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.

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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:

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- 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:

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- 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:

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- 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:

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- Competitive salary package.

- Stable employment and a positive work environment. xhfqzwm

- A comprehensive benefits package including health insurance, subsidized meals, and a pension plan.

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📌 Project Manager - Madrid, Comunidad De Madrid, Spain
🏢 Importante grupo
📍 Madrid