- Design, develop, and validate analytical methods using LC-MS and HPLC/UPLC techniques for small molecules and late-stage APIs.
- Lead 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.
- Train and mentor junior analytical chemists, fostering a culture of continuous learning and development
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
- Master's or Ph.D. in Analytical Chemistry, Pharmaceutical Sciences, or related field.
- Minimum 5 years of relevant experience in a pharmaceutical or contract manufacturing organization.
- Strong expertise in LC-MS and HPLC/UPLC techniques, including method development, troubleshooting, and validation.
- Solid understanding of cGMP principles and regulatory guidelines pertaining to analytical chemistry.
- Experience in analytical development and method optimization for small molecules and late-stage API manufacturing.
- Proficient in data analysis software and laboratory information management systems (LIMS).
- Excellent communication skills and ability to collaborate effectively with cross-functional teams. 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
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Analytical Scientist/Chemist - Providence, United States - Michael Page
Description
About Our Client
My client is a leading Contract Manufacturing and Development Organization (CMDO) that provides comprehensive services in laboratory chemistry, manufacturing, and control for small molecules and late-stage Active Pharmaceutical Ingredient (API) manufacturing. With a global presence and a commitment to excellence, they partner with pharmaceutical companies to deliver high-quality products and innovative solutions to patients worldwide.
Job Description
