More jobs:
Assembly Supervisor
Job in
Nottingham, Nottinghamshire, NG1, England, UK
Listed on 2025-12-30
Listing for:
Meriden Media
Full Time
position Listed on 2025-12-30
Job specializations:
-
Manufacturing / Production
Production Manager, Manufacturing Engineer
Job Description & How to Apply Below
Pharmaceutical Assembly Supervisor
Circa £35k
Permanent Mon-Thu & Fri
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
- 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
- 3-5+ 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
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