Below is a sample job description for the contract job opportunity at Abbott:
OVERVIEW
- Assist and advise in matters regarding technology transfer of established synthesis process.
- Provide advice to determine cost saving measures.
- Investigate problem areas and areas of desirable improvement.
KEY ACCOUNTABILITIES
- Maintain and support the production schedule.
- Undertake new procedures and observe proper safety precautions.
- Responsible for in-process Quality Control testing of manufacturing material as it relates to qualifications, quality inspections and titration.
- Maintain quality systems and proper Good Manufacturing Practices (GMP) /Good Laboratory Practices (GLP).
- Create and follow protocols designed around product improvement.
QUALIFICATIONS
- Familiar with wet bench skills, using pH meters, titrations.
- Some understanding of analytical theories.
- BS in Chemistry or 2 – 5 years’ lab experience or master’s degree.
- Solid use of instruments including HPLC, GC GC/MS, TLC, IR, UV/vis, NMR and AA.
- Strong clinical research and regulatory knowledge including GCPS, Federal Regulations, Clinical Trial & Drug Development Process, Disease/Treatment Broad therapeutic background.
Associated Job Titles: Associate Scientist, Clinical Scientists I-III, Information Scientist, Scientists I-III, Sr. Data Scientist
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional and branded generic medicines.
Working together, Abbott and Talent Solutions partner to deliver top talent for contingent roles at Abbott, building better and healthier lives. Abbott believes all employees are essential to performing the key duties that create life-changing breakthroughs.
- Published on 14 Dec 2023, 7:43 PM
