Quality Control Specialist

Genveon İlaç Sanayi ve Ticaret A.Ş.

QUALIFICATIONS
•University degree in Chemical Engineering or Chemistry

•Minimum 2 years of Analytical Laboratory experience with equipments e.g. HPLC, GC, UV/Vis

•Knowledge of cGMP& cGLP and basic 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

•Preferably good command of English

JOB DESCRIPTION
•Perform main activities according to the SOPs prepared and cGMP/cGLP rules.

•Perform analysis will be given himself/herself, do preparations that is needed related to analyses accurately on time.

•To carry out all of the requirements of an analysis.

•Support quality incidents (deviation, OOS, audits etc.) and HSE incidents (near miss and )

•Use valid and approved test and analysis methods in the department where he/she works.

•Protect privacy of methods and documents used ,  work according to  record management principals  appropriately.

•To support for controlling of data and documents.

•Work providing the health and safety of himself/herself.

•Fulfilling the requirements of ISG within the framework of regulations and rules, attending trainings and obeying the rules.