Head of MSAT Pharma Analytics - #2621743

Barrington James


Date: vor 3 Wochen
Stadt: Frankfurt am Main
Vertragstyp: Ganztags
Arbeitsplan: Volle Tag
Barrington James

The Role

Lead a newly established Manufacturing Science and Analytical Technology (MSAT) Analytics function within a global pharmaceutical organisation. The role is primarily post-launch focused, addressing complex analytical and manufacturing challenges across multiple dosage forms, while contributing to innovation products. The position requires a strong leader who can set direction, solve technical problems pragmatically, and drive cross-functional collaboration to ensure product quality and supply reliability.


Requirements

  • PhD or equivalent in Analytical Chemistry, Chemical Sciences, or Pharmaceutical Sciences
  • Extensive experience in R&D or operations, with a proven track record of developing, validating, and troubleshooting analytical methods across multiple manufacturing sites and product types
  • Expertise in root cause analysis, post-launch product lifecycle management, and navigating technical issues with marketed products
  • Experience across multiple dosage forms; exposure to generic products or a broad spectrum of technologies is advantageous
  • Strong leadership and influencing skills, able to guide teams and cross-functional partners to deliver pragmatic, cost-efficient solutions
  • Skilled in designing and conducting studies to generate actionable data for problem-solving in manufacturing and quality operations
  • Agile, collaborative, and capable of leading through ambiguity
  • Language skills beyond English are not required


Responsibilities

  • Lead and develop a small team of analytical scientists, providing clear direction, accountability, and mentorship
  • Oversee investigation, troubleshooting, and resolution of complex analytical and manufacturing issues
  • Develop, validate, and optimise analytical methods for APIs and finished products across multiple dosage forms
  • Direct studies to generate data for problem identification, documentation, and solution implementation while ensuring compliance with GMP and international standards
  • Collaborate with internal cross-functional teams and external partners to deliver solutions efficiently
  • Provide strategic input for post-launch lifecycle management and regulatory support
  • Promote knowledge transfer and best practices to maintain product quality and ensure supply continuity


To Apply

[email protected]

+441293778666

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