Regulatory Affairs Manager (f/m/d)

Lonza is looking for a Regulatory Affairs Manager to join its Visp manufacturing site in Switzerland. The role will steer regulatory strategy for sophisticated client programmes, ensuring that development, production and market launch run smoothly. The position is temporary for one year, with relocation support available for qualified candidates and their families. The daily work involves directing all regulatory tasks for assigned projects, acting as the lead contact for regulatory planning, timelines and deliverables. You will synchronize activities across internal departments and the global regulatory network, manage submissions, maintain dossiers, and handle interactions with health authorities. The job also requires preparing high‑quality documentation, supporting customers on CMC matters, and keeping stakeholders informed about risks and milestones. A strong scientific background and hands‑on experience in the pharma‑chemical‑biotech sector are essential. The candidate must be comfortable working in cross‑functional, client‑focused settings, translating regulatory and customer expectations into practical actions. Deep knowledge of GMP rules, quality systems and manufacturing processes is required, together with the ability to assess changes, oversee lifecycle activities and ensure consistent application of regulations. Effective communication and stakeholder management across QA, QC, production and supply‑chain teams are also critical. The role offers an agile career path within an inclusive and ethical environment, with performance‑linked compensation and a range of benefits. Working at the Visp site provides exposure to complex molecules such as bioconjugates, and the chance to contribute to continuous improvement and inspection readiness. Fluency in English, German language skills and familiarity with systems like TrackWise, LIMS, Documentum or Veeva are considered advantageous. What the role asks for: - Degree in Chemistry, Biochemistry, Pharmacy or related science - Experience in pharmaceutical, chemical or biotech industry - Background in QC, QA, Regulatory Affairs or Project Management - Proven ability to work cross‑functionally in client‑driven projects - Strong knowledge of GMP regulations and quality systems - Excellent stakeholder management and communication capabilities - Structured, proactive, solution‑oriented work style with ownership - Experience with regulatory submissions, lifecycle management or change assessments (nice‑to‑have) - English and German communication skills (nice‑to‑have) - Familiarity with TrackWise, LIMS, Documentum or Veeva (nice‑to‑have)