close

Did you know that your Internet Explorer is out of date?

To get the best possible experience using our website we recommend that you upgrade to a newer version or download another web browser.
A list of the most popular web browsers can be found below. Just click on the icons to get to the download page.

crome
Google Chrome		 IE
Internet Explorer		 firefox
Mozilla Firefox		 opera
Opera

Your browser will need to close to complete the installation and you will need to manually reload the site when finished
Apply for this job

Name:

Surname:

Email:

Phone:

Cv:

Salary Expectations:

Education:

Experience:

Current Location:

Notice Period:

Write here your cover note:


If you would like us to create a jobseeker account for you, giving you access to
account management, job alerts and one-click applications, then please tick this box

If you are having difficulty you can always email your cv to [email protected]
Details

Quality Control Analyst


Reference:RK2211 Location: Greece
Qualification:DegreeExperience:4-5 Years
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: QC Analyst

Quality Control Analyst
RK2211
Greece


Job Summary:

We are seeking a detail-oriented Quality Control (QC) Analyst. The ideal candidate will have a strong background in High-Performance Liquid Chromatography (HPLC), stability testing, and a solid understanding of FDA and EU guidelines related to Out of Specification (OOS) results and HPLC testing. This role is critical to ensuring product quality and regulatory compliance.


Duties:

• Conduct HPLC analysis of raw materials, in-process samples, and finished products to ensure quality and compliance with specifications.
• Conduct stability testing on HPLC equipment
• Perform stability testing and analysis to evaluate product shelf life and effectiveness.
• Review and interpret data, ensuring accuracy and adherence to established protocols and regulatory requirements.
• Investigate OOS results and prepare comprehensive reports, implementing corrective actions as needed.
• Maintain up-to-date knowledge of FDA and EU regulations regarding quality control and laboratory practices.
• Collaborate with cross-functional teams to support product development and quality initiatives.
• Assist in the validation and calibration of analytical equipment and methods.
• Ensure compliance with laboratory safety and quality standards.
• Document all results and maintain detailed records in accordance with Good Manufacturing Practices (GMP).
• Participate in continuous improvement initiatives to enhance laboratory efficiency and effectiveness.


Education and Experience :

• Bachelor’s degree in Chemistry, Pharmaceutical Sciences, or a related field.
• Minimum 5 years experience in a QC laboratory, preferably within the pharmaceutical industry.
• Strong expertise in HPLC and stability testing methodologies.
• Knowledge of FDA and EU guidance on OOS and analytical testing.
• Excellent analytical and problem-solving skills.


If interested in this posting please feel free to contact Rachel Kent on +353 (0)87 427 8808 or [email protected] for further information.