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Head of Research & Production

On Friday, June 12,

Offer criteria

  • Suisse
  • Permanent contract
  • Full Time
  • Fields of expertise: Documentation , Design , FDA , Laboratory , Feedback from experience See more , Strategy , Immunology , Regulatory Compliance , Publications , QC , External , Process , Tracking , CMC , EMA , Biochemistry , Project management , Production , Process development , Conferences , Maintenance , Pharmaceutical , Consolidation , Clinical trials , Creative Problem Solving , Technology Transfer , Gene therapy , Android , Line management Show less

Company: Michael Page

Job description

  • Operations management for manufacturing operations and line management responsibility for the managers of Rexgenero's Manufacturing and QC groups
  • Oversight of development, maintenance and regulatory compliance of Rexgenero's cell therapy GMP manufacturing facilities in Seville and manufacture of Rexgenero cell and gene therapies for clinical trials
  • Development of and execution of a strategy plan for CMC development and integration in integrated development plan
  • Design of manufacturing processes, QC assays and other product characterization methods
  • Project management of CMC process development for commercial manufacturing of REX-001 and other cell and gene therapies including process closure and integration of electronic quality management systems (eQMS) and process tracking systems
  • Development and integration of eQMS and administration systems for application in GMP manufacture
  • Characterization and of cell therapy attributes and process characteristics relevant to the biological activity and quality of cell and gene therapies
  • Management of technology transfer of REX-001 manufacturing to additional facilities in North America
  • Oversight of preparation of CMC sections for regulatory filings
  • Establishment and management of external relationships for project partnerships in cell and gene therapy CMC development and manufacture
  • Drafting, editing and updating of regulatory materials including IMPD, briefing packages etc.
  • Documentation of projects, processes, technical findings in internal documents and manuscripts for publication in scientific journals

Profile description

  • Degree in relevant cell biology, biochemistry, immunology, pharmacy, pharmaceutical development or related discipline
  • Minimum 10-year experience of pharmaceutical manufacture in a regulated GMP environment
  • Extensive experience with the GMP manufacture of cell and gene therapies
  • Experience of project management of CMC development preferably for cell and gene therapies
  • Extensive experience of documentation of technical findings
  • Experience in line management of laboratory and/or manufacturing personnel
  • Creative problem-solving abilities in CMC development
  • Experience of interaction with local and international pharmaceutical regulators (especially EMA and FDA)
  • Experience of managing technology transfer of complex pharmaceutical manufacturing processes
  • International experience outside of Spain (preferable)
  • Track record of publications in international scientific or technical journals and presenting at scientific conferences
  • PhD in relevant discipline
  • Fluency in written and spoken English, Spanish language to intermediate level or above

Salary and benefits

Salary: salary according to profile


Reference: 314254_MP_CH


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