Qualified Person (12 months fixed term contract)

We are seeking a Qualified Person to certify medicinal products in accordance with EU regulations and company requirements. The role involves coordinating QA operational duties, participating in investigations and risk assessments, and ensuring product release procedures comply with current regulatory and company requirements.

Requirements

• Meets qualification requirements for a QP as listed in EU Directive 2001/83/EC
• Previous experience of certifying medicinal product (previously or currently listed as a QP on an EU manufacturing licence) would be an advantage
• Proven quality experience in pharmaceutical industry encompassing analytical, manufacturing or packaging operations
• Working knowledge of EU and US GMPs
• Proficiency in electronic systems/databases such as documentation, Trackwise, SAP, MES etc.
• Good team working and strong communication skills across functions and organization
• An ability to work flexibly in a changing environment
• Good attention to detail and priority management essential
• Flexibility to learn new skills and take on new tasks and responsibilities

Benefits

• Competitive salaries
• Benefits
• Inclusive environment
• Excellent career progression opportunities
• Work-life balance initiatives