Training Documentation Controller for GMP

PQE Group is seeking an experienced Compliance Support Specialist to bolster GMP compliance for an aseptic manufacturing project in Spain. The role focuses on reviewing and harmonizing quality documentation and SOPs to meet FDA and EU GMP standards, ensuring readiness for audits and inspections. The successful candidate will collaborate with QA,...

We are hiring a Quality Assurance Scientist for our GMP area of Quality Assurance Department.No espere a enviar su solicitud después de leer esta descripción; se espera un gran volumen de candidaturas para esta oportunidad.The QA Scientist will be assigned the following responsibilities:Review and approve the documentation involved in the analytical...

We are hiring a Quality Assurance Scientist for our GMP area of Quality Assurance Department. The QA Scientist will be assigned the following responsibilities: - Review and approve the documentation involved in the analytical activity of the company: CoA, protocols, reports, SOPs, product specifications. - Auditing the analytical documentation issued by...

We are hiring a Quality Assurance Scientist for our GMP area of Quality Assurance Department. The QA Scientist will be assigned the following responsibilities: Review and approve the documentation involved in the analytical activity of the company: CoA, protocols, reports, SOPs, product specifications. Auditing the analytical documentation issued by the...

Current job opportunities are posted here as they become available.Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management,...

We are hiring a Quality Assurance Scientist for our GMP area of Quality Assurance Department. The QA Scientist will be assigned the following responsibilities: Review and approve the documentation involved in the analytical activity of the company: CoA, protocols, reports, SOPs, product specifications. Auditing the analytical documentation issued by the...

Grifols, S.A is seeking a Manufacturing Process Evaluation Specialist within the Product Quality area of the Quality Assurance division to support robust process control and compliant documentation. You will analyze incidents, coordinate corrective actions, review qualification/validation documentation, and prepare audit-ready reports for national and...

KYMOS GROUP in Spain is seeking a motivated Quality Assurance Intern to join our Batch Release team, with a focus on preparing Product Quality Reviews (PQRs) in compliance with EU GMP Annex 21. This internship offers hands-on experience in pharmaceutical quality systems, documentation management, and collaboration with QA professionals in a highly regulated...

KYMOS GROUP in Spain is seeking a motivated Quality Assurance Intern to join our Batch Release team, with a focus on preparing Product Quality Reviews (PQRs) in compliance with EU GMP Annex 21. This internship offers hands-on experience in pharmaceutical quality systems, documentation management, and collaboration with QA professionals in a highly regulated...