Analytical Scientist II: Method Development & Validation
Piramal Pharma Ltd
Lexington (KY)
On-site
USD 65,000 - 85,000
Full time
14 days+
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Job summary
A leading pharmaceutical company located in Lexington, KY is seeking an Analytical Scientist II to conduct complex chemical and physical testing on pharmaceutical materials and finished products. The role involves developing and validating test methods, troubleshooting analytical instruments, and preparing regulatory documents. Candidates should have a relevant degree and at least 2 years of experience in the pharmaceutical industry, preferably with cytotoxic materials. This position offers a collaborative work environment with an emphasis on adherence to quality and compliance standards.
Qualifications
Two plus years’ experience in the pharmaceutical industry or similar.
Experience with potent, cytotoxic materials and parenteral drug products preferred.
Responsibilities
Conduct complex chemical and physical testing of pharmaceutical raw materials.
Develop and validate test methods for analysis.
Troubleshoot analytical instrumentation as needed.
Prepare regulatory documents and communicate with clients.
Skills
Proficiency using chemistry and analytical instrumental technologies
Knowledge of quality and regulatory requirements
Good interpersonal and communication skills
Proficiency with HPLC, GC, KF and dissolution techniques
Education
BS, MS or PhD in Chemistry, Biochemistry or Pharmaceutical Science
BS with 2+ years’ Pharmaceutical industry experience
Job description
A leading pharmaceutical company located in Lexington, KY is seeking an Analytical Scientist II to conduct complex chemical and physical testing on pharmaceutical materials and finished products. The role involves developing and validating test methods, troubleshooting analytical instruments, and preparing regulatory documents. Candidates should have a relevant degree and at least 2 years of experience in the pharmaceutical industry, preferably with cytotoxic materials. This position offers a collaborative work environment with an emphasis on adherence to quality and compliance standards.