As an IPC Specialist, you will be primarily responsible for developing, implementing, and overseeing infection prevention and control policies and procedures in healthcare settings.

Job Responsibilities:

• IPC Specialist will assume full responsibility for all quality assurance matters for the technical operations.
• IPC Specialist will perform all required quality assurance functions, recommend and implement improvements for product manufacturing.
• Ensure line clearance & cleaning checks of the batch manufacturing process.
• Reviews documentation associated manufacture of products on the manufacturing area during production.
• Work closely with manufacturing to address any production issues on shift and ensure appropriate documentation.
• Coordinates and assembly of batch record documentation to assist with disposition.
• Reviews and approves completed manufacturing related documents for batch record disposition.
• Performs in process control sampling, testing and inspection (as AQL) for Toll Products.
• Coordinates activities associated with deviation report and CAPAs to facilitate investigations and assure timely closure.
• Ensures adherence of appropriate cGMP regulations and quality standards.
• Perform or support any other tasks necessary to maintain the product quality and site cGMP compliance as needed.
• Ensures that all activities in his unit or section are done according to the relevant cGMP and ISO standards (ISO 9001, ISO 14001, and ISO 45001).

Qualifications:

• Bachelor's degree in pharmacy or science.
• At least 1 year experience in IPC Pharmaceuticals Industry.

Requirements:

• Good communications skills.
• High accuracy level to guarantee the reliability of results.
• Good in English language (reading, speaking and writing).
• Individuals must be a dynamic and hard-working professional with a background in Quality Assurance and must be detail-oriented and self-motivated.