İş Yerinde
İş Yerinde
Full-Time
2 - 6 years of experience
Quality
Quality
306 application
Full-Time
2 - 6 years of experience
306 application
Quality
Position Summary
Reporting to the Finished Goods Control Section Head in the Quality Operations Department, the candidate will have following responsibilities:
Job Description
· Performing semi-finished, finished goods & stability 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
· Performing analysis control and documentation control according to current procedures
· Performing and reporting AMTE, process validation and cleaning validation studies
· Assisting quality control staff with troubleshooting and resolving unusual problems
· Investigating laboratory issues, identify root cause, and develop corrective and preventative actions
· Supporting other GMP related approaches within Quality Control Department such as annual product reviews and data integrity approaches
Qualifications
· Bachelor of Science / Master of Science or higher qualification in Chemistry, Chemical Engineering, Pharmacy or a related discipline
· Minimum of 5 years of experience as an analyst in a Quality Control 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
· Experience/knowledge in laboratory work practices and procedures
· Strong evidence of problem-solving/trouble-shooting skills
· Good relationship management and change agility
· Ability to adapt to a dynamic work environment and adhere to tight deadlines
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Analist Analist Maaşları Analist Nasıl Olunur? Analist Nedir? Analist İş İlanları