Quality Engineers play a vital role in ensuring the quality and safety of products.
Key Responsibilities
* Generate investigation reports and address Corrective and Preventative Actions (CAPAs) to support continuing production.
* Initiate and complete non-conformance reports (NCRs) as required, coordinating production-related NCRs to close in a timely manner.
* Develop CAPAs that satisfactorily address root cause and follow through on effective corrective actions to prevent reoccurrence of failures.
* Define/Develop Standard Operating Procedures & batch paperwork for equipment/processes in collaboration with Production personnel that incorporates Operational Excellence principles.
* Ensure that work is carried out safely and in compliance with the organization's quality system.
Requirements
* A good understanding of pharmaceutical production and GMP is essential. Prior 'hands-on' experience would be beneficial.
* Degree/Diploma in relevant Science/Engineering/Manufacturing/Pharmaceutical course is necessary.
* Must possess a working knowledge of MS Office Suite.
* Good communication and interpersonal skills are required.
* Strong report writing skills are essential.
* Excellent analytical skills with attention to detail are required.