The Company
Our client is a specialist manufacturing company. For maternity cover, they are recruiting for a Quality Manager.
The Role
Will be site based. In this position, the Quality Manager will be responsible for the management and implementation of improvements to the QA system in support of ISO and EU (GMP) regulatory requirements, investigation of non-conformity, vendor assurance, and final product release. Maintain audit ready status of the QMS. Ensure that improvements to product/process are documented and aligned with ISO and cGMP requirements. Responsible for continuous improvement projects by measuring, analyzing, and improving systems and processes. Responsible for Non-Conformance management, including reporting, investigation, identification of corrective actions, and monitoring the effectiveness of actions taken. Ensure the routine testing of incoming raw materials, mixes, in-process testing, and finished products are performed according to approved specifications and procedures. Responsible for QA batch record review and product release. Ensure quality critical steps are identified and suitably validated. Develop and report quality metrics to Senior Management - monthly Quality Meetings / Management Review / etc. Monitor quality objectives and compile action plan to reach targets. Manage the Internal audit schedule. Conduct external audits to ensure effective supplier management. Lead customer and regulatory audits on-site. Implement preventative actions to improve both process and product performance. Implement best working practices and techniques for quality assurance. Management and responsibility of all validation. Management and responsibility for all aspects of quality. Management of a team of 4.
The Person
Bachelor's Degree in a scientific area. Previous experience of working in a senior quality role within a manufacturing environment. Experience gained within a pharmaceutical or chemical environment is essential. Experience in personnel management and development, ensuring you can direct your team to successful completion of all tasks whilst maintaining good morale. Thorough knowledge of ISO quality systems and validation principles for manufacturing processes. Understanding and application of QMS processes, tools, and techniques. Sound working knowledge of ISO9001 and GMP requirements. Auditor qualifications essential, Lead Auditor status preferred. Experience of validation of systems and processes. Strong leadership, communication, and influencing skills to work effectively across organizational boundaries and influence decision-makers across multiple sites/regions/levels. With good attention to detail, you approach situations with a meticulous eye on safety, quality, and procedures. You will have excellent troubleshooting skills with a focus on finding a solution through to resolution. Good writing and computer skills required for keeping accurate records, writing reports, and standard operating procedures. Will be willing to work on a FTC.
The Benefits
Attractive base salary with plenty of OT opportunity. Working for a forward-thinking growing business. Good company T's and C's.
#J-18808-Ljbffr
Our client is a specialist manufacturing company. For maternity cover, they are recruiting for a Quality Manager.
The Role
Will be site based. In this position, the Quality Manager will be responsible for the management and implementation of improvements to the QA system in support of ISO and EU (GMP) regulatory requirements, investigation of non-conformity, vendor assurance, and final product release. Maintain audit ready status of the QMS. Ensure that improvements to product/process are documented and aligned with ISO and cGMP requirements. Responsible for continuous improvement projects by measuring, analyzing, and improving systems and processes. Responsible for Non-Conformance management, including reporting, investigation, identification of corrective actions, and monitoring the effectiveness of actions taken. Ensure the routine testing of incoming raw materials, mixes, in-process testing, and finished products are performed according to approved specifications and procedures. Responsible for QA batch record review and product release. Ensure quality critical steps are identified and suitably validated. Develop and report quality metrics to Senior Management - monthly Quality Meetings / Management Review / etc. Monitor quality objectives and compile action plan to reach targets. Manage the Internal audit schedule. Conduct external audits to ensure effective supplier management. Lead customer and regulatory audits on-site. Implement preventative actions to improve both process and product performance. Implement best working practices and techniques for quality assurance. Management and responsibility of all validation. Management and responsibility for all aspects of quality. Management of a team of 4.
The Person
Bachelor's Degree in a scientific area. Previous experience of working in a senior quality role within a manufacturing environment. Experience gained within a pharmaceutical or chemical environment is essential. Experience in personnel management and development, ensuring you can direct your team to successful completion of all tasks whilst maintaining good morale. Thorough knowledge of ISO quality systems and validation principles for manufacturing processes. Understanding and application of QMS processes, tools, and techniques. Sound working knowledge of ISO9001 and GMP requirements. Auditor qualifications essential, Lead Auditor status preferred. Experience of validation of systems and processes. Strong leadership, communication, and influencing skills to work effectively across organizational boundaries and influence decision-makers across multiple sites/regions/levels. With good attention to detail, you approach situations with a meticulous eye on safety, quality, and procedures. You will have excellent troubleshooting skills with a focus on finding a solution through to resolution. Good writing and computer skills required for keeping accurate records, writing reports, and standard operating procedures. Will be willing to work on a FTC.
The Benefits
Attractive base salary with plenty of OT opportunity. Working for a forward-thinking growing business. Good company T's and C's.
#J-18808-Ljbffr
