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QC - Technician

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The company

Our client is a professional Pharmaceutical, Biotechnology and Clinical Research organisation, based in Brabant Wallon Belgium. The company is a global biopharmaceutical company headquartered in Brussels, Belgium. That specializes in the therapeutic areas of neurological disorders and immunology. The key element of the evolution of the company is to focus on creating value for the patient. The company uses all the tools, channels and scientific advances available to develop a better understanding of different expressions of a disease and thus better meet the needs of patients.The entire company employs more than 7,500 people in nearly 40 countries.

As part of our growth, within the Quality Control department, you join the team dedicated to NBE (New Biological Entities) as Quality Control Analyst H / F. You perform the analytical tests in accordance with the instructions received under the pre-established conditions of time, technical compliance and safety.

Role description

Perform control of finished pharmaceutical products in bulk or packaged in accordance with pre-established work instructions and procedures
Participate in the program of maintenance and / or qualification of the apparatus of the laboratory according to your competences
Ensure, if necessary, the follow-up of the calibration of the laboratory equipment
Participate in the planning task, and thus ensure, with the help of the supervisor, the follow-up of the schedule so as to respect the deadlines on each batch to be analyzed
Ensure the inventory of consumables and recommend / report in a timely manner the equipment necessary for the operation of the laboratory to avoid any cessation of activity
Participate and ensure compliance with the housekeeping / 5S program of the laboratory.
Participate actively in the investigations to be carried out during non-compliant or aberrant analytical results
Propose to the Laboratory Manager any measure (choice of apparatus, reagents, methods, organization of work, modification of procedures, training needs, etc ...) to reduce delays and costs on the one hand, and to improve the accuracy and accuracy of tests on the other hand

Responsibilities

Qualifications and Experience Required
Graduate, Bachelor or equivalent in the fields of Chemistry, Biochemistry, Biology
Previous experience in an environment subject to GMP, GMP, ICH standards is desired.
Previous experience in a Quality Control Department is an asset
A mastery of chemical analysis techniques including HPLC is required
A mastery of biochemical analysis techniques such as Bioassays, ELISA, electrophoresis gels, capillary electrophoresis is desired
Good handling under aseptic conditions
A good knowledge of technical English read and write is desired

Requirements

You like working in a team but have a great sense of autonomy
Dynamic, active, you are proactive and able to make decisions
You have the attention to detail, quality work and you want to invest yourself
You respect the deadlines and your hierarchy
The QC department sometimes requires very short deadlines, you have the ability to handle the stress if necessary



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SIRE Life Sciences®

Listed by: SIRE Life Sciences®
Listed on: 07-08-2018
Country: Belgium
Region: Waals-Brabant
Employment: Permanent
Expertise: 3 - 5 years
Location Type: On location
Education: Bachelor
Language: English
Sector: Pharmaceutical
Specialisation: Quality

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