Document Control Specialist - Manchester, United Kingdom - Proclinical
Description
Proclinical are partnering with a health technology organisation who are recruiting for an individual to join their team. The opening position is for a Document Control Specialist. This role is on a contract basis.***
Responsibilities:
- Enable actions affiliated with NCE/CAPA/PDV/EXT/SCAR/IACA records.
- Form solid partnerships with personnel at all levels of the organisation both internally and externally.
- You will exercise food judgment in generally outlined practices and policies in selecting strategies and practices for attaining solutions.
- Support in upholding quality hardcopy documents/records for filing in archive.
- To guarantee documents and records are accomplished and uphold correctly, you will interface and mediate with divisions.
- Guarantee conformance to ISO 13485 needs in documentation and records.
- Other duties may be assigned.
Key Skills and Requirements:
- At least 02 years of experience in a document control/quality/regulatory role would be ideal.
- Educated to an alevel degree level, corresponding college courses or work experience.
- Computer literacy.
- Communication skills both verbally and in writing.
- An organised individual with the ability to work well independently and analysis skills.
- A high attention to detail.
- Fluency in the English language.
- Knowhow of Agile EQMS software would be beneficial.
- Familiarity within a regulated setting would be beneficial.
- Expertise on quality management system procedures, for example: corrective actions.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
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