Regulatory Affairs Manager/CMC (m/f/d)

Duration: 30/10/2025, possible extension

Key Responsibilities:

  • Manage timely responses to Health Authority (HA) questions (author/ review)
  • Draft/ review briefing documents to support e.g. scientific advice procedures/ meetings with HA
  • Lead/ coordinate/ communicate/ track/ activities to ensure submission deadlines are met in accordance with procedures: e.g. planning, liaising with Subject Matter Experts (SME) and Projects Managers (PM), collaborate internally/externally on Clients projects
  • Communicate and escalate risks and issues to management and project teams, as applicable;
  • Act as RA Point of Contact or RA team member for assigned projects e.g. attend meetings with clients, provide regulatory advice
  • Change Controls and Deviations
  • Perform Regulatory assessments for change controls and deviations to ensure compliance with internal procedures and regulations
  • Support site-specific regulatory documentation and activities: maintenance of sites facility registrations filings with regulatory agencies and plant-level documentation (e.g. Site Master File and Japan FMA)
  • Participate in process improvement activities/ projects to bring continuous improvement to Regulatory processes e.g. apply Lean methodology

Requirements:

  • Advanced knowledge in Life Sciences (e.g. Molecular and Cell Biology, Biochemistry, Microbiology) and Pharmaceutical Sciences (e.g. injectables): good understanding of manufacturing processes and quality control for biological medicinal products (e.g. Mammalian, Microbial, Conjugates, Vaccines, Sterile products)
  • Strong knowledge of CMC requirements for biologics as well as good procedural knowledge (EU and US; other markets is a plus). In-depth understanding and application of industry standards and global regulations and guidelines
  • Experience (at least 5 years) in authoring high-quality CMC CTD sections (content and format) for drug substance, drug product, and appendices from first-in-human to post-approval for biological medicinal products
  • Good CMC writing skills

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Facts about the job

Field
Other
Country
Switzerland
Location
Basel-Stadt
Contract type
Contracting
Job-ID
860DBN&origin=51001
Company
Coopers Group AG