Quality Document Controller – Medical Devices

SANMINA-SCI TECHNOLOGY INDIA PRIVATE LIMITED; Fermoy; On-site; EUR 32,000 - 42,000; Full time

Job summary

Sanmina Fermoy in Fermoy, Ireland, seeks a Document Controller to manage and control company documents, ensuring compliance with ISO and FDA quality systems.

The role reports to the Quality Lead within the Quality Department and involves maintaining master documentation, change control processes, and supporting internal audits in a manufacturing environment. You will train staff on document control systems, generate reports, and help ensure traceability and regulatory readiness.

Qualifications

• 1-2 years Document Control or related experience.
• Familiarity with ISO and FDA Quality Systems Regulations.
• Proficiency with PC and Microsoft Office Suite.
• Strong problem-solving and communication skills.
• Ability to work effectively in a team and manage multiple tasks.

Responsibilities

• Administers document control procedures to ensure regulatory compliance.
• Maintain master documentation (soft and hard copies) such as SOPs, protocols, forms.
• Ensure current revision documents are available for use in the plant.
• File and retrieve quality records per retention policies.
• Update document control logs and train staff on systems.
• Support external audits and generate reports as required.
• Collaborate with cross-functional teams on documentation improvements.
• Ensure adherence to company policies including safety regulations.

Skills

Document control

Quality Systems Familiarity

Microsoft Office

English proficiency

Organizational skills

Team collaboration

Problem solving

Tools

Agile

Change Management System

Job description

Sanmina Fermoy in Fermoy, Ireland, seeks a Document Controller to manage and control company documents, ensuring compliance with ISO and FDA quality systems.

The role reports to the Quality Lead within the Quality Department and involves maintaining master documentation, change control processes, and supporting internal audits in a manufacturing environment. You will train staff on document control systems, generate reports, and help ensure traceability and regulatory readiness.