QA Batch Release

Solutia; Cerdanyola del Vallés; Presencial; EUR 30.000 - 50.000; Jornada completa

Descripción de la vacante

An established industry player in the life sciences sector is seeking a dedicated QA Scientist to ensure compliance and quality in pharmaceutical manufacturing. This role involves batch review, deviation management, and collaboration during audits. The company promotes a flexible work environment with professional development opportunities, making it an ideal place for those passionate about quality assurance in the pharmaceutical industry. Join a team that values empowerment and innovation in a collaborative setting.

Servicios

Flexible Working Hours

23 Vacation Days

Fully Stocked Canteen

Employee Benefits Flexibility Platform

Professional Development Opportunities

Formación

• 2 years experience in Quality Control or Manufacturing activities.
• High level of English required for this position.

Responsabilidades

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

Conocimientos

Quality Control

GMP Compliance

Deviation Management

Biologicals

English Communication

Educación

Life Sciences Degree

Descripción del empleo

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Direct message the job poster from Solutia

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.

Seniority level

• Seniority level Associate

Employment type

• Employment type Full-time

Job function

• Job function Quality Assurance
• Industries Pharmaceutical Manufacturing

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