QUALITY CONTROL SUPERVISOR PHARMA INDUSTRY - IRELAND
Reporting to the Team Leader from the Department of Pharmaceutical Chemistry, the main responsabilities will be :
Analysis Supervision and Monitoring
Protocol writing and development
Research and analytical troubleshooting
Data review to the relevant regulatory standard, analytical procedures and appropriate documentation.
Responsible for the review of specific technological projects and writing yp the results of these projects accurately, confidentially on time for the clients.
Laboratory reports and investigation reports
Analytical testing when not engaged in Data Review activities.
Updating docuemntations when required
Hankdling any customer related queries where necessary and liaising with their team to problem solve queries if needed
Degree in chemical sciences or related disciplines.
2 years laboratory experience in similar position in the pharmaceutical or related industry.
Essential 2 years analytical experience using HPLC / GC
Experience in studies of stabilities, sample management and analysis.
Experience in validation of methods (preparation of protocols and reports)
Knowledge of GMP / GLP environment
Used to work as a team and focused on goals.
High degree of autonomy.
High level of English
Passionate about quality and customer service
Good communication skills both internally and exernally
It is offered :
To be a part of a motivated and active group.
Full time Permanent Position.