Analytical specialist (level 2)
Location: BelgiumSIRE® 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 organisation, based in Brussels Hoofdstedelijk Gewest Belgium.
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.).
development and validation of new analytical methods and the monitoring of
product stability.
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
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.
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.
The Company
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 thedevelopment and validation of new analytical methods and the monitoring of
product stability.
Responsibilities
Develops analytical methods in accordance with the specificationsVerifies, 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 orientationExperience 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.
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.
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