Senior Scientist – Analytical Development & GMP Expert

Actalent; Iowa (LA); On-site; USD 95,000 - 130,000; Full time

Job summary

Actalent is seeking a Senior Scientist to lead analytical development for APIs, raw materials, and finished products within a GMP-regulated environment. You will validate methods, interpret complex data, and work with cross-functional teams to ensure compliance and quality.

The role emphasizes method development, validation, and technology transfer, with opportunities for growth toward Principal Scientist. Strong expertise in HPLC, GC, MS, and related QA documentation is essential.

Qualifications

• Proven experience in analytical method development and validation for APIs, raw materials, and finished products.
• Hands-on expertise with HPLC, GC, GC/MS, FTIR, and mass spectrometry in a lab setting.
• Strong understanding of GMP regulations and DEA guidelines in a lab environment.
• Experience with document control and data integrity within GMP.
• Ability to lead investigations and manage timelines for major projects.

Responsibilities

• Develop, validate, and implement analytical methods for materials and products.
• Perform analytical testing using HPLC, GC, GC/MS, FTIR, MS.
• Coordinate cross-functional teams to troubleshoot issues and transfer methods to QA/Process Support.
• Draft and review technical documents, reports, and SOPs with high accuracy.
• Lead investigations related to deviations or out-of-spec results and maintain timelines.

Skills

Analytical method development

HPLC

GC

Mass spectrometry

GMP compliance

DEA guidelines

Documentation & data integrity

Cross-functional collaboration

Education

PhD in Chemistry

MS in Chemistry

BS in Chemistry

Tools

HPLC

GC

GC/MS

FTIR

Job description

Actalent is seeking a Senior Scientist to lead analytical development for APIs, raw materials, and finished products within a GMP-regulated environment. You will validate methods, interpret complex data, and work with cross-functional teams to ensure compliance and quality.

The role emphasizes method development, validation, and technology transfer, with opportunities for growth toward Principal Scientist. Strong expertise in HPLC, GC, MS, and related QA documentation is essential.