QA Manager

UQUIFA; Sant Celoni; Híbrido; EUR 45.000 - 65.000; Jornada completa

Descripción de la vacante

A leading pharmaceutical company is seeking a Quality Assurance Manager for its Sant Celoni plant. The role involves managing the quality assurance department, implementing quality standards, ensuring regulatory compliance, and supervising a dedicated team. Candidates should possess a degree in Pharmacy, Chemistry, or Health Science, and have over 5 years of experience in Quality Assurance within pharmaceutical sites. This role offers an indefinite-term contract and a hybrid work model.

Servicios

Indefinite-term contract

Salary package with bonus

Good training plan

Formación

• 5+ years of Quality Assurance experience in Pharmaceutical sites under GMP guidelines.

Responsabilidades

• Implement quality standards to ensure regulatory compliance.
• Ensure and coordinate batch release process.
• Monitor quality analysis for improvements.
• Supervise quality assurance team.
• Train employees on quality system procedures.
• Manage documentation for the Quality Assurance department.
• Analyze quality system indicators (KPIs).
• Manage suppliers of starting materials.
• Ensure compliance with GMP and regulations.
• Support audits by customers and internal audits.

Conocimientos

Fluent in English

Initiative and flexibility

Problem analysis

Cross-functional collaboration

Educación

Degree in Pharmacy, Chemistry or Health Science

Descripción del empleo

About The Role

As a Quality Assurance Manager at Uquifa Spain, you will be responsible for the management of the quality assurance department implementing any quality standards that the company decides at the Sant Celoni plant.

Primary Responsibilities

• Estables and implement the quality standards of the products, processes and systems of the Sant Celoni plant to ensure the required regulatory compliance.
• Ensure, coordinate and certify the batch release process.
• Monitor quality analysis and identify process improvements and process monitoring.
• Supervise and coordinate the quality assurance team.
• Train other employees on quality system procedures.
• Manage the Quality Assurance department's own documentation.
• Collect and analyze quality system indicators (KPI’s) and coordinate periodic meetings for review by the Site Leadership Team.
• Manage suppliers of starting materials and plant GMP services.
• Keep up to date on laws and regulations to ensure compliance with applicable GMP and regulatory requirements.
• Supporting audits by customers and Internal audits.

Experience And Attributes We Value

• Degree in Pharmacy, Chemistry or Health Science.
• 5+ years of Quality Assurance experience in Pharmaceutical sites under GMPs guidelines.
• Fluent in English.
• Full of initiative, flexible, and capable of analyzing problems on.
• Able to operate effectively across multi-functional teams.

What's on Offer

• Indefinite-term contract
• Salary package of fixed salary plus bonus
• Hybrid work
• Good training plan