DPS have a requirement for a number of Quality Management Systems Lead for a Dublin based Pharmaceutical client.
Role Requirements:
All relevant activities on site are conducted in compliance with cGMP and Company Standards
Minimum of 5 years’ experience in Quality Operations and Systems in Pharma/Biopharma industry
Monitor and support the performance of the site Quality Systems according to Company and cGMP standards
In depth knowledge of GMPs and Good Documentation and Data Practices
Extensive level of experience with reviewing and approving documents such as Procedures, Change controls and Investigations ensuring that compliance requirements are being adhered to.
Ability to work independently and effectively in a fast-paced environment delivering to a high quality standard.
Demonstrated knowledge of Quality Management Systems tools, continuous improvement methodologies and in-depth understanding of site processes.
Strong technical aptitude (ability to read & comprehend technical documentation and execute procedures) and demonstrated experience interfacing with regulators is desirable.
Liaise with internal partners to drive deliverables to completion
DPS is an Equal Opportunities Employer.
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