QC Analyst II must have broad knowledge of all the techniques within the laboratory required for the routine support of the  laboratory operations.

• Preparation and testing of In-Process / Finished Product samples, Raw materials and/or environmental monitoring/water samples in accordance with written procedures and best practice.
• Participate in Laboratory investigations and Root Cause Analysis
• Daily up-keep and maintenance of Laboratory Equipment.
• Accurate and timely recording of all information pertinent to the task being performed in the relevant Laboratory Worksheets / Notebooks and LIMS.
• To maintain a high standard of GMP / GLP in the Laboratory.
• To maintain/adhere a high standard of housekeeping, Dress Code and Safety within the Laboratory.
• To write and update SOPs and Protocols and review laboratory data as required
• To review and check own work results for accuracy and presentation.
• To perform a quality/technical review of data generated in the Laboratory
• To report to and be directed by the Laboratory Management.

• Third level qualification in a science discipline.
• Analytical Chemistry / Pharmaceutical Chemistry desirable.
• Knowledge of cGMP and safety standards applicable to a pharmaceutical environment.
• Excellent attention to detail and accuracy.
• Good organisational, communication and interpersonal skills.
• Available to work a shift pattern/on-call as required.
• Responds positively to changing circumstances and priorities.