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Sr. Team Leader - Formulation Development

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Onsite

Sr. Team Leader - Formulation Development

Strides Pharma Science

Sr. Team Leader - Formulation Development

Skills

Risk Management

2 months ago

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Important information


Contract type:

Permanent

Location:

Bengaluru, Karnataka, India

Work mode:

Onsite

Published on:

20 August 2026

What they need


  • Expertise in development of Nasal drug device combination products with different dosage forms like solutions, suspensions etc.,
  • Have good scientific knowledge on Devices requirements and device documentation like design verification, risk management etc. in case of Nasal product.
  • Good knowledge on pump performance parameters for device sameness
  • IVBE correlation for PBE establishment through statistical methods.
  • Expertise in complete development activities of different Topical dosage forms like solutions, cream, lotion, gel, ointment
  • Scientific knowledge and Hands on experience in Q3 parameters characterization like PSD, GSD, Rheology, Viscosity etc., and correlation to product development.
  • Hands on experience in IVRT studies and good understanding on IVPT studies and requirements.
  • Good knowledge on development of transdermal patches and oral films (Sublingual/Buccal)
  • Knowledge on adhesives selection and optimization to match adhesive properties and wearability profiles.
  • Knowledge on IVPT studies and performance evaluation parameters.
  • Responsible for Planning and execution of projects in coordination with CRO as per the committed timelines.
  • Co-ordinate with CRO & project management team to ensure adherence to project timelines.
  • Project execution strategy finalization in coordination with CRO & manager and various cross functional leads to meet the dossier filing timelines.
  • Coordinate with technology transfer / manufacturing department for smooth transfer of new products from CRO to scale-up, exhibit batch and commercialization.
  • Responsible for coordinating with CRO for preparation and review of PDP and PDR and other relevant documents.
  • Responsible for timely availability of documents to support the dossier compilation and regulatory filing.
  • Responsible for addressing regulatory deficiencies in coordination with cross functional teams and CRO

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