Lead Radiochemist
at GE Healthcare
Oslo, Oslo, Norway -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 28 Aug, 2024 | Not Specified | 29 May, 2024 | N/A | Radiochemistry,Analytical Techniques,Manufacturing Processes,Communication Skills,Automation,Regulatory Requirements,Chemistry,Cmc Development,Radiopharmaceuticals | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
JOB DESCRIPTION SUMMARY
As a Lead Radiochemist in the Pharmaceutical Diagnostics Research and Development, Radiochemistry team you will play a pivotal role to identify and develop novel radiolabelled Molecular Imaging (MI) products within a multidisciplinary Chemistry Manufacturing and Controls (CMC) development team. The role requires the development of MI manufacturing methods suitable for clinical translation and registration/commercialisation. Key business areas are neurology, oncology and cardiology, where GE HealthCare provides MI products across the imaging modalities PET and SPECT.
QUALIFICATIONS/REQUIREMENTS
- PhD/MSc in Radiochemistry or Chemistry or equivalent knowledge or experience.
- Hands-on experience in [18F]fluoride and other radionuclide radiolabelling techniques for small and large molecules using direct or synthon-based methods and strong scientific knowledge of the established chemistries used in diagnostic MI products.
- Experience with academic and/or commercial MI product development/production.
- Strong English communication skills.
Responsibilities:
- Developing radiolabelling methods suitable for reliable supply of radiopharmaceuticals through pre-clinical and clinical translation and ultimately for commercial production.
- Defining and performing radiochemistry laboratory experiments and collaborating remotely with others performing the experimental radiochemistry work.
- Working in multidisciplinary scientific teams and with people from across the different functions of the business.
- Authoring suitable scientific reports & documentation to support regulatory documentation packages (e.g., internal development reports, IND, IMPD, NDA, MAA, research publications, etc.).
- Performing projects and technology transfers with academic partners and external contract R&D organisations.
- Providing radiochemistry development expertise to support products across the wide development stages from early development to life-cycle management.
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
Oslo, Norway