Description
Working as part of the Compliance team, the Compliance Officer will be responsible for the following tasks:- Carrying out the review of batch manufacturing documentation relating to oral solid dose production
- Preparing documentation for QP release in a timely manner
- Investigating and close out of deviations while working in close co-operation with other departments
- Identifying and implementing corrective and preventative actions
- Managing Customer Complaints
- Participating in internal and external audits as required
- Being involved in the continuous improvement of Quality systems
- Providing QA support to other departments.
The ideal candidate will fulfil the following criteria:
- Hold a third level degree in a Life science
- Have a minimum of 1 - 2 years' relevant experience in a Quality Assurance, Quality Control, or Production role within the Pharmaceutical or Medical Devices industries
- Demonstrate a thorough knowledge of quality systems, cGMPs and regulatory requirements
- Display a proven ability to effectively work as part of a team
- Have excellent attention to detail with the ability to critically review data and to write professional technical reports
- Display a high level of organisational skills and IT proficiency
If you are interested in this great opportunity and have the relevant skill set and experience please contact me Anna Mooney or apply below with an up to date CV.