Drug Substance Manufacturing Scientist III Position Available In Florence, South Carolina

Tallo's Job Summary: The Drug Substance Manufacturing Scientist III position involves developing and leading full-scale validations for small molecule drug substances. Responsibilities include performing verifications, validations, and qualifications using HPLC, GC, spectroscopy, GC/MS, and LC/MS, troubleshooting methods, and reporting data. Essential skills include extensive experience in method development, GMP practices, and HPLC/GC instrumentation. A Doctorate degree in Chemistry or Life Science, 10+ years of GMP laboratory experience, and proficiency with EMPOWER III are required. The role offers 10 PTO days, 6 holidays, and potential for long-term employment.

Company:
Actalent
Salary:
JobFull-timeOnsite

Job Description

Job Title:

Drug Substance Manufacturing Scientist III Job Description As a Drug Substance Manufacturing Scientist III, you will develop and lead full-scale validations for small molecule drug substances. You will perform verifications, validations, and qualifications using HPLC, as well as developmental work using GC, spectroscopy, GC/MS, and LC/MS. Troubleshooting developmental methods and suggesting improvements based on prior experience will also be key aspects of your role. Reporting data in a controlled format for review will be part of your responsibilities. Responsibilities Develop and lead full-scale validations for small molecule drug substances. Perform verifications, validations, and qualifications using HPLC. Conduct developmental work on small molecule drug substances using GC, spectroscopy, GC/MS, and LC/MS. Troubleshoot developmental methods and suggest improvements. Report data in the required controlled format for review. Essential Skills Extensive experience in method development, API, and drug substances. Proficiency in GMP practices and

HPLC, GC

instrumentation. Experience leading full-scale validations for small molecule drug substances. Additional Skills & Qualifications Doctorate degree in Chemistry or Life Science. 10+ years of experience working in a GMP laboratory with the relevant analytical instrumentation. Experience in a Contract Manufacturing Organization (CMO). Proficiency with

EMPOWER III.

Technical writing experience. Work Environment You will work in a lab environment where you will develop methods to be utilized in drug substance manufacturing. The position offers 10 PTO and 6 holidays, with holiday and vacation pay included. You will work with advanced equipment and instruments, with the opportunity for long-term employment as a consultant. You will be a valued member of the extended R D team.

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