(Senior) QA Expert Manufacturing Release 80-100% (m/f/d) Our Offering Biologics Mammalian Microbial ADCs / Bioconjugates Drug Product mRNA / LNP Expression Technologies Small Molecules Drug Substance (API) Particle Engineering Drug Product Cell & Gene Process Development cGMP manufacturing Allogeneic Autologous Viral Vectors Bioscience Products Capsules & Health Ingredients Pharmaceutical Solutions Nutraceutical Solutions Our Company About Us Purpose and Strategy Leadership History Locations Site Tours Partnering with Us Events News and Media News Releases Images and Videos Logo Guidelines Blog Podcast Journalist Inquiries Investor Relations Shareholder Information Agenda and Events Financial Reporting Annual and Sustainability Report Corporate Governance Ethics and Compliance Investor Inquiries Sustainability Performance People Planet Community Global Quality Responsible Sourcing Careers Overview Life at Lonza What We Offer Career Stories Job Search Join Our Talent Community Recruitment Process Students, Graduates and Apprentices Contact Our Offering Corporate Biologics Mammalian Microbial ADCs / Bioconjugates Drug Product mRNA / LNP Expression Technologies Small Molecules Drug Substance (API) Particle Engineering Drug Product Cell & Gene Process Development cGMP manufacturing Allogeneic Autologous Viral Vectors Bioscience Products Capsules & Health Ingredients Pharmaceutical Solutions Nutraceutical Solutions Back Our Company Corporate About Us Purpose and Strategy Leadership History Locations Site Tours Partnering with Us Events News and Media News Releases Images and Videos Logo Guidelines Blog Podcast Journalist Inquiries Investor Relations Shareholder Information Agenda and Events Financial Reporting Annual and Sustainability Report Corporate Governance Ethics and Compliance Investor Inquiries Sustainability Performance People Planet Community Global Quality Responsible Sourcing Back Careers Corporate Overview Life at Lonza What We Offer Career Stories Job Search Join Our Talent Community Recruitment Process Students, Graduates and Apprentices Back Contact Corporate Back (Senior) QA Expert Manufacturing Release 80-100% (m/f/d) Switzerland, Stein Senior QA Expert Manufacturing Release 80-100% Location – Stein, Switzerland Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of. The primary purpose of the role is to ensure a Right Time in Inspection Readiness for a Big CAPEX project (encompassing a Fill Finish Facility, Laboratories, Warehousing, Shipment and Offices). The role will manage QA operational activities to support departmental projects and objectives according to agreed timelines and standards and ensure compliance with GMP is maintained in Sterile Production Plant Stein. Then, after the project phase, will manage the quality activities as operational QA (e.g. Batch Release, deviation, etc.) Key Responsibilities: Write, review and/or approve deliverables (e.g. procedures, SOPs, cleaning documents, batch documentation, gap assessments, change request, deviation and CAPA) and related data bases (e.g. training, validation) to ensure GMP compliance. Support project and maintain Sterile Production Stein line functions in GMP compliance related issues. Promote and enforce compliance to internal and external guidelines regarding quality and safety. Lead development and evaluation of new tools, processes, quality initiatives & plans, actively participate in continuous improvement. Represent Sterile Production Stein QA in inspections, audits and local and global initiatives. Ensure internal and customer support in regards to global initiatives (e.g. quality alerts) Key requirements: University or academic degree (e.g. Master) in Chemistry, Biology, Pharmacy or equivalent Professional experience in Quality Assurance or Quality Control in a manufacturing environment within Pharmaceutical Industry > 7 years Excellent knowledge of cGMP regulations Sound knowledge in manufacturing of chemical and biological drug products Problem solving skills Sets clear priorities for task for him Customer oriented and collaboration with Process Unit team Ensuring cGMP and regulatory compliance of all relevant operations in the Process Unit Excellent English skills (spoken and written) German is an advantage Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference. Reference: R59178 Apply Ways to Contact Contact Us Regulatory Support Locations Site Tours Partnering with Us Resources Knowledge Center Meet the Experts Upcoming Events Terms & Conditions Terms and Conditions Legal Disclaimer Privacy Policy California CCPA Notice Transparency in Coverage Lonza.com Company Overview News & Media Investor Relations Sustainability Careers © 2024 Lonza. All rights reserved. Cookie Settings