o2h group seeds new ideas in science, technology and green innovation. We work across boundaries and take a collaborative and shared approach to innovation, and therefore we co-invest, co-create and co-execute to bring these ideas to life.
Experience in analysis of Solid Oral - FP, Instrumentation, In-process or Stability. Experience of Analytical Method Validation. Experience of PMQC & Dissolution.
Perform line clearance. In-process venficatoon and batch reconciliation. Investigate deviations, incidents and support CAPA implementation Coordinate equipment qualification, preventive maintenance and calibration activities.
The ideal candidate must have hands-on exposure to ophthalmic formulations, along with practical experience in autoclave operations and batch manufacturing processes. A strong understanding of GMP and quality compliance is essential.
Compilation of high quality Annual Product Reviews / Product Quality Reviews for products manufactured at various manufacturing sites and retrieve data from the Quality and regulatory databases and system
Responsible for execution and review support of Quality Assurance activities including document review, shop-floor QA support, deviation handling, and quality systems support to ensure compliance with cGMP and regulatory requirements.