Roles and Responsibilities Review of batch manufacturing records and the process of manufacture, supporting the decision to release the product in compliance with all licenses and GMP requirements. Liaising with Operations personnel to ensure regulatory and quality requirements are met during routine operations. Supporting and handling deviation / corrective action program. Supporting and handling product complaints investigation and report. Monitoring the production by inspection, ensuring the manufacturing process meets with compliance. Monitoring and aiding the implementation of continuous improvements and process changes. Taking part in internal and external audit, supporting response and improvement. Conducting QA activities including revision of SOPs, QA routine tasks and new projects.
Required Qualifications B.S. Degree in technical field, better major in pharmacy, food science, chemistry etc. Minimum 2-year experience in pharmaceutical industry or a medical device. Personnel with work experience in QA or QC will be preferred. 67Thorough knowledge of national and international GMP requirements. Good command of English reading, writing, speaking and listening. Proficiency in Microsoft Office Suite.
Desired Characteristics Strong oral and written communication skills. Ability to document, plan, market, and execute programs.
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Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support.