# Quality Assurance Systems Officer

**Company:** [Demo S.A.](http://jobs.workable.com/companies/bfFZ3SuxMR5zjdkBWmB1yU.md)
**Location:** Athens, Greece
**Workplace:** on site
**Employment type:** Full-time
**Department:** Quality Assurance

[Apply for this job](http://jobs.workable.com/view/8556b778-389f-4609-9ce3-e40dbc41e0a8)

## Description

At Demo SA, one of the world’s largest pharmaceutical manufacturers in injectable facilities, we are currently looking for a high-performing Quality Assurance Systems Officer.

**Main duties and responsibilities:** 

-   Εvaluations and revaluation of manufacturers, suppliers and third-party sub-contractors, as well as for sending complaints and monitoring of corrective actions.
-   Perform audits according to the relevant standards on behalf of DEMO to manufacturers and suppliers.
-   Evaluate and analyze change control notifications from manufacturers and suppliers. Monitor of completion of relevant actions within DEMO S.A QMS.
-   Issue Technical and Quality Contracts with manufacturers and suppliers. In particular, generation of the document, distribution, review, approval and monitoring of signing of the document.
-   Assist the regulatory department with providing the necessary documentation for supporting regulatory initial submission, variation and renewal applications.
-   Conducting the deviation investigations, the change controls and the reported complaints with their respective investigations, resulting from the processes under his/her supervision, including the follow up of the CAPA plan.
-   Schedule, monitor, perform and archive Internal Inspections.
-   Implement and monitor the progress of the Corrective and Preventive Action Plan resulting from findings/observations of either Internal Audits and/or Audits from customers/organizations/authorities.
-   Issue the Quality Management Review Report. Under this scope, OOS, DIR, Complaints, Audits, CAPAs, Suppliers Complaints, Suppliers List, SOPs list, HR Data, PV Data, Rejected-Produced batches, presentation of customer satisfaction data should be collected, GMP changes should be evaluated and determined.
-   Writes/revises master documents, Forms, Standard Operating Procedures (SOPs), specifications, etc. within the DEMO document management system.
-   Monitor facility pest control service.

## Requirements

-   BSc Degree in Chemical Engineering, Chemistry, Biology or Pharmacy. MSc Degree in Quality Management or relevant field will be considered an asset.
-   Previous Experience in QA sector in Pharmaceutical Industry or in Production.
-   Fluent oral and written skills in Greek & in English.
-   Computer literacy (Microsoft Word, Excel, Access, Outlook), Working knowledge of SAP is desirable.
-   Self-motivated & results oriented with ability to cope with strict timelines.
-   Ability to deliver on complex project requirements and tasks.
-   Ability to work creatively, analytically with attention to detail.
-   Αbility to adapt to a frequently changing schedule.

## Benefits

The Company offers competitive remuneration, continuous learning and development opportunities, and a friendly and challenging working environment.