Praneeth Patlola
This listing was posted on Willhire.
Senior Expert - Parenteral formulation and Process Development Scientist
Location:
Basel
Description:
<p><strong>This is a temporary contractor opportunity at Novartis</strong></p><p>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!</p><p>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. Click here to learn more about Magnit www.magnitglobal.com</p><p>Ready to work with/through Magnit at Novartis? Please read on...<br /><br /><strong>Assignment:</strong></p><ul><li>Lead and drive formulation development and manufacturing activities for assigned projects, ensuring scientific and technological excellence focus on parenteral drug products.</li><li>Collaborate closely with cross-functional teams to align formulation project plans with control strategies, project timelines, and overall development strategies.</li><li>Communicate and exchange knowledge with Biopharmaceutics Experts and internal subject matter experts to incorporate critical factors for absorption and DP-performance into formulation development strategy.</li><li>Generate accurate and comprehensive scientific documentation, including development reports and manufacturing instructions, to support development trials, process transfers, and supply activities</li><li>Ensure compliance with regulatory requirements and support inspections by contributing to filing dossiers, addressing DP-related questions, and representing project/product-related aspects during internal and health authority inspections.</li></ul><p><strong>Background:</strong></p><ul><li>Minimum: Advanced degree in scientific or relevant discipline (Masters or equivalent) .Desirable: Ph.D. in scientific or relevant discipline or equivalent.</li><li>Previous experience (minimum 3 years) in the development of sterile <strong>pharmaceutical formulations</strong>.</li><li>Strong knowledge of relevant GxP regulations and policies related with aseptic/sterile manufacturing.</li></ul><p><strong>Why Novartis: </strong>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! Learn more here: https://www.novartis.com/about/strategy/people-and-culture</p><p><strong>Commitment to Diversity and Inclusion / EEO:</strong> Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.</p><p><strong>Join our Novartis Network:</strong><strong> </strong>If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network</p><p><strong>Accommodation: </strong>If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to Magnit at XXXX@prounlimited.com</p>
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