What are the responsibilities and job description for the Associate Scientist - CE/HPLC position at Infotree Global Solutions?
Description:
Process Development Associate Scientist ( onsite position Standard 8-5 local hours)
Preferred Qualifications
- • Degree in chemistry, biochemistry, pharmaceutical sciences, or related discipline.
- • Excellent laboratory skills with 2 years of experience in industry laboratories supporting
- analysis and characterization of protein therapies.
- • Advanced technical expertise in analytical methodologies used to characterize protein
- therapeutics including CE-SDS, cIEF / icIEF, HIC, SEC, IEX, RP, HILIC, MS, etc.
- • Experienced using CE and LC operation and data analysis software.
- • Working knowledge of data processing and statistical analysis software tools.
- • Ability to independently prioritize, schedule, and manage multiple tasks in order to meet
- deliverables.
- • Ability to work in a matrix team environment and collaborate effectively.
- • Excellent written and oral communication skills.
- • Experience troubleshooting and maintaining laboratory instruments and training others on
- the use of instruments.
- • Experience with use of electronic notebooks.
- • Hands on experience with method qualifications and transfers.
- • Understanding of phase-appropriate GMP compliance and documentation.
Do you want to make an impact by helping advance promising new medicines in development? We have an exciting career opportunity available in our Pivotal Attribute Sciences team at the Client site in Cambridge, MA. In the role of Associate Scientist, you will be responsible for supporting the development of analytical methods, the characterization of protein-based biologic therapies, and process development activities. At Client , our mission to serve patients drives all that we do. Come join us to work alongside talented scientific colleagues to advance Client innovative pipeline of therapies.
- Work in a cross-functional team environment to advance therapies in late-stage development.
- Analyze late-stage protein-based therapies with advanced analytical techniques such as capillary electrophoresis, liquid chromatography, as well as compendial methods, such as pH, Visual Appearance, turbidity, etc.
- Support the development, optimization, and troubleshooting of analytical methods.
- Other duties include data analysis, preparation of electronic notebook records of experimental data, authorship of technical protocols and reports, presentation of results at team meeting, and support for regulatory filings as needed.
- Expert level experience troubleshooting, and maintaining HPLC/UPLC instruments.
- Expertise in the use of Empower software (e.g., custom field creation, writing instrument methods, etc.)
Basic Qualifications
- Master’s degree and 2 year of scientific / pharmaceutical experience OR
- Bachelor’s degree and 4 years of scientific / pharmaceutical experience
Top 3 Must Have Skill Sets:
- • Degree in chemistry ( Master 2 y, Bachelor 4 y), biochemistry, pharmaceutical sciences, or related discipline.
- • Excellent laboratory skills with 2 years of experience in industry laboratories
- • Analytical chemistry/biochemistry experience
- • Experience working in biopharmaceutical industry
- • GMP experience preferred