(m/f/d)
Freelance/temporary employment for a project
Basel
Start date: asap
Reference number: 890604/1
Establish relationships with business stakeholders and lead the development of molecule/product/process/affiliate-level approaches with appropriate measures (CtQ Factors)
Analyze quality data to identify trends and risks, providing insights to business partners
Lead and perform complex audits and quality assessments
Synthesize individual audit issues into systematic conclusions and present findings and associated risks to senior stakeholders, ensuring quality data fulfills regulatory requirements and supports organizational goals
Play a lead role in inspection preparation and management as well as providing training to staff and ensuring relevant materials are prepared for regulatory review
Lead assigned goals and initiatives and drive the development or revision of PDQ processes
Maintain and influence partnerships with senior business stakeholders and PDQ domains
Facilitate cross-functional collaboration to ensure quality standards are met globally
Expert knowledge in GxP regulations (FDA, EU, ICH guidance) and internal policies
Ensure all activities are conducted in compliance with regulatory and company requirements