Description:
QA Resources is currently recruiting for a Validation Engineer on behalf of a leading pharma company based in Cork. This is an initial 9-month contract role.
Responsibilities:
- Working on small validation projects for manufacturing equipment
- Working on thermal validation of component autoclaves / SIP routes / temperature controlled units
- Generation, review and approval of Validation Plans, FAT, SAT IV/FTs, QRAES, and PQs.
- Liaise with cross-functionally and with external vendors regarding equipment User Requirement Specifications, Factory Acceptance Tests to ensure the quality by design principles are being followed.
- Reviews and Approves summary reports.
- Pre-Approval and Post approval of Validation test documents.
Education / Experience:
- BS degree in an engineering or relevant discipline
- Ideally 3+ years of relevant experience in validation activities in pharma.
- Extensive knowledge and demonstrated experience managing Validation activities for pharmaceutical projects
- Demonstrated strong Communication skills.
- In-depth understanding and application of validation principles, concepts, practices, and standards.
- Strong understanding of engineering standards, documentation, and validation lifecycle.
Interested candidates should submit an updated CV.
Please click the link below to apply, call Kellie on 0214297900 or alternatively send an up to date CV to kellie.hackett@qaresources.com
***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland***
To apply for this job please visit qaresources.com.