Parenteral Formulation and Process Development Scientist
Vor 3 Tagen
This is a temporary contractor opportunity at Novartis
Novartis touches the lives of a tenth of the world’s population. Every role here, regardless of contract type, makes an impact on human life
Novartis partners with external managed service provider Magnit Global to offer engaging temporary contractor opportunities like this, to those who are looking for flexibility in their career while looking to gain new skills and experiences providing services to an inclusive global medicines company.
Ready to work with/through Magnit at Novartis? Please read on...
Novartis Pharmaceutical Development specialty unit (PDU specialty F&PD) is seeking a highly motivated Formulation and Process Development Scientist to join our team. The ideal candidate will be responsible for supporting the development of exciting novel pharmaceutical products such as oligonucleotides modalities (ASOs, siRNA) and radioligand therapies. The candidate will plan, perform and document scientific experiments for the preparation and timely delivery of drug products (DP), processes and procedures in collaboration within a multifunctional project team coordinated by a Project leader. Contribute to maintenance of lab instruments/infrastructure.
Key Responsibilities:
- Plan, organize, perform and document scientific experiments in collaboration with project teams and under minimal guidance from more experienced team members (e.g., contribute to interpretation and report results).
- Provide raw data documentation, evaluation and results interpretation. Propose and provide input for the design of next experiments.
- Communicate and address problems, perform literature searches under moderate guidance from more experienced team members.
- Contribute to the maintenance of lab instruments.
- Ensure all own activities are aligned with overall drug development process.
- Ensure training is up-to-date and on time; no overdue training assignments without acceptable cause.
- Ensure strict adherence to HSE rules and guidelines.
Requirements:
- Bachelor's degree in Chemistry, Pharmaceutical Science, or related field with a minimum of 3 years' experience in a pharmaceutical industry setting.
- Good scientific or technical knowledge in parenteral product development, process development, and formulation development. Experience in NBE, Oligo or RLT development preferable.
- Proficient with laboratory and/or technical tools (e.g., lyophilization, Spray drying, analytical equipment, autoclave, etc.).
- Adequate knowledge of software and computer tools.
- Basic presentation skills and scientific/technical writing skills.
- Good communication skills.
Workload: 100% (40 hours per week)
Role type: Onsite
Estimated start date: 3-Feb-2025
Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us
Commitment to Diversity and Inclusion / EEO: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
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