LSC have a great contract opportunity for Validation Engineer to join a leading Biopharmaceutical Facility in Louth.
If you have 4 years of experience and are ready for your next challenge, this could be the perfect project for you!
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
- Execute qualification and validation activities for life cycle approach following validation plans and complying with cGMP and company procedures as part of the design, build and qualification, including ongoing operations to maintain the validated state.
- Author, review, execution and approval of testing protocols and reports. Responsible for project delivery, participate on project teams, vendor enquires and the troubleshooting and monitoring of process systems.
- Perform all duties in accordance with GMP requirements, SOPs and controlled documents.
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- Bachelor degree, in a scientific or engineering field.
- A minimum of 3 - 5 years' experience working in a pharmaceutical or similar GMP environment as part of a validation, MSAT or engineering function.
- Experienced in the execution of commissioning and qualification/validation of facilities, utilities, equipment and instruments.
- Experience in troubleshooting and providing technical and engineering solutions for GMP manufacturing operations and equipment in a biologics processing environment
For our contracting positions in Ireland's pharmaceutical industry, applicants must possess a Stamp 1G or a Stamp 4 visa. We apologize for any inconvenience, as visa sponsorship is not available currently.
Apply via this advert or contact Adam Murphy on 021 4777 329 if you have any more questions about this opportunity!
