Athens, Attica, GreeceFull time
lmw is seeking for a Quality Control Analyst on behalf of a Greek pharmaceutical company located in the North-Western region of Athens.
The company manufactures both sterile and non-sterile products and is focused on exports worldwide.
Develop and qualify new testing methods.
Write technical reports or documentation such as deviation reports, testing protocols, trend analyses, data capture forms, equipment logbooks, or inventory forms.
Revise standard quality control operating procedures.
Review data from contract laboratories to ensure accuracy and regulatory compliance.
Receive and inspect raw materials.
Serve as a technical liaison between quality control and other departments, vendors, or contractors.
Supply quality control data necessary for regulatory submissions.
Participate in internal and external audits as required.
Ensure that lab cleanliness and safety standards are maintained.
Calibrate, validate, or maintain laboratory equipment, identify and troubleshoot equipment problems.
Prepare or review required method transfer documentation including technical transfer protocols or reports.
Perform validations or transfers of analytical methods in accordance with applicable policies or guidelines.
Participate in out-of-specification and failure investigations and recommend corrective actions.
Conduct routine and non-routine analyses of in-process materials, raw materials, environmental samples, finished goods, or stability samples.
Bachelor’s degree in Chemistry
Postgraduate degree is desirable
1+ year of related pharmaceutical laboratory experience in a cGMP environment
Prior experience in method development / validation and / or transfer / verification, protocols, and troubleshooting
Fluency in English
The QC Analyst will be part of the highly qualified QC team in a fast-paced environment that offers competitive remuneration and opportunities to grow.