Job Title: Quality Specialist
We have a great contract opportunity for a Quality Specialist to join a top pharmaceutical company in Tipperary. The site supports the complete pharmaceutical small molecule process from Phase III clinical trials to product release and market support.
About the Project
* Review and approve production and analytical documentation accompanying the release of drug substance, drug product, and packaged finished goods to ensure conformance to appropriate SOPs, GMP, and regulatory requirements, including supporting QP certification.
* Actively communicate and collaborate with functional areas to develop a strong working relationship and understanding of roles and responsibilities.
* Utilise this network to help resolve comments and issues that arise during audit and review.
* Carry out all assignments to the standards of compliance, efficiency, innovation, accuracy, and safety in accordance with Company and regulatory requirements.
About You
* You will be an excellent communicator with strong organizational skills.
* Prior experience in the pharma industry is required.
* The Specialist must possess a degree in a Science or Engineering discipline plus some industrial experience.
* Alternatively, they must possess considerable industrial experience.
* Please note that for our contracting opportunities in the pharmaceutical sector in Ireland, candidates must possess either a Stamp 1G or a Stamp 4 visa.
* We regret that we are unable to provide visa sponsorship at this time.
Requirements
* GMP Quality system
* Quality Assurance