We are currently recruiting for an exciting opportunity in the pharmaceutical industry.
Job Description
The successful candidate will be responsible for compiling relevant documentation from contractors, suppliers and other departments for inclusion in reports. They will also prepare reports for executed protocols for review and approval.
Additionally, they will initiate and implement change control activities in accordance with site procedures, track and resolve exceptions/events/deviations, prioritize MSAT activities in line with the project schedule and coordinate document review and approval.
Other responsibilities include collating and organizing files for turnover to QADC, assisting in the development of training material and participating in cross-functional teams as required.
Domestic and international travel may be necessary.
Required Skills and Qualifications
A bachelor's degree in a scientific or technical discipline is required, along with experience in cleaning validation, large molecule facility management and other validation areas.
Candidates should possess excellent organizational and communication skills, as well as the ability to work effectively in a team environment.
Benefits
This is an excellent opportunity to join a leading multinational organization that is one of the best at what it does.
Applicants should contact Seán McCarthy on +353 (0)87 798 8480 or sean.mccarthy@lifescience.ie for further information.