Scientist

Insight Global; Birmingham (AL); On-site; USD 75,000 - 95,000; Full time

Benefits offered by this job

Healthcare insurance

Bonus opportunities

Paid leave

Job summary

Insight Global is seeking an Analytical Development Scientist in the Birmingham, AL area to perform laboratory testing on raw materials, in-process samples, and finished products within a cGMP environment. The role supports stability studies and validation activities for drug product development with emphasis on regulatory compliance and data integrity.

The position offers bonus opportunities, healthcare insurance, and paid leave, with compensation ranging from $75,000 to $95,000 annually

Qualifications

• BS or MS in chemistry, organic chemistry, or biochemistry.
• 2-3 years of relevant analytical laboratory experience.
• Ability to detect issues beyond routine analysis in methods or instrumentation.
• Basic knowledge of USP/NF, Product Stability requirements, and Process and Method validation.
• Ability to integrate into team-based projects.
• Experience with laboratory instrumentation (HPLC, Dissolution Bath, GC, Karl Fischer, UV/Vis, FT-IR).

Responsibilities

• Perform routine analytical testing, method validation, and process validation per SOPs, cGMP, GLP, GDP, and regulatory guidelines.
• Follow applicable compendial and regulatory standards for analytical procedures, method development, validation, and transfer.
• Troubleshoot laboratory methods and instrumentation, including HPLC and UPLC systems.
• Utilize Empower 3 software to analyze, interpret, and report analytical data.
• Complete assigned work efficiently while maintaining safety, quality, and timelines.

Skills

Analytical testing

Method validation

Data interpretation

Regulatory knowledge

Team collaboration

Education

BS or MS in chemistry, organic chemistry, or biochemistry

Tools

HPLC

UPLC

GC

Karl Fischer titrator

UV/Vis

FT-IR Spectrometer

Job description

The Analytical Development Scientist is responsible for performing laboratory testing on raw materials, in-process samples, and finished products, as well as supporting stability studies and validation activities for drug product development. This role operates in a cGMP environment and requires a strong understanding of pharmaceutical regulations and analytical best practices.

Key Responsibilities

• Perform routine analytical testing, method validation, and process validation in accordance with SOPs, cGMP, GLP, GDP, and regulatory guidelines (FDA, DEA, OSHA)
• Follow applicable compendial and regulatory standards for analytical procedures, method development, validation, and transfer
• Troubleshoot laboratory methods and instrumentation, including HPLC and UPLC systems
• Utilize Empower 3 software to analyze, interpret, and report analytical data
• Complete assigned work efficiently while maintaining a strong focus on safety, quality, and timelines

Requirements

• BS or MS in chemistry, organic chemistry, or biochemistry
• Minimum of 2 - 3 years relevant experience in an analytical laboratory
• Ability to think beyond routine analysis of samples to detect issues with the method, product, or instrumentation
• Basic knowledge of USP/NF, Product Stability requirements, and Process and Method validation.
• Ability to integrate into team-based projects
• Experience with laboratory instrumentation such as HPLC, Dissolution Bath, GC, Karl Fischer titrator, UV/Vis, and FT-IR Spectrometer.
• Strong interpersonal communication and writing skills
• Competency in Microsoft Office Suite

Compensation: Ranges from $75,000 - $95,000 a year annual salary. Bonus opportunities are available. Exact compensation may vary based on several factors, including skills, experience, and education. Benefit packages for this role include: Benefit packages for this role may include healthcare insurance offerings and paid leave as provided by applicable law.