- Compiling Validation Master Plan, Analytical Method Validation protocol, Process Validation protocol, Cleaning Validation protocol, related SOPs.
- Performing process validation, cleaning validation, analytical method validation, PQR, QRM
- Good knowledge of other areas in quality assurance.
Requirements
- MSc in any business related discipline, preferably pharmaceutical engineering or drug quality assurance form a reputable university.
- Minimum of 2 years related experience in a reputable organization.
- Experience with Microsoft office, Visio, Minitab.
- Undertake appropriate technical research.
- Ability to identify and solve problems.
- A high degree of interpersonal skills, time management and organizational skills are necessary.
Experience in written and oral English communication.
