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  • Advanced Scientist - Process Development
  • Volt Life Sciences
  • [Published Fri Feb 15 16:53:00 GMT 2008]

  • Business Type: Drug Development
  • Job Type: Purification & Characterisation Scientist
  • Position Type: Permanent
  • Location: Midlands - Derbyshire
  • Salary: Competitive Package

Background:

We are currently looking for an Advanced Scientist to join the Conventional Drug Delivery process development team, which is dedicated to the latter stages of the product development life cycle of creams and gels. The primary objective of the department is to develop robust manufacturing processes for new formulations and introduce these into the manufacturing environment. As part of this the department is responsible for manufacturing and supplying material for clinical trials and the generation of data to support the regulatory approval process.

In this role you will support the development, process optimisation, scale up, clinical trial supply manufacture, validation and commercialisation of new formulations for topical use. You will assist in the optimisation and development of both bulk product manufacture and filling of the product into single use applicators as well as participate in local and global teams as a technical resource. You will coordinate and perform late phase development activity and clinical trial supply manufacture in line with project plans in conjunction with the designing, performing and reporting of complex laboratory, pilot and full scale development experiments in accordance with GMP, DFSS principles and international regulatory guidance.

Primary Duties:

We are currently looking for an Advanced Scientist to join the Coventional Drug Delivery process development team, which is dedicated to the latter stages of the product development life cycle of creams and gels. The primary objective of the department is to develop robust manufacturing processes for new formulations and introduce these into the manufacturing environment. As part of this the department is responsible for manufacturing and supplying material for clinical trials and the generation of data to support the regulatory approval process.

In this role you will support the development, process optimisation, scale up, clinical trial supply manufacture, validation and commercialisation of new formulations for topical use. You will assist in the optimisation and development of both bulk product manufacture and filling of the product into single use applicators as well as participate in local and global teams as a technical resource. You will coordinate and perform late phase development activity and clinical trial supply manufacture in line with project plans in conjunction with the designing, performing and reporting of complex laboratory, pilot and full scale development experiments in accordance with GMP, DFSS principles and international regulatory guidance.

Qualifications:

To be successful in this role you will either have a BSc in Bio Medical or Life Science Pharmacy or Pharmaceutical Sciences would be ideal or alternatively be a process chemical engineering Graduate with pharmaceutical experience. Experience in a pharmaceutical development environment is desirable, ideally with experience of cream or gel formulations and their manufacture combined with knowledge of pharmaceutical formulation and or scale up processes, preferably with creams or gel formulations.

To apply, please complete the online application or contact us for further information. Please quote reference: ' 40260-PHARM-MCB '

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