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QC Analyst / Perm / Bio / Pharma / nearby Ghent / QMS & ICH

SIRE Life Sciences®

Belgium, zagranica

SIRE Life Sciences®

QC Analyst / Perm / Bio / Pharma / nearby Ghent / QMS & ICH

Location: Belgium
SIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences 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!Our client is a professional Pharmaceutical and Biotechnology organisation, based in Oost-Vlaanderen Belgium.

The Company

They provide high-quality, customized drug development solutions. Our client focuses is to support clients on the earliest phases of their development pathway. Our client is based in Belgium, nearby Ghent. They are looking for a QC Analyst with QA knowledge, are you the one?

Role Description

Our client wishes to enforce its team with a QC Analyst. They are looking for a person who is flexible, problem solving and quality minded. Also do you need to write and speak fluent Dutch and English. Also will you be reporting to the QC Manager.

Curious what your responsibilities will be?

Responsibilities

As a QC Analyst with QA knowledge and maybe with even QA experience, you will be responsible for...

...supporting the maintenance, calibration and qualification of the analytical equipment.
...performing Quality Control activities according to instructions, procedures and protocols in compliance with the GMP principles and the Quality Management System.
...validating analytical methods to support the quality control
...performing Quality Control analyses.
...supporting preparation of the applicable protocols and reports.
...performing ICH compliant stability studies.
...accurately reporting, documenting and reviewing the analytical test results.

Requirements

Exciting about your responsibilities? Read further to know if you match!

Our client ask the following competences and education from their potential employee:
- BSc. Biomedical laboratory technology, Chemistry or Pharmaceutical Sciences.
- A minimum of 3 years relevant professional experience.
- You are fluent in Dutch and English (written and spoken).
- Experience in a regulated Quality Control (HPLC/UPLC, Dissolution) is a must.
- You are punctual and are able to work independently.

Other information

Our client offers you a better position with responsibility within a dynamic company. Also does our client encourage personal development.

Heb je interesse en wil je meer weten over deze functie, reageer dan door op solliciteer te klikken en contact op te nemen met Diana Prieto Reyes
Prosimy o aplikowanie poprzez przycisk znajdujący się po prawej stronie ogłoszenia.
SIRE Life Sciences®

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