and verbal communication skills.

• Perform a variety of analytical tests on raw materials, in-process samples, and finished pharmaceutical products according to established Standard Operating Procedures (SOPs) and pharmacopoeial methods.
• Utilise analytical instrumentation such as HPLC, GC, UV-Vis spectrophotometry, and dissolution apparatus.
• Prepare reagents, standards, and solutions required for testing.
• Accurately record and document all test results, maintaining detailed batch records and laboratory notebooks.
• Evaluate test results against specifications and report any deviations or out-of-specification (OOS) results promptly.
• Calibrate and maintain laboratory equipment, ensuring it is in good working order.
• Assist in the validation and verification of analytical methods.
• Participate in internal quality audits and assist with regulatory inspections.
• Ensure compliance with Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), and other relevant regulatory guidelines.
• Contribute to the investigation of quality issues and OOS results.
• Maintain a safe and clean working environment within the laboratory.
• Support inventory management of laboratory consumables and reagents.
• Engage in continuous professional development to stay updated with analytical techniques and regulatory requirements.

• BSc in Chemistry, Pharmaceutical Science, or a related scientific discipline.
• Previous experience working in a Quality Control laboratory, preferably within the pharmaceutical industry.
• Proficiency in using common analytical laboratory equipment (e.g., HPLC, GC).
• Strong understanding of GMP and regulatory requirements in the pharmaceutical sector.
• Excellent attention to detail and accuracy in data recording and reporting.
• Good understanding of analytical principles and methodologies.
• Ability to follow complex procedures and SOPs accurately.
• Strong organisational and time-management skills.
• Effective communication skills, both written and verbal.
• Ability to work effectively both independently and as part of a team.
• Proficiency in Microsoft Office Suite.

Job Summary

To effectively support the implementation and manage the Bank’s approach to 1st Line Operational Risk including implementation and monitoring of the Training and Competence Scheme and the mandatory aspects of the Leaning and Development programme.

Key responsibilities

• Support Head of Home Finance Distribution building a best in class 'Go To' team for expertise and embed the culture of 'Right First Time” across the Customer and Broker journey.
• Undertake the required Training and Competence and mandatory aspects of Learning and Development assessments, assessing the suitability of advice and customer outcomes
• Liaise with Compliance Monitoring, Internal and External Audits in respect of any annual reviews relating to QC.
• Continuously evaluate and identify training gaps within the Home Finance Distribution teams, recommending changes to procedures and policies. Provide feedback on individual performance objectives and monitor progress.
• Facilitate reporting and presentation of performance metrics against the controls and service frameworks.
• Supporting major incident identification, escalation, and resolution.
• Undertake risk event reviews and analysis root causes analysis and adequacy of actions to address weaknesses. Provide independent assurance of compliance with policies.
• Liaise with Internal Audit and Compliance Monitoring in respect of any scheduled reviews and follow up actions of updating the relevant Procedures and Processes
• Monitor and review Customer and Broker complaints and feedback across platforms to assess any trends and link to processes and procedures improvements.

Skills required

• Good working knowledge of Mortgage and Home Finance regulation
• Knowledge of UK banking (Customer Service, Credit. Financial Crime, Operations) and risk management & controls principles appropriate to the three lines of defence model
• Understanding of compliance with group policies including a strong grasp of Conduct Risk and Consumer Duty knowledge
• Ideally hold a Competent Supervisor status

About us

Founded in 2007, we are a challenger bank that operates in accordance with Shariah principles, with offices in London, Milton Keynes and Wilmslow. We offer personal and corporate savings products and finance for UK residential and commercial property, in addition to sourcing and advising on UK real estate investments.

Additional Details

We offer highly attractive reward package; the typical benefits include:

• 25 days holiday entitlement increasing with service
• Pension plan
• Private medical insurance
• Dental cover
• Income protection
• Life assurance
• Employee referral bonus

Gatehouse Bank is an equal opportunities employer and positively encourages applications from suitably qualified and eligible candidates regardless of sex, race, disability, age, sexual orientation, gender reassignment, religion or belief, marital status, or pregnancy and maternity.

Please be advised that we have an appointed recruitment partner, The Curve Group, to manage our recruitment process and give candidates the best possible experience in pursuing a career with Gatehouse Bank. The personal details you have shared with us may be processed by The Curve Group on behalf of Gatehouse Bank.

The Curve Group is a Recruitment Services and Human Resources business with a mission to transform the working lives of the people and organisations we work with.

We collect and process your personal data for the purpose of providing recruitment and related HR services, in line with our legitimate business interests and legal obligations.

We will retain your data for two years from the last point of contact, after which it will be securely deleted unless you request otherwise.

For more details about how we handle your personal data and your rights, please see our full Privacy Policy:

• Perform routine and non-routine analytical testing of raw materials, intermediates, and finished pharmaceutical products using techniques such as HPLC, GC, UV-Vis, IR, and dissolution testing.
• Develop, validate, and transfer analytical methods in accordance with ICH guidelines and regulatory requirements.
• Prepare and standardise reagents and solutions, ensuring accuracy and traceability.
• Maintain laboratory equipment, perform calibrations, and troubleshoot instrument issues.
• Accurately document all testing procedures, results, and observations in laboratory notebooks and LIMS.
• Review and approve analytical data generated by junior analysts.
• Investigate out-of-specification (OOS) results and deviations, participating in root cause analysis.
• Contribute to the maintenance and improvement of the laboratory's Quality Management System (QMS).
• Ensure compliance with all relevant GMP, regulatory, and safety guidelines.
• Participate in internal and external audits.
• Assist in the training and development of junior QC analysts.
• Stay current with advancements in analytical techniques and pharmaceutical quality control.

• Bachelor's or Master's degree in Chemistry, Pharmaceutical Science, Biochemistry, or a related discipline.
• Minimum of 5 years of experience in a pharmaceutical quality control laboratory environment.
• Extensive hands-on experience with analytical instrumentation, particularly HPLC and GC.
• Thorough understanding of GMP, regulatory guidelines (e.g., FDA, EMA), and pharmacopoeias (e.g., USP, EP).
• Proven experience in method development and validation.
• Strong documentation skills and attention to detail.
• Excellent problem-solving and critical thinking abilities.
• Good communication and interpersonal skills.
• Ability to work effectively both independently and as part of a team.