Bachelor of Science specialized in Chemistry, Microbiology / Bachelor in Pharmacy or similar discipline,
Diploma in Quality Management (SLSI).
DUTIES AND RESPONSIBILITES
Implementation of European Quality Systems, coordinating and conducting internal system audits, assuring continual improvement of the system.
Organizing and carrying out a regular inspection on the production process, reviewing, and verifying products and process conformities against the quality specifications.
Assisting the quality assurance manager to initiate new projects for quality improvement, such as sustainable development.
Analysing data via modern RCA techniques to find out the root cause of any process deviation /customer complaints and propose corrective actions.
Assist Head of Quality to review final Batch records and release quality assured product.
Maintain already established documentation system in a well guided manner.
Perform any other tasks/duties as assigned by manager.
QUALIFICATIONS AND REQUIREMENTS
Bachelor of Science specialized in Chemistry, Microbiology / Bachelor in Pharmacy or similar discipline
Diploma in Quality Management (SLSI).
2-3 years' experience in pharmaceutical manufacturing as Quality Assurance personnel.
Ability to work extended hours as and when required
Ability to read, comprehend, write and communicate effectively in English.
A good team member who can build up a professional relationship with other members and align with company goals.
Working understanding of QC and Microbiological testing procedures and sophisticated techniques.
Working understanding of Pharmaceutical utility systems.
Possess good work ethics and other leadership characters
Self-motivated to build up a career in the pharmaceutical industry.