IMS Coordinator – Quality, Environmental & H&S

Andrews Recruitment Group

Harlow

Vor Ort

GBP 32.000 - 42.000

Vollzeit

14 Tage+

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

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Zusammenfassung

IMS Coordinator – Quality, Environmental & Health & Safety in Harlow, Essex. This role focuses on supporting and continually improving an Integrated Management System covering ISO 9001, ISO 14001 and ISO 45001 standards, not merely document control.

You will work closely with manufacturing teams to investigate issues, identify root causes and drive corrective and preventive actions, audits, data reporting and ongoing system enhancements.

Qualifikationen

  • Experience in manufacturing or production
  • Experience supporting a Quality Management System
  • ISO 9001 knowledge
  • Experience with internal auditing, CAPA, non-conformance management, document control or continuous improvement
  • Attention to detail and good communication across departments

Aufgaben

  • Assist development of an Integrated Management System.
  • Help integrate ISO 9001, ISO 14001 and ISO 45001 systems.
  • Maintain controlled quality documentation and records.
  • Carry out internal audits and document findings.
  • Support root-cause investigations and CAPA activities.
  • Coordinate Corrective and Preventive Actions and manage non-conformances.
  • Monitor CAPA completion and effectiveness and analyze quality data.

Kenntnisse

Quality management
Internal auditing
CAPA
Document control
Continuous improvement
Quality systems

Ausbildung

Internal Auditor qualification

Tools

Microsoft Office

Jobbeschreibung

IMS Coordinator – Quality, Environmental & H&S

Location: Harlow, Essex
Salary: Competitive + Benefits

Are you experienced with ISO 9001, Quality Systems, Internal Auditing or Integrated Management Systems within manufacturing?

We are recruiting for an IMS Coordinator to support and continually improve an Integrated Management System covering Quality, Environmental and Health & Safety standards.

Importantly, this is not simply a document-control position.

You will work directly with manufacturing and operational teams, helping investigate problems, identify root causes and drive corrective actions.

The Role
  • Support the development of an Integrated Management System
  • Help integrate ISO 9001, ISO 14001 and ISO 45001 systems
  • Maintain controlled quality documentation
  • Manage procedures, work instructions, policies and records
  • Carry out internal audits
  • Document audit findings
  • Support root-cause investigations
  • Coordinate Corrective and Preventive Actions
  • Manage non-conformances
  • Monitor CAPA completion and effectiveness
  • Analyse quality-performance data
  • Identify trends and improvement opportunities
  • Assist with risk assessments and inspections
  • Support employee quality and compliance training
  • Work closely with manufacturing teams to improve systems and processes
What We’re Looking For
  • Experience within manufacturing or production
  • Experience supporting a Quality Management System
  • ISO 9001 knowledge
  • Experience with some combination of:
    • Internal auditing
    • CAPA
    • Non-conformance management
    • Document control
    • Continuous improvement
    • Quality systems
  • Strong attention to detail
  • Good communication skills
  • Confident working across different departments
  • Good Microsoft Office and data-reporting capability

An Internal Auditor qualification and exposure to ISO 14001 or ISO 45001 would be advantageous.

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