ppCentrient 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. /p pWe stand proudly at the centre of modern healthcare, as a maker of essential and life‑saving medicines. /p pWith 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. /p pFounded 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. /p h3Quality Assurance Technician /h3 h3The main activities and responsibilities /h3 ul liReview and sign the Certificate of Analysis for Customers, checking CSO when applicable. /li liReview and test preparation shipments. /li liManage internal quality audits and Good housekeeping and propose improvements actions to achieve quality standards. /li liPrepare reports which reflect relevant issues related to quality of manufactured products.



/li liManage and participate to staff GMP's training program from all departments. /li liControl research documentation for investigating mistakes, process change and recovering process. /li liDevelop and coordinate Validation's Plan and Revalidation. /li liSupervise the implementation of stability studies. /li liTracking periodic calibrations of plant's instrumentation. /li liAchieve objectives related to the standards GMP and Good Housekeeping improvements (internal quality audits, validation plans, document control). /li liPrepare annual product reviews according to the products manufactured. /li liUpdate Sop's Quality Management Department. /li liReview methodological analytics. /li liPrepare for new processes VMP. /li liKey user's SAP and other IT quality systems (Quality environment). /li liParticipate on project, committees and subcommittees representing QA role. /li /ul h3The Idóneo Candidate /h3 ul liBachelor degree. /li liFluent in both English and Spanish. /li liKnowledge of audit quality procedures. /li liKnowledge of Quality Control (QC), particularly in the management of OOS. /li liMinimum of 2 years of experience in a similar role. /li /ul h3Terms and reward /h3 pWe 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. /p /p #J-18808-Ljbffr

📌 Quality Assurance Technician (Santa Perpètua de Mogoda)
🏢 Centrient Pharmaceuticals Netherlands
📍 Santa Perpètua de Mogoda