Requirements: English
Company: Tandem Project Management
Region: Dublin, Irlanda
**Summary**: Competitive contracts available for QC Analysts with 1-2 years experience Global Biopharma Dublin.**Responsibilities**:You will be involved in routine QC analysis and related activities in compliance with current cGMP regulations and will support the manufacture of biopharmaceutical product.**Qualifications & Experience**:chemistry/biotechnology or a related scientific discipline.1-2 years QA/QC experience.Previous bio/pharma experience and working knowledge of cGMP.