Centrient
Procesoperator C
Centrient Pharmaceuticals is de toonaangevende producent van bètalactamantibiotica en leverancier van statines van de volgende generatie en anti-schimmelmiddelen. Wij produceren en verkopen tussenproducten, actieve farmaceutische ingrediënten en afgewerkte doseringsvormen. We staan trots in het ce
Quality Assurance Technician
Centrient Pharmaceuticals is the leading manufacturer of beta-lactam antibiotics, and a provider of next generation statins and anti-fungals. We produce and sell intermediates, active pharmaceutical ingredients and finished dosage forms. We stand proudly at the centre of modern healthcare, as a make
Quality Assurance Technician
MS&T Head
•Develop a strategy on a range of technical projects including new product development, process technology transfers, implement operational excellent combine with continuous improvement projects and capital upgrade projects. •Involved in setting and supporting network strategy execution •Drive funct
Technician Mechanical
Centrient Pharmaceuticals is de toonaangevende producent van bètalactamantibiotica en een leverancier van statines van de volgende generatie en antischimmelmiddelen. Wij produceren en verkopen tussenproducten, actieve farmaceutische ingrediënten en afgewerkte doseringsvormen. We zijn een farmaceutis
Technician E&I
Centrient Pharmaceuticals is de toonaangevende producent van bètalactamantibiotica en een leverancier van statines van de volgende generatie en antischimmelmiddelen. Wij produceren en verkopen tussenproducten, actieve farmaceutische ingrediënten en afgewerkte doseringsvormen. We zijn een farmaceutis
Maintenance Engineer E&I
Centrient Pharmaceuticals is the leading manufacturer of beta-lactam antibiotics, and a provider of next generation statins and anti-fungals. We produce and sell intermediates, active pharmaceutical ingredients and finished dosage forms. We are a pharmaceutical company with a clear Purpose: to impro
Lead Technician E&I of Mechanical
Centrient Pharmaceuticals is de toonaangevende producent van bètalactamantibiotica en een leverancier van statines van de volgende generatie en antischimmelmiddelen. Wij produceren en verkopen tussenproducten, actieve farmaceutische ingrediënten en afgewerkte doseringsvormen. We zijn een farmaceutis
Facility & Civil Manager
Centrient Pharmaceuticals is de toonaangevende producent van bètalactamantibiotica en een leverancier van statines van de volgende generatie en antischimmelmiddelen. Wij produceren en verkopen tussenproducten, actieve farmaceutische ingrediënten en afgewerkte doseringsvormen. We zijn een farmaceutis
Specialist, Regulatory Affairs FDF
Supporting the RA-FDF Team and contributing in the regulatory activities in order to achieve the objectives of the department which are: obtaining global approval for CENTRIENT products, including the lifecycle management of the registration dossiers according to business planning. Key Individual Ac
WWTP Supervisor
Manage environment performance of production including wastewater and waste gas to deliver agreed environment target for coverage and MOPEX with full compliance to local and global SHE and quality requirements. In addition, continuously improve performance in all the responsibilities areas under the
Production Manager
•Responsible for SHE& Quality compliance in production department. •Responsible for implementation of safety bi-system in production department. •Department budget and cost management & KPIs including Variable cost / MOPEX / Coverage / Quality •People Management of production department •Continuous
Executive - Quality Assurance
To ensure that the Products provided to the market are tested as per Customer specifications and in compliance with applicable pharmacopoeias as well cGMP/GLP/ICH/USFDA /ISO guidelines. Key Responsibilities: To participate in vendor qualification activities. To participate in Internal/External audit
Officer - Quality Control
Position Description : Position ensures that the products provided to the market are tested as per customer specifications and in compliance with applicable pharmacopoeias as well cGMP/GLP/ICH/USFDA/ISO guidelines. Key Responsibilities: Analysis of Finished products / raw materials/ in process & sta