Join a leader in the field of pharmaceutical science as a Quality Systems Specialist. This is a 12-month hourly rate contract based in Cork, offering a hybrid working model.
Main Responsibilities:
* Support the digitization and automation of existing & new quality systems
* Participate in internal audits
* Manage non-conformances and CAPAs
* Manage change controls
* Support site inspections
* Support site inductions
* Generate metrics & reports from the quality systems
* Ensure & support GMP compliance
Required:
* Degree in Science or Engineering
* 3+ years experience in pharma/biotech/med device industry
* Experience in GMP environment & working within HPRA/FDA regulated environment
* Experience across data analytics techniques/tools such as Tableau, Spotfire, Google Analytics, Rapid Minor, or Python, and intermediate/advanced Excel will be a distinct advantage.
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