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QC product officer

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The company

Our client is a professional Pharmaceutical, Biotechnology and Clinical Research organisation, based in Flandre Orientale Belgium. The company is a leading organization for contract development and production for the pharmaceutical and biotechnology industry.

The company is recognized between four investment banks that offer additional expert services.

Within the Business Unit "Drug Development & Manufacturing" (DDM),
located in Ghent, we are looking for one

Role description

The production officer supports GMP documentation (BRDs, deviations, modifications, CAPAs, SOP / WI, clean-up verification protocols / reports). The production officer carries out GMP production tasks (cleanroom, packaging and label).

Responsibilities

Implement GMP guidelines with documentation to production activities according to the current quality management system (documentation) and the provided training
Stay informed of the GMP Quality Management system. if necessary, switch the procedure documents.
Give input / suggestions about production related processes, efficiency, technical problems
Follow Good Documentation Practice when setting and using GMP batch record documentation
Report and document previous problems during the implementation of GMP production
Keep the training record up-to-date
Design GMP production documentation

Requirements

GMP production
Design-related GMP documents:
(Master) Batch registration documents with respect to the GDP / GMP guidelines for production, primary and secondary packaging and labeling of materials for clinical trials
Non-conformities (deviations, changes, CAPAs, risk assessments)
Procedural documents
Cleaning protocols / reports
Assist (hands-on) during production activities:
Picking and picking verification of materials needed for GMP production
Performance of line clearance and line clearing activities for GMP productions
Preparation of pharmaceutical GMP formulations (such as capsules, liquids, semi-solids, tablets, ...) in a clean room environment using manual and (semi) -automatic techniques
Primary and secondary packaging of GMP materials
Design of clinical labels, printing and quality control
Clinical labeling of GMP materials
Knowledge, experience, profile
Bachelor degree, preferably in the life sciences
Good technical writing skills
Knowledge of GMP / GDP regulations
Hands-on attitude
Fluent in English (written and spoken)
Fluent in Microsoft Office (Word, Excel)
Able to set priorities and manage several in a flexible way.



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SIRE Life Sciences®

Listed by: SIRE Life Sciences®
Listed on: 10-08-2018
Country: Belgium
Region: Oost-Vlaanderen
Employment: Permanent
Expertise: 3 - 5 years
Location Type: On location
Education: Bachelor
Language: Dutch
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

SIRE Life Sciences Deutschland GmbH

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

SIRE Life Sciences UK

702 Howard House Dolphin Square
SW1V3PQ London
+44 7307 179882

SIRE Life Sciences Maastricht

ROOOMS Maastricht
Boschstraat 21
6211 AS Maastricht


SIRE Group GmbH

Platz 3
6039 Root
Luzern
+41 (0)43 508 1743

SIRE Staffing Solutions

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+31 (0) 20 658 9804

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SIRE Healthcare

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Amstelplein 52, 25th floor
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SIRE Finance

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1096 BC Amsterdam
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1096 BC Amsterdam
+31 (0) 85 044 4620

SIRE Staffing

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Amstelplein 52, 25th floor
1096 BC Amsterdam
+31 (0) 85 044 4650

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