Join to apply for the Senior QA Specialist - Project Manager 80-100% (f/m/d) role at Lonza
Today, Lonza is a global leader in life sciences operating across three continents. Our success relies on talented people working together, devising ideas that help businesses and improve lives. We value our employees' careers and encourage innovation, making a meaningful impact on the world.
For our Quality Assurance team in Bioconjugates, Visp, we are seeking a dedicated Senior QA Specialist and Project Manager (f/m/d) to support clinical phase manufacturing and liaise with internal and external stakeholders to uphold Quality standards.
Key Responsibilities
* Ensure production of APIs complies with Good Manufacturing Practice (GMP).
* Support contract manufacturing and advise development, production, and analytical teams on GMP matters.
* Review manufacturing documentation for conformity, process change controls, deviations, and OOS results.
* Act as the quality contact during GMP audits and represent Quality in interactions with clients.
Key Requirements
* University degree in Life Sciences (Microbiology, Biotechnology, Chemistry, etc.).
* Experience in GMP environment, preferably in biopharmaceuticals.
* Strong communication skills and stakeholder management experience.
* Knowledge of TrackWise, SAP, LIMS, DMS is advantageous.
* Fluent in English (spoken and written); German skills at C1 level are required for daily interactions.
At Lonza, we are committed to ethical success, respecting our people and environment. We offer challenges and opportunities to develop solutions that make a global difference. Join us to be part of a team that improves lives worldwide.
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