Pharmaceutical Development Specialist
2 months ago
Viatris empowers people worldwide to live healthier at every stage of life. We do so via:
- Access – Providing high quality trusted medicines regardless of geography or circumstance;
- Leadership – Advancing sustainable operations and innovative solutions to improve patient health;
- Partnership – Leveraging our collective expertise to connect people to products and services.
We are seeking a highly skilled Pharmaceutical Development Specialist to work in the formulation and process group on drug product development projects. This is an exciting opportunity for someone with a strong background in pharmaceutical formulation and manufacturing processes. The successful candidate will be responsible for reliably carrying out laboratory scale formulation and process development activities including documentation and data integrity.
This role will have a significant impact on the development of inhaled dosage forms required for project progression. You will execute experiments to develop the formulation and manufacturing process projects ensuring they meet technical milestones as discussed with supervisor.
- Executes experiments to develop the formulation and manufacturing process projects ensuring they meet technical milestones as discussed with supervisor.
- Actively participates in the matrix team to design, and where required, undertake high quality scientific experimentation to further the development of the formulation and manufacturing process of inhaled dosage forms required for project progression.
- Communicates effectively to supervisor and the wider development team and presents data at technical meetings and project team meetings.
- Analyses test data in the context of manufacturing parameters to understand the impact of formulation and processing on product Quality Attributes.
- Operates laboratory scale equipment for inhalation formulation and process development to manufacture products for analytical testing.
- Contributes practical experience to help define the formulation & manufacturing processes in support of pre-clinical, clinical & pivotal regulatory batch manufacture.
- Contributes to authorship of high-quality technical reports on product development activities.
- Adherence to all applicable policies and procedures, including those relating to EHS, GMP, GCP, Quality and Compliance, consistent with the role.
Paid between £50,000 - £70,000 per annum, depending on experience. Our comprehensive benefits package includes pension scheme, private medical insurance, life assurance and a generous annual leave allowance.
Please note that occasional business travel may be required.
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