Document Control Specialist - Deeside, United Kingdom - ConvaTec
Description
Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence and critical care, and infusion care.
With around 10,000 colleagues, and a promise to be forever caring, our products and services are available in over 100 countries.
Our solutions provide a range of benefits, from infection prevention and protection of at-risk skin, to improved patient outcomes and reduced care costs.
The company is a constituent of the FTSE 100 Index (LSE:CTEC) and in 2021 revenues were over $2 billion.
Every day, our products improve the lives of millions of people around the world. We're hugely proud of this, which is why we're transforming our business to reach millions more.
Join us on our journey to #ForeverCaring as a Document Control Specialist and you'll drive progress that really means something.
Job Summary
A document control specialist is responsible for the timely, accurate and efficient preparation and management of documents.
They control the numbering, sorting, filing, storing and retrieval of both electronic and hard copy documents produced by technical teams, projects, or departments.
This role will be working specifically on projects and support for validations, improvements across the Deeside organization.This is a fixed term role until the end of Q1 2024.
Duties and Responsibilities
- Provides day to day management and maintenance of the EDMS
- Quality checks all documents on project for compliance with global and local procedures prior to issue
- Updates documents as required,
- Proficient in computer software programs such as, word processors, spreadsheet programs, and database systems.
- Conduct company audits to ensure documents are being followed correctly
- Work with auditors to maintain regulatory compliance
- Support training and guidance for the use of EDMS
- Develop procedures so that they are standardized
- Communicate and collaborate with project managers
- Manage the flow of documentation within the organization, Flag issues with documents and closely monitor progress of documents in workflow procedures
- Maintain confidentiality around sensitive information and terms of agreement
- Prepare adhoc reports on projects as needed
Principal Contacts
- Internal: Quality management, Engineering & Manufacturing departments, Global Quality, Technical and quality operations from different sites
- External: Notified bodies
Education/Experience/Qualifications
Requirements:
- Minimum requirements for these courses and posts are GCSE's (59/A-C) including English, and some experience related to this sector.
- Experience of electronic document management systems.
- Ability to analyze data and come to conclusions
- Great time management skills
- Ability to follow procedures exactly
- Good organizational skills
- Experience of Microsoft office suite
- Can work independently without much guidance
- Ability to communicate with team
Desirable but not required:
- Knowledge of ISO13485 & 900
- Knowledge of Documentum
- Root cause analysis
This is stepping up to a challenge.
This is work that'll
move you.
#LI-PD2
#LI-onsite
Beware of scams online or from individuals claiming to represent Convatec
Equal opportunities
Convatec provides equal employment opportunities for all current employees and applicants for employment.
This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law.
Notice to Agency and Search Firm Representatives
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