What are the responsibilities and job description for the Analytical Development Scientist position at EPM Scientific?
Analytical Scientist
Several Positions(up to Sr. Scientist)
Greater Fort Lauderdale Area
Currently partnered with a leading pharmaceutical company dedicated to advancing healthcare through innovative research and development.
This role is responsible for developing, optimizing, and validating analytical methods to support drug development, formulation, and manufacturing processes. The ideal candidate will have a strong background in analytical chemistry, method development, and troubleshooting analytical instrumentation such as HPLC, UPLC, GC, and spectroscopic techniques. We are seeking a highly skilled and motivated Analytical Scientist to join our team and contribute to our mission of improving patient outcomes.
Responsibilities:
- Develop and validate analytical methods for the characterization and quantification of pharmaceutical compounds.
- Conduct routine and non-routine analysis of raw materials, intermediates, and finished products using techniques such as HPLC, GC, LC-MS/MS, and spectroscopy.
- Perform stability testing and support formulation development by providing analytical data.
- Maintain accurate and detailed records of all experiments, results, and procedures in compliance with regulatory requirements.
- Collaborate with cross-functional teams, including R&D, Quality Control, and Regulatory Affairs, to support product development and regulatory submissions.
- Troubleshoot and optimize analytical methods to ensure accuracy, precision, and robustness.
- Prepare technical reports, protocols, and standard operating procedures (SOPs).
- Ensure compliance with Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and other regulatory standards.
Qualifications:
- Bachelors (2-6 years), Master’s (2-5 years), or Ph.D. (0-3years) in Chemistry, Pharmaceutical Sciences, or a related field.
- Proven experience in analytical techniques such as HPLC, GC, LC-MS/MS, and spectroscopy.
- Strong understanding of pharmaceutical development processes and regulatory requirements.
- Excellent problem-solving skills and attention to detail.
- Effective communication skills, both written and verbal.
- Ability to work independently and collaboratively in a fast-paced environment.
- Familiarity with laboratory information management systems (LIMS) is a plus.
Preferred Skills:
- Experience in method development and validation for pharmaceutical applications.
- Knowledge of ICH guidelines and regulatory submission requirements.
- Proficiency in using analytical software and tools.
Benefits:
- Competitive salary and comprehensive benefits package.
- Opportunities for professional growth and development.
- Collaborative and innovative work environment.
Salary : $65,000 - $125,000