Formulation Expert (m/f/d)

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Beschreibung



Formulation Expert (m/f/d)

Reference: -en
Start: asap
Duration: 12 MM++

Main tasks:
  • Job purpose to support drug product manufacturing process related development and supply activities for oral small molecule drug products in Post POC phase.
  • This includes the scientific evaluation and presentation of data, authoring of technical and GMP documentation, integrity checks against raw data and on-site manufacturing support to technical and clinical manufacturing campaigns.
  • You work in a cross-functional team with manufacturing operations, analytics and QA and contribute to the overall Technical Research and Development strategies and goals.
  • You work under minimal guidance of more experienced formulation project leaders.
  • Support drug product formulation development and manufacturing activities at internal or external manufacturing sites for assigned projects in line with the project plan, guidelines and procedures 
  • Collaborate with operational colleagues working on your process at the respectivemanufacturing site
  • Take accountability for formulation and manufacturing process deliverables incl. GMPrelated aspects and change control
  • Author manufacturing instructions for clinical manufacturing campaigns, compile data And interpret results, evaluate data, draw relevant conclusions and contribute to
  • Development reports and Quality risk assessment documents in close collaboration with the project teams
  • Perform document reviews and data integrity checks against raw data
  • Support deviation investigations and drive change control
  • Exchange regularly within your project team as well as seek guidance with internal experts on diverse aspects


Main qualifications
  • This position is ideal for somebody with a pharmaceutical background wishing to gain or expand first experience in the field of pharmaceutical development
  • Master degree or higher in life sciences, ideally in the Pharmaceutical field 
  • Ideally first industrial experience in the development and / or clinical Manufacturing of pharmaceutical formulations for small molecules
  • Fluent in English (oral and written), German is an advantage
  • Interdisciplinary thinking and interest in collaboration with other functions
  • Good knowledge of GMP and GLP
  • Good knowledge of oral solid dosage form technologies and laboratory and/ortechnical tools
  • Good scientific / technical writing skills 
  • Good collaboration skills and team spirit enabling you to work in a matrix environment, Good communication and negotiation skills


Main advantages:
  • Option for extension
  • You will work in an intenational environment
  • You will work in one of the biggest pharmaceutical company of the world



About us:
With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.

My contact at Hays:

My contact person:
Natascha Hanser

Referencenumber:


Make contact:
Email:
Start
ab sofort
Dauer
12 MM++
(Verlängerung möglich)
Von
Hays AG
Eingestellt
27.05.2021
Ansprechpartner:
Hays AG
Projekt-ID:
2122671
Vertragsart
Freiberuflich
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