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.
RESPONSIBILITIES
- 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.
Requirements
- 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
Benefits
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.