What Jobs are available for Manufacturing Companies in Pengam?
Showing 6 Manufacturing Companies jobs in Pengam
Senior Pharmaceutical Quality Control Analyst
CF10 3AA Cardiff, Wales
£40000 Annually
WhatJobs
Posted 4 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company dedicated to advancing healthcare, is seeking a meticulous and experienced Senior Pharmaceutical Quality Control Analyst for their facility in Cardiff, Wales, UK . This role offers a hybrid work model, allowing for a balance of laboratory work and remote data analysis and reporting.
The Senior Pharmaceutical Quality Control Analyst will be responsible for performing a wide range of analytical tests on raw materials, in-process samples, and finished pharmaceutical products to ensure they meet strict quality and regulatory standards. This includes conducting assays, identifying impurities, and verifying product identity and potency using various analytical techniques and instruments.
Key responsibilities include operating and maintaining sophisticated laboratory equipment such as HPLC, GC, UV-Vis spectrophotometers, and dissolution apparatus. You will meticulously document all test procedures, results, and observations in accordance with Good Manufacturing Practices (GMP) and regulatory guidelines. The role also involves method development and validation, troubleshooting analytical issues, and contributing to the continuous improvement of quality control processes. You will play a vital role in ensuring the safety and efficacy of pharmaceutical products.
Qualifications and Experience:
This is a critical role within the pharmaceutical industry, ensuring the highest standards of quality and compliance for life-saving medications. Join a team committed to excellence and innovation in pharmaceutical development.
The Senior Pharmaceutical Quality Control Analyst will be responsible for performing a wide range of analytical tests on raw materials, in-process samples, and finished pharmaceutical products to ensure they meet strict quality and regulatory standards. This includes conducting assays, identifying impurities, and verifying product identity and potency using various analytical techniques and instruments.
Key responsibilities include operating and maintaining sophisticated laboratory equipment such as HPLC, GC, UV-Vis spectrophotometers, and dissolution apparatus. You will meticulously document all test procedures, results, and observations in accordance with Good Manufacturing Practices (GMP) and regulatory guidelines. The role also involves method development and validation, troubleshooting analytical issues, and contributing to the continuous improvement of quality control processes. You will play a vital role in ensuring the safety and efficacy of pharmaceutical products.
Qualifications and Experience:
- 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.
This is a critical role within the pharmaceutical industry, ensuring the highest standards of quality and compliance for life-saving medications. Join a team committed to excellence and innovation in pharmaceutical development.
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0
Senior Pharmaceutical Quality Control Analyst
CF10 1AA Cardiff, Wales
£40000 Annually
WhatJobs
Posted 5 days ago
Job Viewed
Job Description
Our client, a rapidly growing pharmaceutical company, is seeking a highly skilled Senior Pharmaceutical Quality Control Analyst to join their dedicated team. This role, based in **Cardiff, Wales, UK**, offers a hybrid working arrangement, blending essential laboratory work with remote data analysis and reporting. You will be responsible for performing critical quality control testing on raw materials, in-process samples, and finished pharmaceutical products, ensuring compliance with stringent regulatory standards.
Key Responsibilities:
Key Responsibilities:
- 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**.
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1
Senior Quality Control Inspector - Aerospace
BS1 6GU Bristol, South West
£35000 Annually
WhatJobs
Posted 10 days ago
Job Viewed
Job Description
Our client, a leading manufacturer in the aerospace sector, is seeking a meticulous and highly skilled Senior Quality Control Inspector to join their dynamic team in **Bristol, South West England, UK**. This hands-on role is critical to ensuring the highest standards of quality and safety in all manufactured components and assemblies. You will be responsible for conducting detailed inspections of raw materials, in-process components, and finished products, using a variety of precision measuring instruments and techniques. Your expertise will be vital in identifying defects, deviations from specifications, and potential non-conformances, ensuring that all products meet stringent aerospace industry standards and customer requirements. As a Senior Inspector, you will play a key role in interpreting complex engineering drawings, blueprints, and technical specifications. You will document inspection results accurately, generate non-conformance reports, and work collaboratively with production and engineering teams to resolve quality issues. This position involves a significant amount of time on the shop floor, working closely with manufacturing processes. A strong understanding of quality management systems, such as AS9100, is essential. You will also be involved in process audits, contributing to the continuous improvement of quality control procedures. The successful candidate will possess exceptional attention to detail, strong analytical skills, and the ability to work independently while also contributing effectively to a team environment. Our client offers a stable and challenging work environment with opportunities for professional development and advancement within a respected organisation. This is an ideal opportunity for a seasoned quality professional looking to contribute to a critical industry in a key manufacturing hub.
Key Responsibilities:
Key Responsibilities:
- 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.
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2
Senior Quality Control Engineer (Remote)
BS99 4EQ Bristol, South West
£50000 Annually
WhatJobs
Posted 15 days ago
Job Viewed
Job Description
Our client, a leader in precision manufacturing, is seeking a highly experienced Senior Quality Control Engineer to join their dedicated, fully remote quality assurance team. This crucial role focuses on upholding and enhancing the rigorous quality standards of the company's manufactured products. You will be instrumental in developing, implementing, and managing comprehensive quality control systems and processes. Key responsibilities include establishing quality benchmarks, designing and executing inspection and testing procedures, analyzing quality data to identify trends and root causes of defects, and implementing corrective and preventative actions (CAPA). The ideal candidate will possess a deep understanding of quality management systems (QMS), such as ISO 9001, and statistical process control (SPC). A proven track record in quality assurance within a manufacturing environment, particularly in complex industrial products, is essential. You will collaborate closely with engineering, production, and supply chain teams to ensure product conformity throughout the entire lifecycle. Experience with metrology, calibration, and various inspection techniques is required. This role demands strong analytical and problem-solving skills, meticulous attention to detail, and the ability to work autonomously and effectively in a remote setting. Excellent communication and reporting skills are necessary for documenting findings and coordinating quality initiatives. This is an exceptional opportunity for a seasoned QA professional to contribute to maintaining and elevating product excellence for a respected manufacturer, driving quality improvements from a remote work environment.
Responsibilities:
Responsibilities:
- 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.
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3
Senior Pharmaceutical Quality Control Analyst
BS1 1AB Bristol, South West
£45000 Annually
WhatJobs
Posted 24 days ago
Job Viewed
Job Description
Our client, a prominent pharmaceutical company, is seeking an experienced Senior Pharmaceutical Quality Control Analyst to join their dedicated team in Bristol, South West England, UK . This hands-on role is crucial for ensuring the quality, safety, and efficacy of 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 laboratory techniques and instrumentation. This includes HPLC, GC, UV-Vis spectroscopy, and dissolution testing, among others. You will also be involved in method validation, troubleshooting analytical methods, and maintaining laboratory equipment in optimal working condition. The ideal candidate will possess a strong understanding of Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and relevant regulatory guidelines (e.g., MHRA, FDA). Experience with stability testing programs and OOS (Out-of-Specification) investigations is highly desirable. You will meticulously document all experimental procedures, results, and observations in accordance with company SOPs and regulatory requirements. A key aspect of this role involves collaborating with R&D, production, and regulatory affairs departments to resolve quality-related issues and support product lifecycle management. This position requires excellent analytical skills, a keen eye for detail, and the ability to work accurately and efficiently under pressure. You will also contribute to the training and mentoring of junior analysts. This is a fantastic opportunity to advance your career in pharmaceutical quality control within a leading organisation.
Key Responsibilities:
Key Responsibilities:
- Perform analytical testing on raw materials, intermediates, and finished pharmaceutical products.
- Utilise a variety of laboratory instruments including HPLC, GC, UV-Vis, and dissolution apparatus.
- Conduct method validation studies and troubleshoot analytical procedures.
- Ensure compliance with GMP, GLP, and other relevant regulatory standards.
- Accurately document all laboratory activities, results, and deviations.
- Participate in OOS investigations and CAPA (Corrective and Preventive Actions) implementation.
- Maintain laboratory equipment and ensure its calibration and performance.
- Collaborate with cross-functional teams to address quality issues.
- Contribute to the development and continuous improvement of QC processes.
- Train and mentor junior laboratory personnel.
- Bachelor's or Master's degree in Chemistry, Pharmaceutical Science, or a related discipline.
- Significant experience working in a pharmaceutical Quality Control laboratory.
- Proficiency with analytical techniques such as HPLC, GC, and spectroscopy.
- In-depth knowledge of GMP and regulatory requirements in the pharmaceutical industry.
- Experience with method validation and OOS investigations.
- Strong analytical, problem-solving, and critical thinking skills.
- Excellent attention to detail and accuracy.
- Good written and verbal communication skills.
- Ability to work effectively both independently and as part of a team.
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4
Senior Quality Control Engineer - Automotive Manufacturing
BS1 4DJ Bristol, South West
£45000 Annually
WhatJobs
Posted 5 days ago
Job Viewed
Job Description
Our client is seeking a highly skilled and experienced Senior Quality Control Engineer to join their advanced manufacturing facility in Bristol, South West England, UK . This role is crucial in maintaining and improving the quality of manufactured products, ensuring adherence to stringent industry standards and customer expectations. You will be instrumental in developing and implementing quality control systems, processes, and procedures within a fast-paced production environment.
Key Responsibilities:
Key Responsibilities:
- 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.
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