Job Search and Career Advice Platform

Enable job alerts via email!

Assembly Supervisor

Pertemps

Broxtowe

On-site

GBP 35,000

Full time

13 days ago

Generate a tailored resume in minutes

Land an interview and earn more. Learn more

Job summary

A well-established pharmaceutical manufacturer in the UK is seeking a Pharmaceutical Assembly Supervisor to oversee cleanroom operations. The role requires proven experience in GMP-regulated production, strong leadership abilities, and a commitment to quality and compliance. You will lead a skilled team, ensuring production targets are met while maintaining the highest standards of safety and quality. This full-time position offers competitive salary and permanent contract options.

Qualifications

  • 3-5+ years of experience in assembly and leadership in a regulated manufacturing environment.
  • Proven experience as an Assembly Supervisor or similar.
  • Solid understanding of GMP, ISO standards, and cleanroom protocols.

Responsibilities

  • Supervise daily assembly operations in line with GMP and ISO standards.
  • Lead and develop a team of assembly operatives.
  • Plan and monitor production schedules to achieve output targets.
  • Maintain production, inspection, and compliance records.
  • Implement continuous improvement initiatives.
  • Ensure adherence to health, safety, and regulatory standards.
  • Investigate and resolve production issues.

Skills

Leadership and people-management
Analytical and process-driven mindset
Problem-solving skills
Communication skills
Organisational skills
IT proficiency (ERP/MRP, Microsoft Office)
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.

Get your free, confidential resume review.
or drag and drop a PDF, DOC, DOCX, ODT, or PAGES file up to 5MB.