QC Data Review Specialist — GMP, HPLC & Data Integrity

Bial; Trofa; Sur place; EUR 32 000 - 52 000; Plein temps

Résumé du poste

Bial is seeking a QA Data Review Specialist for the Quality Control Laboratory in Portugal. You will review analytical data, calculations, chromatograms and records to ensure GMP compliance and data integrity.

You will support investigations and batch release, contributing to continuous improvements within the lab. The role requires a degree in Pharmaceutical Sciences or related field and 2–3 years of QC lab experience, with hands-on HPLC experience and knowledge of GC, KF and dissolution

Qualifications

• Requires degree in Pharmaceutical Sciences, Chemistry, Biochemistry or related field.
• 2–3 years of QC laboratory experience in pharma.
• Hands-on analytical testing in GMP environment.
• Strong knowledge of GMP and Data Integrity principles.

Responsabilités

• Review analytical raw data, chromatograms, worksheets and lab records to ensure accuracy and traceability.
• Ensure records comply with GMP, pharma standards and internal procedures.
• Collaborate with analysts and supervisors for timely batch release.
• Support GMP implementation and continuous improvement in analytical review processes.
• Participate in audits and inspections and support Quality Control activities.

Connaissances

Data review

GxP compliance

Analytical mindset

Effective communication

Formation

Pharmaceutical sciences degree or related field

Outils

HPLC

GC

KF

Dissolution testing

Description du poste

Bial is seeking a QA Data Review Specialist for the Quality Control Laboratory in Portugal. You will review analytical data, calculations, chromatograms and records to ensure GMP compliance and data integrity.

You will support investigations and batch release, contributing to continuous improvements within the lab. The role requires a degree in Pharmaceutical Sciences or related field and 2–3 years of QC lab experience, with hands-on HPLC experience and knowledge of GC, KF and dissolution