Validation Engineer Haarlem

Validation Engineer

The Company
 Do you want to be a part of one of the leading altruistic pharmaceutical companies whose aim is to improve the health of millions of people around the world? There main mission is to provide everyone with an access to quality and affordable therapy which will enhance their health and help them cope with diseases in a more efficient and easier way. 
 
Role Description
 As a validation engineer you will be responsible for validation/re-qualifications of Equipment including Project work/ Changes/ CAPAS.  You will play a critical role in ensuring compliance with regulatory requirements and industry standards while optimizing operational efficiency and product quality.

Responsibilities
–Lead and participate in equipment qualification activities, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
– Provide technical expertise and guidance on validation-related issues to project teams and stakeholders.
– Collaborate with cross-functional teams to ensure validation activities align with production schedules, project timelines and quality expectations.
– Ensure adherence to Good Manufacturing Practice (GMP) and Good Documentation Practice (GDP) during validation activities.

 Requirements
– Bachelor's or higher degree in a relevant scientific or engineering discipline.
– Experience in validation/CQV within the pharmaceutical industry.
– Knowledge of V-model & SDLC methodologies.
–  Team player with attention to detail and strong can-do mentality.
– Excellent written and verbal communication skills, including the ability to effectively collaborate with multidisciplinary teams

Other Information
Are you interested and would like to apply, feel free to contact me.