The Company
Our clients is one of the leads from the Biotechnology industry who try to improve patients’ lives, by distributing their medicines to hospital and pharmacies in 100 different countries in the world, to over 10 million patients, in Europe, Turkey, Middle East and Africa Regions.

Role Description
As a QA Labeling Specialist, you will be responsible for reviewing and approving Master Data activities, approving artwork for medicinal products, and participating in QA-related projects.

Responsibilities
– Review and approve Master Data activities.
– Conduct QA reviews of operational SOPs and work instructions.
– Ensure compliance with regulatory requirements.
– Screen, categorize, evaluate, reconcile, report, and resolve data integrity issues.
– Refer to technical standards, principles, theories, and precedents as necessary.
– Set project timelines and priorities based on project goals and ongoing tasks.

Requirement
– An MBO or Bachelor's degree in Life Sciences or a related field, or an equivalent combination of education and experience. 
– This is an entry-level position for candidates with a Master's degree in Life Sciences.
– Typically requires 3 years of experience in Quality Assurance or manufacturing within the pharmaceutical or medical device industry.
– Knowledge of Good Manufacturing Practice (GMP), Good Distribution Practice (GDP), and/or Good Clinical Practice (GCP), with the ability to interpret and apply these standards in mostly routine situations.

Other Information
Apply to our vacancy for more details. Looking forward to chatting with you!

53355