30 jul
|
Centrient Pharmaceuticals
|
Madrid
30 jul
Centrient Pharmaceuticals
Madrid
Quality Assurance Technician 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 improvement actions to achieve quality standards
Prepare reports which reflect relevant issues related to the quality of manufactured products
Manage and participate in staff GMP training program from all departments
Control research documentation for investigating mistakes, process change and recovering process
Develop and coordinate Validation Plan and Revalidation
Supervise the implementation of stability studies
Track periodic calibrations of plant’s instrumentation
Achieve objectives related to GMP and Good Housekeeping improvements (internal quality audits, validation plans, document control)
Prepare annual product reviews according to the products manufactured
Update Sops for the Quality Management Department
Review methodical analytics
Prepare for new processes VMP
Key user of SAP and other IT quality systems (Quality environment)
Participate in projects, committees and subcommittees representing QA role
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.
📌 Quality Assurance Technician (Madrid)
🏢 Centrient Pharmaceuticals
📍 Madrid