What Jobs are available for Manufacturing Companies in Risca?

Blue Arrow is recruiting a Quality Control (QC) Analyst to join our clients team based in the Llantrisant area.

Salary : 27,000p.a

Hours : 4 days on, 4 days off, 10-hour shifts from 07:00 to 18:00

Contract : 6 month fixed term contract

Role Overview

As a QC Analyst, you will be responsible for conducting a variety of laboratory tests and analyses to ensure our products meet regulatory standards and client specifications. You will play a key role in monitoring production processes, identifying deviations, and implementing corrective actions to maintain the integrity and safety of our products.

Main Responsibilities

• Perform routine and non-routine analyses of raw materials, in-process samples, and finished products using established analytical techniques (e.g., FPLC, UV-Vis, FTIR, titration, wet chemistry).

• Interpret and report analytical results accurately, maintaining detailed and organised records in compliance with Good Laboratory Practices (GLP) and company SOPs.

• Calibrate, operate, and maintain laboratory equipment, ensuring all instruments are functioning optimally and maintaining calibration logs as required.

• Participate in method development, method validation, and continuous improvement initiatives to optimise laboratory performance.

• Conduct investigations into non-conforming results and work collaboratively to determine root causes and implement effective corrective actions.

• Assist in the preparation and review of technical documents such as SOPs, test methods, specifications, and validation protocols.

• Support internal and external audits by providing necessary documentation, data, and explanations regarding laboratory practices and results.

• Ensure all laboratory activities are conducted in accordance with health, safety, and environmental regulations.

• Collaborate with cross-functional teams, including production, quality assurance, and research and development, to resolve quality issues and drive continuous improvement.

• Stay current with advances in analytical techniques, regulatory requirements, and industry best practices.

Requirements

• Bachelor's degree in chemistry, Biochemistry, Pharmaceutical Science, Microbiology, Food Science, or a related scientific discipline.

• Familiarity with analytical instrumentation (e.g., HPLC, GC, UV-Vis, FTIR) and associated software.

• Strong understanding of GLP, GMP, or ISO standards as applicable to the industry.

• Excellent attention to detail, time management, and organisational skills.

• Strong communication abilities, both written and verbal, and ability to convey technical information clearly.

• Problem-solving skills and an investigative mindset.

• Ability to work independently as well as collaboratively in a fast-paced, team-oriented environment.

• Proficient in using standard office and laboratory software (e.g., Microsoft Office, LIMS).

Desirable Skills

• Experience with method development and validation.

• Knowledge of statistical analysis and data interpretation.

• Familiarity with regulatory submissions and documentation (e.g., MHRA, FDA, EMA).

• Previous experience in root cause analysis and CAPA (Corrective and Preventive Action) processes.

• Additional language skills are an advantage.

If you feel you would be suitable for the above role, please submit your CV for immediate response.

Blue Arrow is proud to be a Disability Confident Employer and is committed to helping find great work opportunities for great people.

• Developing, implementing, and managing the company's quality management system (QMS).
• Establishing and enforcing quality control standards and procedures across all production processes.
• Overseeing incoming material inspection, in-process quality checks, and final product testing.
• Leading and mentoring the quality control team, providing training and performance management.
• Conducting internal audits and facilitating external quality audits (e.g., ISO 9001 certification).
• Analyzing quality data, identifying trends, and implementing corrective and preventive actions (CAPA).
• Collaborating with production and engineering teams to resolve quality issues and improve product design.
• Managing supplier quality assurance and conducting supplier audits.
• Developing and delivering quality training programs for all employees.
• Ensuring compliance with all relevant industry regulations and standards.
• Driving continuous improvement initiatives to enhance product quality and manufacturing efficiency.

• Bachelor's degree in Engineering, Quality Management, or a related technical field.
• Minimum of 7 years of experience in quality control/assurance within the manufacturing industry.
• Proven experience in developing and implementing ISO 9001 or similar quality management systems.
• Strong knowledge of quality tools and methodologies (e.g., Six Sigma, Lean Manufacturing, SPC).
• Excellent leadership, team management, and interpersonal skills.
• Proficiency in data analysis and problem-solving techniques.
• Strong written and verbal communication skills.
• Experience with product testing, inspection, and validation processes.
• Familiarity with regulatory compliance requirements relevant to the industry.
• Relevant certifications (e.g., ASQ Certified Quality Manager) are highly desirable.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Pharmaceutical Science, or a related life science discipline.
• A minimum of 5 years of hands-on experience in pharmaceutical quality control or analytical testing.
• Proficiency in various analytical techniques, including HPLC, GC, Karl Fischer titration, and dissolution testing.
• Strong understanding of GMP, ICH guidelines, and other relevant regulatory requirements.
• Experience with laboratory information management systems (LIMS) is desirable.
• Excellent attention to detail and accuracy in experimental work and data recording.
• Strong problem-solving skills and the ability to troubleshoot analytical instrumentation and methods.
• Effective communication and interpersonal skills, with the ability to collaborate with cross-functional teams.
• Experience in method development and validation is a significant advantage.
• Ability to work independently and manage multiple tasks effectively.

• Perform a range of analytical tests on pharmaceutical raw materials, intermediates, and finished products using techniques such as HPLC, GC, UV-Vis, IR, and titration.
• Develop, validate, and transfer analytical methods according to regulatory guidelines (e.g., ICH).
• Interpret test results, analyse data, and prepare accurate and comprehensive Certificates of Analysis (CoAs).
• Investigate out-of-specification (OOS) results and deviations, identifying root causes and implementing corrective and preventive actions (CAPAs).
• Maintain laboratory equipment, perform calibration and qualification, and ensure compliance with GLP/GMP standards.
• Contribute to the continuous improvement of quality control processes and procedures.
• Collaborate with R&D, production, and regulatory affairs departments to support product development and troubleshooting.
• Ensure all laboratory activities are conducted in compliance with internal SOPs and relevant regulatory requirements (e.g., MHRA, FDA).
• Assist in the training and mentoring of junior QC analysts.
• Prepare and review method validation protocols and reports.
• Manage laboratory documentation and records ensuring data integrity.

• Bachelor's or Master's 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 role.
• Hands-on experience with a variety of analytical techniques, particularly HPLC and GC, is essential.
• Strong understanding of Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP) regulations.
• Experience with method development and validation is highly desirable.
• Excellent analytical and problem-solving skills, with a keen eye for detail.
• Proficiency in data analysis and interpretation, with strong report-writing skills.
• Ability to work effectively both independently and as part of a team.
• Familiarity with laboratory information management systems (LIMS).
• Effective communication skills for cross-departmental collaboration.
• Willingness to work in a hybrid model, with flexibility for on-site laboratory work in **Cardiff, Wales, UK**.

• Perform detailed inspections of incoming materials, in-process work, and final products using advanced metrology equipment.
• Interpret engineering drawings, specifications, and quality standards (e.g., AS9100).
• Identify and document any non-conformities, defects, or deviations from specifications.
• Initiate and manage Non-Conformance Reports (NCRs), working with relevant departments to implement corrective actions.
• Conduct process audits to ensure adherence to quality procedures and standards.
• Maintain accurate and comprehensive inspection records and traceability documentation.
• Collaborate with production, engineering, and quality assurance teams to resolve quality issues.
• Contribute to the continuous improvement of quality control processes and methodologies.
• Ensure compliance with all relevant industry regulations and customer specific requirements.
• Provide guidance and support to junior inspectors and production personnel on quality matters.

• Proven experience as a Quality Control Inspector, preferably within the aerospace or precision engineering industry.
• Demonstrable experience with various inspection tools and techniques (e.g., CMM, micrometers, calipers, visual inspection).
• Strong understanding of engineering drawings, blueprints, and technical specifications.
• Knowledge of quality management systems like AS9100 is essential.
• Ability to interpret and apply industry standards and regulations.
• Excellent analytical, problem-solving, and decision-making skills.
• Strong written and verbal communication skills.
• Meticulous attention to detail and high level of accuracy.
• Ability to work independently and as part of a collaborative team.
• Relevant technical qualifications or certifications (e.g., IPC, NADCAP) are advantageous.

• Develop, implement, and maintain the company's Quality Management System (QMS).
• Establish quality standards and procedures for incoming materials, in-process production, and finished goods.
• Design and execute comprehensive inspection and testing plans.
• Utilize statistical methods (SPC) to monitor and control process quality.
• Analyze quality data, identify root causes of defects, and implement effective CAPA.
• Conduct internal audits to ensure compliance with QMS requirements and relevant standards.
• Collaborate with cross-functional teams to resolve quality issues and improve product reliability.
• Manage calibration programs for measurement and test equipment.
• Prepare detailed quality reports, trend analyses, and performance metrics.
• Stay current with industry best practices in quality control and assurance.

• Bachelor's degree in Engineering, Quality Management, or a related technical field.
• Minimum of 8 years of experience in quality control or quality assurance within a manufacturing setting.
• Extensive knowledge of QMS (e.g., ISO 9001) and SPC principles.
• Demonstrated experience in root cause analysis and CAPA implementation.
• Proficiency in metrology, inspection techniques, and quality tools.
• Strong analytical, problem-solving, and decision-making skills.
• Meticulous attention to detail and commitment to accuracy.
• Excellent written and verbal communication skills.
• Ability to work independently and manage projects effectively in a remote environment.
• Experience in the relevant manufacturing sector is highly desirable.

• Develop, implement, and maintain comprehensive quality control plans and procedures for manufacturing processes.
• Oversee and conduct rigorous quality inspections and testing of raw materials, in-process components, and finished goods.
• Analyse quality data, identify trends, root causes of defects, and implement corrective and preventive actions (CAPA).
• Lead continuous improvement initiatives to enhance product quality, reduce scrap, and improve process efficiency.
• Develop and manage quality documentation, including inspection records, test reports, and quality manuals.
• Collaborate with engineering, production, and supply chain teams to ensure quality is integrated throughout the product lifecycle.
• Manage supplier quality, including audits and performance monitoring, to ensure incoming materials meet specifications.
• Train and mentor junior quality control technicians and line operators on quality standards and procedures.
• Stay up-to-date with relevant industry standards, regulations, and quality management systems (e.g., ISO 9001, IATF 16949).
• Lead internal audits and support external customer audits.
• Drive a strong quality culture throughout the manufacturing operations.
• Utilise statistical process control (SPC) techniques to monitor and control production processes.
• Investigate customer complaints and product non-conformances, implementing effective resolutions.

• Bachelor's degree in Engineering (Mechanical, Electrical, Manufacturing, or related field) or equivalent practical experience.
• Minimum of 5 years of experience in quality control or quality assurance within a manufacturing environment, preferably automotive.
• In-depth knowledge of quality management systems (QMS), such as ISO 9001 or IATF 16949.
• Proficiency in quality tools and methodologies (e.g., SPC, FMEA, Root Cause Analysis, 8D).
• Strong analytical and problem-solving skills with excellent attention to detail.
• Experience with inspection equipment and testing procedures.
• Excellent communication, interpersonal, and leadership skills.
• Ability to read and interpret technical drawings and specifications.
• Proficiency in relevant software, including Minitab, Excel, and QMS databases.
• Experience in supplier quality management is a plus.