Documentational Analyst

Há 1 mês


Oeiras, Portugal GIGROUP Tempo inteiro

Our client is a company that operates in the pharmaceutical industry and is well recognized at a national level, for meeting the health needs of the current scenario, with high quality products in an accessible way.

As part of strengthening their team, they are recruiting a Validation Analyst (M/F) for the Sintra area.

**Your day to day**:

- Manages the purchase orders for all external services, including:
request quotes, issue purchase orders (PDC’s), book services.
- Updates budget control
- Updates Validation documents, such as SOP’s, ASSR’s, VAPR’s
- Assures that documentation related to the functioning of the department, such as protocols, reports, calibration certificates, etc. is updated, easily traceable from the database, and properly filed
- Executes simples IOPQ’s, such as scales, particle counters. Supports the Validation Engineers in qualification activities and issuing reports
- Carries out archiving of the documentation of Validation New Projects
- Reviews and approves Calibration/Validation forms from the Validation Department;
- Controls CAPA’sand change Controls

**Requisitos**:

- Bachelor in Pharmacy;
Biochemistry or similar(preferred)
- Experience
- Fluent in English

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