Analytical Development Scientist II | GMP & Data Analysis

Cambrex Corp.; Charles City (IA); On-site; USD 70,000 - 95,000; Full time

Job summary

Cambrex Corp. is seeking a Scientist II to provide analytical support for multiple project teams.

You will collect and analyze data to support the development, validation and transfer of analytical methods for APIs, intermediates, and raw materials, while strictly following cGMP guidelines. Responsibilities include performing analytical assays, operating HPLC/GC/LC‑MS/FTIR, maintaining notebooks, and ensuring regulatory compliance.

Qualifications

• M.S. in Chemistry or related field with minimum 2 years of experience or B.S. degree with 6 years in a lab environment, pharmaceutical experience preferred.
• Excellent verbal and written communication skills, organizational skills, and ability to work in a diverse team environment are essential.

Responsibilities

• Safely collect analytical data to develop, establish, and validate testing methodologies for raw materials and products.
• Perform analytical chemistry assays based on established methods.
• Operate analytical instruments such as HPLC, GC, GC/MS, LC/MS, FTIR, Titer, and Particle Size Analyzer.
• Maintain laboratory notebooks documenting work.
• Ensure GMP compliance and regulatory SOP adherence.
• Transfer validated methods to QC and Process Support groups.

Skills

Analytical chemistry

Cross‑discipline knowledge

GMP knowledge

Instrument proficiency

Communication

Problem solving

Time management

Teamwork

Documentation

Collaboration

Operational excellence

Change orientation

Education

M.S. in Chemistry or related field with ≥2 years experience

B.S. in Chemistry or related field with ≥6 years experience

Tools

HPLC

GC

GC/MS

LC/MS

FTIR

Titrator

Particle Size Analyzer

Job description

Cambrex Corp. is seeking a Scientist II to provide analytical support for multiple project teams.

You will collect and analyze data to support the development, validation and transfer of analytical methods for APIs, intermediates, and raw materials, while strictly following cGMP guidelines. Responsibilities include performing analytical assays, operating HPLC/GC/LC‑MS/FTIR, maintaining notebooks, and ensuring regulatory compliance.