Are you looking for an exciting opportunity to lead complex engineering projects in a growing, international pharmaceutical company? At ALK, we are on a mission to improve the lives of people living with allergies, and we are seeking a driven and structured Project Manager to join our team.In this role, you'll take ownership of projects and ensure their implementation across production, utilities, and facilities areas. This is a hands-on, cross-functional role for a delivery-focused professional who thrives on managing scope, cost, and timelines, champions GMP and compliance excellence, drives continuous improvement, and enjoys collaborating with stakeholders and vendors alike.Your key responsibilities:The Project Manager leads projects related to pharmaceutical production, utilities, and facilities, ensuring delivery on time and on budget while meeting all quality and compliance expectations.Key responsibilities include:Project Leadership - Lead projects and collaborate with all stakeholders in the scoping, design, sourcing, installation, commissioning, qualification, and handover of equipment for the production areas.Requirements & Specifications - Define equipment requirements and specifications based on process, safety, quality, and customer needs. Establish the general automation requirements for manufacturing, QA, and QC equipment.Technology Evaluation - Evaluate, or assist in evaluating, the technology necessary to support project requirements.Budget & Cost Management - Assist in determining and managing the budget required to support project requirements,



ensuring delivery on time and on cost.Vendor & Subcontractor Management - Manage the efforts of subcontractors and vendors to ensure the correct job priorities and schedules are met, whether delivered by internal or external crews.Quality & Compliance - Take accountability for the quality and compliance aspects of the assigned activities, performing the required actions (risk analysis, documentation, inspection participation, observation responses, SOPs, etc.).Your profile:Degree in Science or Engineering.Candidates should have prior experience in a similar role, ideally within a GMP pharmaceutical/biotech environment.Demonstrated capability of working within GMP frameworks.Knowledge of Quality Systems and Validation standards, policies, procedures, and methodologies.Fluent Spanish and English; excellent technical writing and communication skills.Your skills and attributes:Structured and delivery-focused, comfortable managing multiple projects in parallel.Strong stakeholder management; able to influence and coordinate internal teams and external vendors.Meticulous attention to detail with a pragmatic, risk-based approach to compliance.Confident problem-solver with strong organisational and planning skills.Location: C/ Miguel Fleta, 19 (Madrid, Spain).Reporting line: Projects & Qualification Manager.Work pattern: Regular day shift with a adaptable schedule.We provide:Competitive salary package.Stable employment and a positive work environment.A comprehensive benefits package including health insurance, subsidized meals, and a pension plan.
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📌 Project Manager (Madrid)
🏢 ALK
📍 Madrid