We are looking for aQuality Control Supervisor that will be responsible from the following processes:
QUALIFICATIONS
•University degree in Chemical Engineering or Chemistry
•Minimum 5 years of Analytical Laboratory experience pharmaceutical industry.
•Good leadership skills and experiences.
•Knowledge of cGMP& cGLP and SAP
•Ability to work in a fast-paced changing environment
•Team working and customer-oriented mindset
•Good analytical thinking skills
•Strong interpersonal written and verbal communication skills
•Good knowledge of MS Office applications
•Good command of English is required
JOB DESCRIPTION
•To ensure that GMP requirements defined by MOH are completely and effectively implemented.
•Responsible for all aspects of health, safety, quality, and environment at the responsible area.
•Ensures responsible operations in accordance with local legislation, Guidelines’ / Procedures and Business Continuity Guides. Organization for Emergency preparedness requirements according to global and local requirements at the responsible area
• Planning starting materials sampling and laboratory analyses as a right way
•Review, evaluation and approve of analysis results.
•Release the starting metarials from SAP system
•Reporting of monthyl laboratory datas to Quality Control Manager.
• Leads laboratory investigations and ensure that finding root-cause.
• Support team members to perform right time in all analysis and documentation.
• Protect privacy of documents and methods used.
• Contribute to saving projects.
• Fulfill the responsibilities, which are given by managementat the right time and correctly in conformance with methods, procedures and work flow.