Centrient Pharmaceuticals Netherlands

Purpose of the Role:- Reporting to the Global QA Director CSV and Data Integrity, providing governance and services to Global IT and supporting the global audit programme. Ensure global GMP applications (SAP, Trackwise, Master Control, Veeva and Infrastructure) compliance with CSV and Data Integrity

Centrient Pharmaceuticals es el principal fabricante de antibióticos betalactámicos y proveedor de estatinas y antifúngicos de nueva generación. Producimos y vendemos productos intermedios, ingredientes farmacéuticos activos y formas farmacéuticas acabadas. Nos sentimos orgullosos de estar en el cen

Purpose of the Role : The IT project leader leads IT projects from initiation to business value realization, designs and implements information processes and systems, acts as Subject Matter Expert, and develops the portfolio according to IT and business strategy. Key Responsibilities: Manages projec

The Global Vice President Portfolio Strategy, Product Management & Marketing owns Centrient’s portfolio growth agenda by connecting market opportunities, customer needs, competitive dynamics and operational capabilities into profitable portfolio, pricing and investment decisions. The role serves as

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

Purpose of the Role: Support Global API controller in communicating insightful financial information which can be translated into effective commercial strategy. Preparation of Monthly Business Reporting, Budget, RAF and strategic business plans for the Franchise. Monitor and control the financial pe

The Role is responsible for reviewing the Batch Production Record, Issuance and Reviewing the Product Labels. Release of finished products, Verification activities of finished goods at the sites. Key Individual Accountabilities: Handing & tracking of QMS related activities CAPA, Deviations, Customer

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

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

•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

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

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

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

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

•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

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

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