Analytical Scientist — Method Development & Validation

Piramal Pharma Limited; Sellersville (Bucks County); On-site; USD 70,000 - 95,000; Full time

Job summary

Piramal Pharma Solutions is seeking an Analytical Scientist to develop and validate analytical methodologies using chromatographic, spectroscopic, solid-state, and wet-chemical techniques. The incumbent will support a diverse portfolio across solid and liquid oral dosage forms.

Responsibilities include method development and transfer, QbD implementation, and documentation. The role requires 2+ years of experience and a relevant bachelor's degree, with opportunities to contribute to product

Qualifications

• Bachelor's degree in chemistry, pharmaceutical sciences, or related field; master's preferred.
• 2+ years’ experience developing analytical methods for NCEs and generic drugs in solid and liquid dosage forms.
• Familiarity with chromatographic (HPLC/GC), dissolution, spectroscopic, and solid-state characterization techniques preferred.
• Experience in a client-facing role as the primary contact for external partners on projects.

Responsibilities

• Develop, validate, and transfer analytical methods for NCEs and generics in solid and liquid oral dosage forms.
• Implement QbD principles to analytical method development and prepare necessary documentation.
• Work with methods including dissolution, residual solvents, and finished product analysis.
• Develop methodologies to provide insights to product development teams on mitigation strategies.
• Perform initial and stability testing for R&D batches and demonstration batches.
• Review data and interpret results for technical accuracy.

Skills

Analytical methods

HPLC/GC

QbD

Method transfer

Education

Bachelor's in Chemistry/Pharma

Master's preferred

Tools

HPLC

GC

Dissolutions

Spectroscopy

Solid-state analysis

Job description

Piramal Pharma Solutions is seeking an Analytical Scientist to develop and validate analytical methodologies using chromatographic, spectroscopic, solid-state, and wet-chemical techniques. The incumbent will support a diverse portfolio across solid and liquid oral dosage forms.

Responsibilities include method development and transfer, QbD implementation, and documentation. The role requires 2+ years of experience and a relevant bachelor's degree, with opportunities to contribute to product