Team Lead - Analytical Chemistry - Inhalation

Team Leader - Analytic Chemistry - InhalationAthlone - IrelandReference: 2962
  • Work with a highly successful and expanding CRO
  • Lead a team of analytical chemists conducting inhalation research
  • Have real input into early drug development

Are you a Senior Scientist with line management experience? Have you got a sound background working in an Analytical Laboratory environment? Have you worked with inhalation equipment such as pMDI, DPI, Nasal Sprays and Nebulisers? Our client – a leading CRO providing early drug development services – is looking for an Associate Group Leader to take on a high degree of responsibility at their inhalation laboratories in Athlone, Ireland.

The key to the success of an applicant for this position will lie in the candidate’s ability to demonstrate a familiarity with the direct supervision of technical laboratory staff, alongside a solid understanding of inhalation research and method development in a GMP environment from first-hand experience.

The Candidate:

  • Sound line management experience of technical staff working in an analytical laboratory
  • Full understanding of GMP requirements, client SOPs, ICH guidelines, EP and USP requirements and EMEA and FDA guidelines
  • Educated to Degree level in a relevant subject (i.e. Chemistry)
  • Knowledge and experience in working with inhalation devices and products such as Pressurised Metered Dose Inhalers (pDMI), Dry Powder Inhalers (DPI), Aqueous Nasal Sprays, Nebulisers and Nebuliser solutions
  • Experienced in the review of study protocols, project status reports and final study reports
  • Ability to implement method development strategies and conduct experimental studies, contributing to technical troubleshooting

The Role:

  • Line management of technical staff to include Scientists and Senior Scientists
  • Oversee and be responsible for the overall quality of the study in day to day operations
  • Working within a fully GMP qualified environment, design and deliver inhalation studies in the early drug development phase
  • Allocate, schedule and manage laboratory resources according to the scope of the study
  • Prepare, review and approve study protocols, project status reports, final study reports and other project related documentation
  • Design experimental studies and participate in technical troubleshooting
  • Review and approve laboratory investigations, deviations, QA facility and data audits
  • Assist in regulatory and client led audits

The Salary:

  • In order to secure the services of the right candidate, our client is willing to be flexible
  • A joining fee will be payable to the successful applicant

Zest is working to a tight deadline on this role, so please apply now and your application will be reviewed immediately 

 

Zest Scientific is working to a tight deadline on this position, so please apply now and your application will be reviewed immediately.

Contact: Jason Cox
Email: jason.cox@zestbusinessgroup.com
Telephone: 0114 229 1672