We are recruiting a Manufacturing Science and Technology (MSAT) Senior Scientist at our headquarters and biotech production site in Geneva. Reporting to the Head of MSAT, as part of a team of five and working cross-functionally with a strong presence in the field (production zone), your mission encompasses the development, optimization and continuous improvement of drug product processes and formulations, with a particular focus on lyophilization, encapsulation, dry granulation and intranasal delivery technologies.
Your main responsibilities are as follows:
- Lead development and industrialization of new pharmaceutical products, from formulation and process design to scale-up and validation
- Define development strategies including QTPP, risk assessments, technical requirements, timelines and budgets
- Provide expertise in galenics, formulation, pharmaceutical processes and technology transfer, including CDMO interactions when needed
- Drive optimization of existing manufacturing processes to improve performance, robustness and compliance
- Act as technical expert for troubleshooting, root cause analysis, CAPA implementation and continuous improvement initiatives
- Define Critical Process Parameters (CPPs), Critical Quality Attributes (CQAs) and lead process risk assessments in cross-functional teams
- Manage MSAT Pharma Laboratory activities (equipment qualification, stock management, laboratory support)
- Plan and execute development trials with internal stakeholders (Manufacturing, Quality, Validation, Regulatory CMC), ensuring robust documentation and data analysis
- Ensure full traceability and compliance of development activities in line with GxP requirements
- Contribute to regulatory documentation (e.g. CTD modules) in collaboration with Regulatory CMC
Business travel is required for this position for punctual topics (maximum 5% of working time).
To carry out this mission, we are looking for a person with the following profile:
- Master’s degree in Pharmaceutical Sciences, Biotechnology or equivalent
- At least 8 years of experience related to pharmaceutical process development, formulation development and industrial transposition, with strong expertise in galenics and pharmaceutics
- Proven experience in project management in a cross-functional and GxP environment; experience with regulatory activities is an asset
- Fluent in French with good English skills
- Proficiency in MS Office, with experience using ERP systems (Sage X3 preferred)
To succeed in this role, we are looking for a hands-on, pragmatic and innovation-driven scientist, combining strong technical expertise with a solid business and production mindset. You demonstrate natural leadership, strong communication skills and the ability to collaborate effectively with diverse stakeholders. Entrepreneurial and creative, you continuously seek improvement opportunities and actively contribute to shaping better, more efficient processes. You are solution-oriented, structured, and committed to delivering high-quality results in a dynamic environment.
Are you interested in this opportunity? Apply as soon as possible and join OM Pharma!
OM Pharma is a global Geneva-based biopharmaceutical 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 invests its profits in R&D to develop microbial derived immunotherapeutic products to treat acute and chronic immunological disorders resulting from inflammation and infections.
The company strives to improve the quality of life of patients around the world by providing access to better treatment of immunological imbalances.
For more information, visit the website: ompharma.com.
