Job Description

- Create and manage effective communication and close collaboration with FDO/MOH - Necessary actions and follow-ups to receive related permissions from FDO/MOH - Supervise the implementation of MOH regulations and SOPs for production activities and submission of related reports and technical documents - Validate API and supplier according to GMP standards - Monitor the result of quality control done by reference laboratories - Issue release permission of product distribution - Check and confirm the batch manufacturing records - Focus on continuous improvement of production methods in order to ensure quality and safety of products - Conduct frequent internal audit of production site and warehouses

Requirements

• Education: Pharmacist (Pharm D) • Experience: Minimum of 2 years as a responsible pharmacist in biotech pharmaceutical companies • Capabilities: Good knowledge of GMP and MOH regulation, Production Process and quality control - Strong communication skills – Planning skills – Managerial skills - Fluent in English

Employment Type

  • Full Time

Seniority

Details

Employment type

  • Full Time

Seniority

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