Analytical Scientist

Piramal Pharma Limited

$80K — $95K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in chemistry or related field; master's preferred.
  • 2+ years of experience in developing analytical methods.
  • Experience with New Chemical Entities (NCEs) and generic drug products in oral dosage forms.
  • Familiarity with chromatographic and spectroscopic techniques required.
  • Experience in client-facing roles with external partners.

Responsibilities

  • Develop, validate, and transfer analytical methods for new chemical entities and generic products.
  • Implement Quality by Design (QbD) principles in method development.
  • Work with various analytical methods for product testing and validation.
  • Provide insights to product development teams on analytical methodologies.
  • Perform initial and stability testing for R&D and demonstration batches.
  • Review and analyze data for technical correctness and accuracy.

Benefits

  • Access to continuous professional development and training opportunities.
  • Opportunity to work on a diverse portfolio of drug products.
  • Collaborative work environment with product development teams.
  • Engagement with external partners throughout projects.
Full Job Description
Job Title Analytical Scientist Job Description The incumbent for this position will be responsible for the development and validation of analytical methodologies and performance of tasks using chromatographic, spectroscopic, solid-state, and physical/wet-chemical techniques. - Develop, validate, and transfer of analytical methods for a diverse portfolio of New Chemical Entities (NCEs) and generic drug products in solid and liquid oral dosage forms, including tablets, capsules, suspensions, and solutions.- 30% - Implement Quality by Design (QbD) principles to analytical method development to create robust and reliable methods, preparing all necessary scientific documentation-such as comprehensive reports, technical justifications, and detailed rationales-based on the findings of the QbD study - 20% - Work with various analytical methods including cleaning verification, assay and related substances, BCS Solubility study, dissolution, discriminatory dissolution, doss dumping study, multimedia dissolution study, residual solvents in-process control, and analysis of finished products and excipients - 10% - Developing analytical methodologies to complete all related activities and provide insights to product development teams on mitigation strategies - 20% - Perform initial and stability testing for R&D batches and demonstration batches to support formulation development - 10% - Review/analyze data and information for technical correctness and accuracy; interpret and evaluate results properly - 10% QUALIFICATIONS - Bachelor's degree in chemistry, pharmaceutical sciences, or related field required, master's preferred. - 2+ years' experience developing analytical methods for New Chemical Entities (NCEs) and generic drug products in solid and liquid oral dosage forms, such as tablets, capsules, suspensions, and solutions, within a regulated pharmaceutical environment. - Familiarity with chromatographic (HPLC/GC), Dissolutions, spectroscopic, and solid-state characterization techniques preferred. - Experience in a client-facing role, serving as the primary point of contact for external partners on projects.

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