Job type full-time
Full job description
Millions! novartis made a decision to pursue early discovery research internally to allow us to quickly translate the most impactful discoveries into therapeutics for millions of patients.
Your key responsibilities:
Your responsibilities include, but are not limited to:
Plan and support development of early and late phase nce development of various dosage forms for both documentation aspects and formulation aspects
To support the data integrity checks and documentation support for phad late phase projects/programs
Maintain thorough knowledge and understanding of all standard operating procedures (sops) pertaining to the review process
Maintain thorough knowledge and understanding of gmp/glp/iso requirements as these pertain to work performed in the laboratory
Plan and support entire drug product development process starting with first pre-formulation studies up to the manufacturing process transfer to production and the provision of the required documentation to allow worldwide registration
Strong scientific background wrt biopharmaceutics and its application in dp development
Provide documentation of raw data, evaluation and contribute to interpretation of resultsProvide input for the selection of next experiments
Communicate and address problems, perform safety and literature searches under guidance from more experienced team members.
Meet quality, quantity and timelines in all assigned projects
Commitment to diversity & inclusion:
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
What you’ll bring to the role:
MPharm with 7 to 10 years of experience or phd in science with focus on pharmaceutical sciences and technology (e.gPharmacy, chemistry) with 4+ years of experience
Experience in the pre-formulation, formulation and process development of various drug product dosage forms
Thorough understanding of all the unit operations and equipment for scale-down model development and process characterization is required
Experience in handling data integrity checks and documentation support during the drug product development
Representation of pharmaceutical development as formulation project leader in global cmc teams, functional representative in cross-functional teams
Evaluation and implementation of new methods and technologies, scientific contributions, supervision of research projects and initiation of new research activities
Demonstrated competency and experience in drug product development within the pharmaceutical industry is required.
Successful work experience in a matrix organization is preferred
Why consider novartis?
799 millionThat’s how many lives our products touched in 2019And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives?
We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environmentWhere you’re given opportunities to explore the power of digital and dataWhere you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges.
Imagine what you could do at novartis!
Commitment to diversity & inclusion:
Novartis embraces diversity, equal opportunity and inclusionWe are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusion workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential.
Novartis is an equal opportunities employer and welcomes applications from all suitably qualified persons.
Global drug development
Technical r & d gdd
Nov hltcr shared services ind
Research & development
Posted 19 days ago