Document Control Administrator

JR United Kingdom; Milton Keynes; On-site; GBP 30,000 - 40,000; Full time

Job summary

Une entreprise mondiale de produits médicaux recherche un Document Control and Administrator. Vous serez responsable de fournir un soutien administratif pour le système de gestion de documents électroniques, en assurant que tous les documents qualité soient correctement formatés et alignés avec les normes de l'entreprise. Ce poste requiert une attention exceptionnelle aux détails et des compétences solides en organisation et gestion du temps.

Qualifications

• Expérience avec un système de gestion de qualité, de préférence ISO 13485.
• Aptitude à naviguer dans de grandes bases de données de documents.
• Capacité à travailler sous pression avec un excellent sens de l'organisation.

Responsibilities

• Assurer que tous les documents qualité soient au bon format et selon les procédures.
• Gérer les opérations administratives quotidiennes dans le respect des politiques.
• Prendre en charge l'organisation de réunions de direction sur site.

Skills

Attention to Detail

Organizational Skills

Time Management

Collaboration Skills

Education

University Degree (STEM focused)

Tools

Trackwise

Microsoft Office Suite

Job description

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Client:

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Other

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EU work permit required:

Yes

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Job Views:

3

Posted:

06.06.2025

Expiry Date:

21.07.2025

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Job Description:

• Job Title: Document Control and Administrator
• Contract: Perm
• Location: Abingdon, Oxford

We are working on an exciting opportunity for a Document Administrator to join a global medical products and technologies company. Our client is focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care.

Job Summary

Your role as a Document Controller and Administrator is to provide all Quality Systems administrative support to enable the Oxford team to smoothly transition into the business’s electronic document management system (EDMS). You will ensure that all quality documents and required relevant records are in the correct format and templates for laboratory processes and support functions to work effectively. Although this a desk-based role, you will liaise closely with the laboratory team to ensure document content are correctly captured. You will also work with the quality and business teams as well as project managers.

You will also have a solid track record of successful administrative work and oversee all office administrative duties which will include ownership of ancillary roles including, but not limited to, documentation drafting, shipping, purchasing supplies, maintaining office inventories and scanning lab bench books and lab logbooks. You will be thorough and pay attention to detail and can work well with the team.

Key Duties and Responsibilities

• Ensure all quality documents, including, but not limited to Work Instructions, Technical Documents and SOPs, are in the right templates are formatted correctly and align with the company EDMS whilst adhering to procedures for Document Control.
• Cross-check documents with pre-existing quality documents.
• Provide document drafting, review and approval as part of equipment and software purchase and implementation.
• With the help of management and quality teams link quality work instructions to pre-existing SOPs.
• Ensure smooth day-day administrative operations, in compliance with policies and regulations.
• Take ownership of purchasing reagents, consumables, and equipment.
• Arrange and manage on-site leadership meetings and coordinate all associated accommodation, transport and catering.
• Review and optimize office policies and procedures٫ particularly documentation and filing systems.

Experience required

• STEM focussed (desirable) University Degree (or equivalent)
• Have experience with working in or with a quality management system, preferably to ISO 13485.
• Trackwise experience is highly desired
• Are adept at using and navigating large document repository databases.
• Having worked in/with Regulatory and Validation teams and QA would be beneficial.
• Having drafted User Requirement Specification, Validation Plans and be aware of IQ/OQ/PQ and 21 CFR Part 11 would be advantageous.
• Strong IT skills and knowledge of Microsoft Office Suite, principally, Word.
• Excellent organisational and time-management skills.
• The ability to prioritise tasks and work under pressure.
• Strong attention to detail.
• Having basic lab experience would be an advantage.
• Strong collaboration skills and experience of working within a team.