Job Description
- Design, develop, and validate analytical methods using LC-MS and HPLC / UPLC techniques for small molecules and late-stage APIs.
- Analytical development activities, including method optimization, troubleshooting, and validation studies.
- Ensure compliance with cGMP guidelines and regulatory requirements during analytical testing and method development.
- Collaborate with cross-functional teams, including R&D, Manufacturing, and Quality Assurance, to support product development and process improvement initiatives.
- Perform routine analysis and characterization of samples, interpret data, and generate accurate reports.
MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law.
MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.
The Successful Applicant
- with 1+ years, or with 3+ years of experience in Analytical Chemistry, Pharmaceutical Sciences, or related field.
- Strong laboratory background; experience with LC-MS and HPLC / UPLC.
- cGMP as it relates to analytical chemistry.
- Analytical development and method optimization for late-stage API manufacturing preferred.
- Proficient in developing SOPs, protocols and reports.
- Ability to work cross-functionally across teams efficiently.
What's on Offer
- Competitive base salary
- Great benefits package
- On-site at state of the art facility in Providence
- Great growth potential
- Individual contributor with analytical chemistry group
- Be a part of a billion dollar global CDMO
30+ days ago