We’re currently recruiting for an exciting opportunity with an award-winning pharmaceutical organization based in Dublin. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.

Duties
Develop, review and update engineering, manufacturing, & inspection Standard Operating Procedures.
Liaise with Manufacturing/Inspection/Engineering regarding documentation changes in an effective and timely manner.
Develop protocols for execution in Manufacturing & Inspection in support of change controls, deviations & troubleshooting investigations with support from relevant SMEs.
Involvement in projects as part of continuous process improvement and / or troubleshooting,
Ownership of change controls for Manufacturing/Inspection/Engineering
Liaise with Quality Assurance to ensure that GMP standards are maintained in line with current OS
Support production support team in reducing document turnaround times.
Use specified software packages and standard procedures, responsible for compiling and maintaining all relevant documentation including SOPs.
Provide technical and clerical support to the manufacturing, inspection & engineering teams in the preparation of documentation, collation of data and tracking of SOPs
Ownership of minor deviations as required

Education & Experience

Educated to degree level or equivalent.
Significant experience in Chemistry/Microbiology/Engineering/Validation gained within a biotech, pharma or health care organisation.
Experience working in a GMP environment
Project management experience is desired



If interested in this posting please feel free to contact Jack Caffrey on +353 (0)87 3854921 orjack.caffrey@lifescience.iefor further information.