#

Quality Assurance Analist

SIRE Life Sciences®

Belgium, zagranica

SIRE Life Sciences®

Quality Assurance Analist

Location: Belgium

SIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!

THE COMPANY

Our client is a professional Pharmaceutical organization, based in Antwerpen Belgium.

The passion of the company is to improve the lives of all their patients. They are an healthy and growing organization who is focused to develop new treatments.

ROLE DESCRIPTION

This is an overarching role where you, as QA Analyst, are responsible for the quality assessment and evaluation of locally produced medicines based on the results of the inspections performed and the review and evaluation of the batch documentation. You will work closely with the Production department and support departments and helps to design, continuously improve and follow up control systems, as well as train colleagues and share knowledge within the teams. This function supports the QO Engineer in handling quality deviations and manages the planning to release batches.

RESPONSIBILITIES

As QA Analyst you take care of the continuous improvement and control of the quality processes within the team: for example by writing and adjusting QA-related procedures, reporting atypical incidents that you have established, charting points for improvement in the batch documentation process and other specific assignments.
The following tasks fall under your authority:
- Performing the review of the batch documentation of aseptic bulk and semi-finished products and underlying processes.
- The input of test results in LIMS.
- The QA release of water and bulk locks and underlying processes.
- Follow-up, planning and preparation of batch-related documentation to batch release.
- The preparation of batch-specific certificates.
- The administrative and technical support in, among other things, dealing with deviations in gQTS, together with the QO Engineer.

REQUIREMENTS

- Bachelor or master degree in a life sciences field
- 3 years of experience within a quality or production environment
- Quality minded and knowledge of cGMP
- Fluent in English and Dutch
- Able to work with computer programs like LIMS and SAP (or at least able to learn this in a small amount of time)
- Strong team player who is also able work alone

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Valentijn de Krom.

Prosimy o aplikowanie poprzez przycisk znajdujący się po prawej stronie ogłoszenia.
SIRE Life Sciences®

Czy chcesz otrzymywać oferty pracy na podobne stanowiska?

Utwórz powiadomienie e-mail
Zapisz mnie

Zapisani kandydaci otrzymują informacje jako pierwsi.

Podziel się ze znajomymi