Head Of Analytical – Development

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View: 139

Update day: 17-04-2024

Location: Basel Basel-Stadt BS

Category: Sales

Industry: Staffing Recruiting

Position: Director

Job type: Contract

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Job content

Head Of Analytical – Development12-month contract, full time onsite, BaselExciting new opportunity we have with our global pharmaceutical client based in Basel, Switzerland. Who is looking for a Head of Analytical Development.This position is responsible for strategic planning, delivery of innovated methodologies and execution of all analytical development activities supporting all preclinical programs.The Head of Analytical Development &Technologies Drug Substance & Drug Product will lead early-stage analytical development, method verification and transfer activities necessary for API (Active Pharmaceutical Ingredient) release, as well as lead analytical troubleshooting exercises during technical transfers.The rate of Pay is up to 94 CHF per hour and is based in Basel.
  • Analytical Chemist, Pharmaceutical Chemist or related scientific discipline.
  • BS with 18 +, MS with 14+ or Ph.D with +8 years’ experience in the pharmaceutical industry with increasing scientific and leadership responsibilities in analytical development.
  • Broad knowledge and experience in the development and validation of test methods for small molecule drug substance candidates, physical and chemical characterizations, general analytical analysis, assay/impurity analysis, purity/related substances and PGIs.
  • Skills building and maintaining productive relationships with organizational counterparts such as Toxicology, Preformulation and Preclinical Galenics, Chemical Development, Process Research, Quality Assurance and Regulatory CMC.
  • Scientific knowledge, high level of innovation and experience in analytical science in drug development and associated analytical requirements throughout the development phases.
  • Broad knowledge of the pharmaceutical development process.
  • Knowledge of applicable global drug development and regulatory standards with strong analytical and strategic thinking.
  • Knowledge and application of cGMPs/GLPs, ICH, FDA, and CMC Guidance Documents.
If interested, please feel free to contact myself Ibrahim Bokolo via email: ibokolo@achieva.co.uk or 01727817642.
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Deadline: 01-06-2024

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