Work effectively within cross-functional project teams, including Analytical Development, Quality
Develop, optimize, and author analytical test methods for raw materials, in-process controls
Perform analytical method validations and standard qualification studies, and prepare supporting
Provide analytical support for process development activities, including sample analysis and peer
Conduct scientific investigations and analytical testing to support process development
Author method development reports, stability protocols, and stability reports.

🎯 Requirements

B.Sc. in a related field with a minimum of 5 years relevant experience in pharmaceutical analysis
Excellent skills technical writing and GMP documentation skills.
Excellent problem-solving, planning and organizational skilled coupled with a strong attention to

🎁 Benefits

Excellent full-time benefits including health & dental coverage, life and disability insurance

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