Document Control Specialist

4 months ago


Manchester, United Kingdom Proclinical Full time

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 0-2 years of experience in a document control/quality/regulatory role would be ideal.
- Educated to an a-level 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.
- Know-how 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.

Proclinical Staffing is an equal opportunity employer.

LI-MM1

QACompliance


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