Become part of an innovative team shaping the future of pharmaceutical engineering. You will lead the implementation and validation of critical systems in pharmaceutical production, ensuring compliance with GMP and CQV standards. This role offers an exciting
QPS Engineering AG in Aargau, Switzerland is seeking a Pharmaceutical Engineer to lead implementation and validation of critical systems while ensuring compliance with GMP and CQV standards. You will work with multidisciplinary teams on high-impact projects that enhance
Switzerland, Stein The actual location of this job is in Stein, AG, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. Join Lonza as an Associate Director, Technology Transfer (Global MSAT) and
Your responsibilities include but are not limited to: Supports the preparation and coordination of Annual Product Quality Review activities in accordance with Novartis procedures. Supports third-party management activities and related compliance processes. Contributes to the implementation and
With more than 30 different sterile products supplied to over 120 countries, our site operates in a highly regulated and globally impactful environment. As a postgraduate in the QA Compliance department, you will provide expert support