Location - Limassol, Cyprus

Contract type - Permanent

DUTIES

• Supervise a group of analysts during their daily work to ensure all quality and goals are met and evaluation of their work.
• Testing materials and products under development
• Execution of stability studies and determination of shelf life
• Analytical method development and validation
• Design stability protocols as per the ICH guideline, manage stability analysis, and establish the specifications of the impurities / related
substances for new products.
• Processing / generating of the standard operating procedures (SOP's) and methods of analysis.
• Reviewing of drug master files (DMF) and technical packages


QUALIFICATIONS, SKILLS AND EXPERIENCE

• Bachelor’s degree in Pharmacy or Chemistry
• Previous relevant experience of at least 3 years
• Excellent command of both written and spoken English
• Computer literacy