Pharmaceutical validation professional

Biopharmaceutical Validation Role

LSC has a contract opportunity for Validation Engineer to join a leading facility in Louth.
The ideal candidate will have 4 years of experience and be ready for their next challenge, making this the perfect project for them.

About the Project

Execute qualification and validation activities 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 enquiries 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.

We require applicants to possess a Stamp 1G or a Stamp 4 visa. Please note that we cannot currently offer visa sponsorship.

Key Responsibilities:

* Qualification and validation activities
* Testing protocols and reports
* Project delivery and team participation
* Troubleshooting and system monitoring


* GMP knowledge
* Commissioning and qualification/validation experience
* Engineering skills
* Technical problem-solving abilities