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Job Description
A key member is sought to join a Biopharmaceutical organization in Swords, to contribute to the success of the Downstream Integrated Process Team.
Responsibilities will include ensuring timely delivery of production schedules, maintaining site safety and quality standards, and providing oversight on material management.
Job Requirements
- Own Quality Investigation from identification through root cause analysis
- Provide oversight on day-to-day production quality metrics
- Drive continuous improvement projects
- Act as a link between the shift operations team and days team
- Direct Root Cause Analysis sessions for safety and quality related events
Desirable Qualifications
- A Level 7 Degree in Science, Engineering or other relevant disciplines
- Relevant experience in the Pharmaceutical industry, preferably in Drug Substance
- Experience in change management in a GMP environment
- Experience in technical writing for GMP documentation and quality investigations