Posted on Feb 8, 2021 by Real Staffing Group
My client, a well-known pharmaceutical company based in Dublin are looking for a Validation Engineer to join their MSAT Manager.
You will lead aspects of cleaning validation programmes for the company in order to meet appropriate GMP regulatory and validation requirements. You will also be a Subject Matter Expert in the area of responsibility.
Roles and Responsibilities include:
Plan, co-ordinate and execute cleaning validation studies at site.
Support site VMP activities in area of responsibility
Generate, execute or review Plans/Protocols/Reports/SOPs/WIs/WS associated with cleaning validation activities.
Maintain cleaning validation files
Participate as Validation Representative on Project Teams in area of responsibility.
Participate in Change Control Programme.
Keep abreast of/adhere to regulatory requirements in relation to area of responsibility.
Ensure Project related work is carried out in accordance with the requirements of Group Validation Policies, Guidelines, Site Validation Master Plan and GMP.
Participate in the Self Inspection programme and External Audit.
Generate APQR reports in area of responsibility.
Mentor Validation professionals in area of responsibility.
Contribute to establishing Global standards for Cleaning validation
Education & Experience:
The ideal candidate must have third level qualification (NFQ Level 8 or higher) in Chemistry/Pharmacy/
Biology/Engineering or other appropriate discipline.
Minimum of 3 years relevant experience within quality, production or engineering function in the Pharmaceutical industry
Excellent salary and benefits package on offer with this role
Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Agency in relation to this vacancy| Registered office | London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales