At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.
Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a cooperative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.”
Key Responsibilities
• Work in close partnership with contract research organizations (CROs) for Bio analytical assay development.
• Responsible for TK, PK, ADA & NAB assay development, validation at external contract organizations (CROs) in a regulated (GLP, GCLP) environment to support pre-clinical and clinical studies.
• Lead the evaluation of innate immune responses associated with therapeutic peptides and proteins.
• Lead the assessment of adaptive immune responses associated with therapeutic peptides and proteins
• Serve as the bioanalytical representative at project team meetings and provide scientific and operational oversight of bioanalytical activities conducted at CROs including reagent generation, assay development and validation.
• Work independently and in collaboration with a subject matter expert (SME) representative of the clinical & non-clinical group.
• Identification & screening of CROs for Bioanalytical services.
• Provide guidance to contract organizations (CROs) on assay development, experimental design, troubleshooting and sample analysis.
• Review of method development reports (MDRs), validation reports and bio analytical test procedures (ATPs).
• Responsible for managing the regulatory queries.
• The candidate is expected to draft the technical content for regulatory dossier.