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ANALYTICAL SPECIALIST Braine-l'Alleud

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The company

Our client is a professional Pharmaceutical and Biotechnology organisation, based in Waals-Brabant Belgium. The function of analytical specialist is positioned within the Quality Control Laboratory R&D (SPDC). The laboratory specializes in the development,validation and transfer of analytical methods for all products entering the site.

Analyzed pharmaceutical products are presented in different forms (solution, lyophilized solid, pre-filled syringes, etc.) and in different levels of development from Phase Clinic, Phase I to Phasemarketing. The laboratory also specializes in support via data generation required for the registration dossiers of our new products (determination of the profile ofdegradation, determination of product stability under normal / stressed conditions, etc.).

Role description

The function of the analytical specialist involves the generation of data in the laboratory as part of the
development and validation of new analytical methods and the monitoring of
product stability.

Responsibilities

Develops analytical methods in accordance with the specifications
Verifies, transfers and validates the analytical methods according to the appropriate requirements
Actively participates in stability studies of pharmaceutical products developed in R&D
Actively participate in pharmaceutical product development studies conducted in
R&D (formulation development, freeze-drying cycles, process development)
manufacturing, etc.)
Ensures all activities related to other types of studies in place at the QC laboratory in R&D
Ensures a complete follow-up of the studies under its responsibility in the respect of the procedures applicable

Requirements

Master / engineer with scientific orientation
Experience in the pharmaceutical industry, preferably in the laboratory of analysis or
development is desired.
Analytical Chemistry Oriented.
Good knowledge of current analytical techniques (UV / Visible Spectroscopy,
U / HPLC chromatography, GC, etc.) is essential. Knowledge of Validation Principles
analytical methods as well as pharmacopoeias is an asset.
Knowledge of good manufacturing and documentation practices and the system
quality of type Pharmaceutical Industry is desired.
A mastery of written English (reading) is required.

Other information



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

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SIRE Life Sciences®

Listed by: SIRE Life Sciences®
Listed on: 11-10-2018
Country: Belgium
Region: Waals-Brabant
Employment: Freelance
Expertise: 3 - 5 years
Location Type: On location
Education: Master
Language: French
Sector: Pharmaceutical
Specialisation: Quality

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Contact

SIRE Life Sciences B.V.

Mondriaan Tower
Amstelplein 52, 25th floor
1096 BC Amsterdam
+31 (0) 20 658 9800

SIRE Life Sciences Belgium BVBA

Science 14 Atrium
14b, Rue de la Science
1040 Bruxelles
+32 (0) 2 588 1277

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Fünf Höfe
Theatinerstraße 11
80333 München
+49 (0) 89 3803 8966

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SW1V3PQ London
+44 7307 179882

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