Quality Assurance Supervisor (IPC), Sterile Area - Hikma Pharmaceuticals

About the Job

• Conducting regular investigations to guarantee that workers’ follow safety procedures as required
• Conducting quality audits as required to ensure compliance with GMP, Quality standards, and sterility regulations throughout the field
• Handling the pharmaceutical tailing waste according to the set rules and procedures in this regard
• Carrying out material sampling as needed to conduct QA audits, checking samples’ conformity and taking decisions (Batch Release) of samples’ acceptance
• Performing pre and post-production quality checks and providing related reports accordingly
• Carrying 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
• Ensuring compliance of plant conditions (Humidity, Temperature,…etc) with set guidelines
• Checking machine conformity to standards as well as ensuring periodic maintenance implementation
• Performing other duties related to the job as assigned by the direct supervisor

Job Requirements

• Education: BSc. In Pharmacy, Science or Equivalent.
• Functional Competencies: Audit, Data Analysis, Documenting & Recording Information, Technical Writing, Quality Assurance & Management.
• Behavioral Competencies: Planning & Organizing, Initiative & Drive for Results, Collaboration & Teamwork, Change & Innovation.
• Knowledge of documentation reviews and requirements analysis.

Apply Here