A. Essential Duties and Responsibilities:
- Monitor, control and improve effectively the whole applied operations at every stage of the finished pharmaceutical products
- Work closely with manufacturing to address any production issues on shift and ensure appropriate documentation
- Perform sampling process for all manufacturing and packaging steps according to sampling plan for analysis
- Handle all required quality assurance functions, recommend and implement improvements for product manufacturing
- Apply in process tests to ensure product compliance with established specifications and provide vis-à-vis reports accordingly
- Inspection on the division of the warehouse release area, guarantee area and the reject area with the true identification labels
- Recording any complain from any customer from any product and investigate about the reason of the problem and solving
- Carry out the issuance and weighing process of raw materials to guarantee the conformity of specifications to quality standards, approving the release of materials to production, as well as ensuring compliance of raw material storage with regulatory guidelines
- Monitor GMP & system implementation on daily basis and providing related reports accordingly
- Documentation of validation steps according to the prevailing policies and procedures
- Ensure strict adherence to the relevant cGMP and ISO standards (ISO 9001, ISO 14001, OHSAS 18001
Job Requirements
B. Qualification/Knowledge/Experience:
Level of Education:Life Science Degree
Experience :
Previous experience of Pharmaceutical IPC is mandatory
Language :Fluent English proficiency is mandated
IT Literacy :Professional knowledge of MS-Office
C. Competencies and Behaviors:
- An entrepreneurial winning mentality with strong learning capabilities and loads of energy
- Detailed-oriented personality style
- Ability to manage simultaneous tasks with quality delivery
- Analytical thinking and problem solving
- Striving for continuous improvement
- Able to cope with stress and change