Quality Assurance Specialist Or Ass. Specialist

Centurion İlaç Sanayi ve Ticaret A.Ş.

QUALIFICATIONS AND JOB DESCRIPTION

We are looking for an enthusiastic team member for our Quality Assurance Department who will work as “QA Specialist” or “QA Ass. Specialist” in our Manufacturing Facility located in BOSG, Ankara.

QUALIFICATIONS

 QA SPECIALIST;

• Bachelor’s degree in Chemistry, Pharmacy, Biology Microbiology or a related discipline,
• Min. 3 years experience in pharmaceutical area,
• Up-to-date knowledge of relevant pharmaceutical legislation and GMP / GDP,
• Candidates with analytical mindset and team-work approach will be strongly preferred,
• Strong analytical, communication, decision-making and leadership skills for interaction with external and internal customers and partners,
• Proficieny in MS Office applications,
• Full competency in local languages and a working knowledge of English is a must.

QA ASS SPECIALIST;

• Bachelor’s degree in Chemistry or Chemistry Engineering,
• Preferably 1 years aseptic process experience in pharmaceutical area in Quality Assurance Department,
• Up-to-date knowledge of relevant pharmaceutical legislation and GxP (GMP, GDP, GLP),
• Candidates with analytical mindset and team-work approach will be strongly preferred,
• Strong analytical, communication, decision-making and leadership skills for interaction with external and internal customers and partners,
• Proficieny in MS Office, QMEX and SAP applications,
• Full competency in local languages and a working knowledge of English is a must.

JOB DESCRIPTION

• Providing support to maintain the robust quality assurance system in the company,
• Providing maintenance of Quality Management System to ensure compliance to regulations as well as global and local standards,
• Supporting improvement of processes in Quality Management System,
• Ensuring supplier controls are done to provide product safety and conformity,
• Performing internal and external audits,
• Supporting preparation and uptade of documentation activities in accordance with local GxP (GMP, GDP, GLP) requirements,
• Supporting preparation and issue process of standard forms.