GMP QA Specialist – APQR & Compliance Leader

ALK Nordic A/S; Madrid; Vor Ort; EUR 40.000 - 70.000; Vollzeit

Benefits dieser Stelle

Tailored training and professional growth

Collaborative culture of respect and integrity

Attractive salary and comprehensive benefits

Zusammenfassung

ALK Nordic A/S in Madrid is seeking a Quality Assurance Specialist to ensure compliance with GMPs and enhance product quality in pharmaceutical operations. The ideal candidate will have at least 3 years of experience in the pharmaceutical/biotech industry and a background in Chemistry, Pharmacy, or Biology.

This role includes performing Quality Assurance activities, reviewing technical reports, and supporting comprehensive training within a collaborative and innovative culture.

Qualifikationen

• Minimum of 3 years’ experience in the pharmaceutical/biotech industry.
• Fluent in English, both written and spoken.
• Strong interpersonal and leadership skills in dealing with a variety of cultures.

Aufgaben

• Perform Quality Assurance activities for maintaining internal Quality Systems.
• Review GMP technical and validation reports.
• Support Quality Release activities including Master batch records review.

Kenntnisse

Experience in pharmaceutical/biotech industry

Regulations for sterile medicinal products

Fluent in English

Knowledge of technology transfer projects

Interpersonal and leadership skills

Ausbildung

Studies related to Chemistry, Pharmacy, Biology or equivalent

Tools

SAP

Jobbeschreibung

ALK Nordic A/S in Madrid is seeking a Quality Assurance Specialist to ensure compliance with GMPs and enhance product quality in pharmaceutical operations. The ideal candidate will have at least 3 years of experience in the pharmaceutical/biotech industry and a background in Chemistry, Pharmacy, or Biology.

This role includes performing Quality Assurance activities, reviewing technical reports, and supporting comprehensive training within a collaborative and innovative culture.