Job Description
We are currently recruiting for a highly skilled professional to join our team as a Senior Validation Engineer.
This is an excellent opportunity for individuals who are passionate about quality and reliability in a fast-paced biopharmaceutical environment.
As a Senior Validation Engineer, you will be responsible for executing qualification and validation activities following a lifecycle approach, complying with cGMP and company procedures.
You will author, review, execute, and approve testing protocols and reports, while ensuring all duties are performed in accordance with GMP requirements, SOPs, and controlled documents.
In addition, you will participate on project teams, vendors inquiries, and troubleshooting and monitoring of process systems.
The ideal candidate will have a minimum of 3-5 years of experience working in a pharmaceutical or similar GMP environment, with expertise in commissioning and qualification/validation of facilities, utilities, equipment, and instruments.
Experience in maintaining the validated state, requalification/revalidation (CTUs, Cleanrooms, Clean Equipment etc.) is also essential.
If you are interested in this challenging role, please feel free to contact us for further information.
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