QA Scientist for Batch Release

Solutiaghs; Cerdanyola del Vallés; Presencial; EUR 30.000 - 45.000; Jornada completa

Descripción de la vacante

A scientific-technical services company is seeking a QA Scientist in Cerdanyola del Vallés. The role involves batch review, deviation management, and quality system improvement. The company offers flexible working hours, generous vacation days, and professional development opportunities.

Servicios

Flexible Working Hours

23 vacation days per year

Fully stocked canteen

Access to employee benefits platform

Professional development opportunities

Formación

• 2 years of experience in Quality Control or Manufacturing activities in Quality Assurance.

Responsabilidades

• Verify manufacturing and packaging records for pharmaceutical batch releases.
• Assess deviations and complaints to ensure GMP compliance.
• Support certification of batches for market release.

Conocimientos

Quality Control

GMP compliance

English

Educación

Life Sciences Degree

Descripción del empleo

Solutia Life Sciences (recruitment division of Solutia) specializes in technical and middle management profiles in the pharmaceutical, biotech, and medical device sectors.

We are currently selecting a QA Scientist for a scientific-technical services company serving businesses in the chemical-pharmaceutical and veterinary sectors, located in Cerdanyola del Vallés.

Responsibilities :

• Batch Review : Verify manufacturing and packaging records for pharmaceutical batch releases.
• Deviation & Complaint Management : Assess deviations, OOS / OOT, complaints, CAPA, and Change Controls to ensure GMP compliance.
• Batch Certification : Support certification of batches for market release or clinical trials.
• Quality Agreements : Review agreements with manufacturers and authorization holders, focusing on batch certification.
• Audit Collaboration : Participate in audits and inspections by clients and regulatory bodies.
• Quality System Improvement : Contribute to the ongoing enhancement of the quality system.

Here's what they offer :

• Flexible Working Hours and intensive schedule on Friday.
• 23 vacation days per year plus 24th and 31st of December.
• Fully stocked canteen and rooftop space (coffee, fruits, snacks, and beverages).
• Access to the employee benefits flexibility platform.
• Professional development and collaborative environment and a culture of empowerment.

Requirements :

• Life Sciences Degree
• 2 years of experience in Quality Control or Manufacturing activities in Quality Assurance in the Pharmaceutical Industry.
• Experience on Biologicals will be highly valued.
• A high level of English, both written and spoken is required for this position.