Drug Product MSAT

$75000.00 - $85000.00 per annum
  1. Permanent
Reykjavík
  1. Technical Operations, Validation, Manager
Posted: 13/07/2020
BBBH14513

This vacancy has now expired. Please see similar roles below...

Hobson Prior are currently working with a specialty biopharma organisation who are focused on the advancing and manufacturing biosimilar medicines. Our client is looking for a Drug Product MSAT to join them on a permanent basis in


Job Responsibilities:

  • Work cross functionally to lead/support manufacturing related process improvement, process
  • validation, process change control, deviation investigation and technical troubleshooting to help maintain lean, flexible and agile manufacturing facility.
  • Work cross functionally to plan and implement and review CAPA and change controls related to DP Manufacturing.
  • Aim to continually identify process improvement and waste elimination opportunities to help create and maintain a lean, flexible and agile manufacturing facility.
  • Lead selection and manage vendors of new equipment, services and materials to support DP Manufacturing activities.
  • Adhere to budget and resource management for all assigned projects according to guidance given by management.
  • Formulate and inform strategies for the successful and smooth technical transfer of new processes and products into manufacturing.
  • Inform and manage strategies for process characterisation/ validation.
  • As a trained Trainer, train, coach and mentor. Help to provide guidance and support for less experienced members of staff.
  • Responsible for own continuous professional development to maintain up-to-date knowledge of new Regulatory requirements as well as technical developments relevant to own area of expertise. Proactively share knowledge for the benefit of others.

Key Skills:

  • Team player with strong leadership and organizational skills.
  • Excellent written and verbal communication skills.
  • Proficient in use of a PC and common Microsoft packages such as Word,Visio, Excel.

Requirements:

  • Industry experience in pharmaceutical development and/or manufacturing of finished dosage forms for biopharmaceuticals.
  • Knowledge of GMP, Process Characterization and Validation.

Apply now:

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

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