Key Responsibilities:

• Supports all relevant activities for establishing compliance with national and international regulatory framework, current regulations, and applicable standards for pharmaceutical products Develops, updates and reviews company processes (SOPs), contributing to the desired compliance with the requirements of GMP, ISO standards, customers, and state law.
• Participates in handling of basic quality procedures (Deviations, Change Controls, Customer Complaints, Risk management, etc)
• Communicate with internal and external stakeholders regarding projects, products, materials and other quality related topics
• Keeps records of quality relevant documentation
• Provides support during regulatory and other audit-related activities.

Requirements & Skills:

• University Degree in Chemistry, Engineering, Biology, Pharmacy, or related field.
• Excellent knowledge and handling of both verbal and written English language.
• Good knowledge of MS Office suites (Word, Excel, Power Point, Outlook).
• Ability to work accurately in a busy and demanding environment, following strict deadlines/timescales.
• Previous experience in QA sector.