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Senior Scientist - Pharmaceutical Process Development - Geneva
Vue: 146
Jour de mise à jour: 03-04-2024
Localisation: Meyrin Genève GE
Catégorie: R & D IT - Logiciel
Industrie: Pharmaceuticals
Niveau: Associate
Type d’emploi: Full-time
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le contenu du travail
ResponsibilitiesReporting to the Head of Process Development, your main responsibilities are as follows
In view of our continued global growth we are expanding our production capacities. For this reason we are looking for further support and recruiting our new Senior Scientist specialized in pharmaceutical process development at our biotech production site in Geneva. In this position you are accountable for technical aspect related to pharmaceutical process development (dried forms) and optimization and has an in-depth experience in leading technical.
- Establish optimization / development strategies for pharmaceutical process: lab and pilot scale, scale-up, industrial transposition
- Act as project manager in projects related to pharmaceutical process development
- Plan and execute development trials in collaboration with the concerned departments or CDMO: provide appropriate documentation, protocol, reports, in-depth data analysis
- Act as pharmaceutical process expert to provide the necessary support to production to ensure the robustness and the improvement of current manufacturing processes: troubleshoot, root cause analysis and correct problem with manufacturing and quality teams
- Contribute to maintain a state-of-the-art pharmaceutical development laboratory
- Act as expert on theoretical and applied knowledge of biologics dried forms process and formulation development, and current international guidelines (GMP, ICH, ISO)
- Write protocol, reports, SOP and contribute to write technical parts of CTD in collaboration with RA
- Promote operational excellence in pharmaceutical development (Lean 6 sigma)
- Anticipate innovation in the field of expertise and manage implementation of new technologies
- Adhere to all measures for protection of health and environment which are in the area of responsibility.
- Master degree or PhD in the pharmaceutical field
- At least 5 years’ experience in process development for biologics dried forms
- Minimum of 3 years’ experience in industrial transposition and in pharmaco-technical characterization of dried forms
- Experience in GxP environment
- Applied technical understanding of manufacturing equipment and processes
- Experience in analytical development and implementation of processes, project management, CTD writing and PAT implementation would be assets
- Fluency in French and good knowledge in English
- Ability to work alone as well as in project teams as single Point of Contact
Are you interested in this opportunity? Apply as soon as possible and join OM Pharma!
About Us
OM Pharma is a global Geneva-based Biotech company. It is a leader in the prevention of recurrent respiratory and urinary tract infections and is also active in the treatment of vascular diseases.
It operates worldwide through a strong network of international partners and continues to invest into R&D to develop microbial derived immunotherapeutic products addressing acute and chronic immunological disorders resulting from infections and inflammation. OM Pharma is operating to highest Good Manufacturing Practice (GMP) standards which rely on a high level of Biotech competencies and experienced teams.
The company strives to help patients around the world to live better lives by allowing access to a better management of infectious diseases and immunological imbalances.
For more information, please visit: ompharma.com .
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Date limite: 18-05-2024
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