Senior Scientist I - Analytical Method Development

Cambrex; East Rutherford (NJ); On-site; USD 90,000 - 120,000; Full time

Job summary

Cambrex in East Rutherford, NJ is seeking a Sr. Scientist I (ARD) to execute analytical methods for in-process control, release testing and stability monitoring of drug substances and products.

You will organize routine work independently, evaluate data, and apply method development and validation principles under cGMP guidelines. You will interact with clients to discuss data and methods, design experiments, maintain compliant records, write technical documents, and contribute to SOPs.

Qualifications

• Proven ability to develop and qualify analytical methods.
• Experience writing technical documents and SOPs.
• Familiarity with cGMP regulations and quality systems.
• Experience with method validation and data interpretation.
• Ability to work with clients and present data clearly.

Responsibilities

• Execute analytical methods for in-process control, release testing and stability monitoring under cGMP.
• Independently develop and evaluate methodologies and design experiments.
• Participate in experimental design and testing requirements to demonstrate method suitability.
• Maintain compliant records with minimal supervision.
• Write technical documents with assistance.
• Set up instrumentation and troubleshoot laboratory equipment as needed.
• Lead a sample project with assistance and mentor others.
• Ensure compliance with regulatory guidelines and communicate results to clients.

Skills

Analytical method development

Data interpretation

Troubleshooting

Technical writing

Team collaboration

Attention to detail

Education

S./B.A. Chemistry

Tools

Empower

ChemDraw

Microsoft Word

PowerPoint

Excel

Job description

Cambrex in East Rutherford, NJ is seeking a Sr. Scientist I (ARD) to execute analytical methods for in-process control, release testing and stability monitoring of drug substances and products.

You will organize routine work independently, evaluate data, and apply method development and validation principles under cGMP guidelines. You will interact with clients to discuss data and methods, design experiments, maintain compliant records, write technical documents, and contribute to SOPs.