Project Delivery Partners

The Senior CQV Consultant leads validation activities for pharmaceutical operations, ensuring compliance with global regulatory standards.

The Senior Pharmaceutical Site Transfer Lead directs the full transfer of a pharmaceutical manufacturing facility, including operations, systems, technologies, and regulatory commitments, from the…

The Project Manager will lead cross-functional projects for sterile injectable drug products in Madrid, ensuring timely delivery of milestones in compliance with GMP and global regulatory standards.

The QA Validations Expert will lead validation activities across manufacturing, laboratory, and computerized systems, ensuring compliance with GMP standards and regulatory requirements.

The QA Validations Expert will lead validation activities across manufacturing, laboratory, and computerized systems in Madrid, ensuring compliance with GMP standards and regulatory requirements.

The Senior CQV Consultant will lead validation activities for sterile injectable pharmaceutical operations, ensuring compliance with global regulatory standards.

The QA Validations Expert will lead validation activities for manufacturing, laboratory, and computerized systems in Madrid, ensuring GMP and regulatory compliance.

Efor is seeking an Equipment Automation Specialist to configure, maintain, and troubleshoot automated pharmaceutical equipment such as lyophilizers, bioreactors, autoclaves, and filling lines…

This PI Engineer role in Madrid focuses on monitoring and improving pharmaceutical manufacturing processes using data analysis and digital tools.

PharmEng/Efor is seeking a QA Specialist with at least 5 years of experience in pharmaceutical or biotech quality assurance.

PharmEng / Efor is seeking a QC Specialist with at least 5 years of experience in pharmaceutical Quality Control to support deviation investigations, environmental monitoring, water system validation…

The Quality Assurance Specialist will ensure compliance with FDA, EMA, and GMP standards across pharmaceutical manufacturing and laboratory operations.

Efor is seeking an experienced LIMS Consultant to support a laboratory digitalization project, focusing on the design, configuration, and deployment of a Veeva Vault LIMS solution.

PharmEng / Efor is seeking a Mid-Level EHS Expert based in Madrid to independently manage EHS compliance programs, lead incident investigations, conduct risk assessments, and train staff across…