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Documentation Controller
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Documentation Contro....
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Documentation Controller

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1 Vacancy
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Jobs by Experience

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1-3 years

Job Location

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farranfore - Ireland

Monthly Salary

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Not Disclosed

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Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Req ID : 1643745

We are presently recruiting for a Document Controller / Documentation Specialist for our clients, an Engineering company in County Kerry. You will be Responsible for the timely, accurate and efficient management and implementation of documents including access and revision control aspects and will Drive the Documentation life cycle to ensure schedules are met and quality is maintained. You will ensure that accurate information is distributed throughout an organisation, on time, to the people who need it most. This is a full time, permanent position based in County Kerry.

Responsibilities include:

  • Responsible for the timely, accurate and efficient management and implementation of documents including access and revision control
  • Drive the Documentation life cycle to ensure schedules are met and quality is maintained
  • Work closely with subject matter experts, engineering project teams, support teams, and other stakeholders to create, maintain and approve high-quality documentation
  • Effectively manage documentation projects and deliver customer-focused documentation
  • Creation and revision of Standard operating procedure (SOPs) as required
  • Ensure compliance with all regulatory GMP, Safety and Environmental requirements
  • Participate and comply with Quality Management System (QMS) requirements
Ideal Candidate:
  • Experience working with GMP Documentation Management Systems and/or a willingness to learn GMP validation documentation development
  • Experience in a regulated industry (Pharmaceutical, Manufacturing, Quality, Tech Services) would be advantageous but not essential
  • High level of technical writing skills
  • Proficient in Microsoft Office (Word, Excel, PowerPoint)
  • Highest level of attention to detail and fast delivery
  • Experience of ISO would be advantageous

Salary is based on qualifications and experiences and in the region of 35 - 40,000. If you are interested please apply or email [email protected]



Experience working with GMP Documentation Management Systems and/or a willingness to learn GMP validation documentation development Experience in a regulated industry (Pharmaceutical, Manufacturing, Quality, Tech Services) would be advantageous but not essential High level of technical writing skills Proficient in Microsoft Office (Word, Excel, PowerPoint) Highest level of attention to detail and fast delivery Experience of ISO would be advantageous

Employment Type

Full Time

Company Industry

About Company

0-50 employees
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