CQV Expert
A Senior CQV Consultant will lead validation activities for pharmaceutical manufacturing equipment and processes.
Project Delivery Partners (PDP) is a specialized consultancy providing project management, commissioning, qualification, and validation (CQV) services primarily for the life sciences and…
A Senior CQV Consultant will lead validation activities for pharmaceutical manufacturing equipment and processes.
This senior leader directs the full transfer of pharmaceutical manufacturing facilities, including operations and regulatory commitments.
The Project Manager leads cross-functional projects for sterile injectable drug products. The role ensures milestone delivery in compliance with GMP and global regulatory standards.
The QA Validations Expert leads validation activities for manufacturing and laboratory systems. The role offers professional development and high-impact projects.
The QA Validations Expert leads validation activities for manufacturing and laboratory systems. The role offers professional development and high-impact projects.
This role involves designing and deploying Veeva Vault LIMS solutions for laboratory digitalization. You will configure systems, define business requirements, and ensure GxP compliance.
An EHS Expert will manage compliance programs and drive operational excellence. The role offers international exposure and professional growth opportunities. This is an on-site position in Madrid.
Process improvement engineer ensuring stable, compliant drug manufacturing at a pharma consultancy in Madrid. Monitors KPIs, builds dashboards, and drives GMP-compliant process changes.
A Senior CQV Consultant will lead validation activities for sterile injectable pharmaceutical operations. The role offers exposure to international regulatory environments and high-impact programs.
An Equipment Automation Specialist ensures automated pharmaceutical equipment operates reliably and complies with GMP standards.
Quality Assurance Specialist ensuring GMP, FDA and EMA compliance for pharmaceutical manufacturing. Reviews batch records, audits operations, and manages deviations and CAPAs.
QA Validations Expert leading validation activities across manufacturing, laboratory and computerized systems at a pharmaceutical consultancy in Madrid.
A QA Specialist is needed to oversee GMP compliance and quality records in a pharmaceutical environment. The role involves managing deviations, CAPAs, and batch record reviews.
This role supports critical Quality Control operations within a regulated pharmaceutical environment. You will perform deviation investigations, environmental monitoring, and microbiological testing.
Project Delivery Partners (PDP) is a specialized consultancy providing project management, commissioning, qualification, and validation (CQV) services primarily for the life sciences and pharmaceutical industries. The company supports clients in the design, construction, and regulatory qualification of manufacturing facilities, ensuring compliance with Good Manufacturing Practices (GMP) and other industry standards. With a global footprint, PDP operates across multiple regions, including Europe, the US, and Asia, and is known for its expertise in delivering complex capital projects on time and within budget.
In Spain, PDP has a significant presence, with offices in Madrid and a strong focus on supporting pharmaceutical and biotech projects in the region. The company is actively hiring for a range of roles in Spain, including QA/QC specialists, validation experts, and project managers, many of which are remote or site-based. For international professionals, PDP offers opportunities to work on high-stakes projects in a growing life sciences hub, with a collaborative and dynamic work culture that values technical excellence and cross-border collaboration.
Project Delivery Partners was founded in 2005 to provide specialized project management and validation services to the life sciences industry. Over the years, it has expanded globally, establishing a strong presence in Europe, the US, and Asia, and has become a trusted partner for pharmaceutical companies seeking to build and qualify new facilities. The company continues to grow, focusing on delivering high-quality, compliant solutions.