Gmp Inspector, Inspection

**HPRA**

**Role**: GMP Inspector

**Salary**: €64,614 per annum

**Location**: Dublin - Availability to travel for national and international inspections is a requirement in this role

**Contract**: Three year contract post

**ROLE SUMMARY**
- Reporting to a Senior Inspector, the Inspector will be primarily responsible for assessing the compliance of manufacturers with EU Good Manufacturing Practice (GMP). The role of an Inspector is to evaluate the compliance of sites inspected, in Ireland andabroad, with the requirements of National legislation (in Ireland), European Community Directives, Regulations and Guidance.
- The role involves inspecting, reporting and forming conclusions in respect of the suitability of a site for the activities which it has sought or for which it is already authorised. The Inspector provides technical information and advice to relevant individualsand organisations both internal and external to the HPRA. The Inspector will provide support to the enforcement and execution of national regulations in relation to medicinal products.

**KEY RESPONSIBILITIES**
- Preparing for and performing inspections in accordance with HPRA procedures
- Writing and compiling inspection reports when acting as lead inspector and contributing
- Ensuring that Inspection procedures remain up to date with relevant developments in National, European and International regulations, legislation and guides
- Assisting to ensure that there are effective mechanisms in place to capture, store and communicate key information, experience and knowledge gained by the Inspection section
- Participating in the performance development programme (PDP) within the Inspection section to maximise efficiency gains
- Working with the line manager to agree appropriate performance related targets
- Attending and contributing to meetings of the Compliance department as required
- Liaising with relevant departments of the HPRA to facilitate the evaluation and follow-up of inspection and compliance activities

**QUALIFICATIONS AND EXPERIENCE**
- Third level degree in a relevant scientific discipline
- A minimum of 3 years relevant work experience in one of the following:

- Experience in a facility that manufactures biological active substances or finished medicinal products in any of the following functions: quality assurance, compliance, production, technical services or validation

**If you are interested in this role please feel free to contact Janice on +**

Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Agency in relation to this vacancy| Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England andWales