QA Manager

UQUIFA; Madrid; Híbrido; EUR 45.000 - 60.000; Jornada completa

Descripción de la vacante

A pharmaceutical company in Madrid is seeking a Quality Assurance Manager responsible for implementing quality standards at their Sant Celoni plant. The ideal candidate will have at least 5 years of experience in Quality Assurance within the pharmaceutical sector, ensuring compliance with GMP guidelines. A fixed salary plus bonus and hybrid working conditions are offered.

Servicios

Indefinite-term contract

Salary package of fixed salary plus bonus

Hybrid work

Good training plan

Formación

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

Responsabilidades

• Establish and implement the quality standards to ensure regulatory compliance.
• Coordinate and certify the batch release process.
• Monitor quality analysis and identify process improvements.
• Supervise the quality assurance team.
• Train employees on quality system procedures.
• Manage the Quality Assurance documentation.
• Collect and analyze quality KPI indicators.
• Manage suppliers of starting materials and plant GMP services.
• Ensure compliance with applicable GMP and regulatory requirements.
• Support audits by customers and internal audits.

Conocimientos

Fluent in English

Problem analysis

Initiative

Flexibility

Multi-functional teamwork

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

• Establish 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.
• Support 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