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highest standards of quality and compliance in all aspects of our operations. Job Description: We are seeking a highly skilled and experienced Site Lead (QMS) to join our team. The Site Lead will be responsible for ensuring compliance with regulatory requirements, overseeing MHRA client audits, managing our global Quality Management … System (QMS), and implementing a labelling service. Key Responsibilities: Develop, implement, and maintain a comprehensive Quality Management System (QMS) to ensure compliance with regulatory standards, including MHRA requirements. Lead and manage MHRA client audits, ensuring timely preparation, coordination, and follow-up activities. Develop, implement, and maintain the Quality Management System … interacting with regulatory agencies. Strong knowledge of global regulatory requirements, including MHRA regulations, FDA regulations, and ISO standards. Experience developing and implementing Quality Management Systems (QMS) in a global environment. Preferred Qualifications: Experience implementing labelling services or managing labelling operations within a regulated industry. Certified Quality Auditor (CQA) or equivalent more »

have a wide range of responsibilities, from operational tasks like batch review and production liaison to broader activities such as auditing, supplier management, and QMS implementation. Crucially, you'll also serve as Deputy QA Manager, with some immediate line management duties and close collaboration with the QA Manager to meet more »

and across other functions. Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork. Support and comply with the company's Quality Management System policies and procedures. Maintain regular and reliable attendance. Ability to act with an inclusion mindset and model these behaviors for the organization. Ability to more »

of the relevant regulations Provide reports to management to enable them to monitor system performance. Review and authorise documentation and processes in the Quality Management System to ensure compliance with established quality procedures and applicable regulations and alignment with other related documentation. Identify and collaborate in the implementation of changes more »

Infrastructure, Manufacturing, Chemical, Education and Training, Healthcare, Pharmaceutical, IT, Finance, HR and Support Services markets. We offer this service through the Ten Live Quality Management System which has combined our 60 years + experience in the industry, our partnerships with industry bodies and regulators and a customer-centric quality management more »

throughout our business and ensure we deliver the optimum level of efficiency whilst maintaining the highest quality standards and continuous improvement of our quality management system ISO 9001:2015. We aim to minimize environmental impact of our own systems and help develop environmentally responsible customer solutions. DPS Group recognises its more »

throughout our business and ensure we deliver the optimum level of efficiency whilst maintaining the highest quality standards and continuous improvement of our quality management system ISO 9001:2015. We aim to minimize environmental impact of our own systems and help develop environmentally responsible customer solutions. DPS Group recognises its more »

in our manufacturing and operations teams. Key areas of responsibility: Validation of changes to Manufacturing & QC standard operating processes Document control within a Quality management system to ensure traceable, logical and consistent workflow and procedures. Liaise with appropriate departments to contribute to the rapid and effective investigation of process quality more »

for improvement. Collaborate with manufacturing engineers on customer requirements to ensure compliance within the Production environment. Assist in general Upkeep & continual improvement of the QMS to ensure compliance to EN9100. Develop inspection and risk management methods to analyse product quality inline with customer requirements such as MSA, FMEA, CPK. Perform more »

management and loss prevention initiatives in order to safeguard pharmaceutical products, streamline operations, and minimise risks. KEY RESPONSIBILITIES Develop and oversee a robust quality management system in line with pharmaceutical industry regulations, including Good Distribution Practices (GDP) and Good Manufacturing Practices (GMP). Establish quality policies, procedures, and guidelines to more »

responsibilities will be: Develop and implement quality assurance policies, procedures, and standards specific to defence and naval systems. Establish and maintain a comprehensive quality management system to ensure consistent product quality and reliability. Lead and manage a team of quality assurance professionals, providing guidance, training, and support as needed. Collaborate more »

responsibilities will be: Develop and implement quality assurance policies, procedures, and standards specific to defence and naval systems. Establish and maintain a comprehensive quality management system to ensure consistent product quality and reliability. Lead and manage a team of quality assurance professionals, providing guidance, training, and support as needed. Collaborate more »

to customers Actively participate in document control Direct interaction with customers on quality issues Undertaking Continuous Improvement activities to ensure the integrity of the QMS is maintained Person Specification A-C GCSE Level or equivalent in English and Maths Manufacturing or Operational qualification or relevant proven experience HNC or Degree more »

systems and impact assessment of pertinent change controls. Any other assigned duties. Requirements: Experience with TrackWise, LIMS and Documentum and/or any other QMS systems. Acquaintance global GxP, e.g., FDA CFRs, EU, 'Third countries' other than the UK. Familiarity within a pharmaceutical manufacturing, testing or quality assurance setting in more »

if required Co-ordinate and provide training across functional groups in Quality Procedures, cGMP requirements and QA concepts Trend and report batch review and QMS data Provide support to management during third-party audits Perform internal housekeeping, in-process visits and quality audits Perform external quality audits, supporting Livingston and more »

throughout our business and ensure we deliver the optimum level of efficiency whilst maintaining the highest quality standards and continuous improvement of our quality management system ISO 9001:2015. We aim to minimize environmental impact of our own systems and help develop environmentally responsible customer solutions. DPS Group recognises its more »

Infrastructure, Manufacturing, Chemical, Education and Training, Healthcare, Pharmaceutical, IT, Finance, HR and Support Services markets. We offer this service through the Ten Live Quality Management System which has combined our 60 years + experience in the industry, our partnerships with industry bodies and regulators and a customer-centric quality management more »

that all costs are considered. Providing routine internal commercial and progress reporting in accordance with management time requirements Maintain systems to see that Quality Management System ISO 9001 and 14001 are implemented. Progress all sales opportunities. Develop and pursue new and existing sales leads Ensure No Claims are made on more »

and guidelines including, but not limited to, Code of Business Conduct and Ethics, GDPR, and HIPAA. Support and comply with the company's Quality Management System policies and procedures. Regular and reliable attendance. Ability to work normal schedule of Monday through Friday during normal business hours. Ability to work in more »

or maintaining and archiving documentation Supporting and executing external audits where applicable Supporting management when hosting regulatory audits Working on executing and maintaining the QMS, including but not limited to: Risk Assessments Change Controls CAPAs Deviations Complaints Recalls OOS/OOT The Person: Will have a Degree in a relevant more »

or Quality Manager or Quality Management experience gained within a software development working environment. Experience of ISO9001:2015 quality standard and maintaining a Quality Management System Any knowledge or experience of ISO27001/002 or maintaining an Information Security Management System would be advantageous but not essential. Experience of developing more »

or Quality Manager or Quality Management experience gained within a software development working environment. Experience of ISO9001:2015 quality standard and maintaining a Quality Management System Any knowledge or experience of ISO27001/002 or maintaining an Information Security Management System would be advantageous but not essential. Experience of developing more »

related meetings. Maintaining the divisions central quality and service management documents, which includes conducting regular reviews and updates to policies and procedures. Maintaining the QMS and SMS risk and action logs. Liaising with external and internal auditors, including issuing and reviewing audit reports, maintaining audit finding logs, and proactively following more »

regulations. quality performance metrics, targets, and KPIs to monitor and drive continuous improvement initiatives. Quality Assurance Strategy implement, and maintain robust aviation-specific quality management system in accordance with industry standards and regulatory requirements. effective documentation control, recordkeeping, and configuration management processes to maintain the integrity of quality records and more »

and permanent role in which the successful candidate will be responsible for leading the Quality department, (including Operational Quality Assurance, Supplier Approval, and Quality management system)ensuring compliance with regulatory requirements, and maintaining the highest standards of quality across all aspects of the business. About Torbay Pharmaceuticals At TP we more »