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 maker of essential and life-saving medicines.
With our commitment to Quality, Reliability and Sustainability at the heart of everything we do, our over 1.600 employees work continuously to meet our customers' needs. We work towards a sustainable future by actively participating in the fight against antimicrobial resistance.
Founded 150 years ago as the ‘Nederlandsche Gist- en Spiritusfabriek', our company was known as Gist Brocades. Headquartered in Rotterdam (Netherlands), we have production facilities and sales offices in China, India, the Netherlands, Spain, the United States and Mexico. Centrient Pharmaceuticals is wholly owned by Bain Capital Private Equity, a leading global private investment firm.
Quality Assurance Technician
The Main Activities And Responsibilities
Review and sign the Certificate of Analysis for Customers, checking CSO when applicable
Review and test preparation shipments
Manage internal quality audits and Good housekeeping and propose improvements actions to achieve quality standards
Prepare reports which reflect relevamt issues related to quality of manufactured products
Manage and participate to staff GMP's training program from all departments




Control research documentation for investigating mistakes, process change and recovering process
Develop and coordinate Validation's Plan and Revalidation.
Supervise the implementation of stability studies
Tracking periodic calibrations of plant's instrumentation.
Achieve objectives related to the standards GMP and Good Housekeeping improvements (internal quality audits, validation plans, document control)
Prepare annual product reviews according to the products manufactured
Update Sop's Quality Management Department
Review methodical analytics.
Prepare for new processes VMP
Key user's SAP and others IT quality systems (Quality environment)
Participate on project, committees and subcommittees representing QA role
The Idóneo Candidate
Bachelor degree.
Fluent in both English and Spanish
Knowledge of audit quality procedures
Knowledge of Quality Control (QC), particularly in the management of OOS
Minimum of 2 years of experience in a similar role
Terms and reward
We offer a local contract in a challenging, comprehensive, operational environment, with many opportunities for personal input and growth and plenty of discussions with other professionals. The organization is very flat. You have a lot of freedom and responsibility in an open, direct, and informal atmosphere.
The Procedure
Reference check procedures are part of the Centrient Recruitment & Selection Process. You will be contacted when a reference check is required.
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📌 Quality Assurance Technician (España)
🏢 Centrient Pharmaceuticals
📍 España