Director, Formulation & Process Innovation

Hyper Recruitment Solutions

United Kingdom

On-site

GBP 120,000 - 170,000

Full time

2 days ago
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Job summary

Hyper Recruitment Solutions seeks a Director of Formulation & Process Development to lead strategic formulation development across early clinical phases to commercialisation. You will oversee multi-disciplinary teams, ensure GMP compliance, and drive regulatory submissions to support product approvals and lifecycle management.

The role requires a strong track record in pharmaceutical formulation leadership, cross-functional collaboration, and experience with FDA/EMA/ICH regulatory frameworks,

Qualifications

  • Degree or higher in Pharmaceutical Sciences, Chemistry, or related field.
  • Proven GMP formulation development leadership with global regulatory submissions.
  • Extensive knowledge of FDA, EMA, ICH regulatory requirements.
  • Ability to lead cross-functional teams in fast-paced client-driven settings.

Responsibilities

  • Provide strategic and operational leadership for formulation and process development.
  • Define end-to-end formulation development strategies for early to late-stage products.
  • Lead cross-functional teams across formulation, analytical, manufacturing and quality.
  • Develop and mentor the formulation development team; build high-performance culture.
  • Support client interactions, regulatory inspections, and product approvals.

Skills

Leadership
Cross-functional teams
Regulatory submissions
Client interactions

Education

Degree in Pharmaceutical Sciences or Chemistry

Job description

Hyper Recruitment Solutions seeks a Director of Formulation & Process Development to lead strategic formulation development across early clinical phases to commercialisation. You will oversee multi-disciplinary teams, ensure GMP compliance, and drive regulatory submissions to support product approvals and lifecycle management.

The role requires a strong track record in pharmaceutical formulation leadership, cross-functional collaboration, and experience with FDA/EMA/ICH regulatory frameworks,

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