59 Quality Control jobs in Blyth
Quality Control Manager (Manufacturing)
SR1 1AA Sunderland, North East
£50000 Annually
WhatJobs
Posted 3 days ago
Job Viewed
Job Description
Our client, a leader in advanced manufacturing, is looking for a highly experienced and detail-oriented Quality Control Manager to join their innovative, fully remote team. This critical role will be responsible for establishing, implementing, and maintaining quality control systems and procedures throughout the manufacturing process. You will oversee all aspects of quality assurance, ensuring that products meet stringent internal and external standards and customer specifications. The ideal candidate will have a strong background in quality management within a manufacturing environment, with a deep understanding of quality control methodologies, statistical process control (SPC), and Lean manufacturing principles. Responsibilities will include developing quality control plans, conducting root cause analysis for quality issues, implementing corrective and preventive actions (CAPA), and managing non-conformance reporting. You will also be responsible for training and mentoring quality control personnel, fostering a culture of quality awareness across the organisation. Experience with ISO 9001 or other relevant quality management systems is essential. Excellent analytical, problem-solving, and decision-making skills are required, along with strong communication and leadership abilities to collaborate effectively with production, engineering, and supply chain teams, despite the remote nature of the role. This is a remote-first position, requiring a proactive and self-motivated individual who can manage their workload and drive quality initiatives independently. You will be expected to conduct virtual audits and maintain close communication with on-site teams. We offer a competitive salary, comprehensive benefits, and the opportunity to significantly impact the quality and success of our manufactured products from a remote setting. Join us in upholding the highest standards of quality and driving continuous improvement.
This advertiser has chosen not to accept applicants from your region.
0
Senior Pharmaceutical Quality Control Manager
NE6 1AA Newcastle upon Tyne, North East
£75000 Annually
WhatJobs
Posted today
Job Viewed
Job Description
Our client, a rapidly growing pharmaceutical company committed to improving global health, is seeking an experienced and meticulous Senior Pharmaceutical Quality Control Manager to lead their QC operations in Newcastle upon Tyne, Tyne and Wear, UK . This pivotal role involves overseeing all aspects of quality control testing, ensuring adherence to strict regulatory standards (e.g., GMP, FDA), and maintaining the integrity and safety of pharmaceutical products. You will manage a team of skilled analysts, implement advanced testing methodologies, and contribute significantly to the company's compliance and product excellence.
Key Responsibilities:
The ideal candidate will possess a Master's degree or Ph.D. in Chemistry, Pharmacy, or a related life science discipline. A minimum of 7 years of experience in pharmaceutical quality control, with at least 3 years in a management or supervisory role, is essential. In-depth knowledge of GMP regulations and analytical techniques (HPLC, GC, spectroscopy, wet chemistry) is required. Proven experience in method development, validation, and OOS investigations is critical. Strong leadership, problem-solving, and communication skills are necessary. Experience with pharmaceutical manufacturing processes and quality systems is highly desirable. This is a key leadership position based in Newcastle upon Tyne , offering a competitive salary, excellent benefits, and the opportunity to contribute to life-saving medicines.
Key Responsibilities:
- Lead and manage the day-to-day operations of the Quality Control department, including laboratory testing of raw materials, in-process samples, and finished products.
- Develop, validate, and implement analytical methods according to relevant pharmacopoeias and regulatory guidelines.
- Ensure compliance with Good Manufacturing Practices (GMP) and other applicable regulatory standards.
- Supervise and mentor QC analysts, providing training and performance management.
- Review and approve testing data, batch records, and analytical reports.
- Manage laboratory equipment, ensuring calibration, maintenance, and qualification.
- Investigate Out-of-Specification (OOS) results and deviations, implementing corrective and preventive actions (CAPAs).
- Collaborate with R&D, Production, and Quality Assurance departments to resolve quality issues and support product lifecycle management.
- Maintain accurate and organized laboratory records and documentation.
- Contribute to internal and external audits as a subject matter expert.
- Stay current with scientific advancements and regulatory changes affecting pharmaceutical quality control.
The ideal candidate will possess a Master's degree or Ph.D. in Chemistry, Pharmacy, or a related life science discipline. A minimum of 7 years of experience in pharmaceutical quality control, with at least 3 years in a management or supervisory role, is essential. In-depth knowledge of GMP regulations and analytical techniques (HPLC, GC, spectroscopy, wet chemistry) is required. Proven experience in method development, validation, and OOS investigations is critical. Strong leadership, problem-solving, and communication skills are necessary. Experience with pharmaceutical manufacturing processes and quality systems is highly desirable. This is a key leadership position based in Newcastle upon Tyne , offering a competitive salary, excellent benefits, and the opportunity to contribute to life-saving medicines.
This advertiser has chosen not to accept applicants from your region.
1
Senior Pharmaceutical Quality Control Analyst
NE1 1 Newcastle upon Tyne, North East
£45000 Annually
WhatJobs
Posted 1 day ago
Job Viewed
Job Description
We are seeking a highly skilled and motivated Senior Pharmaceutical Quality Control Analyst to join a leading pharmaceutical company in **Newcastle upon Tyne, Tyne and Wear, UK**. This critical role involves conducting a wide range of laboratory tests on raw materials, in-process samples, and finished pharmaceutical products to ensure compliance with stringent quality standards and regulatory requirements. The Senior Analyst will perform analytical testing using various techniques, including HPLC, GC, UV-Vis, FT-IR, and wet chemistry methods. You will be responsible for method validation and transfer, developing and optimizing analytical methods, and troubleshooting instrument issues. Accurate and meticulous documentation of all test results, deviations, and investigations in compliance with Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP) is paramount. The role also involves reviewing and approving analytical data generated by junior analysts, contributing to internal audits, and participating in regulatory inspections. You will play a key role in the continuous improvement of quality control processes and systems, identifying potential risks and implementing corrective and preventive actions (CAPAs). The ideal candidate will possess a strong understanding of pharmaceutical quality systems, regulatory guidelines (e.g., FDA, EMA), and analytical chemistry principles. Excellent problem-solving skills, attention to detail, and the ability to work independently and as part of a team are essential.
Key Responsibilities:
Qualifications and Experience:
Key Responsibilities:
- Perform analytical testing on raw materials, intermediates, and finished products using various instrumental and wet chemistry techniques (e.g., HPLC, GC, UV-Vis, FT-IR).
- Ensure all testing is conducted in compliance with GMP, GLP, and relevant regulatory guidelines.
- Develop, validate, and transfer analytical methods.
- Troubleshoot and maintain laboratory instrumentation.
- Accurately document and review all experimental data, results, and deviations.
- Investigate out-of-specification (OOS) results and implement corrective actions.
- Review and approve analytical data and reports prepared by junior analysts.
- Participate in internal audits and regulatory inspections.
- Contribute to the continuous improvement of QC processes and laboratory operations.
- Maintain a safe and compliant laboratory environment.
Qualifications and Experience:
- BSc/MSc in Chemistry, Pharmaceutical Science, or a related scientific discipline.
- Minimum 5 years of experience in a pharmaceutical Quality Control laboratory environment.
- Extensive hands-on experience with analytical techniques such as HPLC, GC, spectroscopy, and wet chemistry.
- Strong understanding of GMP, GLP, ICH guidelines, and regulatory requirements.
- Experience with method validation and transfer.
- Proficiency in data analysis and interpretation.
- Excellent documentation skills and attention to detail.
- Strong problem-solving and critical thinking abilities.
- Good communication and interpersonal skills.
- Ability to work independently and collaboratively within a team.
This advertiser has chosen not to accept applicants from your region.
2
Lead Pharmaceutical Quality Control Scientist
SR1 2AY Sunderland, North East
£70000 Annually
WhatJobs
Posted 3 days ago
Job Viewed
Job Description
Our client is seeking an experienced and highly motivated Lead Pharmaceutical Quality Control Scientist to oversee critical quality operations in Sunderland, Tyne and Wear, UK . This role demands a meticulous approach to ensuring that all manufactured pharmaceutical products meet stringent quality standards and regulatory requirements. You will lead a team of QC analysts, manage laboratory activities, develop and validate analytical methods, and contribute to the overall quality strategy of the company. Your expertise will be vital in maintaining compliance and ensuring the safety and efficacy of our products.
Key Responsibilities:
Qualifications:
This hybrid position offers the opportunity to work from our modern facilities in Sunderland, Tyne and Wear, UK , with flexibility for remote work on specific tasks. Our client is committed to scientific excellence and fostering a collaborative research environment.
Key Responsibilities:
- Lead and mentor a team of QC analysts, providing technical guidance and performance management.
- Oversee all routine QC testing of raw materials, in-process samples, and finished products using various analytical techniques (e.g., HPLC, GC, UV-Vis, dissolution).
- Develop, validate, and transfer analytical methods in compliance with ICH guidelines.
- Ensure adherence to Good Manufacturing Practices (GMP) and other relevant regulatory standards.
- Manage laboratory equipment, including calibration, maintenance, and qualification.
- Review and approve analytical data, test results, and QC batch records.
- Investigate out-of-specification (OOS) results and deviations, implementing corrective and preventive actions (CAPAs).
- Collaborate with R&D, manufacturing, and regulatory affairs departments.
- Contribute to regulatory submissions and respond to queries from health authorities.
- Maintain accurate and complete laboratory documentation.
- Implement continuous improvement initiatives within the QC laboratory.
Qualifications:
- MSc or PhD in Chemistry, Pharmaceutical Sciences, or a related discipline.
- Minimum of 7 years of experience in pharmaceutical quality control, with at least 2 years in a supervisory or lead role.
- Extensive hands-on experience with a variety of analytical techniques common in pharmaceutical QC.
- In-depth knowledge of GMP, ICH guidelines, and regulatory requirements for pharmaceuticals.
- Proven experience in method development and validation.
- Strong leadership, communication, and problem-solving skills.
- Proficiency in laboratory information management systems (LIMS).
- Experience with statistical analysis software is beneficial.
- Ability to work effectively in a hybrid environment, balancing on-site laboratory work with potential remote administrative tasks.
This hybrid position offers the opportunity to work from our modern facilities in Sunderland, Tyne and Wear, UK , with flexibility for remote work on specific tasks. Our client is committed to scientific excellence and fostering a collaborative research environment.
This advertiser has chosen not to accept applicants from your region.
3
Senior Pharmaceutical Quality Control Analyst
NE1 4DR Newcastle upon Tyne, North East
£45000 Annually
WhatJobs
Posted 3 days ago
Job Viewed
Job Description
We are seeking a highly motivated and experienced Senior Pharmaceutical Quality Control Analyst to join a dynamic team in Newcastle upon Tyne, Tyne and Wear, UK . This role is crucial in ensuring that our pharmaceutical products meet stringent quality standards and regulatory requirements before they reach patients. The successful candidate will be responsible for performing a wide range of analytical tests on raw materials, in-process samples, and finished products using various laboratory techniques and instrumentation, such as HPLC, GC, UV-Vis spectrophotometry, and Karl Fischer titration.
Key responsibilities include:
The ideal candidate will possess a BSc or MSc in Chemistry, Pharmaceutical Sciences, or a related field, with a minimum of 5 years of experience in a pharmaceutical quality control laboratory environment. A strong understanding of analytical chemistry principles, pharmaceutical manufacturing processes, and regulatory compliance is essential. Excellent problem-solving skills, attention to detail, and the ability to work independently and as part of a team are also required. Proficiency in using standard laboratory software and LIMS is highly desirable. This is a fantastic opportunity to advance your career within the pharmaceutical sector in a hybrid working environment that balances office-based responsibilities with flexible remote work options.
Key responsibilities include:
- Developing, validating, and implementing analytical methods in compliance with ICH guidelines and pharmacopoeial standards (e.g., BP, USP, EP).
- Performing routine and non-routine testing of pharmaceutical products, intermediates, and raw materials.
- Investigating out-of-specification (OOS) results, identifying root causes, and implementing corrective and preventive actions (CAPAs).
- Maintaining accurate and detailed laboratory records, including raw data, calculations, and results, in accordance with Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP).
- Calibrating and maintaining laboratory equipment, ensuring it is fit for purpose and performing as expected.
- Preparing certificates of analysis (CoAs) and other quality-related documentation.
- Contributing to the continuous improvement of QC processes and procedures.
- Providing technical guidance and mentorship to junior analysts.
- Participating in internal and external audits as required.
- Staying up-to-date with the latest advancements in pharmaceutical analysis and regulatory guidelines.
The ideal candidate will possess a BSc or MSc in Chemistry, Pharmaceutical Sciences, or a related field, with a minimum of 5 years of experience in a pharmaceutical quality control laboratory environment. A strong understanding of analytical chemistry principles, pharmaceutical manufacturing processes, and regulatory compliance is essential. Excellent problem-solving skills, attention to detail, and the ability to work independently and as part of a team are also required. Proficiency in using standard laboratory software and LIMS is highly desirable. This is a fantastic opportunity to advance your career within the pharmaceutical sector in a hybrid working environment that balances office-based responsibilities with flexible remote work options.
This advertiser has chosen not to accept applicants from your region.
4
Senior Pharmaceutical Quality Control Analyst
SR1 2AA Sunderland, North East
£40000 Annually
WhatJobs
Posted 3 days ago
Job Viewed
Job Description
Our client, a prominent player in the pharmaceutical industry, is seeking a highly motivated and meticulous Senior Pharmaceutical Quality Control Analyst to join their dynamic team in Sunderland, Tyne and Wear, UK . This role is critical for ensuring the quality, safety, and efficacy of pharmaceutical products through rigorous testing and analysis. You will be responsible for performing a wide range of analytical tests, maintaining laboratory equipment, and ensuring compliance with regulatory standards. This is an excellent opportunity for an experienced analyst looking to advance their career within a leading pharmaceutical company.
Key Responsibilities:
Qualifications and Experience:
This role offers a competitive salary, comprehensive benefits package, and opportunities for professional development within a supportive and challenging work environment. Become a key part of ensuring the highest standards in pharmaceutical manufacturing.
Key Responsibilities:
- Perform comprehensive quality control testing on raw materials, in-process samples, and finished pharmaceutical products using various analytical techniques (e.g., HPLC, GC, UV-Vis, FTIR).
- Develop, validate, and transfer analytical methods according to regulatory guidelines (e.g., ICH).
- Maintain and calibrate laboratory equipment, ensuring optimal performance and accuracy.
- Document all testing activities meticulously in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
- Investigate and resolve Out-of-Specification (OOS) results and deviations, identifying root causes and implementing corrective actions.
- Prepare and review Certificates of Analysis (CoA) and analytical reports.
- Ensure compliance with all company policies, SOPs, and regulatory requirements (e.g., MHRA, FDA).
- Train and mentor junior laboratory personnel on analytical techniques and laboratory procedures.
- Contribute to internal and external audits by providing necessary documentation and explanations.
- Participate in cross-functional team meetings to discuss product quality and process improvements.
- Manage laboratory inventory and ensure adequate stock of consumables and reagents.
Qualifications and Experience:
- Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or a related scientific discipline.
- Minimum of 3-5 years of experience in pharmaceutical quality control or analytical development.
- Proven expertise in chromatographic techniques (HPLC, GC) and spectroscopic methods.
- Strong understanding of GMP, GLP, and relevant regulatory guidelines.
- Experience with method validation and OOS investigations.
- Excellent analytical, problem-solving, and critical thinking skills.
- Proficiency in laboratory information management systems (LIMS) and data analysis software.
- Strong attention to detail and commitment to accuracy.
- Effective communication and interpersonal skills, with the ability to work collaboratively in a team environment.
- Proficiency in English.
This role offers a competitive salary, comprehensive benefits package, and opportunities for professional development within a supportive and challenging work environment. Become a key part of ensuring the highest standards in pharmaceutical manufacturing.
This advertiser has chosen not to accept applicants from your region.
5
Senior Pharmaceutical Quality Control Scientist
SR1 1AA Sunderland, North East
£55000 Annually
WhatJobs
Posted 3 days ago
Job Viewed
Job Description
Our client, a distinguished pharmaceutical company, is actively seeking a highly skilled and meticulous Senior Pharmaceutical Quality Control Scientist to join their expanding, fully remote team. This is a pivotal role dedicated to upholding the highest standards of product quality and compliance within the pharmaceutical industry. You will be responsible for performing complex analytical testing, developing and validating testing methods, and ensuring adherence to stringent regulatory guidelines (e.g., GMP, ICH). This position offers the flexibility of remote work, allowing you to contribute your expertise from anywhere in the UK while working on critical pharmaceutical quality assurance.
Key Responsibilities:
Key Responsibilities:
- Perform advanced analytical testing on raw materials, in-process samples, and finished pharmaceutical products using techniques such as HPLC, GC, UV-Vis, FTIR, and Karl Fischer titration.
- Develop, optimize, and validate analytical methods according to ICH guidelines and regulatory requirements.
- Analyze and interpret complex analytical data, generating comprehensive reports and documenting results accurately.
- Investigate out-of-specification (OOS) results, deviations, and non-conformances, identifying root causes and implementing corrective and preventative actions (CAPAs).
- Ensure all laboratory activities comply with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant regulatory standards.
- Maintain laboratory equipment, ensuring proper calibration, qualification, and maintenance.
- Participate in internal and external audits, providing necessary documentation and support.
- Contribute to the continuous improvement of quality control processes and laboratory operations.
- Stay updated on the latest scientific advancements, regulatory changes, and industry best practices in pharmaceutical quality control.
- Train and mentor junior QC analysts, providing guidance on testing procedures and data interpretation.
- Collaborate with R&D, manufacturing, and regulatory affairs teams to support product development and lifecycle management.
- Prepare and review technical documentation, including Standard Operating Procedures (SOPs) and validation protocols.
- Master's or Ph.D. in Pharmaceutical Sciences, Chemistry, Analytical Chemistry, or a related scientific discipline.
- Minimum of 5 years of hands-on experience in pharmaceutical quality control or analytical development.
- Extensive experience with various analytical techniques, particularly HPLC and GC, is essential.
- Strong understanding of GMP, ICH guidelines, and other relevant regulatory requirements.
- Proven ability to develop, validate, and transfer analytical methods.
- Excellent data analysis and interpretation skills, with meticulous attention to detail.
- Proficiency in LIMS (Laboratory Information Management System) and other relevant software.
- Strong written and verbal communication skills, with the ability to document findings clearly and concisely.
- Experience working remotely and managing laboratory operations or data analysis independently is a significant advantage.
- Ability to work effectively both independently and as part of a distributed team.
This advertiser has chosen not to accept applicants from your region.
Be The First To Know
About the latest Quality control Jobs in Blyth !
6
Senior Pharmaceutical Quality Control Analyst
NE1 1AA Newcastle upon Tyne, North East
£50000 Annually
WhatJobs
Posted 3 days ago
Job Viewed
Job Description
Our client, a rapidly expanding pharmaceutical company renowned for its innovative drug development, is seeking a highly skilled Senior Pharmaceutical Quality Control Analyst. This is a pivotal, fully remote role focused on ensuring the rigorous quality standards of our pharmaceutical products. You will be instrumental in conducting comprehensive analytical testing, validating methodologies, and contributing to regulatory compliance. The ideal candidate will possess extensive experience in pharmaceutical QC, a deep understanding of GMP guidelines, and a meticulous approach to analysis and documentation. This remote position allows you to leverage your expertise from anywhere in the UK.
Responsibilities:
Qualifications:
Responsibilities:
- Perform a wide range of analytical tests on raw materials, in-process samples, and finished pharmaceutical products using various sophisticated instruments (e.g., HPLC, GC, UV-Vis, IR spectroscopy).
- Develop, validate, and transfer analytical methods in accordance with ICH guidelines and regulatory requirements.
- Review and approve analytical data, ensuring accuracy, completeness, and compliance with established specifications.
- Troubleshoot and resolve analytical issues, instrument malfunctions, and out-of-specification (OOS) results.
- Maintain laboratory equipment, ensuring calibration, qualification, and preventative maintenance are performed regularly.
- Author and review analytical protocols, reports, and validation documents.
- Ensure all laboratory activities are conducted in strict adherence to Good Manufacturing Practices (GMP) and other relevant regulatory standards.
- Contribute to the maintenance and improvement of the Quality Management System (QMS).
- Participate in regulatory inspections and internal audits, providing necessary documentation and explanations.
- Assist in the investigation of deviations and implement corrective and preventive actions (CAPAs).
- Mentor and provide technical guidance to junior analysts.
- Stay abreast of advancements in pharmaceutical analysis, regulatory trends, and new technologies.
- Collaborate with R&D and manufacturing teams to support product development and process improvements.
Qualifications:
- MSc or PhD in Analytical Chemistry, Pharmaceutical Sciences, Biochemistry, or a related scientific discipline.
- A minimum of 7 years of hands-on experience in pharmaceutical Quality Control or Analytical Development.
- Extensive experience with chromatographic techniques (HPLC, GC) and spectroscopic methods.
- Thorough understanding and practical application of GMP, ICH guidelines, and pharmacopoeial standards (e.g., USP, EP).
- Proven experience in method development and validation.
- Strong analytical, problem-solving, and critical thinking skills.
- Excellent written and verbal communication skills, with the ability to clearly document complex technical information.
- Proficiency in LIMS and other relevant laboratory software.
- Demonstrated ability to work independently and manage time effectively in a remote setting.
- Experience with stability testing programs.
This advertiser has chosen not to accept applicants from your region.
7
Senior Quality Control Inspector - Automotive Manufacturing
SR5 3NB Sunderland, North East
£40000 Annually
WhatJobs
Posted 3 days ago
Job Viewed
Job Description
Our client, a prominent automotive manufacturing company, is seeking a meticulous and experienced Senior Quality Control Inspector to join their team in **Sunderland, Tyne and Wear, UK**. This role is crucial for ensuring that all manufactured automotive components and finished products meet stringent quality standards and customer specifications. The ideal candidate will possess a keen eye for detail, a thorough understanding of automotive manufacturing processes, and a strong commitment to quality assurance. You will be responsible for performing inspections, conducting tests, and identifying any deviations from quality benchmarks, as well as guiding junior inspectors. Your responsibilities will encompass:
Key Responsibilities:
Qualifications and Experience:
Key Responsibilities:
- Conducting comprehensive inspections of raw materials, in-process components, and finished automotive products using various measurement tools and techniques.
- Interpreting technical drawings, blueprints, and quality standards to verify product conformity.
- Performing dimensional, visual, and functional inspections to identify defects and deviations.
- Utilising precision measuring instruments such as CMMs, calipers, micrometers, and gauges.
- Documenting inspection results accurately and promptly in the quality management system.
- Identifying non-conforming products and initiating the appropriate corrective action process.
- Collaborating with production and engineering teams to resolve quality issues and implement preventative measures.
- Participating in root cause analysis for quality defects and contributing to the development of solutions.
- Ensuring adherence to all relevant quality standards (e.g., IATF 16949) and safety regulations.
- Training and mentoring junior quality control inspectors, providing guidance on inspection techniques and standards.
- Contributing to the continuous improvement of quality control processes and procedures.
Qualifications and Experience:
- Proven experience (4+ years) as a Quality Control Inspector, preferably within the automotive manufacturing sector.
- Solid understanding of automotive manufacturing processes and quality control principles.
- Proficiency in using a wide range of precision measuring equipment and inspection tools.
- Ability to read and interpret technical drawings, specifications, and quality standards.
- Experience with CMM operation and programming is highly desirable.
- Knowledge of quality management systems such as IATF 16949 or ISO 9001.
- Strong attention to detail and analytical skills.
- Good communication and interpersonal skills, with the ability to work effectively in a team.
- A proactive approach to problem-solving and continuous improvement.
- Must be eligible to work in the UK.
This advertiser has chosen not to accept applicants from your region.
8
Quality Assurance Manager
Durham, North East
CK Group- Science, Clinical and Technical
Posted 18 days ago
Job Viewed
Job Description
CK Group are recruiting for a Quality Assurance Manager to join a leading manufacturer of Medical and Technical products who are based in County Durham on a permanent basis.
Location:
The role is based in County Durham and is site based.
Role:
Your Background:
Apply:
For more information, or to apply for this Quality Assurance Manager position please contact Mary Bolt on (phone number removed) or email (url removed). Please quote job reference (Apply online only) in all correspondence.
It is essential that applicants hold entitlement to work in the UK
Location:
The role is based in County Durham and is site based.
Role:
- Take responsibility for overall ownership of the Plant Quality Management System and for monitoring and assuring the quality of all incoming materials, outgoing materials, work in progress materials and also the quality of all physical and transactional processes.
- Design, implement, and maintain quality management systems, policies, and procedures.
- Ensure that the Quality Management system in place conforms with all relevant Quality standards which include ISO 9001, ISO 13485 and ISO 22716
- Manage and update the site Quality Manual and conduct Training
- Ensure the legal compliance of New Products
- Establish standards and processes to ensure that defects are prevented from occurring in the first place
- Contribute to the long-range strategy for quality within the organisation
- Complete Internal Audits to a high standard and follow up by closing actions
- Promote quality awareness and ensure compliance with quality standards, both internal and external
- Supplier audits
- Drive improvements in quality performance across the organisation
Your Background:
- Educated to degree level or above in a relevant field.
- QA experience in an ISO 13485 regulated environment.
- The ability to manage the Quality System and deal with non-conformance appropriately.
- Must be diligent and accurate.
- Skilled in the use of Microsoft Office.
Apply:
For more information, or to apply for this Quality Assurance Manager position please contact Mary Bolt on (phone number removed) or email (url removed). Please quote job reference (Apply online only) in all correspondence.
It is essential that applicants hold entitlement to work in the UK
This advertiser has chosen not to accept applicants from your region.
9