
Engineering • IT Services • Aerospace
ALTEN is a leader in outsourced Engineering and R&D and IT Services, catering to various industries such as aeronautics, automotive, banking, and life sciences. With a workforce of over 57,400 employees across nearly 30 countries, ALTEN specializes in executing complex and technical projects, supporting innovation and technology advancements in multiple sectors. The company focuses on providing engineering services, project management, and IT solutions to enhance client operations and foster sustainable innovation.
10,000+ employees
🚀 Aerospace
November 13
🗣️🇩🇪 German Required

Engineering • IT Services • Aerospace
ALTEN is a leader in outsourced Engineering and R&D and IT Services, catering to various industries such as aeronautics, automotive, banking, and life sciences. With a workforce of over 57,400 employees across nearly 30 countries, ALTEN specializes in executing complex and technical projects, supporting innovation and technology advancements in multiple sectors. The company focuses on providing engineering services, project management, and IT solutions to enhance client operations and foster sustainable innovation.
10,000+ employees
🚀 Aerospace
• Manage the entire product lifecycle of approved medicinal products (e.g., maintenance of marketing authorizations, variation management, manufacturing changes) • Coordinate and implement regulatory changes in collaboration with Regulatory Affairs (RA), Quality Assurance (QA), Production and Supply Chain • Develop strategic plans to extend product life and market presence • Monitor and assess product performance post-launch • Prepare and maintain post-market surveillance (PMS) plans, Periodic Safety Update Reports (PSURs), Risk Management Plans (RMPs) and other regulatory documents • Analyze market and safety data (e.g., complaints, adverse events, recalls) and derive necessary corrective and preventive actions (CAPA).
• Degree in a scientific discipline (e.g., Pharmacy, Chemistry, Biology or related fields) • Relevant professional experience in lifecycle management, regulatory affairs, quality management or pharmacovigilance within the pharmaceutical industry • Strong knowledge of regulatory requirements (EU GMP, GVP, ICH guidelines; AMVO, MDR advantageous) • Experience with change control processes, deviation management and CAPA systems • Analytical thinking, structured working style and strong project management skills • Business-fluent in German and English, both written and spoken.
• Talent management – we support and develop your career • Work–life balance – flexible working hours and the option to work remotely • Fit and relaxed – access to EGYM Wellpass • Enjoy biking – company bike leasing • Green mobility – discounted sustainable transport options • Permanent employment contract • Corporate benefits • Team events
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