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.

Responsibilities.

• 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
  

• 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− Ability to work on own initiative
• Good project management and communication skills.
• Attention to detail.