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Form of workI'm currently looking for a Data and Document Reviewer to global pharmaceutical business based in the County Armagh region. As the Data and Document Reviewer you will be responsible for monitoring and performing all assigned duties for the GMP manufacturing facility, as well as the following:
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Data and Document Reviewer will be varied however the key duties and responsibilities are as follows:
Ensure the appropriate GMP procedures are followed consistently in all areas of work and communicate deviations from GMP procedures effectively.
Prepare and review Data and Documentation accurately and efficiently, ensuring that documentation is in line with the businesses RFT (Right First Time) culture.
Responsible for communicating with internal and external customers and dealing with their requirements.
Be able to identify OOS, OOT, OOP and OOE results to adequately inform the member of staff according to the procedure.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Data and Document Reviewer we are looking to identify the following on your profile and past history:
1. Relevant degree within an Analytical discipline or equivalent level of practical experience.
2. Proven industry experience within a GMP or GLP environment.
3. A working knowledge and practical experience in method development or validation.
Key Words: Documentation, Compliance, GMP GLP Laboratory, Right First Time, Ireland,
