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Scientist - Parenteral formulation and Process Development
View: 97
Update day: 12-04-2024
Location: Basel Basel-Stadt BS
Category: R & D IT - Software
Industry: Pharmaceutical Manufacturing
Position: Mid-Senior level
Job type: Contract
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Job content
This is a temporary contractor opportunity at NovartisNovartis 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. Click here to learn more about Magnit www.magnitglobal.com
Ready to work with/through Magnit at Novartis? Please read on...
This role will have the opportunity to work in cutting edge parenteral formulations and innovation projects to support the development of patient centric drugs, bring transformational medicines to the market as well as an opportunity to work in exciting novel pharmaceutical products such has new modalities and radioligand therapies.
Responsible for the design, plan, perform, interpret and report results of formulation and process development for liquid and lyophilized parenteral drug products of small molecules, biologics (e.g. oligonucleotides) and long acting injectable within a multifunctional project team coordinated by a Project Leader.
Lead and manage all project activities, support team members, participate in sub-teams and contribute to overall TRD strategies and goals.
Major Accountabilities:
- Independently plan, organize, perform and document scientific experiments under minimal supervision.
- Documentation of raw data, evaluate and interpret results; propose and actively support the design of next experiments; supervise project related activities.
- Oversees and write protocols, scientific reports or process (e.g. development reports, support for preparation of regulatory documents).
- Guide and develop new methods or optimize existing methods/processes and contribute to development and implementation of new technologies.
- Communicate, address and solve problems within own and broader area of responsibility; communicate effectively across organizational interfaces; lead the transfer of know how to other departments or external contractors, including troubleshooting and on-site training.
- Participate in function-specific sub teams and fulfill assigned project tasks and responsibilities.
- Ph.D. or Master in pharmaceutical sciences, chemistry, biochemistry, or related fields with parenteral dosage forms industry experience (3-5 years).
- Experience with biologics formulation development, GxP work environment and data and digital knowledge desirable.
- Very good communication skills with, excellent command of English both written and spoken.
- Excellent scientific writing and presentation skills.
- Capability to work independently and in a team environment.
Pay Rate: 34-53 CHF / hour
Contract: 12 months
Start date: November, 2023
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! Learn more here: https://www.novartis.com/about/strategy/people-and-culture
Join our Novartis Network: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
Accommodation: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 directsourceproteam@prounlimited.com or 1.862.778.5441
Commitment to Diversity and Inclusion / EEO
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Deadline: 27-05-2024
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