Finished Product Specialist / Responsible Analyst

• Bachelor of Science/Master of Science or higher qualification in Chemistry, Chemical Engineering, Pharmacy or a related discipline.
• Minimum of 2 years of experience as an analyst in a Quality Control or Research&Development Laboratory in a Pharmaceutical company.
• Solid knowledge of cGMP and GLP requirements in the pharmaceutical environment.
• Excellent verbal and written communication skills both in Turkish and English, and able to work in a matrix environment.
• Strong evidence of problem-solving/trouble-shooting skills.
• Strong analytical skills, good relationship management and change agility.
• Ability to adapt to a dynamic work environment and adhere to tight deadlines.
• No military obligation for male candidates.

İŞ TANIMI

• Performing Finished Goods Analysis according to current procedures and GMP, GLP rules.
• Ensuring that all testing has been performed and recorded according to the approved procedures, and ensuring on time testing completion.
• Conducting Analytical Method Transfer and Analytical Method Validation studies.
• Supporting other GMP related approaches within Quality Control Department such as annual product reviews and data integrity approaches.
• Supporting the equipment calibration plan and the applications used for these equipments within the Quality Operations Department.
• Monitoring and reviewing instrument/ equipment’s qualification or requalification.