(Senior) Manager – Quality operations and Deputy Responsible Person (RP)(m/w/x)

In this role, you will ensure compliance with regulations for Medicinal Products while managing quality tasks and supporting GMP activities. Your day-to-day responsibilities will involve overseeing quality processes, conducting audits, and contributing to continuous improvement efforts.

Anforderungen

• •BA/BS, MA/MS in scientific discipline or related field
• •5 years’ experience in Quality function in pharmaceutical industry
• •Strong understanding of GMPs, GDP, ICH guidelines
• •Significant experience as lead auditor for pharmaceutical manufacturing
• •Experience with regulatory agencies such as Swissmedic, EMA, FDA
• •Prior experience as deputy Responsible Person & interactions with Swissmedic
• •Fluency in English; German and/or French beneficial
• •Ability to work effectively in team-oriented environment
• •Leadership, Drive, Enthusiasm skills
• •Goal-Orientated and commitment to follow up on tasks
• •Decision Making, Problem Solving, Independence skills
• •Flexibility and willingness to travel (up to approx. 25%)
• •Proactive and Self-motivated