Your responsibilities:

• Assists in the development and execution of streamlined business systems, which effectively identify and resolve quality issues.
• Supports departmental, functional, divisional, and corporate quality goals and priorities.
• Acts as team member in supporting quality disciplines, decisions, and practices.
• Builds quality into all aspects of work by maintaining compliance to all quality requirements.
• Execute CAPAs and participate in improvement projects as appropriate.
• Execution of field actions and handling product complaints, document review and Supplier management.
• Managing processes at a Third-Party Logistic (3PL) warehouse.
• In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures.
• Assures that appropriate resources (personnel, tools, etc.) are maintained in order to assure Quality System compliance and adherence to the BSC Quality Policy.
• Establishes and promotes a work environment that supports the Quality Policy and Quality System.

What are we looking for in you:

• A degree qualification in scientific subjects, such as Biological Sciences or Health Sciences.
• Proven experience within Quality Assurance, either from the medical device industry, or from the pharmaceutical sector.  
• Experience of CAPA, managing non-conformances.
• Experience in executing field actions, handling product complaints and documentation reviews.
• Good understanding of governing regulations and experience in managing processes at a Third-Party Logistic (3PL) warehouse.  
• ISO13485 lead auditor experience is beneficial.
• Proactive and innovative team member with problem solving expertise.
• Highly organised with excellent attention to detail.
• Internal and external communication skills.
• English language skills, both written and verbal, at a professional working proficiency level.