Assembly Supervisor

688000482

£35,000 Per Annum

Full Time

Permanent

Toton, Nottinghamshire

Engineering And Technical

Posted 2 hours ago

Expires In 29 Days

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
  • 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
Please click to apply or call 01332 363000 opt 3