Anil Sebastian, PhD, Founder & Principal Consultant

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Founder & Principal Consultant

Anil Sebastian, PhD

Anil Sebastian, PhD, is a biopharmaceutical scientist and technical leader with more than 18 years of experience spanning academic research, biotechnology and industrial bioprocess development. His career has included scientific and leadership roles across bioprocess development at Lonza Biologics, Accord Healthcare, Ivy Farm Technologies, a stealth-mode biotechnology company and Intercytex.

His core technical expertise spans host-cell and cell line development strategy, media development and optimisation, mammalian upstream process development, scale-up and technology transfer. He also brings practical experience in establishing biopharmaceutical development capabilities, including the set-up of cell line development and process development laboratories, with responsibility spanning laboratory infrastructure, equipment implementation, workflows and operational readiness.

Experience

18+ years

Publications

40+ articles & papers

Funding

£3M+ secured

Career highlights

Ivy Farm Technologies

Associate Director, Cell Culture Media & Process Development

Accord Healthcare

Head of Upstream Process Development – established the process development laboratories

Lonza Biologics

Group Leader – inter-site cell line construction governance

Earlier roles

Bioprocess development with a stealth-mode biotechnology company and Intercytex

The University of Manchester

PhD, Chemical Engineering & Biotechnology; postdoctoral research

Regulatory, CMC & compliance

His development experience is complemented by regulatory and CMC exposure, including review and contribution to IND/BLA documentation and scientific support for regulatory submissions and interactions with agencies including the FDA and MHRA. He also has hands-on experience in biosafety and laboratory compliance associated with mammalian cell and genetically modified organism activities.

  • IND/BLA documentation review and contribution
  • Regulatory interactions including FDA and MHRA
  • GMO risk assessments and containment requirements
  • COSHH/BioCOSHH documentation
  • SOP development and equipment/process procedures
  • Qualification activities

Research, funding & memberships

He holds a PhD in Chemical Engineering & Biotechnology from The University of Manchester and has authored or co-authored more than 40 scientific articles and conference publications. During his postdoctoral research, he contributed to securing more than £3 million in research and innovation funding, providing first-hand experience in developing scientifically credible funding propositions and translating complex research programmes into investment cases.

Education

PhD, Chemical Engineering & Biotechnology

Memberships

BioIndustry Association (BIA) & ESACT-UK

Through Z2 Biopharma Solutions, this focused CLD and upstream CMC expertise is complemented by a panel of experienced consultants with broader bioprocess development understanding, supporting wider scientific and cross-functional discussions across biologics development where required.

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Whether you are designing a CLD programme, stuck on an upstream process, preparing for technology transfer, or assessing a biologics asset before you commit.