Ultimate Solutions : Validation Engineer

Fundación Parque Científico de Madrid; Madrid; Presencial; EUR 30.000 - 45.000; Jornada completa

Descripción de la vacante

A leading engineering company seeks a Validation Engineer in Madrid to support clients with regulatory compliance in the pharmaceutical industry. The role involves preparation of validation protocols, management of qualification activities, and a strong grasp of GMP environments. Opportunities for growth and a competitive salary are offered.

Servicios

Training program across Europe

Competitive salary based on experience

Permanent contract

Flexible compensation plan

International and dynamic team

Career Path for growth

Formación

• Degree in Science or Engineering required.
• Previous experience in GMP environments needed.
• Knowledge of GxP, EMA, FDA regulations valued.

Responsabilidades

• Prepare master plans for validation and qualification.
• Write protocols for DQ/IQ/OQ/PQ.
• Conduct qualification activities and assessments.

Conocimientos

Problem Solving

Verbal Communication

Written Communication

Educación

Degree in Science or Engineering

Herramientas

Microsoft Office

Descripción del empleo

Ultimate Solutions is a leading engineering company in automation, serialization, vision solutions, and validation, with offices in Puerto Rico, United States, and Spain . Among its main clients are the top pharmaceutical companies in Europe and the United States.

What are we looking for?

We are looking for the right people : those who want to innovate, achieve, grow, and lead . Do you stand out when solving problems on your own or as part of a team? With us, you can develop and grow your professional career working on a wide range of innovative products across different technologies.

The ideal candidate for this position will be responsible for the implementation, troubleshooting, training, and support services for our clients in Madrid, Spain .

About the position

The Validation Engineer will work in the validation department of Ultimate Solutions to help our clients develop documented evidence so that their systems, processes, and equipment comply with the requirements and specifications appropriate for their intended use and the current regulatory framework of the pharmaceutical industry.

Responsibilities

• Preparation of master plans for qualification / validation, URS, RA
• Writing protocols DQ / IQ / OQ / PQ for packaging equipment and their systems
• Management and execution of qualification activities
• Process risk assessment and adherence to planning
• Report preparation

Requirements

• Degree in Science or Engineering
• Previous experience working in GMP environments and knowledge in equipment qualifications (HVAC, compressed air, and computerized control systems)
• Knowledge of regulations such as GxP, EMA, FDA, and CFR Part 11 and other systems will be valued
• Advanced level of Microsoft Office
• Intermediate level of English – spoken and written
• Skills to solve technical problems and verbal and written communication

What do we offer?

• Training program offered by the company in different locations across Europe
• Competitive salary according to your experience
• Permanent contract and flexible compensation plan
• Be part of a young, international, and dynamic team
• Career Path – opportunities for growth and professional development

If you are interested , please apply for the position through this link .

Other Offers

• 34) 91 116 99 40

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