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A leading scientific equipment manufacturer in East Sussex is seeking a Quality, Safety & Environmental (QSE) Manager. This pivotal role involves overseeing quality assurance and health & safety compliance while implementing and managing ISO standards. The ideal candidate will bring demonstrated experience in a similar role and possess strong communication skills to collaborate across teams. Competitive salary and benefits offered.
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Cpl Life Sciences
East Sussex, United Kingdom
Other
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Yes
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1acd70dc095a
67
12.08.2025
26.09.2025
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Overview
Our client a privately owned company located in East Sussex currently employing just over 60 people. With a core business in the design and manufacture of specialised imaging detectors and systems covering a diverse range of industries from aerospace to biomedical.
Applications for such detectors include the detection of single photons and ultrafast cameras capable of sub-nanosecond exposure times.
A global leader of highly differentiated technologies in scientific and medical research, life sciences, agriculture, recycling, aerospace, defence and security, and industrial markets.
Job Summary
A QSE Manager is required for immediate start to have overall responsibility for Quality Assurance and implementing Health & Safety and Environmental compliance throughout the company.
This includes the maintenance and administration of our Quality Management Standards – ISO 9001 and ISO 14001. This is a key position that will help shape our quality culture and ensure our commitment to continuous improvement in every area of our business.
Key areas of responsibility
• Supervision and development of a small QA team
• Maintain and administer the Quality Management System (QMS), ISO 9001 and ISO 14001.
• Collaborate with cross-functional teams to address quality issues and ensure product and process consistency.
• Monitor and report yield statistics and warranty return numbers within our core product lines. • Co-ordinate 8D corrective actions with support from engineering.
• Oversee quality control processes including incoming inspection, in-process checks and final product evaluation.
• Oversee all aspects of document control.
• Manage internal and external audits and drive corrective and preventative actions.
• Manage the change control system (QCBD).
• Lead the internal MRB meetings and follow up actions.
• Represent the company in quality control matters to outside parties such as customers and suppliers.
• Report and present on company performance against quality targets at Senior Management and Board level.
Qualifications
Experience
Skills & Abilities
Apply
Full name Email address Cover Message (optional) Upload CV Choose File Upload your CV and any other relevant file. Contact via SMS (optional) I would like to be contacted via SMS Privacy Policy I have read and agree to the Clinical Professionals Group Privacy PolicyOverview
Our client a privately owned company located in East Sussex currently employing just over 60 people. With a core business in the design and manufacture of specialised imaging detectors and systems covering a diverse range of industries from aerospace to biomedical.
Applications for such detectors include the detection of single photons and ultrafast cameras capable of sub-nanosecond exposure times.
A global leader of highly differentiated technologies in scientific and medical research, life sciences, agriculture, recycling, aerospace, defence and security, and industrial markets.
Job Summary
A QSE Manager is required for immediate start to have overall responsibility for Quality Assurance and implementing Health & Safety and Environmental compliance throughout the company.
This includes the maintenance and administration of our Quality Management Standards – ISO 9001 and ISO 14001. This is a key position that will help shape our quality culture and ensure our commitment to continuous improvement in every area of our business.
Key areas of responsibility
• Supervision and development of a small QA team
• Maintain and administer the Quality Management System (QMS), ISO 9001 and ISO 14001.
• Collaborate with cross-functional teams to address quality issues and ensure product and process consistency.
• Monitor and report yield statistics and warranty return numbers within our core product lines. • Co-ordinate 8D corrective actions with support from engineering.
• Oversee quality control processes including incoming inspection, in-process checks and final product evaluation.
• Oversee all aspects of document control.
• Manage internal and external audits and drive corrective and preventative actions.
• Manage the change control system (QCBD).
• Lead the internal MRB meetings and follow up actions.
• Represent the company in quality control matters to outside parties such as customers and suppliers.
• Report and present on company performance against quality targets at Senior Management and Board level.
Qualifications
Experience
Skills & Abilities
Apply
Full name Email address Cover Message (optional) Upload CV Choose File Upload your CV and any other relevant file. Contact via SMS (optional) I would like to be contacted via SMS Privacy Policy I have read and agree to the Clinical Professionals Group Privacy PolicyFind our privacy policy here