Validation Specialist

Join a leading pharmaceutical company as a Validation Specialist in the vibrant and historical heart of Spain. As a Validation Specialist, you will play a pivotal role in ensuring the integrity and compliance of pharmaceutical equipment by crafting and executing Operational Qualification (OQ) documentation.

Your expertise as a Validation Specialist will be instrumental in maintaining the highest standards of quality and safety. You will be immersed in a dynamic environment where your meticulous attention to detail and robust validation practices will contribute to the development of life-saving products.

Key Duties and Responsibilities

Your duties as the Validation Specialist will be varied; however, the key duties and responsibilities are as follows :

• Authoring comprehensive OQ protocols and reports, ensuring they meet regulatory requirements and industry standards.
• Conducting and overseeing validation activities, including test execution and data analysis.
• Collaborating with cross-functional teams to ensure seamless integration of validation processes with manufacturing operations.
• Identifying and implementing improvements to validation strategies and methodologies.

Role Requirements

To be successful in your application as the Validation Specialist, we are looking to identify the following on your profile and past history :

• Relevant degree in a scientific or engineering discipline.
• Proven experience in validation within the pharmaceutical sector.
• A working knowledge and practical experience with pharmaceutical equipment and validation processes.

Key Words

Validation / Pharmaceutical / OQ Documentation / Equipment Validation / Compliance / Regulatory Requirements / Quality Assurance / Spain / GMP / Protocol Authoring / Cross-Functional Teamwork

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