General Electric Lead Scientist, Pharmaceutics in Oslo, Norway
Job Description Summary
You will join the Pharmaceutical Development which is scientifically responsible for defining, developing and delivering formulations and materials for diagnostic imaging products. The Pharmaceutical Development team is part of Pharmaceutical Diagnostics R&D, GE Healthcare. Key business areas are neurology, oncology and cardiology, where GE Healthcare provides contrast agents and molecular imaging products across the imaging modalities MRI, X-Ray, Ultrasound, SPECT and PET. The products span across simple solutions, gas bubbles, cassette-based products and freeze-dried formulations. The drug products are for i.v. injection, so sterility assurance and adequate microbiological controls of all materials is a critical part of the development work.
As a Pharmaceutics Scientist you will be contributing to the design and development of products and their interaction with the human body. You will impact departmental operations and be responsible for planning/execution. You will have some autonomy, but you will be focused on execution of activities within an operating discipline covered by standard functional practices and procedures. Some judgment may be required but this is typically with guidance.
GE Healthcare is a leading global medical technology and digital solutions innovator. Our mission is to improve lives in the moments that matter. Unlock your ambition, turn ideas into world-changing realities, and join an organization where every voice makes a difference, and every difference builds a healthier world.
Your role will be to design and develop formulations and production processes, scalable to pre-clinical and clinical studies, and into commercial manufacturing.
You will develop suitable drug product formulations, processes and materials to correct level of quality, specifications and controls. Your duties will include leading work at external parties as well as practical work.
You will provide drug product formulation expertise to support R&D projects in development & marketed products (i.e. regulatory questions, set up manufacturing).
You will contribute to non-clinical safety and clinical studies, through co-ordination with internal and external partners
You will produce and review suitable scientific reports & documentation to support regulatory documentation packages (IND's, IMPD’s, NDA, MAA, etc).
PhD/MSc in Pharmaceutics, or similar
Ability to design and develop new formulations drawing on multidisciplinary input on physical, chemical, biological, and engineering sciences
Self-motivated and able to work independently and as part of a team
Strong oral and written communication skills
Fluent English verbal and written
Strong scientific capability, clear thinking, ability to identify smart ways of working
Experienced with Good Manufacturing Practice (GMP) requirements
Experience from Pharmaceutical Industry or Regulatory Body
Capability of applying appropriate statistical planning and analysis tools as part of formulation development
Experienced in standard office tools like Word, Excel, PowerPoint etc.
Fluent Norwegian verbal and written
Inclusion and Diversity
GE Healthcare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.
Our total rewards
Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support.
Relocation Assistance Provided: No