Validation Engineer

Description

Team Horizon is seeking a Validation Engineer for our client s Technical Operations team in the Northwest. This is a fixed term contract for 12 months and will report to the Validation Team Lead.

This role is a fully on–site position in Ireland, are you willing to relocate? Do you have authorisation to work in the EU?

Why you should apply:

This role will provide you the opportunity to get exposure to a broad range of validation activities on site, and you You will be responsible for co–ordinating the development and maintenance of the company s validation program in compliance with all applicable regulatory and company requirements.

What you will be doing:

Co–ordinate, implement and participate in the site Validation Program. Ensure all computerised systems are qualified in compliance with Data Integrity policies and regulatory requirements. Co–ordinate / direction and participate in the validation of site equipment, facilities, utilities, processes and software in compliance with company policies, FDA, European cGMP and GAMP standards. Generate/maintain Validation Master Plans. Generate /maintain Project Validation Plans. Generate validation plans, write protocols and final reports to cGMP standard. Review / approve of protocols and final reports as required. Manage validation change control process. Adhere to and support all EHS & E standards, procedures and policies.

What you need to apply:

3rd level qualification in a relevant engineering or scientific discipline. A minimum of 2 years experience in a cGMP regulated pharmaceutical manufacturing environment. High level of attention to detail and mental concentration, to ensure accuracy and compliance. Excellent communications skills with the ability to write protocols and reports. Proven problem–solving skills and the ability to adapt to new regulatory requirements. This role is a fully on–site position in Ireland, are you willing to relocate? Do you have authorisation to work in the EU?

Ad ID: 5418387158