Quality Assurance Technician

Centrient Pharmaceuticals Netherlands; Santa Perpètua de Mogoda; Presencial; EUR 28.000 - 42.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Local contract

Growth opportunities

Open atmosphere

Descripción de la vacante

Centrient Pharmaceuticals is seeking a Quality Assurance Technician to join our team in Spain. The role focuses on QA activities, audit procedures, and QC processes within a GMP environment.

The ideal candidate holds a Bachelor's degree, speaks English and Spanish fluently, and has at least two years of relevant experience. The position offers a local contract and opportunities for growth in a global pharma setting.

Formación

• Fluent in English and Spanish.
• Knowledge of audit quality procedures.
• Knowledge of Quality Control (QC).
• Minimum of 2 years of experience in a similar role.

Responsabilidades

• 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 relevant issues related to quality of manufactured products.
• Coordinate Validation plans and Revalidation.
• Supervise the implementation of stability studies.

Conocimientos

Bilingual English and Spanish

Quality Assurance

Audit procedures

Quality Control (QC)

GMP knowledge

Educación

Bachelor's degree

Herramientas

SAP

Descripción del empleo

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 relevant 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 methodological analytics.
• Prepare for new processes VMP.
• Key user's SAP and other IT quality systems (Quality environment).
• Participate on project, committees and subcommittees representing QA role.

The Ideal 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.