Technical Operations Specialist
Our Client is currently has an opportunity for a Technical Operations Specialist. (Hybrid. The successful candidate will have previous GMP experience and will work internally within the Operations and Product Development group and the external support teams to ensure standard, accurate and succinct documentation is in place to ensure compliance with Pharmaceutical Quality Systems. They will be responsible for ensuring that efficient documentation cycles are in place which will support the business execution while maintaining or improving EHS & Quality standards. Main areas of responsibility: • Perform technical writing activities which will support the development of new documentation for new products and processes as well as revising and maintaining current documentation. These would include but not limited to; Procedures, Study protocols, Batch Records, Deviations, Change controls, deficiencies, technical specification/reports, risk assessments, Investigations & CAPA’s. Skillsets Required • Expertise in the use of Microsoft Word. • Excellent interpersonal and team collaboration skills. • Team player with an ability to work well across various departments on site. • Deadline focused individual. Education and Experience. • Minimum Level 6 NFQ qualification in an appropriate discipline with 2 years + relevant experience in the pharma industry. • Understanding of cGMP, Compliance and Regulatory expectations. ** You must have the right to work in Ireland for these roles ** If you have the above skills & experience and you are looking for the next step in your career, please contact Sean.Fahy@cpl.ie.
20 days ago