Validation Engineer
| Job Type | Fixed Term |
| Area | Sligo, Ireland |
| Sector | EngineeringQuality |
| Start Date | |
| Advertiser | Ashling Guthrie |
| Job Ref | 3923 |
| Job Views | 227 |
- 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.
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.
