Document Control Specialist

A global leader in biotechnology, committed to advancing treatments and potential cures for life-threatening illnesses. Working at this company allows you to make a direct impact on patient lives while expanding your skills in the pharmaceutical sector. They foster an open, transparent culture where your contributions are valued from day one. 

Join a growing and international environment where you play a key role in maintaining a compliant document management process. As a Document Control Specialist, you will:

• Manage site document control systems and related workflows
• Review new and updated documents to ensure alignment with global and site procedures
• Support users with electronic document management tools
• Oversee the periodic review of procedures
• Issue batch documentation supporting GMP manufacturing
• Reconcile GMP documents following lifecycle requirements
• Create and issue GMP logbooks
• Manage storage, retention, and archival of GMP records
• Perform tasks according to cGMP, quality systems, and safety policies
• Review and approve SOPs and drive continuous improvement initiatives

• bachelors degree or equivalent experience
• First expierience in a relevant job.
• Preferably familiar with GMP environments
• Knowledge of GxP Quality Systems and relevant guidelines (21 CFR, ICH Q10, EU GMP/GDP, etc.)
• Strong communication, problem-solving and conflict-resolution abilities
• Highly organized, detail-oriented, flexible, and able to manage shifting priorities
• Strong interpersonal skills with the ability to work independently
• Proficient with Microsoft Office