Quality Control Analyst

Job Description:

Catalyx are seeking an experienced candidate to join our team and work as a QC Analyst for our customer site in Cork. Responsibilities: Review and release of Primary and secondary Packaging components. Completion of the associated auxiliary tasks related to this analysis e.g. data review, archiving, liaising with Materials management etc Quality investigation and root cause analysis. Provide Services in a LEAN and 7S environment and adhere to the good lab practices. Comply with safety and quality procedures and participate in internal and external audits as required. Maintain laboratory housekeeping standards. Demonstrate strong scientific and GMP documentation skills. May be required to perform other duties as assigned. Requirements: Degree in relevant field and pharmaceutical industry experience Post-graduate studies as appropriate to augment primary degree. Operational experience of quality laboratories in a fast moving manufacturing environment. Detailed knowledge of quality management systems, pharmaceutical manufacturing operations, requirements for cGLP, pharmacopeial methods and stability. Understand relevant quality/compliance regulations. Adaptable and flexible Strong attention to detail. Application Deadline: Wednesday April 1st

Catalyx are seeking an experienced candidate to join our team and work as a QC Analyst for our customer site in Cork.

Responsibilities:
* Review and release of Primary and secondary Packaging components.
* Completion of the associated auxiliary tasks related to this analysis e.g. data review, archiving, liaising with Materials management etc
* Quality investigation and root cause analysis.
* Provide Services in a LEAN and 7S environment and adhere to the good lab practices.
* Comply with safety and quality procedures and participate in internal and external audits as required.
* Maintain laboratory housekeeping standards.
* Demonstrate strong scientific and GMP documentation skills.
* May be required to perform other duties as assigned.
Requirements:
* Degree in relevant field and pharmaceutical industry experience
* Post-graduate studies as appropriate to augment primary degree.
* Operational experience of quality laboratories in a fast moving manufacturing environment.
* Detailed knowledge of quality management systems, pharmaceutical manufacturing operations, requirements for cGLP, pharmacopeial methods and stability.
* Understand relevant quality/compliance regulations.
* Adaptable and flexible
* Strong attention to detail.
Application Deadline: Wednesday April 1st