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Assembly Supervisor

Meriden Media - Nottingham, England

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Job Description

Pharmaceutical Assembly Supervisor Circa 35k Permanent Mon- Thur 7.00-16.00 & Fri 7.00-13.00 We are recruiting an experienced Pharmaceutical Assembly Supervisor to lead cleanroom operations for a well-established pharmaceutical manufacturer. This is a hands-on leadership role suited to an individual with a strong background in GMP-regulated production, who enjoys driving quality, efficiency, and team performance within a highly controlled environment. You will play a key role in ensuring assembly activities are delivered safely, compliantly, and to the highest quality standards, while supporting and developing a skilled cleanroom team. Key Responsibilities Supervise and coordinate daily cleanroom assembly operations in line with GMP and ISO 7 cleanroom requirements Lead, coach, and develop a team of assembly operatives, including training, performance management, and ongoing competency assessment Plan and monitor production schedules to ensure output targets are achieved without compromising quality or compliance Maintain accurate and auditable production, inspection, and compliance records using digital manufacturing systems Identify, implement, and sustain continuous improvement initiatives to enhance efficiency and reduce waste Ensure strict adherence to health & safety, quality, and regulatory standards at all times Investigate and resolve assembly or process issues to maintain smooth, uninterrupted production Key Requirements Proven experience as an Assembly Supervisor, Team Leader, or similar within a pharmaceutical, cleanroom, or regulated manufacturing environment Strong leadership and people-management capability, with the confidence to lead by example on the shop floor Analytical and process-driven mindset, with experience implementing improvements Confident IT user, with experience of ERP/MRP systems, digital production records, reporting tools, and Microsoft Office Solid understanding of GMP, ISO standards, and cleanroom protocols Excellent problem-solving, communication, and organisational skills Essential Experience 35+ years experience in assembly and people leadership, including direct supervision in a cleanroom or regulated manufacturing environment Strong, hands-on knowledge of Lean manufacturing tools and methodologies Experience working to ISO, GMP, or equivalent regulatory frameworks Ability to manage competing priorities and deliver results in a fast-paced, quality-critical production setting High level of competence in manufacturing documentation and compliance reporting TPBN1_UKTJ

Created: 2025-12-16

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