Analytical Chemist- Method Development & Validation

In this role you drive the validation, transfer and verification of analytical methods for APIs and finished products within a GMP environment. You apply chromatographic techniques to support drug product testing and collaborate with clients and cross-functional teams. You troubleshoot instruments, mentor junior staff and ensure compliant, high-quality method implementations. This position offers the chance to shape method development within a leading life sciences testing network and contribute to reliable product safety and quality.

• comprehensive medical coverage
• dental and vision options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays

• Perform method validations, transfers and verifications for APIs and finished products
• Apply GMP in all responsibilities and use HPLC, GC, UV/Vis and dissolution methods
• Read, interpret and implement diverse analytical procedures
• Conduct analytical investigations and troubleshoot instrumentation
• Train and mentor junior staff in laboratory procedures
• Manage and discuss projects with clients
• Coordinate with vendors when instrument issues arise
• Support cross-functional teams in delivering validated methods to clients

• BS with 4+ years of industry experience, MS with 2+ years, or PhD with 1+ year
• 3+ years of chromatography experience
• 3+ years of LC chromatographic validation in a GMP environment
• Authorization to work in the U.S. without sponsorship

• Excellent communication (oral and written)
• Attention to detail
• Ability to work independently and in a team
• HPLC
• GC
• UV/Vis