Quality Assurance Reviewer 

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 Master Data & Labeling Specialist you will be responsible for Perform review and approval of Master Data related activities, as well as perform approval of artwork for medicinal products and participate in QA related projects.

Responsibilities
– Perform review and approval of Master Data related activities.
– QA Review of operational SOPs and Work Instructions.  
– Ensures compliance within regulatory environment.
– Screens, categorizes, evaluates, reconciles, reports and resolves data integrity issues.
–  Refers to technical standards, principles, theories and precedents as needed.
–  May set project timeframes and priorities based on project objectives and ongoing assignments.

 Requirements
– MBO or Bachelor’s degree in Life Sciences or related field or the equivalent combination of education and/or experience. Entry-level position for master’s degree in Lifesciences.
– Typically 3 years of related Quality Assurance or manufacturing experience in the pharmaceutical or medical device industry
– Good Manufacturing Practice (GMP), Good Distribution Practice (GDP) and/ or Good Clinical Practice (GCP) knowledge with the ability to interpret and apply in mainly routine cases.
– Accurate mindset

Other information
Are you interested? Feel free to contact me!