Senior Formulation Scientist

Canton of Basel-Stadt  ‐ Onsite
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Description

Job Purpose:
We are recruiting for a Formulation Scientist who will oversee formulation development projects and the related manufacturing duties. Experience in Solid Oral Dosage is a must. You will be responsible for formulation and process-design, control strategy, quality risk management, authoring of development documents and manufacturing instructions for technical and GMP manufacture incl. handling of deviation.

Responsibilities:
  • Accountable for all formulation and manufacturing process deliverables including scientific documentation and excipient qualification.
  • Create, own and update formulation project plans aligned with the control strategy.
  • Drive Drug Product development and supply activities with scientific and technological excellence.
  • Closely collaborate with your Drug Product subteam team members understand, identify and manage with them together critical aspects around Drug Substance, Drug Product, packaging and analytics.
  • Drive regular exchange with Biopharmaceutics Experts to understand critical factors for absorption and Drug Product performance and build this understanding into your development strategy.
  • Drive regular exchange with internal SMEs such as the Technology Focus Groups covering pharmaceutical unit operations of your Drug Product and build their guidance into your development strategy.
  • Author Create documents (such as CSF, FMI development reports) and Supply documents (MIs, PHAD application sheets) to allow timely start of development trials, process transfers and supply activities.
  • Contribute to the generation of filing dossiers, answer Drug Product related questions in inspections and support Health Authority requests.
  • Take accountability for the preparation and representation of project/product-related aspects during internal and health authority inspections (e.g. batch production records, project/product-related change requests and deviations, etc.


Requirements:
  • Preferably educated to a PhD level in Scientific or relevant discipline.
  • 5 - 10 years of successful industry experience in the development of pharmaceutical formulations. (ideally oral solid dosage forms), solid understanding of QbD and biopharmaceutics).
  • Interdisciplinary thinking and interest in collaboration with other functions.
  • Excellent scientific knowledge and skills
  • Excellent knowledge of laboratory and/or technical tools (e.g. QbD, statistical software, PAT).
  • Broad and profound understanding of formulation development activities.
  • Strong knowledge of relevant GLP, GMP regulations and policies.
  • Good project management skills.


Kontakt: Luchele Mendes:

Michael Bailey International is acting as an Employment Business in relation to this vacancy.
Start date
03/2019
Duration
03/03/2021
From
Michael Bailey Associates
Published at
08.02.2019
Project ID:
1716648
Contract type
Freelance
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